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肠道肌肉组织缺失:该病变胚胎起源的解剖学证据。

Absent intestinal musculature: anatomic evidence of an embryonic origin of the lesion.

作者信息

McCarthy D W, Qualman S, Besner G E

机构信息

Department of Surgery, Columbus Children's Hospital, OH 43205.

出版信息

J Pediatr Surg. 1994 Nov;29(11):1476-8. doi: 10.1016/0022-3468(94)90148-1.

Abstract

Absent intestinal musculature is a rare entity of uncertain etiology. The diagnosis is confirmed histologically by segmental absence of the intestinal muscularis. The remaining layers of the bowel wall are completely intact, and notably absent are significant inflammation and hemorrhage. The authors report two cases of segmental absence of intestinal musculature presenting as perforations. There was gross or microscopic evidence of diverticula formation at sites of perforation and absent muscle. Based on the anatomic evidence in these specimens and a review of the surgical literature, we propose that the etiology is based on embryologic diverticuli.

摘要

肠道肌肉组织缺失是一种病因不明的罕见病症。通过肠道肌层节段性缺失的组织学检查来确诊。肠壁的其余各层完全完整,且明显不存在显著炎症和出血。作者报告了两例以穿孔形式表现的肠道肌肉组织节段性缺失病例。在穿孔部位和肌肉缺失处有肉眼可见或显微镜下可见的憩室形成证据。基于这些标本中的解剖学证据以及对外科文献的回顾,我们提出病因是胚胎性憩室。

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