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Pulmonary Hypertension in Patients with Common Variable Immunodeficiency.

Pierre ThoréXavier JaisLaurent SavalePeter DorfmüllerAthénaïs BouclyMatthieu DevilderOlivier MeyrignacJérémie PichonJulie MankikianMarianne RiouEmmanuel BoiffardClément BoissinPascal De GrooteCéline ChabanneGagnadoux FredericAnne BergeronNicolas NoelOlivier SitbonMarc HumbertI David Montani
Published in: Journal of clinical immunology (2021)
PH is a possible complication of CVID whose pathophysiological mechanisms, while still unclear, would be due to the inflammatory nature of CVID. CVID-associated PH presents as precapillary PH with multiple possible causes, acting in concert in some patients: a portal hypertension, a pulmonary vascular remodeling, sometimes a pulmonary parenchymal involvement and occasionally an extrinsic compression by mediastinal lymphadenopathies, which would be consistent with its classification in group 5 of the current PH classification.
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