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节段性高安(巨细胞)主动脉炎伴破裂及局限性夹层形成。

Segmental Takayasu (giant cell) aortitis with rupture and limited dissection.

作者信息

Lie J T

机构信息

Department of Pathology, Mayo Clinic, Rochester, MN 55905.

出版信息

Hum Pathol. 1987 Nov;18(11):1183-5. doi: 10.1016/s0046-8177(87)80389-1.

Abstract

Takayasu arteritis is a chronic inflammatory disease of the aorta and its main branches, with variable extents of involvement. Rarely is it sharply localized in an isolated segment of the aorta, and it seldom occurs in an elderly person. Clinically, Takayasu arteritis produces symptoms of vascular insufficiency, predominantly because of the occlusive disease and less commonly because of aneurysmal disease of the affected arteries. An unusual case of segmental Takayasu arteritis confined to the infrarenal abdominal aorta in an elderly woman is described, in which rupture and fatal hemoperitoneum were the initial manifestations of the disease.

摘要

高安动脉炎是一种累及主动脉及其主要分支的慢性炎症性疾病,受累范围不一。该病极少局限于主动脉的单个节段,且很少发生于老年人。临床上,高安动脉炎主要因受累动脉的闭塞性病变而非动脉瘤性病变引发血管功能不全症状。本文描述了一例罕见的老年女性节段性高安动脉炎病例,病变局限于肾下腹主动脉,其最初表现为主动脉破裂和致命性腹腔积血。

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