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原发性精囊弥漫性大 B 细胞淋巴瘤:病例报告及文献复习。

Primary seminal vesicle diffuse large B-cell lymphoma: a case report and review of the literatures.

机构信息

Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.

Department of Oncology, Shanghai Medical College Fudan University, Shanghai, China.

出版信息

Front Immunol. 2024 Oct 30;15:1461090. doi: 10.3389/fimmu.2024.1461090. eCollection 2024.

Abstract

Primary seminal vesicle lymphoma is a remarkably rare condition, predominantly manifesting as diffuse large B-cell lymphoma. Due to its rarity and nonspecific clinical presentations, it is often misdiagnosed or overlooked. Here, we report a case of a 68-year-old male diagnosed with primary seminal vesicle lymphoma, coinciding with prostate cancer. The diagnosis followed initial findings of elevated prostate-specific antigen levels and abnormal magnetic resonance imaging of the prostate and left seminal vesicle. Suspicion of prostate cancer led to a radical resection of both the prostate and seminal vesicle. Subsequent pathological examination and next-generation sequencing post-surgery confirmed the diagnosis of primary seminal vesicle diffuse large B-cell lymphoma, characterized by CD79B mutation type (MCD type). The patient was treated with six cycles of the R-CHOP regimen (rituximab, cyclophosphamide, vincristine, doxorubicin, prednisone), achieving complete metabolic remission as confirmed by positron emission tomography-computed tomography. Fifteen months post-treatment, the patient's condition remains favorable. Through our literature review of additional six cases of primary seminal vesicle lymphoma, we aim to elucidate the typical clinical presentations, imaging features, pathological characteristics, genetic mutations, and therapeutic strategies, aiming to contribute to better detection and management of this rare malignancy. This case underscores the diagnostic challenges and emphasizes the necessity for heightened clinical suspicion and definitive pathological examination in the management of primary seminal vesicle lymphoma.

摘要

原发性精囊淋巴瘤是一种非常罕见的疾病,主要表现为弥漫性大 B 细胞淋巴瘤。由于其罕见性和非特异性临床表现,常被误诊或漏诊。在此,我们报告一例 68 岁男性原发性精囊淋巴瘤合并前列腺癌的病例。诊断依据为前列腺特异性抗原水平升高,前列腺和左侧精囊磁共振成像异常。最初怀疑为前列腺癌,行前列腺和精囊根治性切除术。术后病理检查和下一代测序证实为原发性精囊弥漫性大 B 细胞淋巴瘤,CD79B 突变型(MCD 型)。患者接受了六个周期的 R-CHOP 方案(利妥昔单抗、环磷酰胺、长春新碱、多柔比星、泼尼松)治疗,正电子发射断层扫描-计算机断层扫描证实完全代谢缓解。治疗后 15 个月,患者病情良好。通过对另外 6 例原发性精囊淋巴瘤的文献复习,旨在阐明其典型的临床表现、影像学特征、病理特征、基因突变和治疗策略,以期更好地发现和管理这种罕见的恶性肿瘤。本病例强调了诊断挑战,并强调在原发性精囊淋巴瘤的管理中需要提高临床警惕性和进行明确的病理检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83f3/11557305/93fb5b482538/fimmu-15-1461090-g001.jpg

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