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Clinical Nuclear Medicine, 2018
Abstract Sellar and suprasellar paragangliomas are rare. We report the case of a 19-year-old man with sellar paraganglioma with parasellar and posterior pontine extension, requiring multiple transcranial surgeries and radiotherapy. The lesion was avid on 68Ga DOTANOC PET-CT scan substantiating its neuroendocrine nature.
Manjiri, Karlekar +5 more
openaire +2 more sources
Abstract Sellar and suprasellar paragangliomas are rare. We report the case of a 19-year-old man with sellar paraganglioma with parasellar and posterior pontine extension, requiring multiple transcranial surgeries and radiotherapy. The lesion was avid on 68Ga DOTANOC PET-CT scan substantiating its neuroendocrine nature.
Manjiri, Karlekar +5 more
openaire +2 more sources
The American Journal of the Medical Sciences, 2015
Somkiat, Sangwatanaroj +5 more
openaire +2 more sources
Somkiat, Sangwatanaroj +5 more
openaire +2 more sources
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
Science, 2000B. Baysal +13 more
semanticscholar +1 more source
Pheochromocytoma and paraganglioma—an update on diagnosis, evaluation, and management
Pediatric nephrology (Berlin, West), 2019Amrish Jain, Rossana Baracco, G. Kapur
semanticscholar +1 more source