Occult insulinoma with treatment refractory, severe hypoglycaemia in multiple endocrine neoplasia type 1 syndrome; difficulties faced during diagnosis, localization and management; a case report

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN 1) syndrome is a rare, complex genetic disorder characterized by increased predisposition to tumorigenesis in multiple endocrine and non-endocrine tissues. Diagnosis and management of MEN 1 syndrome is challenging due to its vast heterogeneity in...

Descripción completa

Detalles Bibliográficos
Autores principales: Ranaweerage, Rasika, Perera, Shehan, Sathischandra, Harsha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925226/
https://www.ncbi.nlm.nih.gov/pubmed/35296318
http://dx.doi.org/10.1186/s12902-022-00985-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925226/
https://www.ncbi.nlm.nih.gov/pubmed/35296318
http://dx.doi.org/10.1186/s12902-022-00985-w

Ejemplares similares