A Normotensive Case of Pheochromocytoma With Unusual Presentation of Abdominal Pain

Multiple endocrine neoplasia (MEN) is an inherited, autosomal dominant condition characterized by primary parathyroid hyperplasia, medullary thyroid neoplasm, and pheochromocytoma. It most commonly presents with medullary thyroid cancer and less frequently with other complaints. Pheochromocytoma can...

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Detalles Bibliográficos
Autores principales: Abid, Amina, Siddiqi, Ahmed Imran, Shafiq, Waqas, Irfan, Hira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Endocrinology/Diabetes/Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644892/
https://www.ncbi.nlm.nih.gov/pubmed/38022135
http://dx.doi.org/10.7759/cureus.47063

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644892/
https://www.ncbi.nlm.nih.gov/pubmed/38022135
http://dx.doi.org/10.7759/cureus.47063

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