Clinical features of multiple glomus tumors.


Journal Article

BACKGROUND: While glomus tumors are usually solitary, multiple glomus tumors do occur. The purpose of this study was to review the clinical characteristics and outcomes in a series of patients with multiple glomus tumors presenting to our institution. METHODS: A retrospective review of patients with multiple glomus tumors seen at our institution over the past 25 years was performed. RESULTS: Twenty-two patients with multiple glomus tumors were identified. Initial diagnosis was blue rubber nevus syndrome and hemangioma in 10 and 7 patients, respectively. The mean duration from onset of symptoms until correct diagnosis was 14.6 years. Involvement of an extremity was noted in 90.9% of the patients. An autosomal dominant pattern of inheritance was noted in 13 of 22 patients. The classic triad of symptoms in solitary glomus tumors--pain, pinpoint tenderness, and cold hypersensitivity--was noted in only 1 of the 22 patients; pain and pinpoint tenderness were simultaneously identified in 14 patients, 8 with visible lesions but no symptoms. Symptoms were relieved by surgical excision in most patients. CONCLUSION: Patients with multiple glomus tumors are frequently misdiagnosed. Proper recognition and diagnosis would lead to improved management.

Full Text

Duke Authors

Cited Authors

  • Anakwenze, OA; Parker, WL; Schiefer, TK; Inwards, CY; Spinner, RJ; Amadio, PC

Published Date

  • July 2008

Published In

Volume / Issue

  • 34 / 7

Start / End Page

  • 884 - 890

PubMed ID

  • 18363721

Pubmed Central ID

  • 18363721

Electronic International Standard Serial Number (EISSN)

  • 1524-4725

Digital Object Identifier (DOI)

  • 10.1111/j.1524-4725.2008.34173.x


  • eng

Conference Location

  • United States