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Treatment of familial glomangiomatosis with Nd:YAG laser: a case report.
Baqays, Abdullah; Bulai Livideanu, Cristina; Mazereeuw-Hautier, Juliette; Alkhalaf, Humoud; Jendoubi, Fatma.
Afiliación
  • Baqays A; Department of Dermatology, University Hospital of Toulouse, Toulouse, France.
  • Bulai Livideanu C; Department of Dermatology, University Hospital of Toulouse, Toulouse, France.
  • Mazereeuw-Hautier J; Department of Dermatology, University Hospital of Toulouse, Toulouse, France.
  • Alkhalaf H; Department of Dermatology, Nice University Hospital, Nice, France.
  • Jendoubi F; Department of Dermatology, University Hospital of Toulouse, Toulouse, France.
J Cosmet Laser Ther ; 26(1-4): 81-82, 2024.
Article en En | MEDLINE | ID: mdl-39171935
ABSTRACT
Familial glomangiomatosis is a rare autosomal dominant vascular malformation caused by a mutation in the glomulin GLMN gene. It is characterized by the appearance of multiple glomus tumors composed of dysmature veins surrounded by glomus cells. We present a case of an 11-year-old girl with familial glomangiomatosis successfully treated with NdYAG long-pulse laser. Three sessions of laser treatment were performed, resulting in more than 80% reduction of the lesion and complete disappearance of pain, with no adverse effects reported. This case report demonstrates the excellent risk-benefit ratio of NdYAG long-pulse laser in the treatment of familial glomangiomatosis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tumor Glómico / Láseres de Estado Sólido Límite: Child / Female / Humans Idioma: En Revista: J Cosmet Laser Ther Asunto de la revista: DERMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tumor Glómico / Láseres de Estado Sólido Límite: Child / Female / Humans Idioma: En Revista: J Cosmet Laser Ther Asunto de la revista: DERMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido