• Presse Med · Apr 2021

    Review

    PULMONARY ARTERIAL HYPERTENSION IN SYSTEMIC SCLEROSIS.

    • Benoît Lechartier and Marc Humbert.
    • Lausanne University Hospital, Department of Respiratory Medicine, Lausanne, Switzerland.
    • Presse Med. 2021 Apr 1; 50 (1): 104062.

    AbstractPulmonary arterial hypertension (PAH) is a frequent and severe complication of systemic sclerosis (SSc) due to combined vasculopathy and fibrogenesis. Early diagnosis and treatment are highly challenging in SSc-PAH and require referral to an expert PAH centre. Diagnostic algorithms evolved in the last decade. Novel therapeutic options notably targeting pulmonary vascular remodeling are needed.Copyright © 2021 Elsevier Masson SAS. All rights reserved.

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