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Acromegaly in a patient with a pulmonary neuroendocrine tumor: case report and review of current literature
BACKGROUND: Pulmonary neuroendocrine tumors (NET) form a heterogeneous group of rare diseases. In these tumors, paraneoplastic syndromes have been described to drive the course of the disease, among them acromegaly induced by paraneoplastic secretion of growth hormone-releasing hormone (GHRH). CASE...
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| Publicado en: | BMC Res Notes |
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| Autores principales: | , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4924317/ https://ncbi.nlm.nih.gov/pubmed/27349224 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-016-2132-1 |
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