Beck Adele, Hunter Hannah, Jackson Simon, Sheridan David
University Hospitals Plymouth NHS Trust, Plymouth, UK.
Department of Haematology, University Hospitals Plymouth NHS Trust, Plymouth, UK.
BMJ Case Rep. 2019 Mar 14;12(3):e227821. doi: 10.1136/bcr-2018-227821.
A 17-year-old man with no significant past medical history presented with a 2-week history of worsening jaundice, lethargy, anorexia and progressive right upper quadrant abdominal pain. There were no stigmata of chronic liver disease. Initial investigations were suggestive of cholangitis with large intrahepatic and extrahepatic bile duct strictures but otherwise normal hepatic and splenic appearances. A percutaneous transhepatic cholangiogram with the positioning of drains was performed to alleviate the obstructive jaundice. Within 2 weeks of the first presentation, full blood count revealed a significantly raised white blood count and a subsequent peripheral blood smear and bone marrow were consistent with a diagnosis of acute myeloid leukaemia. Chemotherapy was started after partial improvement of his obstructive jaundice. Complete morphological and cytogenetic remission was obtained 4 weeks after the first cycle of chemotherapy (half dose of daunorubicin and full dose of cytarabine, treated off trial) on control bone marrow. The patient remains in remission.
一名既往无重大病史的17岁男性,出现黄疸加重、嗜睡、厌食及右上腹进行性腹痛2周。无慢性肝病体征。初步检查提示胆管炎伴肝内及肝外大胆管狭窄,但肝脏和脾脏外观正常。进行了经皮经肝胆管造影及引流管置入以缓解梗阻性黄疸。首次就诊后2周内,全血细胞计数显示白细胞计数显著升高,随后外周血涂片和骨髓检查结果符合急性髓系白血病的诊断。在其梗阻性黄疸部分改善后开始化疗。在第一个化疗周期(柔红霉素半量及阿糖胞苷全量,非试验性治疗)4周后,对照骨髓检查显示获得完全形态学和细胞遗传学缓解。患者仍处于缓解状态。