Department of Pathology, The Ohio State University Wexner Medical Center/James Cancer Hospital, Columbus, OH; and.
Department of Pathology and Dermatology, Wake Forest University, School of Medicine, Medical Center Boulevard, Winston-Salem, NC.
Am J Dermatopathol. 2024 Oct 1;46(10):672-674. doi: 10.1097/DAD.0000000000002787. Epub 2024 Jun 28.
Although CD20 expression is typically scarce in mycosis fungoides (MF), it is more commonly associated with T-cell lymphomas. Nevertheless, isolated instances of CD20-positive MF have been documented infrequently. Here, we present a unique case of CD20-positive MF in a 30-year-old man who manifested with a hypopigmented patch on the anterior chest. Histopathological examination revealed epidermotropic infiltrates of small- to medium-sized lymphocytes with hyperchromatic and cerebriform nuclei aligned along the basal and low-mid layers of the epidermis. Immunophenotypic analysis demonstrated neoplastic T cells expressing CD4+, CD8+, and CD3+ with the loss of CD7. Intriguingly, a notable subset of the neoplastic T cells exhibited CD20 expression. This case contributes to the sparse literature on CD20-positive MF and underscores its diagnostic and clinical ramifications. The role of B cells has been more thoroughly characterized in T-cell lymphomas other than MF. However, its significance in MF remains unclear due to the scarcity of reported cases. Some hypotheses propose that the B cells' expression might indicate immune dysregulation or complex interactions within the tumor microenvironment. Another perspective suggests it could signify a progression of the disease towards a more aggressive lymphoma phenotype. Further investigation and documentation of similar cases is imperative to elucidate the clinical features, prognosis, and optimal therapeutic strategies. The long-term prognosis and outcomes in patients with hypopigmented MF and CD20 positivity remain ambiguous, underscoring the necessity for continued research and scrutiny of analogous cases.
虽然 CD20 表达在蕈样肉芽肿(MF)中通常很少见,但它更常与 T 细胞淋巴瘤相关。然而,也有少数孤立的 CD20 阳性 MF 病例被记录下来。在这里,我们报告了一例 30 岁男性的 CD20 阳性 MF 病例,他表现为前胸的色素减退斑块。组织病理学检查显示,小至中等大小的淋巴细胞呈表皮内浸润,核呈深染和脑回状,沿表皮的基底层和中低层排列。免疫表型分析显示,肿瘤性 T 细胞表达 CD4+、CD8+和 CD3+,同时 CD7 缺失。有趣的是,肿瘤性 T 细胞的一个显著亚群表达 CD20。该病例增加了关于 CD20 阳性 MF 的文献,并强调了其诊断和临床意义。B 细胞在 MF 以外的 T 细胞淋巴瘤中的作用已经得到了更深入的研究。然而,由于报道的病例较少,其在 MF 中的意义仍不清楚。一些假说提出,B 细胞的表达可能表明免疫失调或肿瘤微环境中的复杂相互作用。另一种观点认为,它可能标志着疾病向更具侵袭性的淋巴瘤表型的进展。进一步研究和记录类似病例对于阐明其临床特征、预后和最佳治疗策略至关重要。色素减退性 MF 和 CD20 阳性患者的长期预后和结局仍不明确,这突显了对类似病例进行持续研究和审查的必要性。