临床小儿外科杂志
臨床小兒外科雜誌
림상소인외과잡지
JOURNAL OF CLINICAL FEDIATRIC SURGERY
2015年
4期
284-286
,共3页
杨利静%杨合英%贾佳%张大%王家祥%李延安%朱永亮
楊利靜%楊閤英%賈佳%張大%王傢祥%李延安%硃永亮
양리정%양합영%가가%장대%왕가상%리연안%주영량
Hirschsprung 病%外科手术%婴儿,新生
Hirschsprung 病%外科手術%嬰兒,新生
Hirschsprung 병%외과수술%영인,신생
Hirschsprung Disease%Surgical Procedures,Operative%Infant,Newborn
目的:探讨新生儿期疑诊先天性巨结肠的诊断与治疗选择。方法回顾性分析2010年12月至2014年3月我们收治的116例新生儿期疑诊为先天性巨结肠患儿的临床资料。其中10例确诊为先天性巨结肠后于新生儿期行巨结肠根治术;94例先予清洁回流灌肠,症状缓解者,教会家长清洁回流灌肠或扩肛等保守治疗措施后出院,3个月后复查,其中28例排便正常,获痊愈,60例症状未缓解者经确诊后行巨结肠根治术,6例失随访;12例新生儿期清洁回流灌肠效果不佳,一期行肠造瘘术,二期行巨结肠根治术。结果116例疑诊先天性巨结肠患儿中,随访110例,随访率为94.8%,获随访病例中,82例经手术治疗痊愈,28例经保守治疗痊愈;12例大便次数多,伴肛周糜烂,2例排便困难,1例肛门狭窄,1例偶有污粪。结论对新生儿期疑诊为先天性巨结肠患儿,可先行清洁回流灌肠、扩肛等保守治疗,3个月后明确诊断者再择期手术治疗。对长段型或全结肠型巨结肠经回流灌肠等治疗效果不佳者,可先行一期肠造瘘术,二期行巨结肠根治术。
目的:探討新生兒期疑診先天性巨結腸的診斷與治療選擇。方法迴顧性分析2010年12月至2014年3月我們收治的116例新生兒期疑診為先天性巨結腸患兒的臨床資料。其中10例確診為先天性巨結腸後于新生兒期行巨結腸根治術;94例先予清潔迴流灌腸,癥狀緩解者,教會傢長清潔迴流灌腸或擴肛等保守治療措施後齣院,3箇月後複查,其中28例排便正常,穫痊愈,60例癥狀未緩解者經確診後行巨結腸根治術,6例失隨訪;12例新生兒期清潔迴流灌腸效果不佳,一期行腸造瘺術,二期行巨結腸根治術。結果116例疑診先天性巨結腸患兒中,隨訪110例,隨訪率為94.8%,穫隨訪病例中,82例經手術治療痊愈,28例經保守治療痊愈;12例大便次數多,伴肛週糜爛,2例排便睏難,1例肛門狹窄,1例偶有汙糞。結論對新生兒期疑診為先天性巨結腸患兒,可先行清潔迴流灌腸、擴肛等保守治療,3箇月後明確診斷者再擇期手術治療。對長段型或全結腸型巨結腸經迴流灌腸等治療效果不佳者,可先行一期腸造瘺術,二期行巨結腸根治術。
목적:탐토신생인기의진선천성거결장적진단여치료선택。방법회고성분석2010년12월지2014년3월아문수치적116례신생인기의진위선천성거결장환인적림상자료。기중10례학진위선천성거결장후우신생인기행거결장근치술;94례선여청길회류관장,증상완해자,교회가장청길회류관장혹확항등보수치료조시후출원,3개월후복사,기중28례배편정상,획전유,60례증상미완해자경학진후행거결장근치술,6례실수방;12례신생인기청길회류관장효과불가,일기행장조루술,이기행거결장근치술。결과116례의진선천성거결장환인중,수방110례,수방솔위94.8%,획수방병례중,82례경수술치료전유,28례경보수치료전유;12례대편차수다,반항주미란,2례배편곤난,1례항문협착,1례우유오분。결론대신생인기의진위선천성거결장환인,가선행청길회류관장、확항등보수치료,3개월후명학진단자재택기수술치료。대장단형혹전결장형거결장경회류관장등치료효과불가자,가선행일기장조루술,이기행거결장근치술。
Objetive To discuss the choice of operative time for neonatal Hirschsprung 's Disease. Methods A retrospective analysis was given to 1 1 6 cases of children suspected with neonatal Hirschsprung's Disease admitted in the first affiliated hospital of zhengzhou university from December 201 0 to March 201 4.1 0 cases underwent megacolon radical operation immediately;94 cases received the clean reflux enema,after 3 months,symptoms in 28 cases have improved,60 cases underwent megacolon radical operation routinely.6 ca-ses lost follow-up.Due to the dissatisfactory of clean reflux enema,1 2 cases received one-stage intestinal colos-tomy and two-stage megacolon radical operation then.Results 1 1 0 cases of all 1 1 6 cases (94.8%)were giv-en follow-up.82 cases were cured by surgery,28 cases were cured by the support treatment,increased defecate frequency was found in 1 2 cases,defecation difficulty in 2 cases,anal stricture in 1 cases,and fecal inconti-nence in 1 cases. Conclusions Symptoms of children suspected with congenital megacolon in neonatal period are not typical.Patients may have their symptoms improved after receiving 3 months’auxiliary treatment,or their symptoms remain until receiving surgery.If the treatment effect of enema of long or total colonic aganglionosis is not satisfactory,they may receive one-stage intestinal colostomy and two-stage megacolon radical operation.