JP2003102673A - Endoscope - Google Patents

Endoscope

Info

Publication number
JP2003102673A
JP2003102673A JP2002251718A JP2002251718A JP2003102673A JP 2003102673 A JP2003102673 A JP 2003102673A JP 2002251718 A JP2002251718 A JP 2002251718A JP 2002251718 A JP2002251718 A JP 2002251718A JP 2003102673 A JP2003102673 A JP 2003102673A
Authority
JP
Japan
Prior art keywords
endoscope
tip
treatment tool
treatment instrument
raising
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2002251718A
Other languages
Japanese (ja)
Other versions
JP3725849B2 (en
Inventor
Hidenobu Kimura
英伸 木村
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Olympus Corp
Original Assignee
Olympus Optical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Olympus Optical Co Ltd filed Critical Olympus Optical Co Ltd
Priority to JP2002251718A priority Critical patent/JP3725849B2/en
Publication of JP2003102673A publication Critical patent/JP2003102673A/en
Application granted granted Critical
Publication of JP3725849B2 publication Critical patent/JP3725849B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00064Constructional details of the endoscope body
    • A61B1/00071Insertion part of the endoscope body
    • A61B1/0008Insertion part of the endoscope body characterised by distal tip features
    • A61B1/00098Deflecting means for inserted tools

Abstract

PROBLEM TO BE SOLVED: To provide an endoscope by which a treating tool having the endoscope put there-through is guided surely to a desired site. SOLUTION: At a position on a side where an observation optical system is arranged on the guiding surface 29 of a treating tool standing up table 27 arranged within a housing 25 opening at the tip of an insertion part where the observation optical system of the endoscope 1, a projection part 45 projecting is formed at the edge of the guiding surface 29 to guide the treatment tool standing up deviated to the side of the observation optical system to the guiding surface 29 of the standing-up table.

