Kobayashi Hiroyuki, Miyagi Norito
Division of Hematology, Nasu Red Cross Hospital.
Division of Dentistry, Oral and Maxillofacial Surgery, Nasu Red Cross Hospital.
Rinsho Ketsueki. 2017;58(5):443-448. doi: 10.11406/rinketsu.58.443.
A 61-year-old, HIV-negative, immunocompetent woman was admitted to our hospital for significant weight loss, painful swelling of her right cheek, and rapid growth of a tumor in the right hard palate. A CT scan revealed a neoplastic lesion in the right maxillary sinus, extending to the surrounding soft bone tissue and oral cavity, as well as multiple osteolytic lesions in the skull. A pathologic examination revealed that the neoplastic cells in the oral cavity were plasmablasts tending to appear as differentiated plasma cells. The tumor cells strongly expressed CD138, Vs38c, EBER, and MYC, and were negative for CD20 and CD19. The MIB-1 index was 90%, and MYC/IgH fusion gene was detected by fluorescence in situ hybridization analysis. Based on these clinical and pathological findings, we confirmed the diagnosis of plasmablastic lymphoma. This disease has characteristics of aggressive lymphoma originating from differentiated plasma cells. Treatment was initiated with dose-adjusted EPOCH added to a concurrent bortezomib regimen. After completion of four cycles, the patient achieved and sustained complete remission.
一名61岁、HIV阴性、免疫功能正常的女性因体重显著减轻、右侧脸颊疼痛性肿胀以及右上颌硬腭肿瘤迅速生长而入住我院。CT扫描显示右上颌窦有一个肿瘤性病变,延伸至周围的软骨质组织和口腔,以及颅骨上的多个溶骨性病变。病理检查显示口腔中的肿瘤细胞为浆母细胞,倾向于表现为分化的浆细胞。肿瘤细胞强烈表达CD138、Vs38c、EBER和MYC,而CD20和CD19为阴性。MIB-1指数为90%,通过荧光原位杂交分析检测到MYC/IgH融合基因。基于这些临床和病理发现,我们确诊为浆母细胞性淋巴瘤。这种疾病具有源自分化浆细胞的侵袭性淋巴瘤的特征。治疗开始时采用剂量调整的EPOCH方案并联合硼替佐米方案。四个周期结束后,患者实现并维持了完全缓解。