Published October 2017 | Version v1
Journal article

Glomangiomatosis: a case report

  • 1. Rutgers, the State University of New Jersey-New Jersey Medical School, Department of Pathology and Laboratory Medicine, Newark, NJ (United States)
  • 2. Rutgers, the State University of New Jersey-New Jersey Medical School, Department of Orthopaedics, Newark, NJ (United States)
  • 3. Rutgers, the State University of New Jersey-New Jersey Medical School, Department of Radiology, Newark, NJ (United States)

Description

Glomangiomatosis is a benign vascular variant of a glomus tumor. The lesion represents only 5% of glomus tumors with unusual or atypical features and even fewer glomus tumors with typical features. The lesions are most commonly located in the distal extremities and are multiple, deep, extensive, and often pain producing. They develop from small arteriovenous anastamoses and are most often identified in young adults. The lesions may recur. We present a case of a 33-year-old male who presented clinically with multiple slowly enlarging masses of the leg over a 5-year period, of which one caused significant pain. One of the lesions was reported to be present at birth. Imaging studies were performed and were suggestive of neurofibromatosis. Biopsies from multiple lesions led to an eventual diagnosis of multiple glomangiomatosis. (orig.)

Availability note (English)

Available from: http://dx.doi.org/10.1007/s00256-017-2697-3

Additional details

Identifiers

Publishing Information

Journal Title
Skeletal Radiology
Journal Volume
46
Journal Issue
10
Journal Page Range
p. 1427-1433
ISSN
0364-2348
CODEN
SKRADI