GLMN causing vascular malformations: the clinical and genetic differentiation of cutaneous venous malformations

BMJ Case Rep. 2022 Jun 22;15(6):e246114. doi: 10.1136/bcr-2021-246114.

Abstract

Cutaneous venous malformations frequently present with blue-pink lesions on the skin or mucosal surfaces. They can be problematic for patients who experience pain or unsightly lesions and can also be associated with significant bleeding. A proportion of venous malformations have been noted to occur in families, in particular glomuvenous malformations (GVMs). A 'two-hit' occurrence of genetic pathogenic variants appears to explain the appearance of GVMs, with the initial change in the germline copy of GLMN followed by a second somatic hit. Here we discuss a report of siblings experiencing such lesions, which were diagnosed as GVMs by genetic testing. We include a review of the literature regarding the clinical and genetic differences between these groups of venous malformations.

Keywords: Dermatology; Genetic screening / counselling; Interventional radiology; Paediatrics.

Publication types

  • Case Reports

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Glomus Tumor* / diagnosis
  • Humans
  • Paraganglioma, Extra-Adrenal
  • Skin Neoplasms* / pathology
  • Vascular Malformations* / diagnosis
  • Vascular Malformations* / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • GLMN protein, human

Supplementary concepts

  • Glomus vagale tumors