A novel mutation of the glomulin gene in an Italian family with autosomal dominant cutaneous glomuvenous malformations

Exp Dermatol. 2011 Dec;20(12):1032-4. doi: 10.1111/j.1600-0625.2011.01387.x.

Abstract

Glomuvenous malformations (GVM) are hamartomas characterized histologically by glomus cells, which should be distinguished from glomus tumors. Familial GVM are rare, often present as multiple lesions, and exhibit familial aggregation, with autosomal dominant transmission. GVM are caused by mutations of the glomulin (GLMN) gene on chromosome 1p21-p22. Their development is thought to follow the 'two-hit' hypothesis, with a somatic mutation required in addition to the inherited germline mutation. We describe a novel GLMN mutation in an Italian family with GVM in which some members present with the less commonly observed phenotype of solitary lesions. A second somatic 'hit' mutation in GLMN was not discovered in our family. We further provide histological, immunohistochemical and electron microscopic data exhibiting the classic features of GVM. The diagnosis of GVM is critical because of distinction from venous malformations and blue rubber bleb nevus syndrome, which may demonstrate clinical similarities but require different treatment.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Actins / metabolism
  • Adaptor Proteins, Signal Transducing / genetics*
  • Adult
  • Dermis / pathology
  • Family*
  • Fathers
  • Female
  • Frameshift Mutation / genetics*
  • Glomus Tumor / diagnosis
  • Glomus Tumor / genetics*
  • Glomus Tumor / metabolism
  • Glomus Tumor / pathology
  • Heterozygote
  • Humans
  • Italy
  • Leukocytes, Mononuclear / chemistry
  • Paraganglioma, Extra-Adrenal / diagnosis
  • Paraganglioma, Extra-Adrenal / genetics*
  • Paraganglioma, Extra-Adrenal / metabolism
  • Paraganglioma, Extra-Adrenal / pathology
  • Pericytes / metabolism
  • Pericytes / pathology
  • Pericytes / ultrastructure
  • Siblings
  • Subcutaneous Fat / pathology
  • Vimentin / metabolism

Substances

  • Actins
  • Adaptor Proteins, Signal Transducing
  • GLMN protein, human
  • Vimentin

Supplementary concepts

  • Glomus vagale tumors