Co-occurrence of pheochromocytoma and paraganglioma of the organ of Zuckerkandl resected simultaneously by laparoscopy: a rare case report and literature review

Pheochromocytomas (PHEOs) and paragangliomas are generally grouped as rare chromaffin cell tumors. The co-occurrence of PHEOs and paragangliomas of the organ of Zuckerkandl (POZ) is extremely rare. The most common symptom of pheochromocytoma-paraganglioma (PPGL) is hypertension, and open surgery is...

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Detalles Bibliográficos
Autores principales: Chang, Zhi, Shang, Jiwen, Yang, Shushang, Qin, Wuyao, Cui, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037737/
https://www.ncbi.nlm.nih.gov/pubmed/36950957
http://dx.doi.org/10.1177/03000605231161211

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037737/
https://www.ncbi.nlm.nih.gov/pubmed/36950957
http://dx.doi.org/10.1177/03000605231161211

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