Suzuki N, Tsuji H, Nakamura S, Asabe H, Sueishi K, Fujishima M
Second Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Am J Gastroenterol. 1998 Jan;93(1):115-7. doi: 10.1111/j.1572-0241.1998.115_c.x.
A 62-year-old man was admitted to our hospital because of severe jaundice and fever. Physical examination demonstrated hepatosplenomegaly. The laboratory data revealed elevated serum bilirubin, alkaline phosphatase, lactate dehydrogenase, aspartate aminotransferase and alanine aminotransferase, and the reduced hepaplastin test (Normotest). Computed tomography showed hepatosplenomegaly and swelling of the paraaortic lymph nodes. Although he was treated with antibiotics and steroids, he died of hepatic failure 22 days after admission. At autopsy, his liver weighed 1910 grams, and a histological examination of the liver revealed marked infiltration of CD30 (Ki-1) positive lymphoma cells. He was diagnosed as having non-Hodgkin lymphoma, large cell anaplastic type, Ki-1 lymphoma. We herein report our findings of this very rare case of Ki-1 lymphoma associated with hepatic failure.
一名62岁男性因严重黄疸和发热入住我院。体格检查发现肝脾肿大。实验室检查数据显示血清胆红素、碱性磷酸酶、乳酸脱氢酶、天冬氨酸转氨酶和丙氨酸转氨酶升高,凝血酶原时间测定(正常检测)降低。计算机断层扫描显示肝脾肿大和主动脉旁淋巴结肿大。尽管给予了抗生素和类固醇治疗,但他在入院22天后死于肝衰竭。尸检时,他的肝脏重1910克,肝脏组织学检查显示CD30(Ki-1)阳性淋巴瘤细胞明显浸润。他被诊断为非霍奇金淋巴瘤,大细胞间变性型,Ki-1淋巴瘤。我们在此报告这例与肝衰竭相关的非常罕见的Ki-1淋巴瘤病例的研究结果。