Lima M, Silvestre F, Correia J, Oliveira J, Justiça B
Service of Clinical Hematology, Sto Antonio's Hospital, Porto Portugal.
Sangre (Barc). 1996 Oct;41(5):383-6.
We describe a case of 27 year-old female presenting with Kikuchi-Fujimoto's disease whose diagnosis was based on histopathologic and immunophenotypic studies. The illness was characterized by fever, urinary tract infections, skin rash, polyarthritis, generalized lymphadenopathy, pancytopenia, hepatic cytolysis and cholestasis, abnormal coagulation tests and elevated serum lactate dehydrogenase. The lymph node biopsy was consistent with the diagnosis of a histiocytic necrotizing lymphadenitis. Flow cyto-metric studies performed on the affected lymph node, bone marrow aspirate and peripheral blood, revealed a relative expansion of mature activated T lymphocytes, predominantly expressing a CD8 (+) phenotype.
我们报告一例27岁女性的菊池-藤本病病例,其诊断基于组织病理学和免疫表型研究。该疾病的特征为发热、尿路感染、皮疹、多关节炎、全身淋巴结肿大、全血细胞减少、肝细胞溶解和胆汁淤积、凝血试验异常以及血清乳酸脱氢酶升高。淋巴结活检结果符合组织细胞坏死性淋巴结炎的诊断。对受累淋巴结、骨髓穿刺液和外周血进行的流式细胞术研究显示,成熟活化T淋巴细胞相对增多,主要表达CD8(+)表型。