Pitfalls in diagnosing primary cutaneous aggressive epidermotropic CD8+ T‐cell lymphoma
Pitfalls in diagnosing primary cutaneous aggressive epidermotropic CD8+ T‐cell lymphoma
复制标题
诊断原发性皮肤侵袭性表皮性 CD8+ T 细胞淋巴瘤的陷阱
DOI：
10.1111/bjd.17252
复制
发表时间：
2018
影响因子：
10.3
通讯作者：
M. Bekkenk
中科院分区：
文献类型：
--
作者：
N. J. Deenen;L. Koens;E. H. Jaspars;M. Vermeer;R. Willemze;M. D. de Rie;M. Bekkenk
原发性皮肤侵袭性表皮性 CD8+ T 细胞淋巴瘤 (CD8+ CTCL) 是一种罕见的 CTCL 类型，作为临时实体纳入最近的皮肤淋巴瘤分类中。尽管有特定的临床和组织学特征，但初步诊断可能具有挑战性。我们报告了三例 CD8+ CTCL，其临床和组织学与坏疽性脓皮病 (PG) 或 D 型淋巴瘤样丘疹病 (LyP) 相似。本文受版权保护。版权所有。
Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma (CD8+ CTCL) is a rare type of CTCL included as a provisional entity in recent cutaneous lymphoma classifications. Despite specific clinical and histological characteristics, the initial diagnosis can be challenging. We report three cases of CD8+ CTCL presenting with clinical and histological resemblance to pyoderma gangrenosum (PG) or lymphomatoid papulosis (LyP) type D. This article is protected by copyright. All rights reserved.