Personalized management of pheochromocytoma and paraganglioma
S Nölting, N Bechmann, D Taieb… - Endocrine …, 2022 - academic.oup.com
Pheochromocytomas/paragangliomas are characterized by a unique molecular landscape
that allows their assignment to clusters based on underlying genetic alterations. With around …
that allows their assignment to clusters based on underlying genetic alterations. With around …
Clinical practice guideline for screening and management of high blood pressure in children and adolescents
These pediatric hypertension guidelines are an update to the 2004 “Fourth Report on the
Diagnosis, Evaluation, and Treatment of High Blood Pressure in Children and Adolescents.” …
Diagnosis, Evaluation, and Treatment of High Blood Pressure in Children and Adolescents.” …
New perspectives on pheochromocytoma and paraganglioma: toward a molecular classification
A molecular biology–based taxonomy has been proposed for pheochromocytoma and
paraganglioma (PPGL). Data from the Cancer Genome Atlas revealed clinically relevant …
paraganglioma (PPGL). Data from the Cancer Genome Atlas revealed clinically relevant …
Current management of pheochromocytoma/paraganglioma: a guide for the practicing clinician in the era of precision medicine
S Nölting, M Ullrich, J Pietzsch, CG Ziegler… - Cancers, 2019 - mdpi.com
Pheochromocytomas and paragangliomas (PCC/PGLs) are rare, mostly catecholamine-
producing neuroendocrine tumors of the adrenal gland (PCCs) or the extra-adrenal …
producing neuroendocrine tumors of the adrenal gland (PCCs) or the extra-adrenal …
Head and neck paragangliomas: an update on the molecular classification, state-of-the-art imaging, and management recommendations
EP Lin, BB Chin, L Fishbein, T Moritani… - Radiology: Imaging …, 2022 - pubs.rsna.org
Paragangliomas are neuroendocrine tumors that derive from paraganglia of the autonomic
nervous system, with the majority of parasympathetic paragangliomas arising in the head …
nervous system, with the majority of parasympathetic paragangliomas arising in the head …
von Hippel–Lindau disease
P Chittiboina, RR Lonser - Handbook of clinical neurology, 2015 - Elsevier
Abstract von Hippel–Lindau (VHL) disease is an inheritable condition with an incidence of 1
in 36 000 live births. Individuals with VHL develop benign and malignant tumors including …
in 36 000 live births. Individuals with VHL develop benign and malignant tumors including …
Von Hippel-Lindau disease: current challenges and future prospects
Understanding of molecular mechanisms of tumor growth has an increasing impact on the
development of diagnostics and targeted therapy of human neoplasia. In this review, we …
development of diagnostics and targeted therapy of human neoplasia. In this review, we …
Pheochromocytoma and paraganglioma—an update on diagnosis, evaluation, and management
A Jain, R Baracco, G Kapur - Pediatric Nephrology, 2020 - Springer
Pheochromocytomas and paragangliomas (PPGLs) generally grouped together are rare
catecholamine-secreting endocrine tumors. Symptoms of catecholamine excess are non …
catecholamine-secreting endocrine tumors. Symptoms of catecholamine excess are non …
Characteristics of Pediatric vs Adult Pheochromocytomas and Paragangliomas
C Pamporaki, B Hamplova, M Peitzsch… - The Journal of …, 2017 - academic.oup.com
Abstract Context: Pheochromocytomas and paragangliomas (PPGLs) in children are often
hereditary and may present with different characteristics compared with adults. Hereditary …
hereditary and may present with different characteristics compared with adults. Hereditary …
Review of pediatric pheochromocytoma and paraganglioma
R Bholah, TE Bunchman - Frontiers in pediatrics, 2017 - frontiersin.org
Pheochromocytoma (PCC) and paraganglioma (PGL) are rare chromaffin cell tumors which
secrete catecholamines and form part of the family of neuroendocrine tumors. Although a …
secrete catecholamines and form part of the family of neuroendocrine tumors. Although a …