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Metachronous metastatic paraganglioma in jejunum as a rare entity: A case report
Pheochromocytomas and paragangliomas are neuroendocrine tumors that arise from chromaffin cells of adrenal medulla and extra-adrenal paraganglia, respectively. The recurrence of these neuroendocrine tumors as a jejunal mass causing obstruction in the small intestine is an exceptional entity. The pre...
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| Pubblicato in: | Oncol Lett |
|---|---|
| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
D.A. Spandidos
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4314967/ https://ncbi.nlm.nih.gov/pubmed/25663897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2015.2860 |
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