Leiomyosarcoma Originating From Axilla in Neurofibromatosis Type 1: A Rare Occurrence

Neurofibromatosis type 1 (NF1) or von Recklinghausen syndrome is an autosomal dominant disorder that affects the multisystem in the body with complex presentation caused by the neurofibromin gene mutation on chromosome 17. These patients tend to develop soft tissue sarcomas more than the general pop...

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Detalles Bibliográficos
Autores principales: Ullah, Assam, Khan, Salman, Irfan, Muhammad, Majeed, Imad, Khan, Imadullah, Khan, Hameed Haidar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Dermatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10292097/
https://www.ncbi.nlm.nih.gov/pubmed/37378254
http://dx.doi.org/10.7759/cureus.39007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10292097/
https://www.ncbi.nlm.nih.gov/pubmed/37378254
http://dx.doi.org/10.7759/cureus.39007

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