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Marginal zone variant of mantle cell lymphoma: CD5-negative cyclin D1-positive variant posing a diagnostic dilemma.

机译:套细胞淋巴瘤的边缘区变体:CD5阴性细胞周期蛋白D1阳性变体构成诊断难题。

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摘要

Described herein is an unusual case of mantle cell lymphoma (MCL) histologically mimicking marginal zone lymphoma (MZL). An 83-year-old man presented with multiple adenopathies and a hilar mass encroaching on the right lung. A transbronchial biopsy showed small blue cells suspicious for small cell carcinoma. On further analysis the cells were predominantly small cleaved and CD20 positive, suggesting follicular lymphoma, grade 2. An axillary lymph node biopsy showed germinal centers surrounded by monocytoid B cells. Flow cytometry was negative for CD5 and CD23 and the diagnosis of MZL was considered. Because of the aggressive clinical behavior, including extensive necrosis on imaging studies, immunohistochemistry for cyclin D-1 was performed and was positive. Bone marrow was extensively involved and it showed t(11;14), in addition to other complex cytogenetic abnormalities. Differentiating MCL from MZL has prognostic and therapeutic implications, particularly when considering the potential role of targeted therapy and cell cycle modulators.
机译:在此描述的是在组织学上模仿边缘区淋巴瘤(MZL)的套细胞淋巴瘤(MCL)的罕见情况。一名83岁的男性出现多发性腺病,右肺部侵犯肺门。经支气管活检显示小蓝细胞可疑为小细胞癌。在进一步分析中,细胞主要为小裂痕,CD20阳性,提示滤泡性淋巴瘤为2级。腋窝淋巴结活检显示生发中心被单核细胞B细胞包围。 CD5和CD23的流式细胞术阴性,并考虑了MZL的诊断。由于具有侵略性的临床行为,包括在影像学研究中广泛坏死,因此进行了细胞周期蛋白D-1的免疫组织化学检查,结果呈阳性。骨髓广泛参与,除其他复杂的细胞遗传学异常外,还显示t(11; 14)。将MCL与MZL区分具有预后和治疗意义,尤其是在考虑靶向治疗和细胞周期调节剂的潜在作用时。

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