ArticleSkeletal radiology2017
Glomangiomatosis: a case report.
Article in Skeletal radiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed, 6 citations in OpenAlex.
- PET imaging of extradigital glomus tumor: a case report and literature review.Pain management · 2026Review
- Musculoskeletal glomus tumor: a review of 218 lesions in 176 patients.Skeletal radiology · 2025Article
- Flares of Confusion: A Case Report of Uterine Leiomyoma and Angiomatosis Complexity on Imaging.Cureus · 2023Article
- Glomangiomatosis - immunohistochemical study: A case report.World journal of clinical cases · 2022Article
- Glomangiomatosis of the lower leg.Radiology case reports · 2022Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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.
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Registered trials
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