Novel AGL variants in a patient with glycogen storage disease type IIIb and pulmonary hypertension caused by pulmonary veno-occlusive disease: A case report [PDF]
Frontiers in Genetics, 2023 Glycogen storage disease type III (GSD-III) is an autosomal recessive metabolic disorder caused by mutations in the AGL gene, and may develop various types of pulmonary hypertension (PH).
Akito Shindo +10 more
doaj +2 more sources
DIAGNOSTIC SPECIFICS OF PULMONARY VENO-OCCLUSIVE DISEASE
Российский кардиологический журнал, 2012 The authors present the two-year follow-up of a female patient with severe pulmonary hypertension and a rare pathology – pulmonary veno-occlusive disease. Due to the treatment with low-dose prednisolone, in combination with warfarin, coraxan, and oxygen,
E. A. Zhuk +4 more
doaj +1 more source
Clinical features of canine pulmonary veno‐occlusive disease and pulmonary capillary hemangiomatosis
Journal of Veterinary Internal Medicine, 2019 Background Histologic features of pulmonary veno‐occlusive disease (PVOD) and pulmonary capillary hemangiomatosis (PCH) have been described in dogs but without a thorough clinical description.
Carol R. Reinero +5 more
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Late Onset Pulmonary Arterial Hypertension Associated With Features of Pulmonary Veno‐Occlusive Disease and Rare Heterozygous Variants of KDR and EIF2AK4 [PDF]
Pulmonary CirculationThe natural history of late‐onset pulmonary arterial hypertension (PAH) with features of venous/capillary involvement and the associations with rare variants in PAH genes are not well known.
Vasile Foris +11 more
doaj +2 more sources
Reactive Pulmonary Capillary Hemangiomatosis and Pulmonary Veno-Occlusive Disease in a Patient with Repaired Scimitar Syndrome [PDF]
Case Reports in Cardiology, 2016 Pulmonary capillary hemangiomatosis (PCH) is a rare histological substrate within the spectrum of pulmonary arterial hypertension that possibly represents an unusual manifestation of pulmonary veno-occlusive disease (PVOD).
Eva Güttinger +6 more
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Pulmonary veno-occlusive disease misdiagnosed as idiopathic pulmonary arterial hypertension [PDF]
European Respiratory Review, 2009 A 27-yr-old female with a 6-month diagnosis of idiopathic pulmonary arterial hypertension (PAH) confirmed elsewhere was referred to our centre with worsening dyspnoea.
M. Palazzini, A. Manes
doaj +2 more sources
A case of pulmonary veno-occlusive disease: diagnostic dilemmas and therapeutic challenges
Therapeutic Advances in Respiratory Disease, 2013 Pulmonary veno-occlusive disease (PVOD) is a rare cause of pulmonary hypertension (PH). Misdiagnosis of the disease is common since PVOD presents with clinical and radiographic features mimicking idiopathic pulmonary arterial hypertension or even PH due ...
Evdokia Sourla +5 more
doaj +2 more sources
BMC Pulmonary Medicine, 2018 Background Pulmonary tumor thrombotic microangiopathy (PTTM) is a rare cause of pulmonary hypertension that is associated with malignancies and is marked by the presence of non-occlusive tumor emboli and fibrocellular intimal proliferation of small ...
Dante A. Suffredini +6 more
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Targeted therapy in pulmonary veno-occlusive disease: time for a rethink? [PDF]
BMC Pulmonary Medicine, 2019 Background Pulmonary veno-occlusive disease (PVOD) is a rare condition with poor prognosis, and lung transplantation is recommended as the only curative therapy.
Qin Luo +8 more
doaj +2 more sources
Pulmonary hypertension secondary to veno-occlusive disease in a 15-years old boy: a case report.
Critical Care Innovations, 2022 Pulmonary hypertension (PH) is a pathology characterized by a mean arterial pressure of the pulmonary artery greater than 20 mmHg and with a classification system based on its etiologies.
Pedro Pinheiro Barros +4 more
doaj +1 more source