具有结节外表现和异常 CD10 表达的套细胞淋巴瘤 Blastoid 变异。

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Arthy Raman, Sree Rekha Jinkala, Roobashri Murugan, Prabhu Manivannan
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引用次数: 0

摘要

套细胞淋巴瘤(MCL)占非霍奇金淋巴瘤的 3%-10%,其特征为 t (11:14)(q13;q32)。常见表现为全身淋巴结肿大,伴有体重减轻、盗汗和发热。在 MCL 的组织学亚型中,鼓泡变异型 MCL 占所有病例的 10%-15%。由于囊泡型 MCL 与大 B 细胞淋巴瘤相似,因此仅根据其形态诊断囊泡型 MCL 具有挑战性。因此,免疫分型和分子研究有助于正确诊断。我们报告了一名被诊断为囊泡状变异型 MCL 的老年男性。他出现了播散性软组织和皮下结节,CD10表达异常。出现结节外部位和CD10异常表达意味着总体预后较差。CD10阳性的MCL可能被误诊为大B细胞淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Blastoid Variant of Mantle Cell Lymphoma with Extranodal Presentation and Aberrant CD10 Expression.

Blastoid Variant of Mantle Cell Lymphoma with Extranodal Presentation and Aberrant CD10 Expression.

Blastoid Variant of Mantle Cell Lymphoma with Extranodal Presentation and Aberrant CD10 Expression.

Mantle cell lymphoma (MCL) constitutes 3%-10% of non-Hodgkin lymphoma and is characterized by t (11:14)(q13;q32). The common presentation is generalized lymphadenopathy with weight loss, infrequently night sweats, and fever. Among histological subtypes of MCL, the blastoid variant of MCL constitutes 10%-15% of all the cases. It is challenging to diagnose the blastoid variant of MCL based on its morphology alone as it mimics large B-cell lymphoma. Hence, the immunophenotyping and molecular studies aid in its correct diagnosis. We report an elderly man diagnosed with blastoid variant MCL. He presented with disseminated soft-tissue and subcutaneous nodules, and showed aberrant CD10 expression. Presentation of the extranodal site and aberrant CD10 expressions carries an overall poor prognosis. CD10-positive MCL can be mistaken for large B-cell lymphoma.

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