Description

【発明の詳細な説明】 【0001】 【発明の属する技術分野】本発明は、挿入部の先端部に
形成したチャンネルの先端開口部に処置具の導出方向を
規制する起上台を設けた内視鏡に関する。 【0002】 【従来の技術】挿入部の先端部にチャンネルの先端を開
口し、この開口部に起上台を設け、この起上台により処
置具の導出方向を規制するようにした内視鏡が知られて
いる(特開平8−154890号公報)。 【0003】 【発明が解決しようとする課題】この特開平8−154
890号公報の内視鏡は、チャンネルに挿通した処置具
を内視鏡の挿入部先端から突き出した際、処置具が、処
置具起上台の側面に接する先端構成部の壁と、処置具起
上台の側面に挟まれるように保持され易く、処置具起上
台の誘導溝に沿うことなく起上操作されることがある。
そして、処置具がある角度まで起上された時点で、誘導
溝に落ち込む、いわゆる処置具の飛びが発生する。この
ような現象が起こることがある。この場合、内視鏡検査
中に目的部位への処置具の誘導が難しくなり、検査に支
障をきたす。 【0004】本発明は上記事情に着目してなされたもの
で、その目的とするところは、内視鏡に挿通した処置具
を、挿入部先端から目的部位に向けて確実に誘導できる
ようにした内視鏡を提供する事にある。 【0005】 【課題を解決するための手段】本発明は、内視鏡の観察
光学系が配された挿入部先端部分に開口して形成された
処置具起上台用収容室と、上記内視鏡の操作部側に設け
られ、処置具が挿通される挿通口と、上記内視鏡内部に
形成され、上記収容室と上記挿通口とを連通する処置具
用案内路と、上記収容室に起上操作可能に設けられ、処
置具を誘導する誘導面を有した処置具起上台と、上記処
置具起上台の誘導面の上記観察光学系が配される側に位
置する稜部に突き出して形成され、上記処置具を上記誘
導面に誘導するための突出部と、を具備した事を特徴と
する内視鏡である。 【0006】 【発明の実施形態】図1乃至図18を用いて、本発明の
一実施形態について説明する。 【0007】(構成)図1は本発明の第1の実施形態に
係る内視鏡1と各種の外部装置を組み込んだシステムの
全体を示す斜視図である。外部装置としては、光源装置
2、画像処理装置3、モニタ4、入力用キーボード5、
吸引ポンプ装置6、吸引瓶7等の機器があり、これらの
機器はキャリア8付きの棚9に設置されている。 【0008】内視鏡1は挿入部12、操作部13および
ユニバーサルコード14を備える。挿入部12は可撓管
部15、湾曲部16および先端部17の各構成部分より
なる。 【0009】操作部13にはユニバーサルコード14の
一端が接続され、ユニバーサルコード14の他端にはコ
ネクタ18が設けられている。コネクタ18は上記外部
装置の一つである光源装置2に接続される。コネクタ1
8にはライトガイド管や電気接点部が設けられている。 【0010】先端部17の構成について、図2乃至図1
2を用いて詳細に説明する。先端部17は先端部本体と
しての先端硬質部21と、これの周囲を覆うように樹脂
等の非導電性材質より形成された先端カバー22とが設
けられ、先端カバー22は先端硬質部21に接着等にて
固定されている。 【0011】先端硬質部21には処置具挿通用案内路と
してのチャンネル(挿通孔)23と連続して形成され、
処置具等の導入を先端側へ案内する導入案内路24が形
成されている。この導入案内路24の先端側には先端硬
質部21と先端カバー22とにて形成される空間部であ
る収容室25が設けられている。この収容室25は処置
具挿通用チャンネル23の先端開口部を構成する。 【0012】また、収容室25内には上記チャンネル2
3を通じて導入される鉗子やカテーテル等の処置具26
を所望の位置へ起上させるための処置具起上台27が納
められている。 【0013】処置具起上台27はその一端が先端硬質部
21に設けられた起上台回動支点28により枢着されて
いる。起上台回動支点28は、導入案内路24の先端開
口部分の下側部位に位置しており、収容室25内におい
て処置具起上台27の他端側部分が回動するように処置
具起上台27を起伏動作自在に取り付けている。処置具
起上台27には上記導入案内路24より連続するように
形成した断面略V字状の溝によって、処置具26を誘導
するための誘導面29が形成されている。 【0014】処置具起上台27の、誘導面29が形成さ
れていない側の一面である起上台裏面31において回動
先端の近くで、処置具起上台26の左右側端近傍にはそ
れぞれ起上台裏面31に対して垂直に突出して形成され
ている左右一対のワイヤ支持壁33が設けられている。
この左右一対のワイヤ支持壁33には処置具起上台27
を起上させるための起上ワイヤー34の先端部が貫通し
て回動自在に連接されている。左右一対のワイヤ支持壁
33の間に位置する起上ワイヤー34の部分には脱落防
止用のパイプ35が外装されている。このパイプ35は
起上ワイヤー34に固着されている。 【0015】起上ワイヤー34は挿入部12内に挿通さ
れるガイドパイプ36を通じて操作部13に導かれ、後
述する起上操作機構に接続される。 【0016】また、先端カバー22には起上台裏面31
と相対する位置において、起上台回動支点28の位置に
向かう滑らかな斜面として形成されるスロープ部41が
形成されている。このスロープ部41には図6(a)お
よび図6(b)で示すように、洗滌用のブラシ等を起上
台裏面31へ誘導するための溝部であるブラシ誘導面4
2を形成するようにしても良い。図6(a)はスロープ
部41の斜視図、図6(b)はそのスロープ部41の図
6(a)に示すX面に沿った横断面図である。 【0017】処置具起上台27の起上台裏面31は、図
2で示す如く、処置具起上台27を最大に起上させた際
において、上記ワイヤ支持壁33の部分を除き、挿入部
12の先端部17の長手方向に対する角度θが、約90
度、(または80度〜100度の範囲)に形成されてい
る。 【0018】また、ワイヤ支持壁33の下端は、処置具
起上台27を最大に起上させた際において、先端カバー
22の開口部端より上部に偏位するように形成されてい
る(図2中の距離Cにて指示)。 【0019】収容室25において、処置具起上台27を
最大に起上させた際の起上台裏面31から、この起上台
裏面31と対向する先端カバー22の面までの距離Aは
収容室25の上部開口端で最大となるように形成されて
いる(図2を参照)。つまり、収容室25にて構成され
る空間にあって処置具起上台27の裏面と垂直な断面で
の断面積が開口端にて最大となる様に構成される。 【0020】また、図10の点線で示すように、処置具
起上台27を寝かせた状態において、収容室25の一面
であり、起上台裏面31と対向する面は、起上台回動支
点28の部位に向かい傾斜する斜面として形成される上
記スロープ部41である。 【0021】処置具起上台27を最大起上させた際にお
いて、起上台裏面31と対向する収容室25の面は挿入
部12の先端部17の長手方向に対して約90度に形成
されるが、この面と、処置具起上台27を寝かせた状態
にした際において、起上台裏面31と対向する面とは曲
面44にて連接される。また、収容室25を形成する各
壁面は互いに接するすべての接線部において曲面を構成
するように形成される。 【0022】また、処置具起上台27を最大起上させた
際において、処置具起上台27の裏面と、上記裏面が対
向する収容室25の面までの距離が処置具起上台27の
回動支点に向かって短く狭くなるように形成されてい
る。 【0023】図3で処置具起上台27の横断面形状(図
2中のB−B断面)を示すが、処置具起上台27の誘導
面29が形成される面側であって、後述する観察光学系
の対物レンズ及び照明レンズが配される側方の部位に
は、薄肉のヘラ状の形態である突出部45が誘導面29
を形成する斜面の稜部よりも突き出して延出形成されて
いる。この突出部45の内側面は処置具起上台27の中
心側に傾斜し、上記誘導面29に連続する斜面である突
出部誘導面46を形成している。突出部誘導面46の勾
配は上記誘導面29の勾配よりも大きく急に形成されて
いる。 【0024】尚、この突出部誘導面46としては斜面で
はなく、凸状または凹状の曲面によって形成されるもの
であっても良い。 【0025】図2に示すように、突出部45の稜線は処
置具起上台27が最大に起上した時の状態で、先端部1
7の各構成部分と干渉しないような形状に形成されてい
る。また、図10で示すように、突出部45の頂部48
は処置具起上台27の起上動作を行う際の軌跡が太破線
のようになる。頂部48の軌跡が先端カバー22の稜線
部49より起上台回動支点28寄り内側に来るように形
成されている。 【0026】一方、図7で示すように、内視鏡1の先端
部17において、先端硬質部21には収容室25の片
側、ここでは右側に位置して照明レンズ51と対物レン
ズ52が先端部17の長手方向の前後に一列に位置して
配設され、側視タイプの内視鏡1を構成している。 【0027】体腔内に照明光を拡開照射する照明レンズ
51にはライトガイド(ファイバーバンドル)53が接
続され、対物レンズ52にはプリズム54や結像レンズ
55を介して撮像部56が接続されている。これらはい
ずれも先端硬質部21に取り付けられている。撮像部5
6は図示しないCCD等の撮像素子や付属回路素子が組
み込まれている。 【0028】図7、図8、図9、図11および図12で
示す如く、先端硬質部21にはライトガイド53を配置
する収納溝57がその先端硬質部21の長手方向に沿っ
て細長く形成されている。そして、ライトガイド53を
納めた後に収納溝57内にはRTVゴム等の充填剤58
が充填され、この後に収納溝57の開口部分がLGカバ
ー59で覆われる。 【0029】また、図12に示すように、先端硬質部2
1の湾曲部16が接続される端側で、湾曲部16の外皮
部材61の端部が配される位置には薄肉のリング状部材
であるリング部材62が接着等にて固定されている。全
周においてそのリング部材62の一端には先端カバー2
2の端部が被嵌されており、当該外嵌される部分は接着
剤等が液密的に配されている。 【0030】なお、このリング部材62としては図7で
示すように、先端カバー22の後端を全周において延接
して形成した延接部63として構成するものであっても
良い。 【0031】外皮部材61はその内周面がリング部材6
2(または延接部63)の外周に密着するように配され
ており、その部位において外皮部材61の外周には糸状
部材64が巻回され、糸状部材64の外周には接着剤6
5を塗布した後に、包皮部材66が加熱溶融されて配さ
れている。 【0032】ここにおいて、上記外皮部材61の内径
を、上記リング部材62(または延接部63)の外径の
90%以下となるように形成されている。後述する図1
3の構成においても同様であるが、外皮部材61の両端
部で先端硬質部21及び後述する可撓管口金85に取り
付くべき範囲の内径は先端硬質部21及び可撓管口金8
5の外径の90%以下となるように形成される。また、
外皮部材61の湾曲部16を外層する範囲の内径はブレ
ード67の外径の90〜110%となるように形成され
ている。 【0033】ここで、外皮部材61は先端硬質部21に
取り付くべき範囲の内径を小さくし、これ以外は同一の
内径にて形成されていても良い。その際において、後述
する可撓管口金85の外径は、(可撓管口金85の外
径)×0.9≧ (外皮部材61の内径)の式が成り立
つように形成されている。 【0034】ところで、上記ライトガイド53は、挿入
部12、操作部13およびユニバーサルコード14内を
通じてコネクタ18まで導かれる。撮像部56に接続さ
れる図示しない電気配線も挿入部12、操作部13およ
びユニバーサルコード14内を通じてコネクタ18まで
導かれる。電気配線はコネクタ18の電気接点部に接続
した接続ケーブル19を介して画像処理装置3に接続さ
れる。そして、撮像部56で得た撮像信号を画像処理装
置3にて映像信号に変換し、モニタ4に表示するように
なっている。 【0035】一方、図1で示す如く、内視鏡1の操作部
13には上記挿入部12の湾曲部16を上下/左右方向
に湾曲させるための湾曲操作部71、対物レンズ52の
外表面に水や空気等の流体を噴き付けてそのレンズ面の
清掃を行うノズル72に選択的に気体と液体を噴出させ
るための送気送水ボタン73、先端部17に先端が開口
したチャンネル23を通じて選択的に体腔内の粘液等を
回収するための吸引操作ボタン74、上記チャンネル2
3に通じる挿入口部75が配設されている。尚、上記チ
ャンネル23の先端開口部は処置具起上台27を配置す
る収容室25を兼ねる。 【0036】内視鏡1の内部にはノズル72に流体を供
給する流体管路76及び回収した流体が通る吸引管路
(上記チャンネル23がこれを兼ねる。)が配設されて
いる。 【0037】挿入部12の湾曲部16は、例えば図13
で示すようにも構成される。すなわち一列に配置した複
数の湾曲コマ81がリベット82を用いて回動自在に組
み合わされて芯材83を構成しており、この芯材83の
外周には金属又は化学繊維のワイヤを編組して筒状に形
成された上記ブレード67が外装され、そのブレード6
7の両端部は湾曲部16の両最端部に配設される湾曲コ
マ81に接着または半田等にて固定されている。ブレー
ド67にはチューブ体よりなる上記外皮部材61が外装
されている。湾曲部16を構成する最先端の湾曲コマ8
1には先端部17を構成する金属又は硬質の樹脂よりな
る先端硬質部21が接続される。また、先端硬質部21
には絶縁性を有する材料にて形成されたキャップ状の部
材である先端カバー22が接着等にて一体的に固着され
る。 【0038】また、挿入部12の可撓管部15は帯状の
金属を螺旋状にて形成された図示されない螺旋管、金属
線又は化学繊維を筒状に編組形成した図示されないブレ
ード、樹脂よりなる図示されない外皮を積層して構成さ
れている。 【0039】可撓管部15の先端には金属等よりなる可
撓管口金85が接着または半田等にて固定されており、
この可撓管口金85を介して湾曲部16を構成する手元
側端の湾曲コマ81が接続固定されている。図14で示
すように、可撓管口金85の一端と、可撓管部15の最
外層を構成する外皮層との隙間には接着剤等よりなる充
填剤84が全周にわたり隙間なく液密的に配されてい
る。 【0040】また、例えば、外皮部材61の先端は、先
端硬質部21の外周に密着するように外装され、その先
端部は先端カバー22の後端部に当接されるように配さ
れている。そして、図14で示すように、先端硬質部2
1を外装している外皮部材61の先端部分には絹または
化学繊維等よりなる糸状部材86が巻回されている。外
皮部材61の後端部分は可撓管口金85の外周に密着す
るように外装され、その後端部分は可撓管部15の外皮
層の先端部分に当接されるように配されている。可撓管
口金85を外装している外皮部材61の後端部には絹ま
たは化学繊維等よりなる糸状部材86が巻回されてい
る。 【0041】そして、外皮部材61の端部に巻回されて
いる糸状部材86はその引張力が2N以上にて外皮部材
61を外部より縛るように巻回して締め付ける。また、
糸状部材86の巻き数は4巻き以上とする。さらに、糸
状部材86にはその全域にわたり接着剤87を塗布す
る。接着剤87を塗布した後、糸状部材86の外周には
ウレタン等の熱可塑性樹脂よりなる包皮部材88を配す
る。 【0042】ここで、接着剤87はその粘度が8.5P
s・s以下である。包皮部材88はその融点が外皮部材
61の樹脂の融点よりも低い樹脂材にて形成されてい
る。また、糸状部材86及び包皮部材88のうち少なく
とも包皮部材88は可撓管部15の外観色と類似の色よ
りなる。包皮部材88は外観色に類似のものにとどまら
ず、黒色でも良い。接着剤87についても可撓管部15
の外観色に類似または黒色である。包皮部材88はリン
グ状の形態にて形成されていても良いし、帯状のシート
状に形成されていても良い。 【0043】上記包皮部材88は接着剤87の外周に取
り付ける際して、図示されない熱収縮チューブ材にてそ
の外周が全て覆われ、図示されない加熱機器等により熱
収縮チューブを加熱収縮すると同時に溶融し、組み付け
られる。 【0044】包皮部材88が帯状のシート状にて形成さ
れている場合、接着剤87の外周に包皮部材88を巻き
付け、包皮部材88が重なる部位を半田こて等の加熱機
器等にて加熱する事で、本部位にリング状に配するよう
にする。 【0045】また、図16で示すように、包皮部材88
は糸状部材86に接する層に黒色包皮部材89、外部に
露呈される層に無色(半透明)である透明包皮部材90
の2層により構成しても良い。 【0046】図17および図18で示すように、内視鏡
1の操作部13には上記処置具起上台27を操作する起
上ワイヤー34を操作するための起上台作動機構91が
内蔵されている。 【0047】すなわち、操作部13の内部において、そ
の起上ワイヤー34の基端には金属等の硬質の棒状材質
よりなるワイヤ固定部材92が半田等にて一体的に固着
されている。ワイヤ固定部材92の基端部分には凹部よ
りなる係止溝93が形成されている。このワイヤ固定部
材92の基端部分には係止溝93が形成された範囲をす
べて嵌挿できる金属等の硬質のブロック体よりなる、リ
ンク部材94が挿入してあり、係止溝93にはリンク部
材94に設けられた雌ネジ95に螺合された固定ネジ9
6の先端部が挿入係止している。これにより、ワイヤ固
定部材92はリンク部材94に連結される。 【0048】リンク部材94は操作部13の基盤となる
ベース97の長手方向に進退自在に配されている。リン
ク部材94には、上記湾曲操作部71に隣接して設けた
起上操作ノブ98に連接されたアーム99が連結されて
いる。アーム99はリンク部材94に棒状の軸部材であ
るリンク軸100により回動自在に連接されている。リ
ンク軸100の、ベース97に対向しない側の一端に
は、C型またはE型とめ輪等よりなる係止部材101が
係合してある。図示されるように係止部材101が、湾
曲操作部カバー103の端部よりも把持部カバー104
側に位置するようにアーム99の長さ等が設定されてい
る。 【0049】(作用・効果)処置具起上台27を起上す
る場合、操作部13の起上操作ノブ98を回動操作す
る。起上操作ノブ98が回動することにより、起上ワイ
ヤー34が進退し、これに応じて処置具起上台27は起
上台回動支点28を支点として回動し、起伏動作を行
う。 【0050】図2で示した如く、処置具起上台27が最
大に起上した時、起上台裏面31と、これに対向する先
端カバー22の一面により形成される、収容室25の空
間は開口端部にて最も大きく開口し、また、起上台裏面
31の面が先端部17の長手方向に対し、略垂直に位置
する。このため、図4に示すように、先端部17の鉛直
上方より収容室25内の全域を眼で容易に捉える事がで
きる。また、収容室25はその開口部端が最も大きく開
口するため、その収容室25への洗浄等のアプローチが
容易である。 【0051】収容室25を形成する各壁面は互いに接す
るすべての接線部において曲面を構成するように形成さ
れる。このため、その収容室25内には鋭角な隅部が無
く、汚れが溜まり難い。 【0052】さらに、図2で示すように、処置具起上台
27に設けられたワイヤ支持壁33の下端面は先端カバ
ー22の開口端面より距離Cだけ上方部位に来ており、
先端部17の先端側よりワイヤ支持壁33の下端面を眼
で捉える事が出来る。ワイヤ支持壁33の下端面におい
ても先端側よりアプローチが容易である。 【0053】スロープ部41の面にブラシ誘導面42を
設けている場合には、洗滌ブラシ等で起上台裏面31と
スロープ部41を洗滌する際、狙った位置にブラシを誘
導し易い。 【0054】よって、収容室25及びワイヤ支持壁33
の下端部の洗滌性がよく、先端カバー22を先端硬質部
21より取り外す事無く、処置具起上台27の起上台裏
面31及び収容室25の各面を隅々まで容易に洗浄する
事が可能となる。 【0055】従って、先端カバー着脱の煩わしさ、検査
時に先端カバーがずれて視野を遮ると言った不具合が無
くなる。加えて、収容室25内の隅部に汚物が溜まりに
くく、隅部の洗浄性も良くなる。 【0056】ところで、図5に示される如く、収容室2
5内に処置具案内用チャンネル23を通じて導かれてき
た処置具26は処置具起上台27の誘導面29を通り、
チャンネル23の開口部へと延出されるが、処置具26
がPTFE等の樹脂にて形成されたものである場合、そ
の処置具26のシース部には曲がり癖がつき易い。ま
た、処置具26の先端部を対物レンズ52の中心に向か
せるべく、そのシース部に積極的に曲がり癖をつけてい
る事もある。 【0057】このような場合、処置具26の導出先端は
処置具起上台27の中心に位置せず、先端部17の照明
レンズ51側へ向く事となる。例えば、図8で示すよう
に、処置具26の先端が処置具起上台27において対物
光学系収容領域側に片寄ってしまう場合がある。このよ
うな場合、処置具起上台27をさらに起上させて行く
と、処置具26は誘導面29には収まらず、処置具起上
台27と先端部17の部材との間に挟まれて持ち上がる
ことになる。しかし、処置具26の一部が案内路24の
近傍において誘導面29内に収まっているため、処置具
起上台27がある起上角度まで持ち上がると、処置具2
6の先端部も誘導面29に飛び込むように収まる。この
現象を処置具26の飛びと呼ぶことにする。 【0058】しかし、此処での処置具起上台27の先端
側には突出部45が形成されているため、処置具起上台
27の起上動作の初期の段階(起上角が小さい位置)で
処置具26の先端を突出部誘導面46に続く誘導面29
に導くことができる。 【0059】以上の如く、処置具が誘導面29に収まり
易く、内視鏡での観察時に処置具先端の位置が決まり易
く、検査処置がやり易い。加えて、処置具起上台27に
形成された突出部45が先端カバー22より突出しない
ため、その突出部45にて患者粘膜を損傷する事も無
い。また、突出部45には突出部誘導面46が形成され
ていることで、処置具26を突出部誘導面46及び誘導
面29へと導き易くなる。 【0060】また、図3に示すように、誘導面29の勾
配よりも突出部誘導面46の勾配が大きい事から、誘導
面29の処置具起上台27に対する幅を狭くする事が無
く、その突出部45の高さを十分に高く取れるようにな
る。 【0061】上記突出部45は処置具起上台27を最大
に起上した時でも、先端硬質部21が構成される各部に
接しない様に形成されているため、処置具起上台27の
繰り返し起上動作により突出部45に大きな応力が加わ
る事が無い。 【0062】突出部45の最も突出する頂部48は処置
具起上台27の起上動作のいずれにおいても、先端カバ
ー22の最も突出している稜線部49より突出する事が
ない。 【0063】外皮部材61の内径が可撓管口金85及び
先端硬質部21の外径の90%以下である事より、その
外皮部材61は可撓管口金85及び先端硬質部21の外
周面に密着する。 【0064】また、外皮部材61の外周より糸状部材8
6を巻き付ける事で、外皮部材61の内周面と先端硬質
部21及び可撓管口金85の外周面にて湾曲部16を液
密に保つ事が出来る。 【0065】糸状部材86の外周に配された接着剤87
により包皮部材88が接着固定される。また、包皮部材
88は加熱溶融される事で、包皮部材88の端部が滑ら
かに可撓管部15、先端カバー22及び外皮部材61の
外周が連続的につながるように形成される。 【0066】包皮部材88は加熱溶融する際に、その外
周を熱収縮チューブにて覆われた状態で溶融されるた
め、全周に渡りほぼ同一の形状に熱成型する事が出来
る。 【0067】また、包皮部材88を帯状のシート形態と
する事で可撓管部15の径が異なる複数の機種において
も同一の部材にて対応させる事が出来る。 【0068】包皮部材88は可撓管部15の外皮樹脂の
融点より低いため、可撓管部15の外皮樹脂を破損する
事無く包皮部材88のみを溶融させる事が出来る。接着
剤87は低粘度の接着剤であるため、糸状部材86の隙
間部への浸透が良く、包皮部材88の下層全域をむらな
く接着出来る。包皮部材88は黒または可撓管部15の
外観と類似色であるため、内視鏡の挿入部12の外観を
損ねる事が無い。 【0069】先端硬質部21において、ライトガイド5
3を配置する収納溝57はLGカバー59によって覆わ
れているが、通常、LGカバー59の縁部と、収納溝5
7の開口部には少なからず段が出来てしまう。 【0070】しかし、上記構成ではリング部材62(ま
たは延接部63)を先端硬質部21の外周に配する事
で、上記LGカバー59とLG収納溝57により形成さ
れる段部を無くし、外皮部材61の取付け部の凹凸を無
くす事が出来る。 【0071】さらに、リング部材62が先端カバー22
に外嵌するように構成されているため、リング部材62
と先端カバー22の間は液密的に構成されている。 【0072】外皮部材61はリング部材62(または延
接部63)に密着するように配されており、外皮部材6
1はリング部材62及び外皮部材61と延接部63の間
も液密的に構成されている。 【0073】外皮部材61の両端部において、糸状部材
86を巻回する事のみで湾曲部16を液密構造とする事
ができる。加えて、高技能を有さず、簡便な作業にて外
皮部材61の両端固定部を滑らかに形成する事が出来
る。 【0074】側視タイプの内視鏡においても、外皮部材
61を糸状部材86にて巻回する事で液密構造とする事
が出来る。加えて、図16で示す構成によれば、消毒薬
による化学変化及び衝撃などによる物理的変化により包
皮部材88に劣化が生じても、糸状部材86により物理
的に外皮部材61と延接部63が液密構造となっている
ため、外皮部材61の両端固定部において電気的な絶縁
性を常に確保する事が出来る。 【0075】また、上記起上台作動機構91において、
リンク軸100を係止し、リンク部材94とアーム99
を回動自在に連接するための構成部品である係止部材1
01が、ベース97と対向しない位置にあり、かつアー
ム99の端部より把持部カバー104側に配されている
ため、把持部カバー104を取り外す、または内視鏡の
可撓管部15側へずらす事のみで、係止部材56が外部
より容易に確認し、アプローチできる。 【0076】ワイヤ固定部材92が繰り返しの使用によ
りリンク部材94の内部に位置する係止溝93において
破損した場合、把持部カバー104を取り外す、または
内視鏡の可撓管部15側へずらす事のみで係止部材10
1を露呈する事が出来る。 【0077】さらに、アプローチも容易である事から、
係止部材101を容易に着脱する事が出来、これによ
り、リンク部材94及びワイヤ固定部材92を交換する
事で、破損に対する修理が簡便に行える。 【0078】本発明は上述した実施形態のものに限定さ
れるものではない。また、以下に列記する事項またはそ
の任意の組み合わせの事項が得られる。 【0079】<付記> 付記項1;内視鏡の挿入部先端に開口した処置具起上台
用収容室と、上記内視鏡の操作部側に設けられ、処置具
が挿入される挿通口部と、上記内視鏡に設けられ、上記
収容室と上記挿入口部とを連通する案内路と、上記収容
室に起上可能に設けられ、上記案内路を通じて挿通され
た処置具を導出方向へ誘導する誘導面を有する処置具起
上台とを有する内視鏡において、処置具起上台が起上操
作されたとき、処置具起上台の誘導面の裏面と、上記裏
面が対向する収容室の面までの距離が、処置具起上台が
露出されない領域における収容室の開口端において最大
となる様に構成されている事を特徴とする内視鏡。 【0080】付記項2;付記項1において、処置具起上
台の誘導面の裏面と、上記裏面が対向する収容室の面ま
での距離が処置具起上台の回動支点に向かって短くなる
ように形成されていることを特徴とする内視鏡。 付記項3;付記項1において、処置具起上台の誘導面の
裏面と、収容室にて構成される空間にあって処置具起上
台の誘導面の裏面と垂直な断面での断面積が開口端にて
最大となる様に構成されている事を特徴とする内視鏡。 【0081】付記項4;付記項3において、処置具起上
台の誘導面の裏面と垂直な断面での断面積が処置具起上
台の回動支点に向かって狭くなるように形成されている
ことを特徴とする内視鏡。 付記項5;付記項1において、上記収容室の各面の隣接
する稜線部は曲面にて形成されている事を特徴とする内
視鏡。 付記項6;付記項1において、処置具起上台の誘導面の
裏面に対向する収容室の構成面は、内視鏡挿入部の先端
に向かった軸方向に対し、鋭角な斜面として、処置具起
上台の回動支点に向かい形成されている事を特徴とする
内視鏡。 【0082】付記項7;付記項1において、処置具起上
台の誘導面の裏面は、処置具起上台が最大角度まで起上
操作された時、先端部の開口面に対し略垂直になるよう
に形成されている事を特徴とする内視鏡。 付記項8;付記項7において、略垂直とは、開口面と処
置具起上台の裏面との成す角度が80度以上である事を
特徴とする内視鏡。 付記項9;付記項1において、処置具起上台の誘導面の
裏面が対向する、上記収納室の面は、その収納室の開口
側から処置具起上台の回動支点に向かって滑らかに傾斜
している事を特徴とする内視鏡。 【0083】付記項10;内視鏡の挿入部先端に開口し
た収容室と、上記内視鏡の操作部側に設けられた送液ま
たは処置具が挿通される挿通口と、上記収容室と上記挿
通口とを連通する案内路と、上記収容室に起上操作可能
に設けられ処置具を誘導する誘導面を有する処置具起上
台とを有する内視鏡において、処置具起上台の誘導面の
観察光学系が配される側に位置して起上台の一部を起上
台の誘導面を形成する斜面の稜線部よりも突き出して突
出部を形成した事を特徴とする内視鏡。 【0084】付記項11;付記項10において、突出部
は、処置具起上台の長手方向の中央部近傍に設けられて
いる事を特徴とする内視鏡。 付記項12;付記項10において、突出部は、誘導面の
横方向に垂直な断面形状を誘導面の内側方向に斜面を有
する直角三角形に近似した形状である事を特徴とする内
視鏡。 付記項13;付記項10において、突出部は、処置具起
上台の起上操作において、収容室より突出しない様に形
成されている事を特徴とする内視鏡。 【0085】付記項21;可撓管部と、可撓管部の先端
に連結された湾曲部と、湾曲部の先端に連結された先端
構成部とからなる挿入部を有し、上記湾曲部の外皮を形
成する外皮部材の両端部をそれぞれ可撓管の先端部と先
端構成部の基端部とに固定してなる内視鏡において、外
皮の両端部の外周面を糸状部材にて巻回し、上記糸状部
材の外周面に、包皮部材を配し、上記包皮部材は加熱溶
融することでその外表面を、挿入部の外表面に対し滑ら
かに配した事を特徴とする内視鏡。 【0086】付記項22;付記項21において、包皮部
材は熱可塑性樹脂にて形成されている事を特徴とする内
視鏡。 付記項23;付記項21において、糸状部材には、包皮
部材を配する前に、接着剤が塗布されている事を特徴と
する内視鏡。 付記項24;付記項22において、熱可塑性樹脂はポリ
ウレタンである事を特徴とする内視鏡。 【0087】付記項25;付記項22において、熱可塑
性樹脂はその融点が、可撓管に使用の樹脂の融点以下で
ある事を特徴とする内視鏡。 付記項36;付記項21において、包皮部材は、黒色で
ある事を特徴とする内視鏡。 付記項27;付記項21において、包皮部材は、糸状部
材に接する面を黒色の層とし、外部に露呈される面を透
明の層とする2層構造体である事を特徴とする内視鏡。 付記項28;付記項27において、包皮部材の外部に露
星される層の融点は、糸状部材に接する層の融点よりも
低い事を特徴とする内視鏡。 【0088】付記項29;付記項23において、接着剤
は低粘度である事を特徴とする内視鏡。 【0089】付記項30;付記項29において、接着剤
の粘度は8.5Ps・s以下である事を特徴とする内視
鏡。 付記項31;付記項23において、接着剤の色は黒色で
ある事を特徴とする内視鏡。 付記項32;付記項21において、包皮部材は細長のシ
ート状である事を特徴とする内視鏡。 付記項33;付記項21において、糸状部材は黒色であ
る事を特徴とする内視鏡。 【0090】付記項34;付記項21において、外皮部
材の少なくとも両端固定部の内径は、上記両端固定部の
取り付くべき構成部材の外径以下である事を特徴とする
内視鏡。 付記項35;付記項21において、糸状部材は外皮に4
回以上巻回されている事を特徴とする内視鏡。 付記項36;付記項21において、糸状部材は2N以上
の引張力にて巻回されている事を特徴とする内視鏡。 付記項37;付記項21において、先端構成部は、本体
である先端硬質部と、先端硬質部を覆い、樹脂等よりな
る先端カバーより構成され、先端硬質部の少なくとも外
皮部材が取り付く全周には、リング状の部材が液密的に
配されていることを特徴とする内視鏡。 付記項38;付記項37において、リング状の部材は全
周において、その一端を先端カバーと液密的に接続され
ている事を特徴とする内視鏡。 【0091】付記項39;付記項37において、リング
状部材は、金属箔よりなる薄肉の部材である事を特徴と
する内視鏡。 【0092】付記項10〜14の従来技術としては、特
開平8−154890号公報がある。付記項21〜39
の従来技術としては、実公昭62−23444号公報お
よび特開平9−299319号公報のものがある。 【0093】特開平8−154890号公報の問題点
は、挿入部に挿通した処置具が、内視鏡先端から突出し
た際に、先端構成部の処置具起上台の側面に接する壁
と、処置具起上台に挟まれるように保持された場合、処
置具は、処置具起上台の誘導溝に沿うことなく起上操作
され、ある角度まで起上された時点で、誘導溝に落ち込
む、いわゆる処置具の飛びが発生する。 【0094】この場合、内視鏡検査中に目的部位への処
置具の誘導が出来ず、検査に支障をきたすと言う点にあ
る。 【0095】・実公昭62−23444号公報の問題点
は、外套皮の表面より突出したリング状バンドの端部
