Csomor J, Bognár A, Benedek S, Sinkó J, Fekete S, Krenács L, Matolcsy A, Reiniger L
1st Department of Pathology and Experimental Cancer Research, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
J Clin Pathol. 2008 Jun;61(6):770-2. doi: 10.1136/jcp.2007.054585.
Primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma is a rare and provisional entity, characterised by cutaneous involvement and aggressive clinical behaviour. The case is here presented of a young woman with concurrent cutaneous and systemic involvement. Despite multi-agent chemotherapy, only partial remission could be achieved, and the patient died from therapy-resistant respiratory and circulatory failure. This case report is intended to add to the data collected on this rare entity, with only about 20 cases as yet described.
原发性皮肤侵袭性亲表皮CD8 + 细胞毒性T细胞淋巴瘤是一种罕见的暂定实体,其特征为皮肤受累及侵袭性临床行为。本文报告了一名年轻女性同时出现皮肤和全身受累的病例。尽管采用了多药化疗,仍仅实现了部分缓解,患者最终死于治疗抵抗性呼吸和循环衰竭。本病例报告旨在补充关于这一罕见实体收集的数据,目前仅有约20例病例被描述。