[丛状纤维组织细胞瘤]

[Plexiform fibrohistiocytic tumor].

作者信息

Naoum Christina, Trennheuser Lukas, Krahl Dieter, Toberer Ferdinand

机构信息

Hautklinik, Universitätsklinikum Heidelberg, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Deutschland.

Gemeinschaftspraxis für Dermatologie, Allergologie, Phlebologie, Ästhetische Lasermedizin, Operative Dermatologie und Dermatoonkologie Dres. Trennheuser Saarlouis, Wadgassen, Deutschland, Provinzialstr. 59, 66787.

出版信息

Dermatologie (Heidelb). 2023 Jun;74(6):453-456. doi: 10.1007/s00105-023-05126-5. Epub 2023 Mar 6.

DOI:10.1007/s00105-023-05126-5

PMID:36879141

Abstract

Plexiform fibrohistiocytic tumors are rare, low-to-moderate malignant soft tissue tumors that occur primarily in children and adolescents and are located on the upper extremity. The diagnosis must be made histologically. We report on a young woman who presented a growing, painless lesion on the cubital fossa. Histopathology as well as the standard of treatment are discussed.

摘要

丛状纤维组织细胞瘤是一种罕见的、低至中度恶性的软组织肿瘤，主要发生于儿童和青少年，位于上肢。必须通过组织学进行诊断。我们报告了一名年轻女性，其在肘窝处出现了一个逐渐增大的无痛性病变。文中讨论了组织病理学及治疗标准。