に、本部位が引っ掛かりとならない様に接着剤等を塗布
し滑らかにせねばならなかった。しかし、この作業は挿
入部に出るところであるため、滑らかに仕上げる作業に
は高技能を有するものであり、作業者によるバラツキが
大きくなると言う点にある。 【0096】・特開平9−299319号公報の問題点
は、外皮部材が接する可撓管部もしくは先端構成部に熱
可塑性樹脂を構成しなくてはならず、そのため熱可塑性
樹脂の構成厚さ分だけ挿入部の径が大きくなってしま
う。また、外皮部材の一部を熱可塑性樹脂にて形成し、
組み付け時に加熱溶融するため、外皮部材が部分的に薄
くなる可能性があり、本部位が引っ張り等のストレスに
より破損し易くなると言う点にある。 【0097】付記項10〜14の目的は、挿入部に挿通
した処置具を、目的部位に確実に誘導する事を目的とす
る。付記項21〜33の目的は、高技能を要せず、外皮
部材の両端固定部を先端構成部及び可撓管に対し滑らか
に仕上げる事にある。付記項34〜39の目的は、挿入
部において、外皮部材の両端部の防水性を保持する事に
ある。 【0098】付記項10〜14の効果は、先端より処置
具を引っかかりなく誘導し、突出させる事に加え、処置
具起上台へ形成された誘導溝に処置具を確実に誘導し、
内視鏡による検査及び処置に係わる作業をスムーズに行
うようにする事に有る。付記項21〜33の効果は、外
皮部材を先端構成部及び可撓管に対し、確実に液密固定
する事に加え、固定部の外部に露呈される面を、高技能
を要せず簡便に、かつ滑らかに仕上げる事が出来ると言
う事に有る。付記項34−39の効果は、外皮部材の両
端部を糸状部材のみにて、作業者の技術的な差異によら
ず確実に液密固定できると言う事に有る。 【0099】 【発明の効果】以上説明したように本発明は、処置具起
上台に突出部を設けたから、処置具起上台で処置具を起
上するとき、側方にずれて起上する処置具を処置具起上
台の誘導面に誘導して収め、挿入部に挿通した処置具を
目的部位に確実に誘導できるようになる。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention
The leading direction of the treatment channel is
The present invention relates to an endoscope provided with a raising table for regulation. 2. Description of the Related Art An end of a channel is opened at an end of an insertion portion.
And an elevator is provided in this opening, and the processing is performed by the elevator.
Endoscopes that regulate the direction in which the fixture is led out are known
(JP-A-8-154890). [0003] Japanese Patent Application Laid-Open No. Hei 8-154
The endoscope disclosed in Japanese Patent No. 890 is a treatment tool inserted through a channel.
When the treatment tool is protruded from the distal end of the insertion section of the endoscope,
The wall of the tip component that is in contact with the side of the
It is easy to be held so that it is sandwiched between the sides of the upper stand, and the treatment tool rises
There is a case where the operation is performed without standing along the guide groove of the table.
Then, when the treatment tool is raised to a certain angle,
The so-called jump of the treatment tool which falls into the groove occurs. this
Such a phenomenon may occur. In this case, endoscopy
It is difficult to guide the treatment tool to the target site during
Cause obstacles. [0004] The present invention has been made in view of the above circumstances
The purpose is to use a treatment tool inserted through the endoscope.
Can be reliably guided from the tip of the insertion section to the target site.
It is an object of the present invention to provide an endoscope. SUMMARY OF THE INVENTION [0005] The present invention relates to an endoscope observation system.
Opened at the tip of the insertion section where the optical system is located
Provided on the accommodation room for the treatment instrument raising table and on the operation unit side of the endoscope
And the insertion port through which the treatment tool is inserted and the inside of the endoscope.
A treatment tool formed and communicating the accommodation chamber and the insertion port
Guide path and the storage room are provided so as to be able to be raised.
A treatment tool raising table having a guide surface for guiding the device,
Position the guide riser on the side where the observation optical system is located on the guide surface.
The treatment instrument is formed so as to protrude from the ridge to be placed.
And a protrusion for guiding to the conductive surface.
Endoscope. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Referring to FIGS.
An embodiment will be described. FIG. 1 shows a first embodiment of the present invention.
Of the system incorporating the endoscope 1 and various external devices.
It is a perspective view showing the whole. As an external device, a light source device
2, image processing device 3, monitor 4, input keyboard 5,
There are devices such as a suction pump device 6, a suction bottle 7, etc.
The equipment is installed on a shelf 9 with a carrier 8. The endoscope 1 includes an insertion section 12, an operation section 13,
A universal cord 14 is provided. The insertion part 12 is a flexible tube
From each component of the portion 15, the bending portion 16, and the tip portion 17
Become. The operation unit 13 has a universal cord 14
One end is connected, and the other end of the universal cord 14 is
A connector 18 is provided. The connector 18 is external
It is connected to a light source device 2 which is one of the devices. Connector 1
8 is provided with a light guide tube and an electric contact portion. FIGS. 2 to 1 show the structure of the tip portion 17. FIG.
This will be described in detail with reference to FIG. The tip 17 is in contact with the tip body.
Tip hard portion 21 and a resin
And a tip cover 22 made of a non-conductive material such as
The tip cover 22 is attached to the tip hard portion 21 by bonding or the like.
Fixed. The distal end hard portion 21 has a guide path for inserting a treatment instrument.
Channel (insertion hole) 23 and is formed continuously.
An introduction guideway 24 that guides the introduction of the treatment tool etc. to the distal end side is shaped.
Has been established. The leading end of the introduction guide path 24 has a hard tip.
A space formed by the material portion 21 and the tip cover 22.
An accommodation room 25 is provided. This accommodation room 25 is a treatment
The distal end opening of the tool insertion channel 23 is formed. The channel 2 is provided in the accommodation room 25.
Treatment tools 26 such as forceps and catheters introduced through
A treatment instrument raising table 27 for raising the patient to a desired position is provided.
Is being used. One end of the treatment instrument raising table 27 has a hard end portion.
21 and is pivotally connected to a fulcrum rotation fulcrum 28 provided at
I have. The elevating platform rotation fulcrum 28 is opened at the end of the introduction guide path 24.
It is located in the lower part of the mouth, and
So that the other end portion of the treatment instrument raising table 27 rotates.
The raising table 27 is attached so as to freely move up and down. Treatment tool
The elevator 27 is connected to the guideway 24 so as to be continuous.
The treatment instrument 26 is guided by the formed V-shaped groove.
A guiding surface 29 is formed. The guide surface 29 of the treatment instrument raising table 27 is formed.
Pivot on the back of the elevator 31
Near the distal end, near the left and right ends of the treatment instrument raising table 26,
Each is formed so as to project perpendicularly to the back surface 31 of the elevator.
A pair of left and right wire support walls 33 is provided.
The pair of left and right wire support walls 33 is provided with the treatment instrument raising table 27.
The tip of the raising wire 34 for raising
And are rotatably connected. A pair of left and right wire support walls
The part of the raising wire 34 located between 33
A stopping pipe 35 is provided. This pipe 35
It is fixed to the raising wire 34. The raising wire 34 is inserted through the insertion portion 12.
Is guided to the operation unit 13 through the guide pipe 36,
It is connected to the raising operation mechanism described below. The front cover 22 has a back surface 31 of the elevator.
At the position opposite to
The slope portion 41 formed as a smooth slope toward
Is formed. FIG. 6A shows the slope portion 41.
And raising the brush for cleaning as shown in FIG.
Brush guide surface 4 which is a groove for guiding to back surface 31
2 may be formed. Fig. 6 (a) shows the slope
FIG. 6B is a perspective view of the slope portion 41, and FIG.
FIG. 6A is a cross-sectional view along the X plane shown in FIG. The back surface 31 of the raising table 27 of the treatment tool raising table 27 is shown in FIG.
As shown by 2, when the treatment instrument raising table 27 is raised up to the maximum
, Except for the wire support wall 33,
12 with respect to the longitudinal direction of the tip 17 is about 90
Degrees (or in the range of 80 to 100 degrees)
You. The lower end of the wire support wall 33 is provided with a treatment tool.
When the elevator 27 is raised up to the maximum, the tip cover
22 is formed so as to be deviated upward from the end of the opening.
(Instructed at the distance C in FIG. 2). In the accommodation room 25, the treatment instrument raising table 27 is
From the back surface 31 of the erecting platform when raised up to the maximum,
The distance A to the surface of the tip cover 22 facing the back surface 31 is
It is formed so as to be maximum at the upper open end of the accommodation chamber 25.
(See FIG. 2). That is, it is constituted by the accommodation room 25.
In a space perpendicular to the back surface of the treatment instrument raising table 27
Is configured such that the cross-sectional area becomes maximum at the open end. As shown by a dotted line in FIG.
One side of the accommodation room 25 with the elevator 27 laid down
The surface facing the back surface 31 of the elevator is a pivot support for the elevator.
Formed as a slope that slopes towards point 28
This is the slope section 41. When the treatment instrument raising table 27 is raised up to the maximum,
And the surface of the storage room 25 facing the elevator back surface 31 is inserted.
Formed at about 90 degrees to the longitudinal direction of the tip 17 of the part 12
However, this surface and the treatment instrument raising table 27 are laid down.
When it is set to the
The connection is made at the surface 44. In addition, each of the chambers 25 is formed.
Walls have curved surfaces at all tangents that touch each other
It is formed so that. The treatment instrument raising table 27 is raised up to the maximum.
At this time, the back surface of the treatment instrument raising table 27 and the back surface
The distance to the surface of the accommodation room 25 facing
It is formed to be short and narrow toward the pivot point.
You. FIG. 3 shows a cross-sectional shape of the treatment instrument raising table 27 (see FIG. 3).
2 BB section in FIG. 2), but guidance of the treatment instrument raising table 27
A surface side on which the surface 29 is formed;
On the side where the objective lens and illumination lens
The projecting portion 45 having a thin, spatula-like shape is
Is formed to protrude beyond the ridge of the slope to form
I have. The inner surface of the projecting portion 45 is inside the treatment instrument raising table 27.
A projection that is inclined toward the center and is a slope that is continuous with the guiding surface 29.
An exit guiding surface 46 is formed. The slope of the protrusion guiding surface 46
The distribution is formed larger and steeper than the gradient of the guide surface 29.
I have. The projecting portion guiding surface 46 is a slope.
Not formed by a convex or concave curved surface
It may be. As shown in FIG. 2, the ridge line of the projecting portion 45 is
In the state where the fixture raising stand 27 is raised up to the maximum, the tip 1
7 is formed in a shape that does not interfere with each component.
You. Further, as shown in FIG.
Indicates a locus indicated by a bold broken line when the treatment instrument raising table 27 is raised.
become that way. The trajectory of the top 48 is the ridgeline of the tip cover 22
Formed so that it comes closer to the inside of the lift base fulcrum 28 than the part 49
Has been established. On the other hand, as shown in FIG.
In the part 17, a piece of the accommodation chamber 25 is
Side, here on the right side, the illumination lens 51 and the objective lens
Are located in a line in front and back of the tip portion 17 in the longitudinal direction.
The endoscope 1 is disposed and constitutes a side-view type endoscope 1. Illumination lens for expanding and illuminating the body cavity with illumination light
A light guide (fiber bundle) 53 is connected to 51.
The objective lens 52 has a prism 54 and an imaging lens.
An imaging unit 56 is connected via 55. These yes
The displacement is also attached to the distal end hard portion 21. Imaging unit 5
Reference numeral 6 denotes an image pickup device such as a CCD (not shown) and an accessory circuit device.
It is embedded. Referring to FIGS. 7, 8, 9, 11 and 12, FIG.
As shown, a light guide 53 is arranged on the distal end hard portion 21.
Storage groove 57 is formed along the longitudinal direction of the distal end hard portion 21.
It is elongated. And the light guide 53
After being filled, a filler 58 such as RTV rubber is
After that, the opening of the storage groove 57 is covered with the LG cover.
-59. Further, as shown in FIG.
At the end side to which the first bending portion 16 is connected, the outer skin of the bending portion 16
A thin ring-shaped member is provided at the position where the end of the member 61 is disposed.
Is fixed by bonding or the like. all
In the circumference, one end of the ring member 62 has a tip cover 2
2 is fitted, and the outer fitting part is bonded.
Agents and the like are arranged in a liquid-tight manner. The ring member 62 is shown in FIG.
As shown, the rear end of the tip cover 22 extends all around.
Even if it is constituted as the extension portion 63 formed by
good. The outer skin member 61 has an inner peripheral surface which is the ring member 6.
2 (or the extension 63) so as to be in close contact with the outer periphery thereof.
The outer periphery of the outer skin member 61 is thread-like
The member 64 is wound, and the adhesive 6
5 is applied, the foreskin member 66 is heated and melted and arranged.
Have been. Here, the inner diameter of the outer skin member 61
Of the outer diameter of the ring member 62 (or the extension portion 63).
It is formed so as to be 90% or less. FIG. 1 to be described later
The same applies to the configuration of FIG.
To the distal end rigid portion 21 and the flexible tube cap 85 described later.
The inner diameter of the area to be attached is the tip hard portion 21 and the flexible tube cap 8.
5 is formed so as to be 90% or less of the outer diameter. Also,
The inner diameter of the outer portion of the outer surface of the curved portion 16 of the outer cover member 61 may vary.
Formed so as to be 90 to 110% of the outer diameter of the cable 67.
ing. Here, the outer skin member 61 is attached to the distal end hard portion 21.
Reduce the inside diameter of the area to be mounted, and keep the same
It may be formed with an inner diameter. At that time,
The outer diameter of the flexible pipe base 85 is (outside of the flexible pipe base 85).
Diameter) × 0.9 ≧ (Inner diameter of outer skin member 61)
It is formed like one. The light guide 53 is inserted
In the section 12, the operation section 13 and the universal cord 14,
Through this, it is led to the connector 18. Connected to the imaging unit 56
The electrical wiring (not shown) is also inserted into the
And the connector 18 through the universal cord 14
