| Literature DB >> 17396092 |
Mehdi Ouaïssi1, Igor Sieleznieff, Nicolas Pirrò, Marie-José Payan, Jean-Baptiste Chaix, Bernard Consentino, Bernard Sastre.
Abstract
Paragangliomas are rare tumors arising from extraadrenal chromaffin cells. These tumors are most commonly found in the adrenal gland but other locations are possible. A 79-year-old woman with abdominal pain underwent computed tomography (CT scan). Surgery was indicated because of the increase in the size of the tumor. Histopathological examination revealed a non secreting paraganglioma in the left retroperitoneum. Paragangliomas are rare neuroendocrine tumors. They have a greater potential for malignancy than pheochromocytomas due to metastases or local recurrence making surgical excision the treatment of choice.Entities:
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Year: 2007 PMID: 17396092 DOI: 10.1016/s0399-8320(07)89380-8
Source DB: PubMed Journal: Gastroenterol Clin Biol ISSN: 0399-8320