一例罕见的弥漫大b细胞淋巴瘤(DLBCL)起源于腮腺的干燥综合征患者

Oncology, Gastroenterology and Hepatology Reports Pub Date : 2016-11-20 DOI:10.5530/OGH.2017.6.1.6

Suresh Babu Mallekavu Chikkadasappa, G. Kanakasetty, Rajeev Lakkavalli Krishnappa, S. Rao

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引用次数: 0

摘要

原发性唾液腺淋巴瘤很少见，NHL占所有结外淋巴瘤的5%，占所有唾液腺肿瘤的2%。多数为低级别淋巴瘤，以MALT淋巴瘤最为常见。DLBCL淋巴瘤并不常见，大多数被认为是由于潜在的低级别淋巴瘤的转化，假设出现在那些有唾液炎和干燥综合征。我们报告一个罕见的病例DLBCL在病人治疗干燥综合征。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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A Rare Case of a Diffuse Large B-Cell Lymphoma (DLBCL) arising From The Parotid Gland In a Patient With Sjogren’s Syndrome

Primary lymphoma of the salivary gland is rare, with NHL being 5% of all extra nodal lymphomas and 2% of all salivary gland tumors. Most are low grade lymphomas with MALT lymphomas being the most common. DLBCL lymphomas are uncommon with most thought to be due to transformation from underlying low-grade lymphomas, postulated to arise in those with sialedinitis and Sjogren’s syndrome. We report a rare case of DLBCL in a patient on treatment for Sjogren’s Syndrome.

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Oncology, Gastroenterology and Hepatology Reports

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