Be guided. Electrical wiring is connected to the electrical contact of connector 18
Connected to the image processing apparatus 3 via the connection cable 19
It is. Then, the imaging signal obtained by the imaging unit 56 is converted into an image processing device.
So that it is converted to a video signal by the device 3 and displayed on the monitor 4.
Has become. On the other hand, as shown in FIG.
13 has a curved portion 16 of the insertion portion 12 in the up / down / left / right direction.
Of the bending operation unit 71 and the objective lens 52 for bending
Spraying a fluid such as water or air onto the outer surface
Gas and liquid are selectively ejected to the nozzle 72 for cleaning.
The water supply button 73 for opening, the tip is opened to the tip part 17
Mucus and the like in the body cavity selectively through the channel 23
Suction operation button 74 for collection, channel 2
An insertion port 75 leading to 3 is provided. In addition,
The distal end opening of the channel 23 is provided with a treatment instrument raising table 27.
Also serves as a storage room 25. A fluid is supplied to the nozzle 72 inside the endoscope 1.
Supply fluid line 76 and suction line through which recovered fluid passes
(The channel 23 also serves as this.)
I have. The bending portion 16 of the insertion portion 12 is, for example, as shown in FIG.
It is also configured as shown in FIG. In other words, multiple
A number of curved pieces 81 are rotatably assembled using rivets 82.
The core 83 is combined to form the core 83.
A metal or chemical fiber wire is braided on the outer periphery to form a cylinder.
The blade 67 thus formed is exteriorized, and the blade 6
7 are provided at both ends of the bending portion 16.
It is fixed to the mask 81 by bonding or soldering. Bray
The outer skin member 61 composed of a tube body is externally
Have been. State-of-the-art bending piece 8 constituting bending section 16
1 is made of a metal or hard resin constituting the tip portion 17.
Is connected. In addition, the tip hard portion 21
Is a cap-shaped part made of an insulating material
The tip cover 22, which is a material, is integrally fixed by bonding or the like.
You. The flexible tube 15 of the insertion section 12 has a belt-like shape.
Spiral tube (not shown) made of metal in a spiral shape, metal
Braid (not shown) formed by braiding wire or chemical fiber into a cylindrical shape
(Not shown) made of resin and resin.
Have been. The distal end of the flexible tube 15 can be made of metal or the like.
The flexible tube cap 85 is fixed by bonding or soldering,
A hand that constitutes the curved portion 16 via the flexible tube cap 85
A curved piece 81 at the side end is connected and fixed. As shown in FIG.
As described above, one end of the flexible tube base 85 and the
The gap between the outer layer and the outer layer is filled with an adhesive or the like.
The filler 84 is arranged in a liquid-tight manner over the entire circumference without any gap.
You. For example, the tip of the outer skin member 61 is
It is externally attached so as to be in close contact with the outer periphery of the
The end is arranged to be in contact with the rear end of the tip cover 22.
Have been. Then, as shown in FIG.
In the tip portion of the outer skin member 61 which covers 1, silk or
A thread member 86 made of chemical fiber or the like is wound. Outside
The rear end portion of the skin member 61 is in close contact with the outer periphery of the flexible tube cap 85.
The outer end of the flexible tube 15 is
It is arranged to be in contact with the tip of the layer. Flexible tube
At the rear end of the outer skin member 61 that covers the base 85,
Or a thread member 86 made of chemical fiber or the like is wound.
You. Then, it is wound around the end of the outer cover member 61.
The thread member 86 is a skin member when its tensile force is 2N or more.
Wrap and tighten 61 so as to bind it from the outside. Also,
The number of turns of the thread member 86 is four or more. In addition, yarn
An adhesive 87 is applied over the entire area of the member 86.
You. After applying the adhesive 87, the outer periphery of the thread member 86
A wrapping member 88 made of a thermoplastic resin such as urethane is provided.
You. Here, the adhesive 87 has a viscosity of 8.5P.
s · s or less. The melting point of the foreskin member 88 is the outer skin member
61 is made of a resin material having a melting point lower than the melting point of the resin.
You. In addition, less of the thread member 86 and the foreskin member 88
Both of the foreskin members 88 are similar in color to the appearance color of the flexible tube portion 15.
It becomes. The foreskin member 88 is not limited to the one similar in appearance color.
Instead, it may be black. The adhesive 87 is also used for the flexible tube portion 15.
Is similar in appearance color or black. The foreskin member 88 is phosphorus
May be formed in a belt-like form, or a belt-like sheet.
It may be formed in a shape. The wrapping member 88 is attached to the outer periphery of the adhesive 87.
When attaching, use a heat-shrinkable tubing material (not shown).
Is completely covered and heated by a heating device (not shown).
Heat shrinks the shrink tubing and melts at the same time as the assembly
Can be The foreskin member 88 is formed in a belt-like sheet shape.
Wrap the wrapping member 88 around the adhesive 87
A heater such as a soldering iron is used to attach a portion where the foreskin member 88 overlaps.
By heating with a container etc., arrange it in a ring shape at this part
To As shown in FIG. 16, the foreskin member 88
Is a black foreskin member 89 on the layer in contact with the thread member 86,
A transparent foreskin member 90 that is colorless (semi-transparent) in the exposed layer
May be constituted by two layers. As shown in FIG. 17 and FIG.
The first operating unit 13 is provided with an operating device for operating the treatment instrument raising table 27.
The elevator operating mechanism 91 for operating the upper wire 34
Built-in. That is, inside the operation unit 13,
The base end of the raising wire 34 is made of a hard rod-like material such as metal.
Wire fixing member 92 is integrally fixed with solder or the like.
Have been. The base end of the wire fixing member 92 is a recess.
A locking groove 93 is formed. This wire fixing part
In the base end portion of the material 92, the area where the locking groove 93 is formed is formed.
It is made of a hard block made of metal or the like that can be all inserted.
Link member 94 is inserted, and a link portion is provided in the locking groove 93.
Screw 9 screwed into a female screw 95 provided on the material 94
6 are inserted and locked. This allows the wire
The fixing member 92 is connected to a link member 94. The link member 94 serves as a base of the operation unit 13.
The base 97 is disposed so as to be able to advance and retreat in the longitudinal direction. Rin
The lock member 94 is provided adjacent to the bending operation section 71.
The arm 99 connected to the raising operation knob 98 is connected.
I have. The arm 99 is a rod-shaped shaft member for the link member 94.
Are rotatably connected by a link shaft 100. Re
At one end of the link shaft 100 which is not opposed to the base 97.
Is a locking member 101 composed of a C-type or E-type
Engaged. As shown, the locking member 101 is
The gripper cover 104 is larger than the end of the music operation unit cover 103
The length of the arm 99 is set so that it is located on the side
You. (Operation / Effect) Raise the treatment instrument raising table 27.
The operating knob 98 of the operating section 13 is rotated.
You. When the raising operation knob 98 is rotated, the raising
The treatment tool raising table 27 is raised accordingly.
It rotates about the upper table rotation fulcrum 28 as a fulcrum, and performs an undulating operation.
U. As shown in FIG. 2, the treatment instrument raising table 27 is
When raised up, the back of the raising base 31 and the point facing it
The empty space of the accommodation room 25 formed by one surface of the end cover 22.
The opening is the largest at the opening end, and the back of the elevator
31 is positioned substantially perpendicular to the longitudinal direction of the tip 17.
I do. For this reason, as shown in FIG.
The whole area inside the accommodation room 25 can be easily grasped with eyes from above.
Wear. The accommodation chamber 25 has the largest open end at the opening end.
The approach such as cleaning to the accommodation room 25
Easy. The walls forming the storage chamber 25 are in contact with each other.
Are formed to form curved surfaces at all tangents
It is. Therefore, there is no sharp corner in the accommodation room 25.
And it is difficult for dirt to collect. Further, as shown in FIG.
The lower end surface of the wire support wall 33 provided on the
-22 is located above the opening end surface by a distance C,
The lower end surface of the wire support wall 33 is viewed from the distal end side of the distal end portion 17.
Can be caught. On the lower end surface of the wire support wall 33
However, the approach is easier than the tip side. A brush guide surface 42 is provided on the surface of the slope portion 41.
If provided, the back of the elevator 31 with a cleaning brush or the like
When cleaning the slope 41, guide the brush to the target position.
Easy to guide. Therefore, the accommodation room 25 and the wire support wall 33
The lower end of the head has good cleaning properties.
The back of the treatment tool elevator 27 without removing it from the elevator 21
The surface 31 and each surface of the accommodation room 25 are easily cleaned to every corner.
Things become possible. Therefore, the trouble of attaching and detaching the tip cover, the inspection
There is no problem that the top cover sometimes shifts and blocks the field of view
It becomes. In addition, dirt accumulates in the corners of the accommodation room 25.
Also, the cleanability of the corners is improved. By the way, as shown in FIG.
5 is guided through the treatment tool guide channel 23.
The treatment instrument 26 passes through the guide surface 29 of the treatment instrument raising table 27,
The treatment tool 26 extends to the opening of the channel 23.
Is made of a resin such as PTFE,
The sheath portion of the treatment tool 26 tends to be bent. Ma
In addition, the distal end of the treatment instrument 26 is directed toward the center of the objective lens 52.
To make the sheath part bend aggressively.
Sometimes. In such a case, the leading end of the treatment instrument 26 is
Lighting of the distal end portion 17 without being located at the center of the treatment instrument raising table 27
It will face the lens 51 side. For example, as shown in FIG.
The distal end of the treatment tool 26 is
There is a case where the optical system is shifted toward the optical system housing area. This
In such a case, the treatment instrument raising table 27 is further raised.
The treatment tool 26 does not fit on the guide surface 29, and the treatment tool rises.
Lifted up between the base 27 and the member of the tip 17
Will be. However, a part of the treatment tool 26
The treatment tool is located in the guide surface 29 in the vicinity.
When the raising table 27 is lifted to a certain raising angle, the treatment tool 2
6 also fits so as to jump into the guide surface 29. this
The phenomenon will be referred to as a jump of the treatment tool 26. However, the tip of the treatment instrument raising table 27 here
Since the protruding portion 45 is formed on the side,
In the initial stage of the raising operation of 27 (the position where the raising angle is small)
A guide surface 29 that connects the distal end of the treatment tool 26 to the protrusion guide surface 46
Can be led to. As described above, the treatment tool fits on the guiding surface 29.
Easy to determine the position of the tip of the treatment tool during observation with an endoscope
And the inspection procedure is easy. In addition, the treatment instrument raising table 27
The formed protrusion 45 does not protrude from the tip cover 22
Therefore, there is no possibility that the mucous membrane of the patient is damaged by the protrusion 45.
No. Further, a protrusion guiding surface 46 is formed on the protrusion 45.
The treatment instrument 26 is guided by the projection guiding surface 46 and the guiding
It is easier to guide to the surface 29. Further, as shown in FIG.
Since the inclination of the protrusion guiding surface 46 is larger than the inclination,
No reduction in the width of the surface 29 with respect to the treatment instrument raising table 27
The height of the protrusion 45 can be made sufficiently high.
You. The protruding portion 45 extends the treatment instrument raising table 27 to the maximum.
Even when standing up to
Since it is formed so as not to contact, the treatment instrument raising table 27
A large stress is applied to the protruding portion 45 by the repeated raising operation.
Nothing to do. The most protruding top 48 of the protrusion 45 is
In any of the raising operations of the raising table 27, the tip cover is
-22 protruding from the most protruding ridge 49
Absent. The inner diameter of the outer shell member 61 is
Because it is 90% or less of the outer diameter of the hard tip portion 21,
The outer skin member 61 is provided outside the flexible tube base 85 and the distal end hard portion 21.
Adhere to the peripheral surface. Further, the thread-like member 8
6, the inner peripheral surface of the outer skin member 61 and the tip end are hardened.
The curved part 16 is formed on the outer peripheral surfaces of the part 21 and the flexible pipe base 85 by liquid.
Can be kept dense. The adhesive 87 arranged on the outer periphery of the thread member 86
Thus, the foreskin member 88 is bonded and fixed. Also, foreskin member
88 is heated and melted so that the end of the foreskin member 88 is smoothed.
Of the crab flexible tube portion 15, the tip cover 22, and the outer skin member 61
The outer periphery is formed so as to be continuously connected. When the foreskin member 88 is heated and melted,
Melted while the circumference is covered with a heat-shrinkable tube
It can be thermoformed into almost the same shape over the entire circumference
You. The foreskin member 88 is formed in a belt-like sheet form.
By doing so, in a plurality of models with different diameters of the flexible tube
Can also be handled by the same member. The wrapping member 88 is made of a resin of the outer skin of the flexible tube portion 15.
Since the melting point is lower than the melting point, the outer cover resin of the flexible tube portion 15 is damaged.
Only the foreskin member 88 can be melted without any trouble. Bonding
