Batra Rashmi, Medeiros Bruno C, Zehnder James L, Warnke Roger A, Natkunam Yasodha
Department of Pathology and Internal Medicine, Stanford University School of Medicine, Stanford, CA 94305-5324, USA.
Appl Immunohistochem Mol Morphol. 2012 May;20(3):325-30. doi: 10.1097/PAI.0b013e318233d72a.
A 19-year-old male patient presented with intermittent high fever and left cervical lymphadenopathy. The lymph node biopsy findings were interpreted as "Epstein-Barr virus (EBV)-associated lymphoproliferative disorder consistent with infectious mononucleosis." No molecular studies were performed at that time. The patient was followed without treatment. Five months later, the patient again presented with fever, lymphadenopathy, and splenomegaly. The lymph node biopsy showed features of a diffuse large B-cell lymphoma. Molecular studies on this lymph node biopsy showed a clonal EBV population, although polymerase chain reaction studies failed to reveal a clonal B-cell or T-cell population. A concurrent bone marrow biopsy showed features consistent with hemophagocytic syndrome. He had elevated ferritin, soluble interleukin-2 receptors and persistent EBV viremia. The patient responded to Rituxan for a short period with undetectable EBV levels. Subsequent right cervical lymph node, liver, and jejunal biopsies showed involvement by diffuse large B-cell lymphoma and the patient expired soon thereafter.
一名19岁男性患者出现间歇性高热和左颈部淋巴结肿大。淋巴结活检结果被解释为“符合传染性单核细胞增多症的爱泼斯坦-巴尔病毒(EBV)相关淋巴增殖性疾病”。当时未进行分子研究。该患者未接受治疗进行随访。五个月后,患者再次出现发热、淋巴结肿大和脾肿大。淋巴结活检显示为弥漫性大B细胞淋巴瘤特征。对该淋巴结活检进行的分子研究显示存在克隆性EBV群体,尽管聚合酶链反应研究未能揭示克隆性B细胞或T细胞群体。同时进行的骨髓活检显示符合噬血细胞综合征的特征。他的铁蛋白、可溶性白细胞介素-2受体升高,EBV病毒血症持续存在。该患者对利妥昔单抗短期内有反应,EBV水平检测不到。随后的右颈部淋巴结、肝脏和空肠活检显示有弥漫性大B细胞淋巴瘤累及,患者此后不久死亡。