Bilateral Pheochromocytoma with Germline MAX Variant without Family History

Recently, the genetic background of pheochromocytomas/paragangliomas (PPGLs) has been rapidly revealed. These tumors have been referred to as the “ten percent tumor”; however, the frequency of genetic variants of PPGLs has turned out to be more common than expected. PPGLs are potentially hereditary...

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Detalles Bibliográficos
Autores principales: Hata, Shinnosuke, Asano, Mai, Tominaga, Hiroyuki, Hamaguchi, Masahide, Hongo, Fumiya, Usui, Takeshi, Konishi, Eiichi, Fukui, Michiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9149808/
https://www.ncbi.nlm.nih.gov/pubmed/35645312
http://dx.doi.org/10.3390/clinpract12030035

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9149808/
https://www.ncbi.nlm.nih.gov/pubmed/35645312
http://dx.doi.org/10.3390/clinpract12030035

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