Idiopathic Pulmonary Hilar Fibrosis: An Unusual Cause of Pulmonary Hypertension

RAUL E. ESPINOSA; WILLIAM D. EDWARDS; EDWARD C. ROSENOW; HARTZELL V. SCHAFF

doi:10.1016/S0025-6196(12)60636-3

Idiopathic Pulmonary Hilar Fibrosis: An Unusual Cause of Pulmonary Hypertension

RAUL E. ESPINOSA, WILLIAM D. EDWARDS, EDWARD C. ROSENOW, HARTZELL V. SCHAFF

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Abstract

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.

Original language	English (US)
Pages (from-to)	778-782
Number of pages	5
Journal	Mayo Clinic proceedings
Volume	68
Issue number	8
DOIs	https://doi.org/10.1016/S0025-6196(12)60636-3
State	Published - 1993

ASJC Scopus subject areas

Medicine(all)

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10.1016/S0025-6196(12)60636-3

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title = "Idiopathic Pulmonary Hilar Fibrosis: An Unusual Cause of Pulmonary Hypertension",

abstract = "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.",

author = "ESPINOSA, {RAUL E.} and EDWARDS, {WILLIAM D.} and ROSENOW, {EDWARD C.} and SCHAFF, {HARTZELL V.}",

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AU - ROSENOW, EDWARD C.

AU - SCHAFF, HARTZELL V.

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N2 - 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.

AB - 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.

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Idiopathic Pulmonary Hilar Fibrosis: An Unusual Cause of Pulmonary Hypertension

Abstract

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