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Translate this page into:

Case Report
01 (
03
); 029-032
doi:
10.1055/s-0038-1656477

Idopathic Pulmonary Hypertension Mimicking Pulmonary Veno-Occlusive Disease – A Case Report.

Resident, Department of Cardiology, NIMS, India
Resident, Department of Cardiology, NIMS, India
Address for correspondence nagendra.kulari@gmail.com
Licence
This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Disclaimer:
This article was originally published by Thieme Medical and Scientific Publishers Private Ltd. and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Abstract

PVOD is rare cause of pulmonary artery hypertension which is associated with worse prognosis and limited treatment options apart from lung transplantation. Differentiating IPAH patients from PVOD is sometimes difficult relying on catheterization data alone. But differentiation between these two diseases is important as there are many evolved treatment options for IPAH. Here we are reporting a case of IPAH where catheterization data shows conflicting results which on further evaluation diagnosis confirmed as idiopathic pulmonary hypertension.


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