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[Granulomatosis and primary immunodeficiency in adulthood].

Authors :
Pavic M
Pasquet F
Fieschi C
Malphettes M
Sève P
Source :
La Revue de medecine interne [Rev Med Interne] 2013 Mar; Vol. 34 (3), pp. 154-8. Date of Electronic Publication: 2012 Mar 15.
Publication Year :
2013

Abstract

Primary immunodeficiency with granulomatosis in the adulthood mainly concern common variable immunodeficiency (CVID). Hypogammaglobulinemia in the adulthood is usually related to a secondary immunodeficiency. When a patient presents with the association of a hypogammaglobulinemia and a granulomatosis, an opportunistic infection must first be ruled out. For unknown reasons, about 10% of the patients affected by CVID also present with granulomatosis. Lesions usually affect the pulmonary tract or the mediastinum. Half of these patients are also affected by an autoimmune cytopenia. Treatment is not codified. Severe pulmonary complications can occur in about 50% of the patients.<br /> (Copyright © 2012 Société nationale française de médecine interne (SNFMI). Published by Elsevier SAS. All rights reserved.)

Details

Language :
French
ISSN :
1768-3122
Volume :
34
Issue :
3
Database :
MEDLINE
Journal :
La Revue de medecine interne
Publication Type :
Academic Journal
Accession number :
22425132
Full Text :
https://doi.org/10.1016/j.revmed.2012.02.005