Rudniki C, Kessler E, Zarfati M, Turani H, Bar-Ziv Y, Zahavi I
Department of Medicine C, Hasharon Hospital, Petah-Tiqva, Israel.
Acta Haematol. 1988;79(2):99-102. doi: 10.1159/000205730.
Kikuchi's disease is characterized by lymphadenopathy in young patients and may be mistaken for malignant disease both clinically and histologically. We report the case of a 26-year-old man with persistent fever for 3 weeks and splenomegaly, in whom pancytopenia developed afterwards. A bone marrow aspiration was normal. Blood, urine, throat, stool and bone marrow cultures were negative as were serological tests for lues, Toxoplasma, Epstein-Barr virus and Widal's test. An abdominal CT scan showed enlarged retroperitoneal lymph nodes and an exploratory laparotomy was performed. Two lymph nodes were excised and a wedge biopsy of the liver was performed. The histological findings in the lymph nodes were compatible with the diagnosis of Kikuchi's disease. The patient became afebrile on the 2nd postoperative day without any treatment. He has been well for 4 months after discharge.
菊池病的特点是年轻患者出现淋巴结病,在临床和组织学上都可能被误诊为恶性疾病。我们报告一例26岁男性病例,该患者持续发热3周并伴有脾肿大,随后出现全血细胞减少。骨髓穿刺结果正常。血液、尿液、咽喉、粪便和骨髓培养均为阴性,梅毒、弓形虫、EB病毒血清学检测及肥达试验也均为阴性。腹部CT扫描显示腹膜后淋巴结肿大,遂进行了剖腹探查术。切除了两个淋巴结,并对肝脏进行了楔形活检。淋巴结的组织学检查结果符合菊池病的诊断。患者术后第2天未经任何治疗即退热。出院后4个月来一直状况良好。