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

Abstract 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 excessi...

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Автори:	Yumiko Hori, Katsutoshi Hirose, Michio Ozeki, Kenji Hata, Daisuke Motooka, Shinichiro Tahara, Takahiro Matsui, Masaharu Kohara, Hiroki Higashihara, Yusuke Ono, Kaishu Tanaka, Satoru Toyosawa, Eiichi Morii
Формат:	Artigo
Мова:	Inglês
Опубліковано:	BMC 2022-01-01
Серія:	Diagnostic Pathology
Предмети:	Fibro-adipose vascular anomaly FAVA PIK3CA mTOR Vascular anomaly Lymphatic malformation
Онлайн доступ:	https://doi.org/10.1186/s13000-022-01199-3
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