The role of the adrenalectomy in the management of pheochromocytoma: the experience of a Portuguese referral center
Purpose Pheochromocytoma is a rare neuroendocrine tumor. Despite the low incidence,
these tumors are of indisputable importance. This study aimed to analyze the management …
these tumors are of indisputable importance. This study aimed to analyze the management …
Characteristics and genetic testing outcomes of patients with clinically suspected paraganglioma/pheochromocytoma (PGL/PCC) syndrome in Singapore
KR Ting, PY Ong, SOG Wei, R Parameswaran… - Hereditary Cancer in …, 2020 - Springer
Background Hereditary paraganglioma (PGL) and pheochromocytoma (PCC) syndromes
are rare conditions, with limited data on spectrum of causative gene variants of these …
are rare conditions, with limited data on spectrum of causative gene variants of these …
Differences between Patients with Sporadic and Familial Pheochromocytoma—Is It Possible to Avoid Genetic Testing in Certain Patients?
MC Muñoz, B Febrero, M Abellán, AM Hernández… - Biomedicines, 2024 - mdpi.com
Background: Pheochromocytoma (PHEO) is a rare neuroendocrine tumour with a strong
genetic link, which therefore may modify its clinical behaviour and prognosis. The aim of the …
genetic link, which therefore may modify its clinical behaviour and prognosis. The aim of the …
Carotid body tumor with neck metastasis due to germline SDHB variant: a case report and literature review
T Mikoshiba, K Yoshihama, F Ito, M Sekimizu… - International Cancer …, 2021 - Springer
Carotid body tumor involving the succinate dehydrogenase subunit B (SDHB) variant
reportedly had a higher frequency of metastasis than other variants of succinate …
reportedly had a higher frequency of metastasis than other variants of succinate …
Pheochromocytoma: a retrospective study from a single center
NA Soares, MTPF Pacheco, ML Matos… - Endocrine …, 2021 - sciendo.com
Objectives. Pheochromocytoma (PCC) is a neuroendocrine tumor derived from chromaffin
tissue more frequently found in the adrenal medulla. Many discoveries over the last decade …
tissue more frequently found in the adrenal medulla. Many discoveries over the last decade …
[PDF][PDF] Hypertension cure and reducing pill burden after adrenalectomy for endocrine hypertension of adrenal origin: a comparative study from an Asian and UK Cohort
C Durand, TC Vasciuc, CH Tai, R Orpean, F Eatock… - World, 2021 - wjoes.com
Background: The cure rate of endocrine hypertension following adrenalectomy is
heterogeneous. Our aim of the study was to investigate the etiology and cure rate of …
heterogeneous. Our aim of the study was to investigate the etiology and cure rate of …
A 15-year pheochromocytoma and paraganglioma experience in a single centre: a Singapore perspective
Y Lee, LYR Tan, SAKKA Shakoor - Singapore Medical Journal, 2022 - journals.lww.com
Methods: We identified patients with positive histopathological confirmations of PCC and
PGL who were treated at a tertiary Singapore hospital between January 2000 and …
PGL who were treated at a tertiary Singapore hospital between January 2000 and …
[PDF][PDF] CONDUCTING AN ENVIRONMENTAL SCAN OF THE CANCER GENETICS SERVICES IN AN IRISH CONTEXT UNDERPINNED BY A MIXED METHODS …
J Hegarty, SJ Flaherty, S Egan, MM Jones, C Odisigo… - 2021 - cancer.ie
CHAPTER 2 INDIVIDUAL, SERVICE AND NATIONAL-LEVEL BARRIERS AND
FACILITATORS TO CANCER GENETIC TESTING AND COUNSELLING: A SYSTEMATIC …
FACILITATORS TO CANCER GENETIC TESTING AND COUNSELLING: A SYSTEMATIC …
Hereditary Pheochromocytoma and Paraganglioma Syndrome
D Liu - Handbook of Tumor Syndromes, 2020 - taylorfrancis.com
Pheochromocytoma and paraganglioma (PPGL) are rare tumors that affect the adrenal
medulla, and extra-adrenal locations, respectively. Although a majority (60%) of PPGL arise …
medulla, and extra-adrenal locations, respectively. Although a majority (60%) of PPGL arise …