Total colonic Hirschsprung's disease: a 28-year experience

被引:78
作者
Wildhaber, BE [1 ]
Teitelbaum, DH [1 ]
Coran, AG [1 ]
机构
[1] Univ Michigan, Sch Med, CH Mott Childrens Hosp, Sect Pediat Surg, Ann Arbor, MI 48109 USA
关键词
total colonic Hirschsprung's disease; endorectal pull-through;
D O I
10.1016/j.jpedsurg.2004.09.033
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: The aim of this study was to review outcomes after surgical treatment of total colonic Hirschsprung's disease ITCH). Methods: Twenty-five records of patients with TCH treated between 1974 and 2002 were reviewed. Follow-up data were collected using a standardized questionnaire. Objective functional outcome was assessed using a scoring system. Results: Twenty patients had aganglionosis of the colon and distal ileum, 5 of whom had a more extensive condition. One of these 5 patients underwent an endorectal pull-through (ERPT), I underwent intestinal transplantation, and 3 died. Four of the remaining 20 patients underwent a primary ERPT, 16 received a stoma as neonates followed by ERPT in 12, and a Martin-Duhamel procedure or Swenson's operation in 3 (median age, 10.5 months); I remains with an ostomy. Postoperative complications included enterocolitis (55%), anal stricture (25%), and perineal excoriation (20%). Mean follow-up were 17.5 years (+/-11.1 years). Eighty-nine percent were free of recurrent enterocolitis. Frequency of bowel movements is I to 5 per day in 82% of the patients, 18% have 6 or more bowel movements per day. Occasional soiling is noted in 40% (one third of those requiring nighttime diapers). Overall functional outcome was good in 83%. Those patients with the longest follow-up periods had the best stooling scores (P = .04). Conclusions: Surgical treatment of TCH is associated with a number of complications including recurrent enterocolitis and anal strictures. Long-term outcome is quite favorable. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:203 / 206
页数:4
相关论文
共 14 条
[1]   SURGICAL MANAGEMENT OF TOTAL COLONIC AND PARTIAL SMALL INTESTINAL AGANGLIONOSIS [J].
CORAN, AG ;
BJORDAL, R ;
EEK, S ;
KNUTRUD, O .
JOURNAL OF PEDIATRIC SURGERY, 1969, 4 (05) :531-+
[2]   Recent advances in the management of Hirschsprung's disease [J].
Coran, AG ;
Teitelbaum, DH .
AMERICAN JOURNAL OF SURGERY, 2000, 180 (05) :382-387
[3]   ENTEROCOLITIS ASSOCIATED WITH HIRSCHSPRUNGS-DISEASE - A CLINICAL RADIOLOGICAL CHARACTERIZATION BASED ON 168 PATIENTS [J].
ELHALABY, EA ;
CORAN, AG ;
BLANE, CE ;
HIRSCHL, RB ;
TEITELBAUM, DH .
JOURNAL OF PEDIATRIC SURGERY, 1995, 30 (01) :76-83
[4]   Long-term morbidity in total colonic aganglionosis [J].
Hoehner, JC ;
Ein, SH ;
Shandling, B ;
Kim, PCW .
JOURNAL OF PEDIATRIC SURGERY, 1998, 33 (07) :961-965
[5]   More than 10 years' follow-up of total colonic aganglionosis - Severe iron deficiency anemia and growth retardation [J].
Ikawa, H ;
Masuyama, H ;
Hirabayashi, T ;
Endo, M ;
Yokoyama, J .
JOURNAL OF PEDIATRIC SURGERY, 1997, 32 (01) :25-27
[6]  
JORDAN FT, 1981, ANN SURG, V194, P70, DOI 10.1097/00000658-198107000-00012
[7]   MORBIDITY ASSOCIATED WITH TOTAL COLON HIRSCHSPRUNGS-DISEASE [J].
LEVY, M ;
REYNOLDS, M .
JOURNAL OF PEDIATRIC SURGERY, 1992, 27 (03) :364-367
[8]   Hirschsprung's disease: functional and psychological follow up comparing total colonic and rectosigmoid aganglionosis [J].
Ludman, L ;
Spitz, L ;
Tsuji, H ;
Pierro, A .
ARCHIVES OF DISEASE IN CHILDHOOD, 2002, 86 (05) :348-351
[9]   AGANGLIONOSIS AND RELATED DISORDERS [J].
QUALMAN, SJ ;
MURRAY, R .
HUMAN PATHOLOGY, 1994, 25 (11) :1141-1149
[10]  
RESCORLA FJ, 1992, ARCH SURG-CHICAGO, V127, P934