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先天性右侧膈疝合并肺叶外肺隔离症,通过后外侧和前外侧缺损:一例报告

Congenital right diaphragmatic hernias through posterolateral and anterolateral defects associated with extralobar pulmonary sequestration: a case report.

作者信息

Urushihara N, Nakagawa Y, Kawashima K, Fukazawa T, Watanabe Y, Todani T

机构信息

Department of Pediatric Surgery, National Iwakunt Hospital, Yamaguchi, Japan.

出版信息

J Pediatr Surg. 1997 Jan;32(1):101-2. doi: 10.1016/s0022-3468(97)90106-8.

Abstract

Multiple diaphragmatic hernias in the unilateral diaphragm are extremely rare. The authors report a neonate with diaphragmatic hernias through two defects in the right diaphragm: a posterolateral defect without a hernia sac and an anterolateral defect with one. After excision of the anterolateral hernia sac, each defect was closed. Histology studies showed extralobar pulmonary sequestration in the removed hernia sac. The presence of sequestrated pulmonary tissue indicates the possibility of interference with the closure of the pleuroperitoneal canal and muscularization in the diaphragm, which may result in multiple defects.

摘要

单侧膈肌出现多个膈疝极为罕见。作者报告了一名患有膈疝的新生儿,其右侧膈肌存在两个缺损:一个是无疝囊的后外侧缺损,另一个是有疝囊的前外侧缺损。切除前外侧疝囊后,分别对每个缺损进行了修补。组织学研究显示,切除的疝囊中存在肺叶外隔离症。隔离肺组织的存在表明,其可能干扰胸膜腹膜管的闭合以及膈肌的肌化,进而可能导致多个缺损。

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