1型神经纤维瘤病患者出现多发性甲下血管球瘤的罕见病例。

A rare case of multiple subungual glomus tumours in a neurofibromatosis type 1 patient.

作者信息

Yuen J, Bavan L, Graham A

机构信息

Department of Trauma and Orthopaedics, Buckinghamshire Healthcare Trust, UK.

出版信息

Hand Surg. 2015;20(1):159-60. doi: 10.1142/S0218810415720065.

DOI:10.1142/S0218810415720065

PMID:25609293

Abstract

Glomus tumours are uncommon lesions of the digit. They tend to be solitary. Only a small number of multifocal cases have been published, most of which are linked to an underlying genetic disorder. Here we report an unusual case of multifocal glomus tumours in the same hand in a patient suffering from neurofibromatosis type 1.

摘要

血管球瘤是手指的罕见病变。它们往往是单发的。仅有少数多灶性病例被报道，其中大多数与潜在的遗传疾病有关。在此，我们报告一例患有1型神经纤维瘤病的患者同一只手出现多灶性血管球瘤的罕见病例。