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 …
Pheochromocytoma and paraganglioma
HPH Neumann, WF Young Jr… - New England journal of …, 2019 - Mass Medical Soc
Pheochromocytoma and Paraganglioma Pheochromocytoma and paraganglioma are
related tumors that differ mainly in location; pheochromocytomas are adrenal, and …
related tumors that differ mainly in location; pheochromocytomas are adrenal, and …
[HTML][HTML] New developments in existing WHO entities and evolving molecular concepts: The Genitourinary Pathology Society (GUPS) update on renal neoplasia
Abstract The Genitourinary Pathology Society (GUPS) reviewed recent advances in renal
neoplasia, particularly post-2016 World Health Organization (WHO) classification, to provide …
neoplasia, particularly post-2016 World Health Organization (WHO) classification, to provide …
Report from the international society of urological pathology (ISUP) consultation conference on molecular pathology of urogenital cancers: III: molecular pathology of …
Renal cell carcinoma (RCC) subtypes are increasingly being discerned via their molecular
underpinnings. Frequently this can be correlated to histologic and immunohistochemical …
underpinnings. Frequently this can be correlated to histologic and immunohistochemical …
Overview of the 2022 WHO classification of familial endocrine tumor syndromes
This review of the familial tumor syndromes involving the endocrine organs is focused on
discussing the main updates on the upcoming fifth edition of the WHO Classification of …
discussing the main updates on the upcoming fifth edition of the WHO Classification of …
Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement
D Taïeb, S Nölting, ND Perrier, M Fassnacht… - Nature Reviews …, 2024 - nature.com
Adult and paediatric patients with pathogenic variants in the gene encoding succinate
dehydrogenase (SDH) subunit B (SDHB) often have locally aggressive, recurrent or …
dehydrogenase (SDH) subunit B (SDHB) often have locally aggressive, recurrent or …
A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: Beyond phaeochromocytoma and paraganglioma
J MacFarlane, KC Seong, C Bisambar… - Clinical …, 2020 - Wiley Online Library
The citric acid cycle, also known as the Krebs cycle, plays an integral role in cellular
metabolism and aerobic respiration. Mutations in genes encoding the citric acid cycle …
metabolism and aerobic respiration. Mutations in genes encoding the citric acid cycle …
[HTML][HTML] Pheochromocytoma/paraganglioma: recent updates in genetics, biochemistry, immunohistochemistry, metabolomics, imaging and therapeutic options
K Antonio, MMN Valdez, L Mercado-Asis, D Taïeb… - Gland …, 2020 - ncbi.nlm.nih.gov
Pheochromocytomas and paragangliomas (PPGLs), rare chromaffin/neural crest cell tumors,
are commonly benign in their clinical presentation. However, there are a number of cases …
are commonly benign in their clinical presentation. However, there are a number of cases …
[HTML][HTML] Expanding the clinicopathological spectrum of succinate dehydrogenase-deficient renal cell carcinoma with a focus on variant morphologies: a study of 62 …
Most succinate dehydrogenase (SDH)-deficient renal cell carcinomas (RCCs) demonstrate
stereotypical morphology characterized by bland eosinophilic cells with frequent …
stereotypical morphology characterized by bland eosinophilic cells with frequent …
Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours
Pituitary neuroendocrine tumours (PitNETs) associated with paragangliomas or
phaeochromocytomas are rare. SDHx variants are estimated to be associated with 0.3–1.8 …
phaeochromocytomas are rare. SDHx variants are estimated to be associated with 0.3–1.8 …