Since the agent 87 is a low-viscosity adhesive, the space between the thread members 86 is
It has good penetration into the space, and the entire lower layer of the foreskin member 88 is even.
It can be glued well. The foreskin member 88 is made of black or flexible tube 15.
Since the color is similar to the appearance, the appearance of the insertion section 12 of the endoscope is changed.
There is no damage. In the distal end hard portion 21, the light guide 5
The storage groove 57 for arranging 3 is covered with an LG cover 59.
However, usually, the edge of the LG cover 59 and the storage groove 5
There are not a few steps in the opening 7. However, in the above configuration, the ring member 62 (or
Or the extended contact portion 63) is arranged on the outer periphery of the distal end hard portion 21.
Formed by the LG cover 59 and the LG storage groove 57.
Stepped portion, and no unevenness in the mounting portion of the outer skin member 61
I can do it. Further, the ring member 62 is
The ring member 62
The space between the end cover 22 and the end cover 22 is liquid-tight. The outer skin member 61 is a ring member 62 (or
The contact member 63) is arranged so as to be in close contact therewith.
1 is between the ring member 62 and the outer skin member 61 and the extension contact portion 63
Are also liquid-tight. At both ends of the outer cover member 61, a thread-like member
Make the curved part 16 a liquid-tight structure only by winding 86
Can be. In addition, they do not have high skills,
The fixed portions at both ends of the leather member 61 can be formed smoothly.
You. The outer member is also used in the side-view type endoscope.
A liquid-tight structure by winding 61 with a thread-like member 86
Can be done. In addition, according to the configuration shown in FIG.
Wrapping due to chemical changes due to
Even if the skin member 88 is deteriorated, the physical
The outer skin member 61 and the extension portion 63 have a liquid-tight structure
Therefore, electrical insulation is provided at both ends of the outer cover member 61.
Sex can always be secured. Further, in the raising table operating mechanism 91,
The link shaft 100 is locked, and the link member 94 and the arm 99 are locked.
Locking member 1 as a component for rotatably connecting
01 is located at a position that does not face the base 97 and
Is disposed closer to the grip cover 104 than the end of the
Therefore, remove the grip cover 104 or use the endoscope.
Only by shifting to the flexible tube 15 side, the locking member 56
You can check and approach more easily. When the wire fixing member 92 is repeatedly used.
In the locking groove 93 located inside the link member 94,
If damaged, remove the grip cover 104, or
Only by shifting the endoscope to the flexible tube portion 15 side, the locking member 10
1 can be revealed. Further, since the approach is easy,
The locking member 101 can be easily attached and detached.
And replace the link member 94 and the wire fixing member 92.
As a result, repair for damage can be easily performed. The present invention is limited to the embodiment described above.
It is not something to be done. In addition, the items listed below or
Are obtained. <Additional remarks> Additional remarks 1; treatment instrument raising table opened at the distal end of the insertion section of the endoscope
Treatment chamber provided on the operation unit side of the endoscope
Is provided in the endoscope and the insertion port portion into which the
A guideway communicating the accommodation chamber with the insertion opening,
It is provided so that it can be raised in the room, and is inserted through the guideway.
Treatment instrument having a guide surface for guiding a broken treatment instrument in the leading-out direction
In an endoscope having an upper table, the treatment tool raising table is raised.
When it is made, the back of the guide surface of the treatment instrument
The distance to the surface of the accommodation room where the surface faces
Maximum at the open end of the containment chamber in the unexposed area
An endoscope characterized in that it is configured to be: Additional Item 2: The treatment instrument according to Additional Item 1,
The back of the guide surface of the table and the surface of the accommodation room
Distance decreases toward the fulcrum of the treatment instrument raising table
An endoscope characterized by being formed as follows. Additional Item 3; In Additional Item 1, the guide surface of the treatment instrument raising stand
Raising the treatment tool in the space consisting of the back and the accommodation room
The cross-sectional area at the cross section perpendicular to the back surface of the guide surface of the table is at the open end
An endoscope characterized by being configured to be the largest. Additional Item 4: The treatment instrument according to the additional item 3,
The cross-sectional area at the cross section perpendicular to the back of the guide surface of the table rises the treatment tool
It is formed so that it becomes narrower toward the pivot point of the table.
An endoscope characterized in that: Supplementary Note 5: In Supplementary Note 1, adjacent to each surface of the accommodation room
The characteristic feature is that the ridge line portion that is formed is a curved surface
Endoscope. Supplementary item 6: In Supplementary item 1, the guide surface of the treatment instrument raising stand
The constituent surface of the storage room facing the back is the tip of the endoscope insertion section
The treatment tool as an acute slope with respect to the axial direction
Characterized in that it is formed facing the rotation support point of the upper stand.
Endoscope. Additional Item 7; In the additional item 1, the treatment instrument is raised.
On the back side of the guide surface of the table, the treatment tool raising table rises to the maximum angle.
When operated, it is almost perpendicular to the opening surface of the tip
An endoscope characterized by being formed in. Additional Item 8; In the additional item 7, substantially perpendicular means that the opening surface is
Make sure that the angle between the back of the fixture raising stand and the back is 80 degrees or more.
Endoscope that features. Supplementary Item 9: In Supplementary Item 1, the guide surface of the treatment instrument raising stand
The surface of the storage room, whose back surface faces, is the opening of the storage room.
Smoothly inclines from the side toward the fulcrum of the treatment instrument raising table
An endoscope characterized by doing. Additional Item 10: Opening at the end of the insertion section of the endoscope
And a liquid feeder provided on the operation section side of the endoscope.
Or the insertion port through which the treatment instrument is inserted,
Guideway communicating with the entrance, and can be raised in the storage room
Up of a treatment instrument having a guide surface for guiding the treatment instrument provided on the
In an endoscope having a table, the guide surface of the treatment tool raising table
Raise a part of the elevator that is located on the side where the observation optical system is located
Projecting beyond the ridgeline of the slope that forms the guide surface of the platform
An endoscope characterized by forming a projection. Additional Item 11: In the additional item 10, the protrusion
Is provided near the longitudinal center of the treatment instrument raising table.
An endoscope characterized by being Additional Item 12; In Additional Item 10, the protruding portion is a guide surface.
Cross section perpendicular to the lateral direction has a slope inward of the guiding surface
Characterized by a shape approximating a right triangle
Endoscope. Additional Item 13; In Additional Item 10, the protruding portion may be
When raising the upper stand, make sure that it does not protrude from the storage chamber.
An endoscope characterized by being made. Additional Item 21; Flexible Tube and Tip of Flexible Tube
And a tip connected to the tip of the bending part
It has an insertion part consisting of a constituent part and forms the outer skin of the bending part.
The ends of the outer shell member to be formed are
In an endoscope fixed to the base end of the end component,
Wrap the outer peripheral surfaces of both ends of the leather with a thread-like member, and
A foreskin member is arranged on the outer peripheral surface of the material, and the foreskin member is heated and melted.
By melting, the outer surface slides against the outer surface of the insertion section.
An endoscope characterized by being arranged in a crab. Additional Item 22; In Additional Item 21, the foreskin portion
The material is characterized by being formed of thermoplastic resin
Endoscope. Additional Item 23; In Additional Item 21, the thread-like member includes a foreskin.
The feature is that adhesive is applied before arranging the members
Endoscope. Additional Item 24; In Additional Item 22, the thermoplastic resin is
An endoscope characterized by being urethane. Item 25; The thermoplastic resin according to Item 22;
The melting point of the conductive resin is lower than the melting point of the resin used for the flexible tube.
An endoscope characterized by something. Additional Item 36; In Additional Item 21, the foreskin member is black.
An endoscope characterized by something. Additional Item 27; In Additional Item 21, the foreskin member is a thread-like portion.
The surface in contact with the material is a black layer, and the surface exposed to the outside is transparent.
An endoscope having a two-layer structure having a bright layer. Additional Item 28; In Additional Item 27, the outside of the foreskin member is exposed.
The melting point of the starred layer is higher than the melting point of the layer in contact with the thread-like member.
An endoscope characterized by being low. Item 29; The adhesive according to Item 23,
Is an endoscope characterized by low viscosity. Additional Item 30; The adhesive according to Additional Item 29, wherein
Is characterized by having a viscosity of 8.5 Ps · s or less.
mirror. Item 31; In Item 23, the color of the adhesive is black.
An endoscope characterized by something. Additional Item 32; In Additional Item 21, the foreskin member may be an elongated
An endoscope characterized in that it is in the shape of a tube. Additional Item 33; In Additional Item 21, the thread-like member is black.
Endoscope characterized by the fact that Additional Item 34; In Additional Item 21, the outer skin portion
The inner diameter of at least both ends fixed part of the material is
It is characterized by being smaller than the outer diameter of the component to be attached
Endoscope. Additional Item 35; In Additional Item 21, the thread-like member may have 4
An endoscope characterized by being wound more than once. Additional Item 36; In Additional Item 21, the thread-like member is 2N or more.
An endoscope that is wound by a tensile force. Additional Item 37; In Additional Item 21, the distal end component is a main body.
And cover the hard tip,
At least outside the hard tip section.
A ring-shaped member is liquid-tight around the entire circumference where the leather member is attached.
An endoscope, wherein the endoscope is arranged. Additional Item 38; In Additional Item 37, the ring-shaped member
In the circumference, one end is connected liquid-tight with the tip cover.
Endoscope characterized by the fact that it is. Additional Item 39; In Additional Item 37, the ring
The member is a thin member made of metal foil.
Endoscope. The prior arts of the additional items 10 to 14 include the following.
There is JP-A-8-154890. Supplementary items 21 to 39
Japanese Patent Publication No. 62-23444 discloses a conventional technique.
And JP-A-9-299319. Problems with JP-A-8-154890
When the treatment instrument inserted through the insertion section projects from the endoscope end
Wall that comes into contact with the side of the treatment tool
If the instrument is held so that it is
The fixture can be raised without operating along the guide groove of the treatment tool raising table.
When it is raised to a certain angle, it falls into the guiding groove
That is, a so-called jump of the treatment tool occurs. In this case, during the endoscopic examination, the processing to the target site is performed.
The equipment cannot be guided, which may hinder the inspection.
You. Problems with Japanese Utility Model Publication No. 62-23444
Is the end of the ring-shaped band protruding from the surface of the mantle
And apply an adhesive etc. to prevent this part from getting caught
It had to be smooth. However, this work
Because it is about to enter the entrance, for work that finishes smoothly
Is highly skilled, and there is no
The point is that it gets bigger. Problems with JP-A-9-299319
Heat is applied to the flexible tube or the tip component that the skin member contacts.
Must be made of thermoplastics, and therefore thermoplastic
The diameter of the insertion part is increased by the thickness of the resin composition.
U. Also, a part of the outer shell member is formed of a thermoplastic resin,
The outer shell is partially thin because it is heated and melted during assembly.
This part may be subject to stress such as tension.
The point is that it is easier to break. The purpose of the additional items 10 to 14 is to insert
The purpose is to guide the treated instrument to the target site without fail.
You. The purpose of Supplementary Notes 21 to 33 is that high-skill
The fixed part at both ends of the member is smooth with respect to the tip part and the flexible tube.
To finish. The purpose of additional items 34 to 39 is to insert
In the part, to maintain the waterproofness of both ends of the outer member
is there. The effects of additional items 10 to 14 can be obtained by treating
In addition to guiding and protruding the tool without getting caught, treatment
Guide the treatment tool into the guide groove formed on the tool raising table,
Smoothly perform the work related to inspection and treatment by endoscope
It is to do. The effects of Additional Items 21 to 33 are
Reliable liquid-tight fixation of the skin member to the tip component and the flexible tube
In addition to the
Can be finished easily and smoothly without the need for
There is. The effect of Additional Items 34-39 is due to the
Due to the technical differences of the workers,
It is that it can be fixed in a liquid-tight manner without fail. As described above, the present invention provides a treatment instrument
Since the projection is provided on the upper table, the treatment tool is
When raising the treatment tool, raise the treatment tool that is shifted to the side.
Guide the treatment tool inserted into the insertion section
Guidance can be reliably obtained at the target site.

