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原发中枢神经系统结外 NK/T 细胞淋巴瘤,鼻型伴 CD20 表达:病例报告及文献复习。

Primary central nervous system extranodal NK/T-cell lymphoma, nasal type with CD20 expression: Case report and review of the literature.

机构信息

Department of Pathology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Department of Radiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

出版信息

Neuropathology. 2024 Jun;44(3):222-229. doi: 10.1111/neup.12954. Epub 2023 Nov 14.

Abstract

Primary central nervous system (PCNS) extranodal NK/T-cell lymphoma, nasal type (ENKTCL), is an exceedingly rare tumor. To the best of our knowledge, only 27 cases and only one reported aberrant CD20 expression have been documented in the literature. Here we present a second case of PCNS ENKTCL with aberrant CD20 expression in a 43-year-old immunocompetent Chinese female. The patient presented with tremors, weakness in the right upper limb, and a slow reaction. Magnetic resonance imaging revealed multiple brain lesions. A histological examination revealed a diffuse distribution of intermediate-sized pleomorphic lymphocytes with angiocentric growth. The tumor cells expressed CD2, CD3, CD56, T-cell intracellular antigen-1, granzyme B, and Epstein-Barr virus-encoded RNAs (EBERs), with additional partial and weak CD20 and CD30 expression. Despite a confirmatory pathological diagnosis, the patient refused treatment and was discharged, ultimately dying from the disease. In the literature review, the clinical, immunohistochemical, EBERs, treatment, and prognostic features of PCNS ENKTCL were summarized. Although PCNS ENKTCT is extremely rare, it does occur and should always be included in differential diagnoses. CD20 expression should be evaluated routinely with relevant markers. The accumulation of cases is crucial for developing an effective treatment strategy for this rare and aggressive malignancy.

摘要

原发性中枢神经系统(PCNS)结外 NK/T 细胞淋巴瘤,鼻型(ENKTCL)是一种非常罕见的肿瘤。据我们所知,文献中仅报道了 27 例病例,仅有 1 例报道存在异常 CD20 表达。在这里,我们报告了第二例异常 CD20 表达的 PCNS ENKTCL 病例,患者为 43 岁免疫功能正常的中国女性。患者表现为震颤、右上臂无力和反应迟钝。磁共振成像显示多个脑部病变。组织学检查显示中等大小多形性淋巴细胞弥漫分布,呈血管中心性生长。肿瘤细胞表达 CD2、CD3、CD56、T 细胞内抗原-1、颗粒酶 B 和 Epstein-Barr 病毒编码的 RNA(EBERs),部分和弱表达 CD20 和 CD30。尽管有明确的病理诊断,但患者拒绝治疗并出院,最终死于该疾病。在文献复习中,总结了 PCNS ENKTCL 的临床、免疫组织化学、EBERs、治疗和预后特征。尽管 PCNS ENKTCT 非常罕见,但确实存在,应始终包括在鉴别诊断中。应常规评估 CD20 表达,并结合相关标志物进行评估。积累更多病例对于制定这种罕见且侵袭性恶性肿瘤的有效治疗策略至关重要。

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