Oct 11, 2003

Common variable immunodeficiency: 17 observations in the adult

La Revue de médecine interne
C Bloch-MichelJ-L Pellegrin

Abstract

Common variable immunodeficiency (CVID) is an immune defect characterized by primary hypogammaglobulinemia. Most of the time, clinical manifestations that reveal CVID are recurrent bacterial infections, but auto-immune or granulomatous events may occur. This retrospective study was conducted on 17 patients fulfilling the classical CVID definition. Lymphocyte activation level was evaluated in 12 patients through HLA-DR expression on lymphocytes subsets. This study includes 17 patients, 7 men and 10 women. The mean age at the first clinical manifestation is 23 years and the mean age at diagnosis is 39 years. Recurrent upper and lower bacterial respiratory tract infections are common to all patients. Abdominal infection due to Mycobacterium avium-intracellulare complex is found in one patient. Digestive events are dominated by chronic diarrhea caused by giardiasis, nodular lymphoid hyperplasia or villous atrophy. Seven patients developed auto-immune conditions (insulin dependent diabetes, idiopathic thrombocytopenic purpura (ITP), rheumatoid arthritis) and 7 patients have a splenomegaly. Non caseating granulomas in the spleen or in lymph node biopsies are found in 3 patients. Ten patients have a T lymphopenia, 2 have a B lymphopen...Continue Reading

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Mentioned in this Paper

T-Lymphocyte
Immune System Diseases
Spleen
Lymphocytes as Percentage of Blood Leukocytes (Lab Test)
Lymphopenia
Neoplasms
IS 23
Etiology
Lymphocyte Activation
Lymph Node Tissue

About this Paper

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