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先天性胸骨裂。1例罕见病例报告。

Congenital bifid sternum. Report of an unusual case.

作者信息

Teitelbaum S A, Fonkalsrud E W

机构信息

Department of Surgery, UCLA School of Medicine 90024.

出版信息

J Thorac Cardiovasc Surg. 1988 Jul;96(1):162-5.

PMID:3290586
Abstract

This article presents the case of a child with an unusual type of cleft sternum characterized by fusion superiorly between the clavicles and inferiorly at the xiphoid with wide intervening separation. The defect was successfully corrected at age 17 months by surgical closure of the cleft primarily, which had not been achieved previously in a patient at this late age.

摘要

本文介绍了一名患有特殊类型胸骨裂的儿童病例,其特征为锁骨上方和剑突下方融合,中间有较宽的间隙。该缺陷在17个月大时通过一期手术闭合裂隙成功矫正,此前在这个年龄较大的患者中尚未实现过。

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