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赫尔曼斯基-普德拉克综合征

The Hermansky-Pudlak syndrome.

作者信息

Parker M S, Rosado Shipley W, de Christenson M L, Slutzker A D, Carroll F E, Worrell J A, White J G

机构信息

University of Texas Southwestern Medical Center at Dallas, Department of Diagnostic Radiology 75235, USA.

出版信息

Ann Diagn Pathol. 1997 Dec;1(2):99-103. doi: 10.1016/s1092-9134(97)80014-7.

Abstract

Hermansky-Pudlak Syndrome (HPS) is a rare, inheritable disorder characterized by the classic triad of oculo-cutaneous albinism, platelet dysfunction, and ceroid deposition. An associated complication is pulmonary fibrosis with progressive restrictive lung disease. This report discusses the lung involvement often seen in this condition correlated with radiography, computed tomography, high-resolution computed tomography, and the underlying pathology, by means of two such afflicted siblings. The elder died of respiratory failure while awaiting lung transplantation. The younger sibling is currently undergoing evaluation for transplantation.

摘要

赫尔曼斯基-普德拉克综合征(HPS)是一种罕见的遗传性疾病,其特征为眼皮肤白化病、血小板功能障碍和类蜡样脂褐质沉积这一典型三联征。一种相关并发症是伴有进行性限制性肺病的肺纤维化。本报告通过两名患此病的同胞兄妹,探讨了这种疾病中常见的肺部受累情况与X线摄影、计算机断层扫描、高分辨率计算机断层扫描以及潜在病理学之间的关系。年长的同胞兄妹在等待肺移植时死于呼吸衰竭。年幼的同胞兄妹目前正在接受移植评估。

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