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Cystic adrenal mass revealing a pheochromocytoma in the setting of multiple endocrine neoplasia: A case report

Pheochromocytoma, a neuroendocrine tumor, represents a rare medical condition characterized by the excessive secretion of catecholamines. These tumors often exhibit distinctive features on imaging studies, notably appearing hypervascular. Furthermore, they may present as cystic masses with thin wall...

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Hlavní autoři: Hajar Zebbakh, Kaoutar Imrani, Taha Yassine Aaboudech, Zakia Bernoussi, Nabil MoatassimBillah, Ittimade Nassar
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2024-08-01
Edice:Radiology Case Reports
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On-line přístup:http://www.sciencedirect.com/science/article/pii/S1930043324002905
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