原发性皮肤γ/δ t细胞淋巴瘤。骨髓肉芽肿的不典型病例。

Guy Shalom, Ronit Gurion, Daniel Benharroch
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引用次数: 2

摘要

背景:原发性皮肤γ/δ t细胞淋巴瘤是一种罕见的外周t细胞淋巴瘤,最近才与皮下泛膜炎样t细胞淋巴瘤区分开来,以其侵袭性而闻名。主要观察:我们在此报告一例原发性皮肤γ/δ t细胞淋巴瘤,患者为35岁男性,伴有骨髓肉芽肿,这是该淋巴瘤的一个意想不到的特征。病人接受联合化疗。获得部分缓解,随后复发。然后进行异体干细胞移植,完全缓解。结论:骨髓肉芽肿可能是原发性皮肤γ/δ t细胞淋巴瘤的伴发特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary cutaneous γ/δ T-cell lymphoma. An atypical case with bone marrow granulomas.

Primary cutaneous γ/δ T-cell lymphoma. An atypical case with bone marrow granulomas.

Primary cutaneous γ/δ T-cell lymphoma. An atypical case with bone marrow granulomas.

Primary cutaneous γ/δ T-cell lymphoma. An atypical case with bone marrow granulomas.

Background: Primary cutaneous γ/δ T-cell lymphoma is a rare variant of peripheral T-cell lymphoma which has been only recently set apart from subcutaneous panniculitis-like T-cell lymphoma and is known for its aggressive nature.

Main observation: We hereby report a case of primary cutaneous γ/δ T-cell lymphoma in a 35-year-old man with bone marrow granulomas, an unexpected feature in this lymphoma. The patient was treated with combination chemotherapy. Partial response was obtained, followed by relapse. Allogeneic stem cell transplantation was then carried out, and full remission was achieved.

Conclusion: Bone marrow granulomas can be an accompanying feature in primary cutaneous γ/δ T-cell lymphoma.

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