【図面の簡単な説明】 【図1】本発明の一実施形態に係る内視鏡と各種の外部
装置を組み込んだシステムの全体を示す斜視図。 【図2】本発明の一実施形態に係る内視鏡の先端部の、
処置具起上台に沿う縦断面図。 【図3】図2中のB−B線に沿う部分の断面図。 【図4】本発明の一実施形態に係る内視鏡の先端部の平
面図。 【図5】本発明の一実施形態に係る内視鏡の先端部の一
使用状態の平面図。 【図6】(a)は処置具起上台におけるスロープ部の斜
視図、(b)はそのスロープ部を図4(a)に示すX面
に沿って切断した横断面図。 【図7】本発明の一実施形態に係る内視鏡の先端部の、
照明レンズと対物レンズに沿って切断した縦断面図。 【図8】本発明の一実施形態に係る内視鏡の先端部の横
断面図。 【図9】本発明の一実施形態に係る内視鏡の先端部の横
断面図。 【図10】本発明の一実施形態に係る内視鏡の先端部の
処置具起上台に沿って切断し、処置具起上台の起上動作
を示す縦断面図。 【図11】本発明の一実施形態に係る内視鏡の先端部
の、照明レンズと対物レンズに沿って切断した縦断面
図。 【図12】図11中、D−D線に沿う部分の横断面図。 【図13】本発明の一実施形態に係る内視鏡の湾曲管部
の縦断面図。 【図14】本発明の一実施形態に係る内視鏡の先端部、
湾曲管部および可撓管部の外装接続部の縦断面図。 【図15】本発明の一実施形態に係る内視鏡の先端部、
湾曲管部および可撓管部の外装接続部の縦断面図。 【図16】本発明の一実施形態に係る内視鏡の先端部、
湾曲管部および可撓管部の他の形式の外装接続部の縦断
面図。 【図17】本発明の一実施形態に係る内視鏡の起上台作
動機構を示すための操作部の断面図。 【図18】本発明の一実施形態に係る内視鏡の起上台作
動機構を示すための操作部の断面図。 【符号の説明】 1…内視鏡、12…挿入部、13…操作部、14…ユニ
バーサルコード、15…可撓管部、16…湾曲部、17
…先端部、21…先端硬質部、22…先端カバー、23
…チャンネル、24…導入案内路、25…収容室、26
…処置具、27…処置具起上台、28…起上台回動支
点、29…誘導面、34…起上ワイヤー、45…突出
部。
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a perspective view showing an entire system incorporating an endoscope and various external devices according to an embodiment of the present invention. FIG. 2 illustrates a distal end portion of an endoscope according to an embodiment of the present invention.
FIG. 4 is a vertical cross-sectional view along a treatment instrument raising table. FIG. 3 is a sectional view of a portion along the line BB in FIG. 2; FIG. 4 is a plan view of a distal end portion of the endoscope according to one embodiment of the present invention. FIG. 5 is a plan view of one state of use of the distal end portion of the endoscope according to one embodiment of the present invention. 6 (a) is a perspective view of a slope portion of the treatment instrument raising stand, and FIG. 6 (b) is a cross-sectional view of the slope portion cut along the X plane shown in FIG. 4 (a). FIG. 7 shows a distal end portion of the endoscope according to one embodiment of the present invention.
FIG. 4 is a longitudinal sectional view cut along the illumination lens and the objective lens. FIG. 8 is a cross-sectional view of a distal end portion of the endoscope according to one embodiment of the present invention. FIG. 9 is a cross-sectional view of a distal end portion of the endoscope according to one embodiment of the present invention. FIG. 10 is a vertical cross-sectional view of the distal end portion of the endoscope according to one embodiment of the present invention, taken along a treatment instrument raising table and showing a raising operation of the treatment instrument raising table. FIG. 11 is a longitudinal sectional view of the distal end portion of the endoscope according to one embodiment of the present invention, cut along the illumination lens and the objective lens. FIG. 12 is a cross-sectional view of a portion along the line DD in FIG. 11; FIG. 13 is a longitudinal sectional view of a bending tube part of the endoscope according to one embodiment of the present invention. FIG. 14 is a distal end portion of an endoscope according to one embodiment of the present invention,
FIG. 4 is a vertical cross-sectional view of an external connection portion of a curved tube portion and a flexible tube portion. FIG. 15 shows a distal end portion of an endoscope according to one embodiment of the present invention,
FIG. 4 is a vertical cross-sectional view of an external connection portion of a curved tube portion and a flexible tube portion. FIG. 16 shows a distal end portion of an endoscope according to one embodiment of the present invention,
The longitudinal section of other types of exterior connection parts of a curved tube part and a flexible tube part. FIG. 17 is a cross-sectional view of an operation unit for illustrating a raising table operation mechanism of the endoscope according to one embodiment of the present invention. FIG. 18 is a cross-sectional view of an operation unit for illustrating a raising table operating mechanism of the endoscope according to one embodiment of the present invention. [Description of Signs] 1 endoscope, 12 insertion section, 13 operation section, 14 universal cord, 15 flexible tube section, 16 bending section, 17
... tip part, 21 ... tip hard part, 22 ... tip cover, 23
... channel, 24 ... introduction guideway, 25 ... accommodation room, 26
... Treatment instrument, 27. Treatment instrument raising table, 28. Lifting table rotation fulcrum, 29. Guide surface, 34. Lifting wire, 45.

