Bravo-Jaimes Katia Marisa
Universidad Nacional Mayor de San Marcos. Lima, PerÚ.
Rev Gastroenterol Peru. 2015 Jul-Sep;35(3):256-7.
Hemophagocytic lymphohistiocytosis is a rare cause of acute liver failure. It requires a high level of clinical suspicion to reach the diagnosis and avoid fatal outcomes. The case of a 13-year old patient with fever, anasarca, jaundice, lymphadenopathy and encephalopathy is presented. Laboratory studies showed anemia, thrombocytopenia, hyperbilirubinemia, hyperferritinemia, elevated INR, and hemophagocytic phenomenon in centrifugated ascitic fluid. Bone biopsy showed mixed cellularity Hodgkin lymphoma. This report discusses diagnostic criteria, etiology and management of hemophagocytic limphohistocytosis, as well as its association with acute liver failure.
噬血细胞性淋巴组织细胞增生症是急性肝衰竭的罕见病因。需要高度的临床怀疑才能做出诊断并避免致命后果。本文介绍了一名13岁患者,有发热、全身性水肿、黄疸、淋巴结病和脑病的病例。实验室检查显示贫血、血小板减少、高胆红素血症、高铁蛋白血症、国际标准化比值升高,且在离心后的腹水中出现噬血细胞现象。骨髓活检显示为混合细胞型霍奇金淋巴瘤。本报告讨论了噬血细胞性淋巴组织细胞增生症的诊断标准、病因和管理,以及它与急性肝衰竭的关联。