PIK3CA mutation correlates with mTOR pathway expression but not clinical and pathological features in Fibfibroipose vascular anomaly (FAVA)

BACKGROUND: Fibro-adipose vascular anomaly (FAVA) is a rare and new entity of vascular anomaly. Activating mutations in the phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) gene were identified at a frequency of 62.5% in FAVA cases. The PIK3CA mutations excessively act...

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Detalles Bibliográficos
Autores principales: Hori, Yumiko, Hirose, Katsutoshi, Ozeki, Michio, Hata, Kenji, Motooka, Daisuke, Tahara, Shinichiro, Matsui, Takahiro, Kohara, Masaharu, Higashihara, Hiroki, Ono, Yusuke, Tanaka, Kaishu, Toyosawa, Satoru, Morii, Eiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802443/
https://www.ncbi.nlm.nih.gov/pubmed/35094709
http://dx.doi.org/10.1186/s13000-022-01199-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802443/
https://www.ncbi.nlm.nih.gov/pubmed/35094709
http://dx.doi.org/10.1186/s13000-022-01199-3

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