原发性皮肤CD8+侵袭性表皮细胞毒性t细胞淋巴瘤1例

IF 0.5 JEADV clinical practice Pub Date : 2024-08-13 DOI:10.1002/jvc2.519
Tomomichi Shimizu, Nobuhiro Takahashi, Aya Okaniwa, Reiko Saito, Akio Kondoh, Fumikazu Yamazaki, Shunsuke Nagase, Naoya Nakamura, Kazuya Takeuchi, Tomotaka Mabuchi
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引用次数: 0

摘要

我们报告一位65岁的日本女性,原发皮肤CD8+侵袭性表皮细胞毒性t细胞淋巴瘤,是一种罕见的类型,预后较差。口服贝沙罗汀和伏立他汀无效,计划进行造血干细胞移植。我们强调原发性皮肤CD8+侵袭性表皮细胞毒性t细胞淋巴瘤应在可行的情况下用骨髓移植治疗。
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 case of primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma

A 65-year-old Japanese woman with primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma, a rare type with a poor prognosis, is presented. Oral bexarotene and vorinostat were ineffective, and hematopoietic stem cell transplantation was scheduled. We stress that primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma should be treated with bone marrow transplantation when available.

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