Pheochromocytoma in the organ of Zuckerkandl with distant skeletal metastases – A case report

Pheochromocytoma in the organ of Zuckerkandl with distant skeletal metastases – A case report

Pheochromocytomas are rare catecholamine-secreting neuroendocrine tumors that originate from chromaffin cells in the adrenal medulla. They cause severe hypertension and various clinical manifestations. While most arise in the adrenal medulla, some occur in extra-adrenal locations.We present a case r...

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Bibliographic Details
Main Authors: Abdul Rehman Ahmad Akhtar, MBBS, Zayed Mohiyuddin, MBBS, Muiz Khan Tareen, MD, Kamran Malik, MBBS
Format: Article
Language:English
Published: Elsevier 2024-04-01
Series:Radiology Case Reports
Subjects:
Pheochromocytoma
Paraganglioma
Zuckerkandl
Bone metastasis
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043324000281

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http://www.sciencedirect.com/science/article/pii/S1930043324000281

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