
When you hear hoofbeats, think zebras – pulmonary veno‐occlusive disease: A case report
Author(s) -
Scelsi Laura,
Lanzillo Giuseppe,
Arbustini Eloisa,
D'Armini Andrea,
Greco Alessandra,
Meloni Federica,
Turco Annalisa,
Valentini Adele,
Oltrona Visconti Luigi,
Ghio Stefano
Publication year - 2022
Publication title -
pulmonary circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.791
H-Index - 40
ISSN - 2045-8940
DOI - 10.1002/pul2.12095
Subject(s) - medicine , pulmonary veno occlusive disease , pulmonary hypertension , disease , pathology , consanguinity , cardiology , pediatrics
Pulmonary veno‐occlusive disease (PVOD) is a rare disease. It may be idiopathic or associated, in particular, with connective tissue disease, or it may develop after radiation exposure; in heritable forms of PVOD, the inheritance is autosomal recessive due to the presence of homozygous or compound heterozygous pathogenic variants in the EIF2AK4 gene. We describe the case of a young man whose PVOD was initially misdiagnosed as chronic thromboembolic pulmonary hypertension despite worsening after riociguat, nonspecific computed tomography pulmonary angiogram findings, and parental consanguinity could suggest an autosomal recessive disease. The correct diagnosis and the correct treatment are crucial given the high mortality rate of this disease.