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Pneumologia ; 64(3): 55-7, 2015.
Article in English | MEDLINE | ID: mdl-26738373

ABSTRACT

The neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a genetic disorder. The café-au-lait spots and neurofibromas are the most common manifestations. Respiratory symptoms are rare in this disease, described as neurofibromas, infiltrative lesions, cysts, bubbles or emphysema. Pulmonary hypertension is rarely reported. It is due to the plexiform lesions in pulmonary arterioles or to parenchymal lung lesions reducing the vascular bed. We report a case of idiopathic precapillary pulmonary hypertension in a young patient with Von Recklinghausen's disease.


Subject(s)
Anticoagulants/therapeutic use , Endothelin Receptor Antagonists/therapeutic use , Hypertension, Pulmonary/drug therapy , Hypertension, Pulmonary/genetics , Neurofibromatosis 1/complications , Phosphodiesterase Inhibitors/therapeutic use , Adult , Antihypertensive Agents/therapeutic use , Drug Therapy, Combination , Epoprostenol/therapeutic use , Female , Humans , Hypertension, Pulmonary/diagnosis , Pericardial Effusion/genetics , Treatment Failure , Treatment Outcome
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