Atypical ovarian carcinoid tumor with widespread skeletal metastases: a case report of multiple endocrine neoplasia type 1 in a young woman

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited condition affecting multiple endocrine organs, resulting in significant morbidity and decreased life expectancy. Early tumor identification allows for timely patient management, reduces morbidity, and impro...

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Detalles Bibliográficos
Autores principales: Lou, Lei, Zhou, Lixia, Wang, Wenyan, Li, Huina, Li, Yuehong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857273/
https://www.ncbi.nlm.nih.gov/pubmed/31727021
http://dx.doi.org/10.1186/s12885-019-6332-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857273/
https://www.ncbi.nlm.nih.gov/pubmed/31727021
http://dx.doi.org/10.1186/s12885-019-6332-7

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