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[胸腹肠重复畸形。病例报告]

[Thoraco-abdominal intestinal duplications. Case report].

作者信息

Schwöbel M G, Uhlschmid G

出版信息

Schweiz Med Wochenschr. 1982 Apr 17;112(16):571-5.

PMID:7079697
Abstract

The case of a 22-year-old patient with a thoracoabdominal duplication of the alimentary tract is described. The chest radiograph, with a large cyst in the posterior mediastinum and vertebral abnormalities and a barium swallow showing the abdominal part of the duplication, were diagnostic. At operation a malrotation of the midgut was found and the duplication was resected, leaving esophagus and small bowel intact. An explanation for association of the two malformations - vertebral abnormalities and malrotation - was sought in the literature, particularly that concerning embryogenesis. The following conclusions were reached: 1. Duplications of the alimentary tract are a heterogeneous group with three different embryological faults in development. 2. According to the so-called notochordal theory, vertebral abnormalities and malrotation of the midgut are usual and should be expected in thoracoabdominal duplications of the alimentary tract.

摘要

本文描述了一名22岁患有胸腹部消化道重复畸形患者的病例。胸部X光片显示后纵隔有一个大囊肿且伴有椎体异常,吞钡检查显示了重复畸形的腹部部分,这些检查具有诊断意义。手术中发现中肠旋转不良,切除了重复畸形部分,食管和小肠保持完整。在文献中,特别是关于胚胎发生学的文献中,寻找了两种畸形(椎体异常和旋转不良)关联的解释。得出以下结论:1. 消化道重复畸形是一组异质性疾病,在发育过程中有三种不同的胚胎学缺陷。2. 根据所谓的脊索理论,椎体异常和中肠旋转不良在胸腹部消化道重复畸形中很常见,应该预料到。

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引用本文的文献

1
Thoracoabdominal duplication accompanied by intestinal malrotation: a case report and literature review of a rare congenital anomaly in an infant.胸腹重复畸形伴肠旋转不良:一例婴儿罕见先天性异常的病例报告及文献综述
Ann Med Surg (Lond). 2024 Jan 10;86(2):1166-1172. doi: 10.1097/MS9.0000000000001654. eCollection 2024 Feb.