The Challenge of Diagnosing and Managing Pulmonary Arterial Hypertension in Systemic Sclerosis with Interstitial Lung Disease

The Challenge of Diagnosing and Managing Pulmonary Arterial Hypertension in Systemic Sclerosis with Interstitial Lung Disease

Pulmonary hypertension (PH) in patients with Systemic Sclerosis (SSc) may stem from a variety of underlying causes, thus making a correct diagnosis and management difficult. The main challenges lie in the distinction between pulmonary arterial hypertension (PAH, group 1) and PH due to interstitial l...

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Bibliographic Details
Main Authors: Elisabetta Zanatta, Martina Perazzolo Marra, Giulia Famoso, Elisabetta Balestro, Chiara Giraudo, Fiorella Calabrese, Federico Rea, Andrea Doria
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Pharmaceuticals
Subjects:
systemic sclerosis
pulmonary arterial hypertension
interstitial lung disease
Online Access:https://www.mdpi.com/1424-8247/15/9/1042

Internet

https://www.mdpi.com/1424-8247/15/9/1042

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