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EB病毒相关浆母细胞淋巴瘤的头颈部和眼部表现:硼替佐米、EPOCH和鞘内注射甲氨蝶呤的临床及影像学反应

Cephalic and ocular manifestations of EBV-associated plasmablastic lymphoma: Clinical and radiological response to bortezomib, EPOCH, and intrathecal methotrexate.

作者信息

Theodory Bassam, Harrison Skyler, Bhatt Vivek V, Sharifi Steve, Nam Jerry I, Bhanu Shiv, Bui Duy Quang

机构信息

University of California, Riverside, School of Medicine, Riverside, CA, USA.

Department of Radiology, Riverside Community Hospital, Riverside, CA, USA.

出版信息

Radiol Case Rep. 2024 Jul 24;19(10):4273-4279. doi: 10.1016/j.radcr.2024.07.011. eCollection 2024 Oct.

DOI:10.1016/j.radcr.2024.07.011
PMID:39155935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11327500/
Abstract

Plasmablastic lymphoma (PBL) is a rare and aggressive type of lymphoma, particularly affecting HIV-positive and immunocompromised individuals, with a median diagnosis age of 49 years. Cases of this malignancy in HIV-negative individuals are less common and rarely involve the bone marrow. While traditional chemotherapy regimens such as cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) were previously utilized in the management of such malignancy, the National Comprehensive Cancer Network currently recommends more intensive approaches. We present a rare stage IV Epstein-Barr virus (EBV)-positive PBL with a nasal cavity tumor extending into the left orbital sinus and encapsulating segments of the optic nerve in a 38-year-old young immunocompetent adult, without a significant past medical history. Treatment consisted of 6 cycles of Bortezomib in combination with dose-adjusted EPOCH (etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin) and intrathecal methotrexate which exhibited significant clinical and radiological improvement suggesting the potential efficacy of this regimen. Vision returned to baseline, the mass size reduced significantly, and headaches improved. Given this outcome, it is highly encouraged to emphasize the need for further exploration of this treatment in larger clinical trials.

摘要

浆母细胞淋巴瘤(PBL)是一种罕见且侵袭性强的淋巴瘤,尤其易发生于HIV阳性和免疫功能低下的个体,中位诊断年龄为49岁。HIV阴性个体发生这种恶性肿瘤的病例较少见,且很少累及骨髓。虽然传统化疗方案如环磷酰胺、阿霉素、长春新碱和泼尼松龙(CHOP)以前曾用于治疗这种恶性肿瘤,但美国国立综合癌症网络目前推荐采用更强化的治疗方法。我们报告了一例罕见的IV期爱泼斯坦-巴尔病毒(EBV)阳性PBL,患者为一名38岁免疫功能正常的年轻成人,鼻腔肿瘤延伸至左眼眶窦并包绕部分视神经,既往无重大病史。治疗包括6个周期的硼替佐米联合剂量调整的EPOCH(依托泊苷、泼尼松、长春新碱、环磷酰胺和阿霉素)以及鞘内注射甲氨蝶呤,治疗后临床和影像学均有显著改善,提示该方案具有潜在疗效。视力恢复至基线水平,肿块大小显著缩小,头痛症状改善。鉴于这一结果强烈建议在更大规模的临床试验中进一步探索这种治疗方法的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90de/11327500/cdf6121e60f1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90de/11327500/677e112d5f54/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90de/11327500/cdf6121e60f1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90de/11327500/677e112d5f54/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90de/11327500/cdf6121e60f1/gr2.jpg

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