Acromegaly caused by a GHRH-producing pancreatic neuroendocrine tumor: a rare manifestation of MEN1 syndrome

SUMMARY: Multiple endocrine neoplasia type 1 NM_001370259.2(MEN1):c.466G>C(p.Gly156Arg) is characterized by tumors of various endocrine organs. We report on a rare, growth hormone-releasing hormone (GHRH)-releasing pancreatic tumor in a MEN1 patient with a long-term follow-up after surgery. A 22-...

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Detalles Bibliográficos
Autores principales: Koivikko, Minna, Ebeling, Tapani, Mäkinen, Markus, Leppäluoto, Juhani, Raappana, Antti, Ahtiainen, Petteri, Salmela, Pasi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Insight into Disease Pathogenesis or Mechanism of Therapy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897594/
https://www.ncbi.nlm.nih.gov/pubmed/35199646
http://dx.doi.org/10.1530/EDM-21-0079

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897594/
https://www.ncbi.nlm.nih.gov/pubmed/35199646
http://dx.doi.org/10.1530/EDM-21-0079

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