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A rare case of an ACTH/CRH co-secreting midgut neuroendocrine tumor mimicking Cushing's disease
Ectopic ACTH/CRH co-secreting tumors are a very rare cause of Cushing’s syndrome and only a few cases have been reported in the literature. Differentiating between Cushing’s disease and ectopic Cushing’s syndrome may be particularly difficult if predominant ectopic CRH secretion leads to pituitary c...
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| Publié dans: | Endocrinol Diabetes Metab Case Rep |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Bioscientifica Ltd
2017
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5488327/ https://ncbi.nlm.nih.gov/pubmed/28680643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-17-0058 |
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