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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-...
Autores principales: | Koivikko, Minna, Ebeling, Tapani, Mäkinen, Markus, Leppäluoto, Juhani, Raappana, Antti, Ahtiainen, Petteri, Salmela, Pasi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2022
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Materias: | |
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 |
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