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从 MD 安德森癌症中心档案库:浆母细胞淋巴瘤表现为免疫功能正常患者的肾脏肿块:病例报告和文献复习。

From the archives of MD Anderson Cancer Center: Plasmablastic lymphoma presenting as a kidney mass in an immunocompetent patient: Case report and literature review.

机构信息

Department of Pathology, The University of Texas Medical Branch, Galveston, TX, USA.

Department of Radiology, The University of Texas Medical Branch, Galveston, TX, USA.

出版信息

Ann Diagn Pathol. 2023 Dec;67:152186. doi: 10.1016/j.anndiagpath.2023.152186. Epub 2023 Jul 29.

Abstract

BACKGROUND

Plasmablastic lymphoma (PBL) is a rare, aggressive large B-cell lymphoma with plasmablastic or immunoblastic morphology and a terminally differentiated B-cell immunophenotype. PBL often presents at extranodal sites, commonly the oral cavity of immunocompromised patients with human immunodeficiency virus (HIV) and/or Epstein-Barr virus (EBV) infection. Cases of PBL arising outside the oral cavity in previously healthy immunocompetent patients are rare.

CASE REPORT

We report a 65-year-old HIV- and EBV-negative man who presented with abdominal pain, fatigue, and vomiting. Imaging studies showed a 30 × 18 cm bulky lobulated mass located within the left kidney with surrounding para-aortic lymphadenopathy. Serum and urine protein electrophoresis revealed a monoclonal gammopathy of IgA lambda type. Biopsy of the mass showed PBL. Bone marrow lumbar puncture evaluations also showed evidence of PBL. The patient was treated with chemotherapy and radiation with initial improvement; however, he died 14 months after initial diagnosis.

CONCLUSIONS

Based on our literature review, this case of PBL is one of the few reported to present as a kidney mass in immunocompetent, HIV- and EBV-negative patient. Distinguishing PBL from plasma cell myeloma (PCM) can be challenging. Knowledge of clinical features including presence of CRAB (hypercalcemia, renal failure, anemia, bone lesions) or bone marrow infiltration by mature clonal plasma cells is helpful to establish a diagnosis of PCM. Genetic features of PCM (typical translocations or mutations) also can be helpful in distinguishing plasmablastic transformation of PCM and from PBL. The case we report also highlights the need for more studies to identify specific immunohistochemical and molecular markers to improve PBL diagnosis in immunocompetent patients.

摘要

背景

浆母细胞淋巴瘤(PBL)是一种罕见的侵袭性大 B 细胞淋巴瘤,具有浆母细胞或免疫母细胞形态和终末分化的 B 细胞免疫表型。PBL 常发生于结外部位,常见于免疫功能低下的人类免疫缺陷病毒(HIV)和/或 EBV 感染患者的口腔。在既往健康的免疫功能正常患者中,口腔外发生的 PBL 病例较为罕见。

病例报告

我们报告了一例 65 岁男性,HIV 和 EBV 均为阴性,表现为腹痛、乏力和呕吐。影像学研究显示,左肾内有一个 30×18cm 的块状分叶状肿块,周围有腹主动脉旁淋巴结肿大。血清和尿液蛋白电泳显示 IgA lambda 型单克隆丙种球蛋白病。肿块活检显示为 PBL。骨髓腰椎穿刺评估也显示有 PBL 证据。该患者接受了化疗和放疗,初始情况有所改善;然而,他在初始诊断后 14 个月死亡。

结论

根据我们的文献复习,本例 PBL 是少数几例报告的在免疫功能正常、HIV 和 EBV 阴性患者中表现为肾肿块的病例之一。将 PBL 与浆细胞骨髓瘤(PCM)区分开来可能具有挑战性。了解包括 CRAB(高钙血症、肾衰竭、贫血、骨病变)或成熟克隆性浆细胞骨髓浸润在内的临床特征有助于建立 PCM 的诊断。PCM 的遗传特征(典型易位或突变)也有助于区分 PCM 的浆母细胞转化和 PBL。我们报告的病例还强调需要更多的研究来确定特定的免疫组织化学和分子标志物,以提高免疫功能正常患者的 PBL 诊断水平。

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