Department of Infectious Diseases, Hedi Chaker Hospital, Sfax 3029, Tunisia.
Mediterr J Hematol Infect Dis. 2012;4(1):e2012050. doi: 10.4084/MJHID.2012.050. Epub 2012 Aug 9.
A 22-year-old man was admitted to our hospital because of fever, skin rash and epistaxis. Physical examination revealed fever (39.5°C), generalized purpura, lymphadenopathy and splenomegaly. Blood tests showed pancytopenia. Bone marrow aspiration and biopsy showed hemophagocytosis with no evidence of malignant cells. Anti rubella IgM antibody were positive and the IgG titers increased from 16 to 50 UI/mL in 3 days. Therefore, he was diagnosed to have rubella-associated hemophagocytic syndrome. We report herein the first case in a man and the sixth case of rubella-associated hemophagocytic syndrome in the literature by search in Pub Med till March 2012.
一位 22 岁男性因发热、皮疹和鼻出血而入院。体格检查发现发热(39.5°C)、全身紫癜、淋巴结病和脾肿大。血液检查显示全血细胞减少。骨髓抽吸和活检显示噬血细胞现象,但无恶性细胞证据。风疹 IgM 抗体阳性,3 天内 IgG 滴度从 16 增加到 50 UI/ml。因此,诊断为风疹相关性噬血细胞综合征。通过在 Pub Med 中检索至 2012 年 3 月,我们报告了首例男性病例和第 6 例文献报道的风疹相关性噬血细胞综合征病例。