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Publikováno v:
BMJ Case Rep
A 32-year-old man with congenital X-linked agammaglobulinaemia (XLA) immunodeficiency, receiving weekly intravenous immunoglobulin since childhood, was admitted for painful and ulcerative proliferative lesion with purulent exudate in the right ankle,
Autor:
Marcio Tavares, Valentim Lopes, Narciso Oliveira, Joana Sotto Mayor, Teresa Pimentel, Vanessa Palha, Elisa Condez, Carla Ferreira
Publikováno v:
Journal of Medical Cases
Castleman disease is a rare lymphoproliferative disorder. Co-presentation with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes (POEMS syndrome) has been documented in 11-30% of Castleman disease cases. POEMS syndrom