Claims (1)

【特許請求の範囲】 【請求項1】 内視鏡の観察光学系が配された挿入部先
端部分に開口して形成された処置具起上台用収容室と、 上記内視鏡の操作部側に設けられ、処置具が挿通される
挿通口と、 上記内視鏡内部に形成され、上記収容室と上記挿通口と
を連通する処置具用案内路と、 上記収容室内に起上操作可能に設けられ、処置具を誘導
する誘導面を有した処置具起上台と、 上記処置具起上台の誘導面の上記観察光学系が配される
側に位置する稜部に突き出して形成され、上記処置具を
上記誘導面に誘導するための突出部とを具備した事を特
徴とする内視鏡。
Claims: 1. An accommodation space for a treatment tool raising base formed to open at a distal end portion of an insertion portion provided with an observation optical system of an endoscope, and an operation unit side of the endoscope. An insertion port through which the treatment tool is inserted, a treatment tool guide path formed inside the endoscope and communicating the storage chamber and the insertion port, and a raising operation into the storage chamber is enabled. A treatment tool raising table having a guiding surface for guiding the treatment tool, and a projection formed on a ridge located on a side of the guiding surface of the treatment tool raising table on which the observation optical system is arranged, and An endoscope comprising: a projection for guiding a tool to the guide surface.
JP2002251718A 2002-08-29 2002-08-29 Endoscope Expired - Fee Related JP3725849B2 (en)

