Suppr超能文献

需要进行掌骨截肢的角化棘皮瘤。

Keratoacanthoma necessitating metacarpal amputation.

作者信息

Hamm J C, DeFranzo A J, Argenta L C, White W

机构信息

Department of Pathology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, N.C. 27103.

出版信息

J Hand Surg Am. 1990 Nov;15(6):980-6. doi: 10.1016/0363-5023(90)90028-p.

Abstract

Keratoacanthoma is usually considered a benign self-limiting lesion. First described in 1888 by Hutchinson, it most commonly involves the face and hands. It is usually controlled by complete soft tissue excision. A variant, subungual keratoacanthoma, affects bone by pressure erosion of the distal phalangeal tip. We report a case of keratoacanthoma clinically involving a metacarpal and phalanges with a radiologic and physical appearance at variance with previous reports. After multiple recurrences following erosion and cryosurgery, as well as attempted digit salvage with Mohs' surgery, ray amputation was required. The world literature pertaining to keratoacanthoma is reviewed and discussed.

摘要

角化棘皮瘤通常被认为是一种良性的自限性病变。1888年由哈钦森首次描述,它最常累及面部和手部。通常通过完整的软组织切除来控制。一种变异型,即甲下角化棘皮瘤,可通过远端指骨尖端的压力侵蚀影响骨骼。我们报告一例角化棘皮瘤,临床上累及掌骨和指骨,其影像学和体格检查表现与既往报道不同。在侵蚀和冷冻手术后多次复发,以及尝试用莫氏手术挽救手指后,需要进行截指手术。对有关角化棘皮瘤的世界文献进行了回顾和讨论。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验