Department of Surgery, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
J Pediatr Surg. 2012 Aug;47(8):1566-71. doi: 10.1016/j.jpedsurg.2012.01.002.
Segmental absence of the intestinal musculature (SAIM) is a known but clinically rare entity involving partial or complete absence of the intestinal muscularis propria. Clinical presentation is consistent with peritonitis, and treatment involves an emergent laparotomy, bowel resection, and reanastamosis or possible ostomy creation. Diagnosis results from histopathologic evaluation of the resected intestinal specimen. Most of the publications are case reports.
We retrospectively reviewed all surgical pathology files at a tertiary pediatric hospital from 2003 to 2010, identifying children who were noted to have absence of intestinal musculature on pathology. Patients meeting criteria were reviewed in detail, and data regarding clinical presentation, diagnostic testing, radiologic findings, treatment, and outcome were recorded.
Five patients were identified between 2003 and 2010 who received the diagnosis of SAIM. Patient age ranged from 1 to 99 days of life. All children were born preterm by cesarean section, had a mean birth weight of 828 ± 338 g, and were intubated after birth.
The 5 patients presented are reviewed and contrasted with previous cases presented in the literature. Theories of pathogenesis and classification are discussed, and the cases are labeled as primary versus secondary SAIM.
肠肌段缺失(SAIM)是一种已知但临床上罕见的疾病,涉及肠固有肌层的部分或完全缺失。临床表现与腹膜炎一致,治疗方法包括紧急剖腹手术、肠切除、再吻合或可能的造口术。诊断结果来自切除肠标本的组织病理学评估。大多数出版物都是病例报告。
我们回顾了 2003 年至 2010 年在一家三级儿科医院的所有外科病理学档案,确定了在病理学上有肠肌缺失的儿童。详细回顾符合标准的患者,并记录有关临床表现、诊断测试、影像学发现、治疗和结果的数据。
2003 年至 2010 年间,共诊断出 5 例 SAIM 患者。患者年龄为 1 至 99 天。所有儿童均通过剖宫产早产,出生体重平均为 828±338g,出生后插管。
对 5 例患者进行了回顾,并与文献中报道的以往病例进行了对比。讨论了发病机制和分类的理论,并将这些病例标记为原发性和继发性 SAIM。