Virdi Verinderjit S, Cheema Ajaiwant S
Trop Gastroenterol. 2003 Apr-Jun;24(2):99-101.
Intestinal perforation as a presentation of Hirschsprung disease is rare, occurring mostly in infants less than 3 months of age, usually those with long-segment disease. Hirschsprung disease may also be associated with other anomalies, that complicate the management and prognosis. Identifying Hirschsprung disease as a cause of perforation will thus help in deciding the site of colostomy and looking for associated anomalies. We report a case of Hirschsprung disease with multiple intestinal perforations and bilateral multicystic kidney disease.
肠穿孔作为先天性巨结肠病的一种表现较为罕见，主要发生在3个月以下的婴儿，通常是患有长段型疾病的婴儿。先天性巨结肠病也可能与其他异常相关，这会使治疗和预后变得复杂。因此，将先天性巨结肠病确定为穿孔的原因有助于决定结肠造口术的位置并寻找相关异常。我们报告一例患有多处肠穿孔和双侧多囊肾病的先天性巨结肠病病例。
