Results 111 to 120 of about 73,068 (324)
Robot assisted laparoscopic excision of a paraganglioma: new therapeutic approach
International Brazilian Journal of Urology, 2014 The Paraganglioma is the most common extra-adrenal pheochromocytoma arising from neural crest (1) (It will better to write: The paraganglioma is an extra-adrenal pheocromocytoma arising from the neural crest. 10% of pheocromocytomas are extra-adrenal and
G. Cochetti +6 more
doaj +1 more source
[Retroperitoneal paraganglioma].
Boletin. Sociedad de Cirugia del Uruguay, 1998 Presented at session 13th July ...
Rodríguez Juanotena, Jorge +2 more
openaire +2 more sources
Veterinary and Comparative Oncology, EarlyView.ABSTRACT Canine phaeochromocytomas (PCCs) are neuroendocrine tumours with malignant potential. Metastatic disease remains the sole definitive evidence of malignancy. Histopathological criteria to predict long‐term survival have not been established in dogs.
Marit F. van den Berg +6 more
wiley +1 more source
Case Reports in Endocrinology, 2014 Pheochromocytoma and paraganglioma are rare in the pediatric population occurring in approximately 1 in 50,000 children. While some cases are sporadic, they have commonly been associated with syndromes such as von Hippel-Lindau, multiple endocrine ...
Heather Choat +4 more
doaj +1 more source
Immunohistochemistry and Mutation Analysis of SDHx Genes in Carotid Paragangliomas [PDF]
, 2020 Anastasiya V. Snezhkina +14 more
openalex +1 more source
Mapping of succinate dehydrogenase losses in 2258 epithelial neoplasms. [PDF]
, 2014 Losses in the succinate dehydrogenase (SDH) complex characterize 20% to 30% of extra-adrenal paragangliomas and 7% to 8% of gastric GISTs, and rare renal cell carcinomas.
Biernat, Wojciech +9 more
core +1 more source
Genetic testing and surveillance guidelines in hereditary pheochromocytoma and paraganglioma
Journal of Internal Medicine, 2018 Pheochromocytoma and paraganglioma (PPGL) are rare tumours and at least 30% are part of hereditary syndromes. Approximately 20% of hereditary PPGL are caused by pathogenic germ line variants in genes of the succinate dehydrogenase complex (SDHx), TMEM127
A. Muth +9 more
semanticscholar +1 more source
Head &Neck, Volume 48, Issue 2, Page E14-E19, February 2026.ABSTRACT Background Carotid body tumor (CBT) is a rare type of paraganglioma in head and neck region, with a high risk of surgical bleeding and nerve damage. Here we applied a new imaging tool termed “Flight Plan for Embolization” (FPFE) technique to better identify tumors' feeding arteries so that better dissection and bleeding control can be made to ...
Haotian Huanggu +4 more
wiley +1 more source
Effectiveness of 18F-FDG PET/CT in finding lung metastasis from a retroperitoneal paraganglioma [PDF]
Asia Oceania Journal of Nuclear Medicine and BiologyA 50-year-old woman was diagnosed with iron deficiency anemia on general medical examination. Further, contrast-enhanced abdominal CT and magnetic resonance imaging revealed a large hypervascular mass with internal degeneration and necrosis in the ...
Tomonori Chikasue +11 more
doaj +1 more source
Gene Profile of Adipose Tissue of Patients with Pheochromocytoma/Paraganglioma [PDF]
, 2022 Judita Klímová +16 more
openalex +1 more source