| Literature DB >> 28478106 |
Annick A J M van de Ven1, Maximilian Seidl2, Vanessa Drendel3, Annette Schmitt-Graeff3, Reinhard E Voll4, Anne Rensing-Ehl1, Carsten Speckmann5, Stephan Ehl5, Klaus Warnatz4, Florian Kollert6.
Abstract
A patient with autoimmune lymphoproliferative disorder (ALPS) developed IgG4-related disease. In retrospect, he had high levels of serum IgG4 for several years prior to presenting with IgG4-related pancreatitis. These high IgG4 levels were masked by hypergammaglobulinemia, a common feature of ALPS. We next screened 18 ALPS patients; four of them displayed increased levels of IgG4. Hence, IgG4-related disease should be considered in ALPS patients, especially in those manifesting lymphocytic organ infiltration or excessive hypergammaglobulinaemia. Screening of IgG4-related disease patients for ALPS-associated mutations would provide further information on whether this disease could be a late-onset atypical presentation of ALPS.Entities:
Keywords: ALPS; Hypergammaglobulinemia; IgG4; IgG4-related disease; Pancreatitis
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Year: 2017 PMID: 28478106 DOI: 10.1016/j.clim.2017.05.003
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969