Multiple glomus tumours: Clinical, ultrasonographic and histopathologic findings of a rare disease

Author:

Wiese Bárbara1ORCID,Acevedo Patricia F.1,Franceschett Rodrigo A.2,Riedel Leila3,Issa Maria Cláudia A.4

Affiliation:

1. Department of Dermatology Fluminense Federal University Rio de Janeiro Brazil

2. Department of Pathology Fluminense Federal University Rio de Janeiro Brazil

3. Private Office Rio de Janeiro Brazil

4. Department of Internal Medicine Fluminense Federal University Rio de Janeiro Brazil

Abstract

AbstractGlomus tumour is a rare benign neoplasm originating from the glomus body, clinically presenting as a violet‐coloured, painful nodule more sensitive when exposed to cold or hot. This hamartoma is typically solitary and predominantly affects the limbs, extremities and nail beds. The appearance of multiple tumours and lesions not placed in the extremities is rare and frequently misdiagnosed. At dermoscopy, it appears as a homogeneous, structureless, purplish area surrounded by a whitish region. Skin ultrasound shows a well‐defined, round, hypoechoic mass. We report a case of numerous blue‐purplish painful nodules distributed in the trunk and arms while sparing the extremities, with typical dermoscopy and ultrasound findings. A biopsy was performed, confirming the diagnosis of glomangioma. We call attention to this rare condition to help dermatologists make this diagnosis when facing multiple painful nodules.

Publisher

Wiley

Reference6 articles.

1. Extradigital glomus tumor: dermoscopic description and histopathological correlation

2. Tumor glômico ‐ Retrospectiva de nove casos: do diagnóstico ao tratamento;Ferreira C;Revista Brasileira de Ortopedia [Internet],2000

3. Extradigital glomic tumor of the forearm. About a case and review of literature

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