血管免疫母细胞t细胞淋巴瘤累及同侧腮腺及侧颈1例

Seok Jung Hong, Mi Ji Lee, Seung Woo Kim
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引用次数: 0

摘要

血管免疫母细胞t细胞淋巴瘤(AITL)是一种罕见的恶性淋巴瘤(ML)亚型,仅占所有非霍奇金淋巴瘤(NHL)的1 - 2%。虽然腮腺的ML是罕见的,大多数是b细胞型。在腮腺和侧颈同时发生的AITL以前未见报道。它被归类为具有侵袭性临床特征的高度恶性肿瘤,预后比任何其他类型的NHL都差。我们最近遇到一位72岁的男性,在同侧腮腺尾部和外侧颈部有多发肿块,最终诊断为AITL。我们报告独特和罕见的疾病实体与简要的文献回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Angioimmunoblastic T-cell Lymphoma Involving the Ipsilateral Parotid and Lateral Neck
Angioimmunoblastic T-cell lymphoma (AITL) is a rare subtype of malignant lymphoma (ML), accounting for only 1 to 2% of all non-Hodgkin’s lymphoma (NHL). Although ML of the parotid gland is rare, the majority are B-cell types. The AITL occurring synchronously in the parotid gland and lateral neck has not been reported earlier. It is classified as a high-grade malignancy with aggressive clinical features, and the prognosis is worse than any other type of NHL. We recently encountered a 72-year-old man with multiple mass on the ipsilateral parotid tail and lateral neck, and he was finally diagnosed as AITL. We report the unique and rare disease entity with a brief literature review.
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