Comparison of longstanding pediatric-onset and adult-onset Crohn's disease

被引:42
作者
Freeman, HJ [1 ]
机构
[1] Univ British Columbia Hosp, Dept Med Gastroenterol, Vancouver, BC V6T 1WS, Canada
关键词
clinical behavior of Crohn's disease; Crohn's disease; granulomatous colitis; natural history of Crohn's disease; vienna classification;
D O I
10.1097/00005176-200408000-00011
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: Limited information is available on the characteristics of longstanding Crohn's disease with onset in childhood or adolescence. Materials and Methods: In this retrospective study, 224 patients with pediatric-onset Crohn's disease were compared to a group of patients with disease diagnosed as adults. Results: More than 50% of the patients in the pediatric-onset group were followed for more than a decade, with a mean follow-up of 12.2 years. There were 96 male (42.9%) and 128 female (57.1%) patients. Most had disease diagnosed in adolescence. The female predominance, similar to adult-onset disease, was noted only among patients with disease diagnosed in adolescence (13-19 years), not in childhood. Disease most often involved both ileum and colon (128 of 224; 57.1%). Isolated ileal or colonic disease was less common. Upper gastrointestinal tract disease was present in 42 of 224 (18.8%) patients. The incidence of strictures (28.6%) and penetrating complications (46.4%) was similar to that of adults followed for the same period of time. Conclusion: In pediatric-onset Crohn's disease, female-predominance emerges during adolescence. Pediatric-onset disease is more extensive than adult-onset disease. When followed for an extended period of time, it has high rates of disease complexity, with strictures and penetrating complications similar to adult-onset disease. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:183 / 186
页数:4
相关论文
共 25 条
[1]   Adult height in patients with early onset of Crohn's disease [J].
Alemzadeh, N ;
Rekers-Mombarg, LTM ;
Mearin, ML ;
Wit, JM ;
Lamers, CBHW ;
van Hogezand, RA .
GUT, 2002, 51 (01) :26-29
[2]   The genetics of inflammatory bowel disease [J].
Bonen, DK ;
Cho, JH .
GASTROENTEROLOGY, 2003, 124 (02) :521-536
[3]   The immunological and genetic basis of inflammatory bowel disease [J].
Bouma, G ;
Strober, W .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (07) :521-533
[4]   INCREASED RISK OF INFLAMMATORY BOWEL-DISEASE ASSOCIATED WITH ORAL-CONTRACEPTIVE USE [J].
BOYKO, EJ ;
THEIS, MK ;
VAUGHAN, TL ;
NICOLBLADES, B .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1994, 140 (03) :268-278
[5]   Defining complex contributions of NOD2/CARD15 gene mutations, age at onset, and tobacco use on Crohn's disease phenotypes [J].
Brant, SR ;
Picco, MF ;
Achkar, JP ;
Bayless, TM ;
Kane, SV ;
Brzezinski, A ;
Nouvet, FJ ;
Bonen, D ;
Karban, A ;
Dassopoulos, T ;
Karaliukas, R ;
Beaty, TH ;
Hanauer, SB ;
Duerr, RH ;
Cho, JH .
INFLAMMATORY BOWEL DISEASES, 2003, 9 (05) :281-289
[6]  
BURBIGE EJ, 1975, PEDIATRICS, V55, P866
[7]  
COOKE WT, 1980, Q J MED, V49, P363
[8]   CHRONIC REGIONAL ENTEROCOLITIS (MB CROHN) IN CHILDREN AND ADOLESCENTS [J].
EHRENPREIS, T ;
GIERUP, J ;
LAGERCRANTZ, R .
ACTA PAEDIATRICA SCANDINAVICA, 1971, 60 (02) :209-+
[9]   PROGNOSIS OF CROHNS-DISEASE WITH ONSET IN CHILDHOOD OR ADOLESCENCE [J].
FARMER, RG ;
MICHENER, WM .
DIGESTIVE DISEASES AND SCIENCES, 1979, 24 (10) :752-757
[10]   Natural history and clinical behavior of Crohn's disease extending beyond two decades [J].
Freeman, HJ .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2003, 37 (03) :216-219