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儿童和青少年克罗恩病手术后的生长、病程及预后

Growth, course, and prognosis after surgery for Crohn's disease in children and adolescents.

作者信息

Homer D R, Grand R J, Colodny A H

出版信息

Pediatrics. 1977 May;59(5):717-25.

PMID:857237
Abstract

Surgery is often performed because of growth failure when Crohn's disease occurs in children and adolescents, but the long-term responses of such therapy are not known. Thirty-seven children and adolescents were followed from 2 to 26 years after resections for Crohn's disease. Twenty-eight patients had disease that involved both the colon and terminal ileum; disease was limited to the small intestine in eight patients and to the stomach in one. At the time of surgery 16 patients were at or below the third percentile for weight and only 16 had reached puberty (all of these were older than 14.5 years). Fourteen patients (11 prepubertal, 3 pubertal) had severe impairment of linear growth; height and was at or below the third percentile or linear growth was absent for more than a year. At the time of the first operation, seven patients had incomplete resections and have had persistent disease. The remaining 30 patients had complete resections as determined by gross and histological criteria. Of these, 12 have had recurrences and 18 have been free of disease. Of the 11 prepubertal patients with preoperative linear growth failure, only two had catch-up growth after surgery. The remaining nine and all of the pubertal patients have either failed to grow or have maintained their height in their preoperative percentile. Catch-up growth after surgery for Crohn's disease occurs only in those children who are operated on before puberty and in whom there is no early recurrence. The recurrence rate for this group of patients was 30%; most recurrences occurred within two years of the initial resection. Growth failure, therefore, may be considered an important indication for surgery in the prepubertal child with Crohn's disease, but it probably is not an indication after onset of puberty.

摘要

儿童和青少年克罗恩病出现生长发育迟缓时通常会进行手术治疗,但这种治疗的长期效果尚不清楚。37例儿童和青少年在因克罗恩病接受切除术后随访了2至26年。28例患者的病变累及结肠和回肠末端;8例患者的病变局限于小肠,1例局限于胃。手术时,16例患者的体重处于或低于第3百分位数,只有16例进入青春期(所有这些患者年龄均超过14.5岁)。14例患者(11例青春期前,3例青春期)存在严重的线性生长障碍;身高处于或低于第3百分位数,或线性生长停滞超过1年。首次手术时,7例患者切除不完全,疾病持续存在。其余30例患者根据大体和组织学标准进行了完整切除。其中,12例复发,18例无疾病复发。11例术前有线性生长障碍的青春期前患者中,术后只有2例实现了追赶生长。其余9例以及所有青春期患者术后要么没有生长,要么身高维持在术前的百分位数。克罗恩病手术后的追赶生长仅发生在青春期前接受手术且无早期复发的儿童中。该组患者的复发率为30%;大多数复发发生在初次切除后的两年内。因此,生长发育迟缓可能被视为青春期前克罗恩病患儿手术的重要指征,但青春期后可能并非手术指征。

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