Nasolabial Ulcerated Placard Revealing a Primary Cutaneous Aggressive Epidermotropic CD8+ T-cell Lymphoma.

Q3 Medicine
Case Reports in Dermatological Medicine Pub Date : 2022-08-09 eCollection Date: 2022-01-01 DOI:10.1155/2022/5672783
J B Ntihebuwayo, F Hali, A Kerouach, H Rachadi, S Chiheb, F Marnissi
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引用次数: 0

Abstract

Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma is a rare entity representing less than 1% of cutaneous lymphomas. It has an aggressive clinical manifestation with a poor prognosis. It is characterized by cytotoxic and epidermotropic CD8+ proliferation. It also expresses the TIA-1 marker. We report a new case for its display and aggressive character, diagnostic difficulty, and good therapeutic response to chemotherapy. This is a 62-year-old female patient admitted to the hospital for a nasolabial ulcerated placard evolving for two years. Clinical examination revealed submandibular lymph nodes. The specimen analysis associated with anatomoclinical manifestation was concluded for a primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma. Tumor extent assessment did not show any secondary localization. The blood tests and serology were unremarkable. The patient had benefited from a CHOEP-type multidrug therapy protocol with complete healing of the lesion after three courses of chemotherapy.

Abstract Image

Abstract Image

Abstract Image

鼻唇溃疡牌显示原发性皮肤侵袭性表皮性CD8+ t细胞淋巴瘤。
原发性皮肤侵袭性表皮性CD8+ t细胞淋巴瘤是一种罕见的实体,占皮肤淋巴瘤的不到1%。它具有侵袭性临床表现,预后差。其特点是细胞毒性和表皮性CD8+增殖。它也表达TIA-1标记物。我们报告一个新病例的表现和侵袭性,诊断困难,和良好的治疗反应,化疗。这是一名62岁的女性患者,因鼻唇溃疡而住院两年。临床检查发现下颌下淋巴结。标本分析与解剖临床表现相结合,结论为原发性皮肤侵袭性表皮性CD8+ t细胞淋巴瘤。肿瘤范围评估未发现继发定位。血液检查和血清学检查均无异常。患者受益于choep型多药治疗方案,经过三个疗程的化疗,病变完全愈合。
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
24
审稿时长
15 weeks
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