韩国儿童结肠息肉病的临床、内镜及病理表现

M. Lim, J. Seo, J. Ko, H. Yang, G. Kang, W. Kim
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引用次数: 3

摘要

目的:结肠息肉病在儿童中较少见。有关儿童结肠息肉病的临床资料有限。结肠息肉病患儿的并发症包括大量息肉、息肉的恶性转化和肠外肿瘤。我们研究了韩国儿童结肠息肉病的临床谱、内镜特征和组织学表现。方法:回顾性分析1987 ~ 2009年37例儿童多发性结肠息肉的临床资料。诊断结肠息肉病时的平均年龄为8.0±3.2岁。结果:Peutz-Jeghers综合征22例,少年性息肉病综合征7例,家族性腺瘤性息肉病6例,淋巴样息肉病2例。儿童结肠息肉病最常见的临床表现是便血。7例患儿有结肠息肉病家族史。结肠息肉病的结肠镜检查结果随息肉的大小和数量而变化。Peutz-Jeghers综合征患儿息肉多呈多小叶状和带梗。儿童期息肉病综合征的息肉以圆形和带足为主。对于FAP患儿,结肠被小的、无根的息肉覆盖。淋巴样息肉病患者有多发无根性息肉。手术切除息肉14例(38%)。13例患儿(35%)行肠段切除术。4例FAP患者行全结肠切除术。四名患有Peutz-Jeghers综合征的儿童患有肠外肿瘤。未发现息肉的恶性转化。结论:结肠息肉病患儿应进行仔细的初步评估,并定期重新评估。韩国儿科胃肠病学杂志2010;13: 154∼163)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical, Endoscopic and Pathologic Findings of Colonic Polyposis in Korean Children
Purpose: Colonic polyposis is less common in children than in adults. The clinical data pertaining to colonic polyposis in children are limited. Children with colonic polyposis have complications associated with numerous polyps, malignant transformation of the polyps, and extraintestinal neoplasms. We studied the clinical spectrum, endoscopic characteristics, and histologic findings of colonic polyposis in Korean children. Methods: We reviewed the clinical data of 37 children with multiple colonic polyps between 1987 and 2009. The mean age at the time of diagnosis of colonic polyposis was 8.0±3.2 years. Results: Peutz-Jeghers syndrome, juvenile polyposis syndrome, familial adenomatous polyposis (FAP), and lymphoid polyposis was diagnosed in 22, 7, 6, and 2 children, respectively. The most common clinical presentation in children with colonic polyposis was hematochezia. A family history of colonic polyposis was noted in 7 children. The colonoscopic findings of colonic polyposis varied with the size and number of polyps. The majority of polyps were multi-lobulatd and pedunculated in children with Peutz-Jeghers syndrome. The polyps in children with juvenile polyposis syndrome were primarily round and pedun- culated. For the children with FAP, the colon was carpeted with small, sessile polyps. There were multiple sessile polyps in the patients with lymphoid polyposis. Surgical polypectomy was performed in 14 children (38%). Intestinal segmental resection was performed in 13 children (35%). Four patients with FAP underwent total colectomy. Four children with Peutz-Jeghers syndrome had extraintestinal neoplasms. No malignant transformation of polyp was identified. Conclusion: Children with colonic polyposis should undergo a careful initial evaluation and require periodic re-evaluation. (Korean J Pediatr Gastroenterol Nutr 2010; 13: 154∼163)
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