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Presenting manifestations of hemophagocytic syndrome in a male patient with systemic lupus erythematosus.
Taki, Hirofumi; Shinoda, Koichiro; Hounoki, Hiroyuki; Ogawa, Reina; Hayashi, Ryuji; Sugiyama, Eiji; Tobe, Kazuyuki.
Afiliación
  • Taki H; First Department of Internal Medicine, University of Toyama, 2630 Sugitani, Toyama, Toyama 930-0194, Japan. htaki-tym@umin.ac.jp
Rheumatol Int ; 30(3): 387-8, 2010 Jan.
Article en En | MEDLINE | ID: mdl-19381636
Hemophagocytic syndrome (HPS) is an unusual but sometimes fatal disorder. We reported a case of 21-year-old man who developed HPS and SLE simultaneously. Febrile pancytopenia, hyperferritinemia, and abnormal liver function tests were observed. Hemophagocytic cells were observed by means of bone marrow biopsy and diagnosed as HPS. The patient was treated with high-dose prednisolone, resulting in an excellent outcome. Early diagnosis of HPS by bone marrow biopsy is important for the successful treatment.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfohistiocitosis Hemofagocítica / Lupus Eritematoso Sistémico Tipo de estudio: Etiology_studies / Screening_studies Límite: Adult / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Rheumatol Int Año: 2010 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Alemania
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfohistiocitosis Hemofagocítica / Lupus Eritematoso Sistémico Tipo de estudio: Etiology_studies / Screening_studies Límite: Adult / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Rheumatol Int Año: 2010 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Alemania