PubMed · 2010 · 43 citations · 6 references
CVID is a multisystemic disease that should be managed by a multidisciplinary team. Intravenous immunoglobulin therapy and antibiotics do not seem to have a suppressive effect on granulomatous or inflammatory manifestations. More comprehensive studies based not only on peripheral blood but also on immunohistological analysis are necessary to shed light on the pathogenesis of these life-threatening complications.
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Peter F. Köhler, Robert I. Cook, W. Robert Brown et al. · Journal of Allergy and Clinical Immunology · 1982 · 55 citations · Full text
Primary Immunodeficiency, Common Variable Hypogammaglobulinemia, Lymphoid Neoplasia +13
Extranodal marginal zone (MALT) lymphoma in common variable immunodeficiency.
Ingrid M.E. Desar, Monique Keuter, John Raemaekers et al. · PubMed · 2006 · 37 citations