Lam-Tse W K, van den Berg L, Dawson L, van Ravenswaay Claasen H H, Hart W, Maartense E
Reinier de Graaf Gasthuis, afd. Inwendige Geneeskunde, Delft.
Ned Tijdschr Geneeskd. 2008 Mar 15;152(11):606-14.
An 82-year-old man was admitted with a 1-week history of chilling fever and dry cough. Laboratory tests revealed pancytopenia and elevated levels of C-reactive protein and lactic dehydrogenase (LDH). Screening for infectious diseases was negative. A bone marrow biopsy showed aspecific findings. The combination of pancytopenia, persistent fever, elevated LDH and hepatomegaly (demonstrated by ultrasound examination of the abdomen) was suggestive of the haemophagocytic syndrome. This was confirmed by very high levels of ferritin and soluble interleukin-2 receptor in the blood. In addition, re-examination of the bone marrow showed several haemophagocytic histiocytes. A polymerase chain reaction for Epstein-Barr virus (EBV) revealed a very high viral load. Since the patient had a history of an increased level of anti-EBV immunoglobulin-G, this was explained by a reactivation of the EBV infection. On the sixth day in hospital the patient developed signs of bilateral pneumonia and subsequent multiple organ failure. Despite intensive treatment the patient died. Autopsy revealed no haematological or other malignancies, but did show haemophagocytosis in many organs. It was then concluded that the patient had a virus-associated haemophagocytic syndrome, due to a reactivation of EBV, for which no underlying cause was found.
一名82岁男性因寒战发热和干咳1周入院。实验室检查显示全血细胞减少,C反应蛋白和乳酸脱氢酶(LDH)水平升高。传染病筛查为阴性。骨髓活检显示非特异性结果。全血细胞减少、持续发热、LDH升高和肝肿大(腹部超声检查证实)提示噬血细胞综合征。血液中极高水平的铁蛋白和可溶性白细胞介素-2受体证实了这一点。此外,再次骨髓检查显示有多个噬血细胞组织细胞。爱泼斯坦-巴尔病毒(EBV)聚合酶链反应显示病毒载量极高。由于该患者有抗EBV免疫球蛋白G水平升高的病史,这可解释为EBV感染的重新激活。住院第6天,患者出现双侧肺炎体征,随后发展为多器官功能衰竭。尽管进行了强化治疗,患者仍死亡。尸检未发现血液系统或其他恶性肿瘤,但许多器官确实显示有噬血细胞现象。随后得出结论,该患者患有与病毒相关的噬血细胞综合征,原因是EBV重新激活,未发现潜在病因。