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Application Number Priority Date Filing Date Title
JP2002251718A JP3725849B2 (en) 2002-08-29 2002-08-29 Endoscope

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Application Number Priority Date Filing Date Title
JP2002251718A JP3725849B2 (en) 2002-08-29 2002-08-29 Endoscope

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP20461499A Division JP3806546B2 (en) 1999-07-19 1999-07-19 Endoscope

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JP3725849B2 JP3725849B2 (en) 2005-12-14

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006212278A (en) * 2005-02-04 2006-08-17 Pentax Corp Manufacturing method of insertion flexible tube, insertion flexible tube and endoscope
JP2007159854A (en) * 2005-12-14 2007-06-28 Pentax Corp Insertion part and endoscope
JP2009195456A (en) * 2008-02-21 2009-09-03 Hoya Corp Bend structure of endoscope

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018160811A1 (en) 2017-03-03 2018-09-07 Boston Scientific Scimed, Inc. Device tip

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6393905U (en) * 1986-12-10 1988-06-17
JPH0856900A (en) * 1994-06-13 1996-03-05 Asahi Optical Co Ltd Endoscope

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6393905U (en) * 1986-12-10 1988-06-17
JPH0856900A (en) * 1994-06-13 1996-03-05 Asahi Optical Co Ltd Endoscope

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006212278A (en) * 2005-02-04 2006-08-17 Pentax Corp Manufacturing method of insertion flexible tube, insertion flexible tube and endoscope
JP2007159854A (en) * 2005-12-14 2007-06-28 Pentax Corp Insertion part and endoscope
JP2009195456A (en) * 2008-02-21 2009-09-03 Hoya Corp Bend structure of endoscope

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Publication number Publication date
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