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An atypical case of ectopic ACTH syndrome in an adolescent boy
Ectopic adrenocorticotropic hormone (ACTH) syndrome (EAS) is exceedingly rare in children and scarcely reported. Pancreatic neuroendocrine tumours (NETs) can rarely lead to secretion of ectopic ACTH. A 14-year-old boy presented with hyperpigmentation, hypertension and intermittent abdominal pain, an...
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| Publicado no: | Oxf Med Case Reports |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7202052/ https://ncbi.nlm.nih.gov/pubmed/32395251 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omaa017 |
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