Chiheb Soumiya, Mouradi Maha, Hali Fouzia
Department of Dermatology Venerology, Hospital Ibn Rochd University Hassan II, Casablanca, Morocco.
Skin Appendage Disord. 2021 Nov;7(6):468-474. doi: 10.1159/000516302. Epub 2021 Aug 6.
Superficial acral fibromyxoma is a relatively rare benign slow-growing soft-tissue tumor, first described by Fetsch's group [. 2001;32:704-14]. Since then, around three hundred publications have concerned this relatively new entity. The tumor involves peri- and subungual regions of fingers and toes in middle-aged adults with slight male predominance. This acral fibrous tumor is poorly known, and in certain cases, histology results may suggest myxoid dermatofibrosarcoma, which carries a completely different prognosis. In this article, we discuss the clinicopathologic features of this acral fibrous tumor through the report of 5 cases including 1 particular clinical presentation that revealed as a retronychia in a young woman.
浅表性肢端纤维黏液瘤是一种相对罕见的良性、生长缓慢的软组织肿瘤,由费奇团队于2001年首次描述[《现代病理学》2001年;32:704 - 14]。从那时起,大约有三百篇出版物涉及这个相对较新的实体。该肿瘤累及中年成年人手指和脚趾的甲周及甲下区域,男性略占优势。这种肢端纤维性肿瘤鲜为人知,在某些情况下,组织学结果可能提示黏液样皮肤纤维肉瘤,其预后完全不同。在本文中,我们通过报告5例病例(包括1例年轻女性表现为逆甲的特殊临床表现)来讨论这种肢端纤维性肿瘤的临床病理特征。