IDIOPATHIC PULMONARY HILAR FIBROSIS - AN UNUSUAL CAUSE OF PULMONARY-HYPERTENSION

被引：12

作者：

ESPINOSA, RE

EDWARDS, WD

ROSENOW, EC

SCHAFF, HV

机构：

[1] MAYO CLIN ROCHESTER,DIV CARDIOVASC DIS & INTERNAL MED,ROCHESTER,MN

[2] MAYO CLIN ROCHESTER,DIV THORAC & CARDIOVASC SURG,ROCHESTER,MN

[3] MAYO CLIN ROCHESTER,DIV ANAT PATHOL,ROCHESTER,MN

[4] MAYO CLIN ROCHESTER,DIV THORAC DIS & INTERNAL MED,ROCHESTER,MN

来源：

MAYO CLINIC PROCEEDINGS | 1993年 / 68卷 / 08期

关键词：

D O I：

10.1016/S0025-6196(12)60636-3

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

A 37-year-old man with progressive exertional dyspnea had pulmonary hypertension associated with pulmonary arterial and venous obstruction. An autopsy revealed that the cause of death was idiopathic pulmonary hilar fibrosis, a variant of mediastinal fibrosis. Pulmonary hilar fibrosis can mimic thromboembolic pulmonary hypertension, pulmonary veno-occlusive disease, and pulmonary venous hypertension.

引用

页码：778 / 782

页数：5

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