Gu Ruo-Lan, Xiang Ming, Suo Jing, Yuan Jing
Department of Hematology, The Third Hospital of Hebei Medical University, Shijiazhuang, Hebei 050051, P.R. China.
Mol Clin Oncol. 2019 Aug;11(2):135-138. doi: 10.3892/mco.2019.1877. Epub 2019 Jun 12.
This case report describes a case of an unusual initial presentation of acute lymphoblastic leukemia in a previously healthy 15-year-old boy. He initially presented with a 6-day history of tiredness, decreased oral intake, nausea, vomiting, and jaundice (yellow sclera and dark urine) with evidence of acute hepatic failure, presenting as an increase in alanine aminotransferase (ALT)/aspartate aminotransferase (AST)/total bilirubin and a decrease in prothrombin activity. A complete serological evaluation for liver disease was negative. The levels of serum AST and ALT declined following hepatoprotective treatment. Bone marrow biopsy was diagnostic, revealing 68.15% blasts with markers consistent with acute B-cell lymphoblastic leukemia. This case report emphasizes that acute hepatic failure may be the initial presentation of ALL in an adolescent.
本病例报告描述了一名既往健康的15岁男孩急性淋巴细胞白血病不寻常的初始表现。他最初表现为6天的疲倦、口服摄入量减少、恶心、呕吐和黄疸(巩膜黄染和深色尿液),伴有急性肝衰竭的证据,表现为丙氨酸转氨酶(ALT)/天冬氨酸转氨酶(AST)/总胆红素升高以及凝血酶原活性降低。对肝病进行的全面血清学评估结果为阴性。经过保肝治疗后,血清AST和ALT水平下降。骨髓活检确诊,发现68.15%的原始细胞,其标志物与急性B淋巴细胞白血病一致。本病例报告强调,急性肝衰竭可能是青少年ALL的初始表现。