Cargando…
Paraganglioma of the tongue with SDHB gene mutation in a patient with Graves’ disease
We report a case of an apparently sporadic paraganglioma of the tongue with a germ‐line mutation in a female patient with asymptomatic Graves’ disease. The tongue is an unusual primary location. Genetic testing is mandatory in all cases. Thyroid gland dysfunction and autoimmune phenomena could be as...
Autores principales: | Duran Alvarez, Marcela Adriana, Tavarez Rodriguez, Juan Jose, Robledo, Mercedes |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452525/ https://www.ncbi.nlm.nih.gov/pubmed/30997073 http://dx.doi.org/10.1002/ccr3.2065 |
Ejemplares similares
-
Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients
por: Huang, Yiqiang, et al.
Publicado: (2018) -
Identification of a novel SDHB c.563 T > C mutation responsible for Paraganglioma syndrome and genetic analysis of the SDHB gene in China: a case report
por: Chen, Heye, et al.
Publicado: (2020) -
Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers
por: Eijkelenkamp, Karin, et al.
Publicado: (2016) -
A Multifocal Paraganglioma in an African Male Due to an Underlying SDHB Mutation
por: Siddiqui, Nida Mishraz, et al.
Publicado: (2021) -
SDHB-Associated Paraganglioma in a Pediatric Patient and Literature Review on Hereditary Pheochromocytoma-Paraganglioma Syndromes
por: Choat, Heather, et al.
Publicado: (2014)