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肺毛细血管血管瘤病:临床病理回顾

Pulmonary capillary hemangiomatosis: a clinicopathologic review.

作者信息

Eltorky M A, Headley A S, Winer-Muram H, Garrett H E, Griffin J P

机构信息

Department of Pathology, University of Tennessee, Memphis 38163.

出版信息

Ann Thorac Surg. 1994 Mar;57(3):772-6. doi: 10.1016/0003-4975(94)90595-9.

Abstract

Pulmonary capillary hemangiomatosis is a locally aggressive benign vascular neoplasm of the lung characterized by the presence of numerous cytologically benign thin-walled capillary-sized blood vessels proliferating diffusely through the pulmonary interstitium, in and around pulmonary vessels and airways. Pulmonary capillary hemangiomatosis is a rare disease characterized by pulmonary hypertension and a slowly progressive clinical course; it is frequently misdiagnosed clinically as primary pulmonary hypertension and veno-occlusive disease. The purpose of this review is to describe the clinical, radiologic, and histologic features of this rare form of pulmonary vascular neoplasm, which may present considerable diagnostic problems to both the clinician and the histopathologist. Fourteen cases of pulmonary capillary hemangiomatosis have been previously reported. In this review we describe the fourth case of pulmonary capillary hemangiomatosis in which the diagnosis was made antemortem, as well as the fourth to undergo lung transplantation.

摘要

肺毛细血管瘤病是一种具有局部侵袭性的肺良性血管肿瘤,其特征是存在大量细胞学上良性的薄壁毛细血管大小的血管,这些血管在肺间质、肺血管内及周围以及气道中弥漫性增殖。肺毛细血管瘤病是一种罕见疾病,其特征为肺动脉高压和缓慢进展的临床病程;临床上常被误诊为原发性肺动脉高压和静脉闭塞性疾病。本综述的目的是描述这种罕见的肺血管肿瘤的临床、放射学和组织学特征,这可能给临床医生和组织病理学家带来相当大的诊断难题。此前已报道过14例肺毛细血管瘤病病例。在本综述中,我们描述了第4例生前确诊的肺毛细血管瘤病病例,也是第4例接受肺移植的病例。

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