Co-occurrence of VHL and SDHA Pathogenic Variants: A Case Report
Von Hippel Lindau (VHL) syndrome presents with cerebellar and spinal
hemangioblastomas, renal cell cancer, neuroendocrine pancreatic tumor, and …
hemangioblastomas, renal cell cancer, neuroendocrine pancreatic tumor, and …
Challenges and controversies in adrenal surgery: A practical approach
In this issue of Current Problems in Surgery, 11 endocrine surgeons tackle 8 clinical
conundrums occasionally faced by all of us who practice contemporary adrenal surgery; …
conundrums occasionally faced by all of us who practice contemporary adrenal surgery; …
Outcomes of systemic treatment according to germline mutational status in patients with metastatic pheochromocytoma and paraganglioma
YG Park, I Park, Y Kim, HS Lee, W Lee, S Yoon… - Clinical Genitourinary …, 2024 - Elsevier
Introduction Metastatic disease affects approximately 15% to 17% of patients with
pheochromocytomas and paragangliomas (PPGLs). Unfortunately, treatment options for …
pheochromocytomas and paragangliomas (PPGLs). Unfortunately, treatment options for …
Metabolomics in paraganglioma: applications and perspectives from genetics to therapy
Metabolites represent the highest layer of biological information. Their diverse chemical
nature enables networks of chemical reactions that are critical for maintaining life by …
nature enables networks of chemical reactions that are critical for maintaining life by …
Pheochromocytoma and paraganglioma in children and adolescents
T Stachowicz-Stencel, N Pasikowska… - Acta Biochimica …, 2023 - abp.ptbioch.edu.pl
Pheochromocytoma (PPC) and paraganglioma (PGL) are the tumors that rarely occur in the
pediatric population (PPGL). Both originate from chromaffin cells, pheochromocytoma is …
pediatric population (PPGL). Both originate from chromaffin cells, pheochromocytoma is …
[HTML][HTML] Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma
Pheochromocytoma and paraganglioma (PPGL), are rare neuroendocrine tumors arising
from the adrenal medulla and extra-adrenal paraganglia, respectively. Up to about 60% are …
from the adrenal medulla and extra-adrenal paraganglia, respectively. Up to about 60% are …
[PDF][PDF] 嗜铬细胞瘤/副神经节瘤的诊疗进展
冯瑞颖， 刘金波 - 临床内科杂志, 2023 - lcnkzz.com
嗜铬细胞瘤/副神经节瘤的诊疗进展 Page 1 [DOI]10.3969/j.issn.1001⁃9057.2023.04.004 http:/
/www.lcnkzz.com/CN/10.3969/j.issn.1001⁃9057.2023.04.004 ·综述与讲座· 嗜铬细胞瘤/副神经节 …
/www.lcnkzz.com/CN/10.3969/j.issn.1001⁃9057.2023.04.004 ·综述与讲座· 嗜铬细胞瘤/副神经节 …
[HTML][HTML] Consanguineous couple with SDHD gene mutations: Diagnosis, treatment, and implications of family genetic testing
J Braegelmann, A Mathew, D Führer‐Sakel… - Clinical Case …, 2024 - ncbi.nlm.nih.gov
Paragangliomas and pheochromocytomas are rare entities. A significant proportion of cases
are hereditary and occur as part of paraganglioma/pheochromocytoma (PGL/PCC) …
are hereditary and occur as part of paraganglioma/pheochromocytoma (PGL/PCC) …
Large Paraganglioma of the Larynx—Surgical Resection With Laryngeal Framework Preservation
J Sotirović, N Baletić, A Dimić… - Ear, Nose & Throat …, 2024 - journals.sagepub.com
Large Paraganglioma of the Larynx—Surgical Resection With Laryngeal Framework
Preservation - Jelena Sotirović, Nenad Baletić, Aleksandar Dimić, Biserka Vukomanović …
Preservation - Jelena Sotirović, Nenad Baletić, Aleksandar Dimić, Biserka Vukomanović …
Composite pheochromocytoma of the adrenal gland—a review of published cases
J Costa, M Jácome, P Souteiro, C Santos, AL Cunha - Virchows Archiv, 2023 - Springer
Composite pheochromocytoma (CP) is a rare adrenal tumor, composed of ordinary
pheochromocytoma and neuroblastic components. There is a paucity of information in the …
pheochromocytoma and neuroblastic components. There is a paucity of information in the …