Cargando…
Coexistence of Multiple Endocrine Neoplasia Type 2B and Chilaiditi Sign: A Case Report
We present a 15-year-old female patient with medullary thyroid carcinoma, marfanoid habitus, and mucosal ganglioneuromatosis. Our case had a RET protooncogene mutation ser836 polymorphism in exon 14 and ser904 polymorphism in exon 15. Our patient is thought to be atypical MEN2B due to the absence of...
Autores principales: | Çetin, Deniz, Ünübol, Mustafa, Soyder, Aykut, Güney, Engin, Coşkun, Adil, Özbaş, Serdar, Ünsal, Alparslan, Erkuş, Muhan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483661/ https://www.ncbi.nlm.nih.gov/pubmed/23119190 http://dx.doi.org/10.1155/2012/360328 |
Ejemplares similares
-
Polymyalgia rheumatica as the first presentation of parathyroid carcinoma
por: Unubol, Mustafa, et al.
Publicado: (2013) -
Chilaiditi sign
por: Yagnik, Vipul D.
Publicado: (2010) -
Adrenal incidentaloma and the Janus Kinase 2 V617F mutation: A case-based review of the literature
por: Unubol, Mustafa, et al.
Publicado: (2013) -
Chilaiditi's sign secondary to Richter's hernia or Chilaiditi's syndrome?
por: Shakya, Vikal Chandra
Publicado: (2015) -
Beware of Chilaiditi sign!!
por: Danve, Abhijeet, et al.
Publicado: (2015)