Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants
Patients with germline SDHD pathogenic variants (encoding succinate dehydrogenase
subunit D; ie, paraganglioma 1 syndrome) are predominantly affected by head and neck …
subunit D; ie, paraganglioma 1 syndrome) are predominantly affected by head and neck …
Neurofibromatosis 1 French national guidelines based on an extensive literature review since 1966
C Bergqvist, A Servy, L Valeyrie-Allanore… - Orphanet Journal of …, 2020 - Springer
Neurofibromatosis type 1 is a relatively common genetic disease, with a prevalence ranging
between 1/3000 and 1/6000 people worldwide. The disease affects multiple systems with …
between 1/3000 and 1/6000 people worldwide. The disease affects multiple systems with …
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline
JWM Lenders, QY Duh, G Eisenhofer… - The Journal of …, 2014 - academic.oup.com
Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and
paraganglioma (PPGL). Participants: The Task Force included a chair selected by the …
paraganglioma (PPGL). Participants: The Task Force included a chair selected by the …
Imaging of pheochromocytoma and paraganglioma
JA Carrasquillo, CC Chen, A Jha, A Ling… - Journal of Nuclear …, 2021 - Soc Nuclear Med
Imaging plays a critical role in the management of pheochromocytomas and
paragangliomas and often guides treatment. The discovery of susceptibility genes …
paragangliomas and often guides treatment. The discovery of susceptibility genes …
Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment
VL Martucci, K Pacak - Current problems in cancer, 2014 - Elsevier
Pheochromocytomas (PHEOs) are rare neuroendocrine tumors that arise from the
chromaffin cells of the adrenal glands. Paragangliomas (PGLs), the extra-adrenal …
chromaffin cells of the adrenal glands. Paragangliomas (PGLs), the extra-adrenal …
Current approaches and recent developments in the management of head and neck paragangliomas
D Taïeb, A Kaliski, CC Boedeker, V Martucci… - Endocrine …, 2014 - academic.oup.com
Head and neck paragangliomas (HNPGLs) are rare neuroendocrine tumors belonging to
the family of pheochromocytoma/paraganglioma neoplasms. Despite advances in …
the family of pheochromocytoma/paraganglioma neoplasms. Despite advances in …
Prospective comparison of 68Ga-DOTATATE and 18F-FDOPA PET/CT in patients with various pheochromocytomas and paragangliomas with emphasis on sporadic …
Abstract Purpose Pheochromocytomas/paragangliomas (PHEOs/PGLs) overexpress
somatostatin receptors and recent studies have already shown excellent results in the …
somatostatin receptors and recent studies have already shown excellent results in the …
Paragangliomas of the head and neck
S Woolen, JJ Gemmete - Neuroimaging Clinics, 2016 - neuroimaging.theclinics.com
Paragangliomas make up a family of neoplasms that develop from the paraganglia tissues,
which are themselves of neural crest origin and have similar functions and histologic …
which are themselves of neural crest origin and have similar functions and histologic …
15 years of paraganglioma: imaging and imaging-based treatment of pheochromocytoma and paraganglioma
F Castinetti, A Kroiss, R Kumar… - Endocrine-related …, 2015 - erc.bioscientifica.com
Although anatomic imaging to assess the precise localization of pheochromocytomas/
paragangliomas (PHEOs/PGLs) is unavoidable before any surgical intervention on these …
paragangliomas (PHEOs/PGLs) is unavoidable before any surgical intervention on these …
Pheochromocytoma: a genetic and diagnostic update
LB Mercado-Asis, KI Wolf, I Jochmanova, D Taïeb - Endocrine practice, 2018 - Elsevier
ABSTRACT Objective: Pheochromocytomas and paragangliomas (PPGLs) are
neuroendocrine tumors derived from adrenal or extra-adrenal locations, respectively. Upon …
neuroendocrine tumors derived from adrenal or extra-adrenal locations, respectively. Upon …