Metastatic Pheochromocytoma Diagnosed with (131) I-MIBG SPECT/CT Imaging in a Patient with Pathogenic VHL Mutation

Pheochromocytoma is a rare catecholamine secreting neuroendocrine tumor arising from chromaffin cells of adrenal medulla with approximate prevalence of 0.1 to 0.6% in patients suffering from hypertension. Hypertensive control followed by surgical resection remains the primary treatment of choice. Al...

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Detalles Bibliográficos
Autores principales: Vankadari, Kousik, Boddula, Raman, Hegde, Aditya Gajanan, Chinte, Chimutai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical and Scientific Publishers Pvt. Ltd. 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056124/
https://www.ncbi.nlm.nih.gov/pubmed/35502282
http://dx.doi.org/10.1055/s-0042-1746177

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056124/
https://www.ncbi.nlm.nih.gov/pubmed/35502282
http://dx.doi.org/10.1055/s-0042-1746177

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