hiv阴性、免疫功能正常患者发生上颌骨浆母细胞淋巴瘤1例

Mohd Zulkimi Roslly , Anis Suhana Hashim
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引用次数: 0

摘要

浆母细胞淋巴瘤(PBL)是一种罕见的侵袭性淋巴瘤,属于b细胞非霍奇金淋巴瘤的一种亚型。PBL于1997年首次被描述为与人类免疫缺陷病毒(HIV)和eb病毒(EBV)感染密切相关。它也与其他免疫抑制条件有关,如移植后的免疫抑制治疗状态、癌症史和高龄。我们报告了一例PBL病例,患者健康,hiv阴性,免疫功能正常,表现为b症状,右上颌疼痛和肿胀,最终诊断为浆母细胞淋巴瘤。进行了广泛的诊断检查以排除免疫抑制条件。唯一有意义的发现是既往EBV感染的证据,这可能是一个易感因素。患者经经筹性EPOCH治疗后再进行R-EPOCH化疗,随访病情明显好转。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plasmablastic Lymphoma of maxilla in an HIV-negative, immunocompetent patient: A case report on unusual occurrence
Plasmablastic Lymphoma (PBL) is a rare and aggressive form of lymphoma that is classified as a subtype of B-cell, non-Hodgkin Lymphoma. First described in 1997, PBL has been strongly linked to Human Immunodeficiency Virus (HIV) and Epstein-Barr Virus (EBV) infections. It is also known to be associated with other immunosuppressive conditions such as post-transplantation state with its immunosuppressive therapy, history of cancer, and advanced age. We reported a case of PBL in a healthy, HIV-negative, and immunocompetent patient who presented with B-symptoms and right maxillary pain and swelling, which was finally diagnosed as Plasmablastic Lymphomas. Extensive diagnostic workups were conducted to rule out immunosuppressive conditions. The only significant finding was evidence of prior EBV infection, which may have served as a predisposing factor. The patient was treated with empirical EPOCH followed by R-EPOCH chemotherapy, showing notable disease improvement during subsequent follow-up.
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