Tai Chi-Ming, Liu Chun-Jen, Yao Ming
Division of Gastroenterology, Department of Internal Medicine, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei.
J Formos Med Assoc. 2005 Jul;104(7):507-10.
Virus-associated hemophagocytic syndrome (VAHS) is a rare complication in acute hepatitis A virus (HAV) infection. There is no standard therapy for VAHS and the clinical course is variable. Data on the use of intravenous immunoglobulin (IVIG) in the treatment of HAV-associated VAHS is limited. We report a previously healthy, 32-year-old man who presented with general malaise, fever, chills and splenomegaly. Laboratory examination showed marked elevation of aminotransferase, leukopenia and thrombocytopenia. Acute hepatitis A was documented by the presence of immunoglobulin M anti-HAV and compatible liver biopsy findings. Bone marrow examination revealed extensive hemophagocytosis. IVIG was administered after the diagnosis of HAV-associated VAHS. His symptoms and laboratory abnormalities improved, and following a smooth recovery he was discharged 1 month after admission.
病毒相关性噬血细胞综合征(VAHS)是甲型肝炎病毒(HAV)急性感染中一种罕见的并发症。VAHS尚无标准治疗方法,其临床病程多变。关于静脉注射免疫球蛋白(IVIG)用于治疗HAV相关性VAHS的数据有限。我们报告一名既往健康的32岁男性,他出现全身乏力、发热、寒战和脾肿大。实验室检查显示转氨酶显著升高、白细胞减少和血小板减少。免疫球蛋白M抗-HAV阳性及符合的肝活检结果证实为急性甲型肝炎。骨髓检查发现广泛的噬血细胞现象。在诊断为HAV相关性VAHS后给予IVIG治疗。他的症状和实验室异常情况得到改善,经过顺利康复,入院1个月后出院。