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高安动脉炎与降主动脉及腹主动脉先天性缩窄:批判性综述

Takayasu's arteritis and congenital coarctation of the descending thoracic and abdominal aorta: a critical review.

作者信息

Lande A

出版信息

AJR Am J Roentgenol. 1976 Aug;127(2):227-33. doi: 10.2214/ajr.127.2.227.

Abstract

A critical reappraisal of the clinical, arteriographic, and pathologic features of Takayasu's arteritis and so-called congenital aortic coarctations at atypical sites is presented. It is concluded that as an isolated cardiovascular abnormality, cases of atypical congenital coarctations of the descending thoracic and abdominal aorta are probably rare. The majority of atypical aortic coarctations previously reported in the United States and Europe as congenital lesions apparently represent unrecognized cases of Takayasu's arteritis.

摘要

本文对高安动脉炎以及非典型部位所谓先天性主动脉缩窄的临床、血管造影和病理特征进行了批判性重新评估。得出的结论是,作为一种孤立的心血管异常,降主动脉和腹主动脉非典型先天性缩窄的病例可能很少见。在美国和欧洲,先前作为先天性病变报道的大多数非典型主动脉缩窄显然代表了未被识别的高安动脉炎病例。

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