Nasta Sunita D, Carrum George M, Shahab Imran, Hanania Nicola A, Udden Mark M
Division of Cancer Medicine, University of Texas M.D. Anderson Cancer Center, Houston, USA.
Leuk Lymphoma. 2002 Feb;43(2):423-6. doi: 10.1080/10428190290006260.
We describe an HIV-infected 44-year-old man who presented 1 month after discontinuation of HAART therapy with a large mass extending from the mediastinum, enclosing the heart and extending through the diaphragm to the epigastric region. Biopsies subsequently revealed a highly aggressive non-Hodgkin's lymphoma (NHL) producing sheets of cells with an organoid distribution. The cells had abundant basophilic cytoplasm and a plasmacytic appearance. Although immunohistochemistry failed to show either B- or T-cell markers, antigens consistent with plasma cells were found. An immunoglobulin heavy chain clonal rearrangement was identified by PCR analysis. These studies were supportive of a diagnosis of a plasmablastic lymphoma. While awaiting the results of these tests, the patient was reinitiated on his HAART regimen. He was found on follow-up a month later to have complete resolution of his bulky mediastinal mass. He remained free of disease for 3 months with subsequent rectal and abdominal recurrence. Treatment with CHOP chemotherapy with filgrastim support was begun which resulted in another remission. Plasmablastic lymphoma is now reported in some studies to account for 2.6% of all HIV-related NHL. Originally described in 1997 in a series of 16 patients, this entity is highly associated with HIV infection in its later stages. Often, patients present with oral or jaw lesions with a rapidly progressive course. The tumors have the morphologic appearance of a plasmacytoid tumor with high proliferative index. Markers are positive mainly for LCA, CD79a, VS38C, and CD138. Co-infection with HHV-8 and EBV has not been consistently reported. Therapy with standard regimens has variable response. One case has been reported with a 3.5 year disease free survival. The regression of disease after resumption of HAART therapy alone in this patient suggests that HAART has an important role in the treatment of lymphoma in the HIV infected patient.
我们描述了一名44岁的HIV感染男性,他在停用高效抗逆转录病毒治疗(HAART)1个月后就诊,有一个巨大肿块,从纵隔延伸,包绕心脏并穿过膈肌至中上腹区域。活检随后显示为一种高度侵袭性的非霍奇金淋巴瘤(NHL),产生呈器官样分布的细胞片。这些细胞有丰富的嗜碱性细胞质和浆细胞样外观。尽管免疫组化未显示B细胞或T细胞标志物,但发现了与浆细胞一致的抗原。通过聚合酶链反应(PCR)分析鉴定出免疫球蛋白重链克隆性重排。这些研究支持浆母细胞淋巴瘤的诊断。在等待这些检查结果期间,患者重新开始HAART治疗方案。1个月后的随访发现,他纵隔的巨大肿块完全消退。他无病生存3个月,随后出现直肠和腹部复发。开始采用含非格司亭支持的CHOP化疗,这导致了又一次缓解。现在一些研究报道浆母细胞淋巴瘤占所有HIV相关NHL的2.6%。该实体最初于1997年在一组16例患者中被描述,与HIV感染后期高度相关。患者通常表现为口腔或颌部病变,病程进展迅速。肿瘤具有浆细胞样肿瘤的形态学外观,增殖指数高。标志物主要对白细胞共同抗原(LCA)、CD79a、VS38C和CD138呈阳性。尚未一致报道与HHV-8和EBV的共同感染。采用标准方案治疗反应不一。有一例报道无病生存3.5年。该患者仅恢复HAART治疗后疾病消退,提示HAART在HIV感染患者淋巴瘤治疗中具有重要作用。