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首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Plasmablastic lymphoma following combination treatment with fludarabine and rituximab for nongastric mucosa-associated lymphoid tissue lymphoma: a case report and review of literature
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Plasmablastic lymphoma following combination treatment with fludarabine and rituximab for nongastric mucosa-associated lymphoid tissue lymphoma: a case report and review of literature

机译:氟达拉滨联合利妥昔单抗联合治疗非胃黏膜相关淋巴样组织淋巴瘤后的成纤维细胞淋巴瘤:1例并文献复习

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Plasmablastic lymphoma (PBL) is an uncommon malignancy which predominantly occurs in the oral cavity of human immunodeficiency virus (HIV)-positive patients. Sporadic cases have been published describing PBL in immunocompetent patients as well as in immunodeficient patients following immunosuppressive therapy or transplantation. We hereby reported a case of PBL in a 69-year-old, HIV-negative male subjected to combination treatment with fludarabine and rituximab for nongastric mucosa-associated lymphoid tissue (MALT) lymphoma. The diagnosis of PBL was made with tumor cells of immunoblasts or plasmablasts morphology strongly positive for MUM-1, EMA and CD138, and partly positive for CD38, and negative for CD20, BCL-6, and CD56, and approximately 80% of which were positive for Ki-67. The case presented PBL after MALT, and a history of chemotherapy including fludarabine and rituximab led to the potential immunocompromised state. The patient died 5 months after the diagnosis of PBL.
机译:浆母细胞性淋巴瘤(PBL)是一种罕见的恶性肿瘤,主要发生在人类免疫缺陷病毒(HIV)阳性患者的口腔中。已经发表了零星病例,描述了免疫功能正常的患者以及免疫抑制治疗或移植后免疫缺陷患者的PBL。我们在此报告一例69岁的HIV阴性男性,接受氟达拉滨和利妥昔单抗联合治疗非胃粘膜相关淋巴样组织(MALT)淋巴瘤的病例。 PBL的诊断是通过免疫母细胞或浆母细胞形态的肿瘤细胞对MUM-1,EMA和CD138呈强阳性,对CD38呈部分阳性,对CD20,BCL-6和CD56呈阴性,其中约80%为Ki-67呈阳性。该病例在MALT后出现PBL,包括氟达拉滨和利妥昔单抗在内的化疗史导致了潜在的免疫功能低下。该患者在诊断为PBL后5个月死亡。

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