原发性皮肤cd8阳性t细胞淋巴瘤-蕈样肉芽肿性真菌病:罕见病例报告。

IF 2 Q2 MEDICINE, GENERAL & INTERNAL
Sharmila Patil, Manjyot Gautam, Divya Shetty, Surekha Bhalekar, S Sudhamani
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引用次数: 0

摘要

蕈样肉芽肿性真菌病(GMF)是一种罕见的t细胞皮肤淋巴瘤亚型。由于缺乏明显的临床特征,GMF可能会给诊断带来挑战,从而导致诊断延迟。诊断是基于组织病理学和免疫组织化学的结果。在此,我们报告一位82岁男性,头皮、面部、前臂、躯干和双侧下肢瘙痒病变6个月。组织学上为cd8阳性的GMF。GMF是一种罕见的蕈样真菌病亚型
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 CD8-positive T-cell lymphoma-granulomatous mycosis fungoides: A rare case report.

Granulomatous mycosis fungoides (GMF) is a rare subtype of T-cell cutaneous lymphoma. Due to the lack of distinct clinical features, GMF may pose a diagnostic challenge, which results in diagnostic delay. The diagnosis is based on histopathological and immunohistochemical findings. Herein, we present an 82-year-old male with itchy lesions over the scalp, face, forearms, trunk, and bilateral lower limbs for 6 months. Histologically, it was a CD8-positive GMF. GMF is a rare subtype of mycosis fungoides with <100 cases in the literature, and most of these cases showed a CD4-positive phenotype. CD8-positive GMF is extremely rare. We observed that it commonly affects elderly females. The patients often present with nodules and do not carry an adverse prognosis.

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来源期刊
International Journal of Health Sciences-IJHS
International Journal of Health Sciences-IJHS MEDICINE, GENERAL & INTERNAL-
自引率
15.00%
发文量
49
审稿时长
8 weeks
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