Medullary carcinoma of the thyroid - an unusual case of hyalinizing trabecular adenoma - like variant (encapsulated) [PDF]
, 2012 Medullary thyroid carcinoma is a neoplasm occurring in sporadic and familial patterns. A rare variant of medullary thyroid carcinoma shows microscopic features similar to hyalinizing trabecular adenoma of thyroid.
Madhusmita Jena, Vidya Bhat
core +2 more sources
Primary hyperparathyroidism in a domestic shorthair cat following I131 radioiodine therapy
Journal of Small Animal Practice, EarlyView.A 12‐year‐old male neutered domestic shorthaired cat presented for further assessment of a cervical mass, having undergone radioiodine therapy for treatment of hyperthyroidism 2 years prior to presentation. Initial cytological diagnosis of the mass was supportive of a carcinoma and laboratory results were consistent with primary hyperparathyroidism ...
E. Ruane +3 more
wiley +1 more source
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
Mistakes in medical ontologies: Where do they come from and how can they be detected? [PDF]
, 2004 We present the details of a methodology for quality assurance in large medical terminologies and describe three algorithms that can help terminology developers and users to identify potential mistakes.
Ceusters, Werner +3 more
core
A Paraganglioma in a Hypertensive Patient with Unilateral Renal Hypoplasia [PDF]
, 2015 We report the case of a 46-year-old hypertensive Japanese female with renal insufficiency related to unilateral renal hypoplasia. The patient was found to have developed paraganglioma in the retroperitoneal space over a 5-year period.
Hagiya, Hideharu +9 more
core +1 more source
Review of Pediatric Pheochromocytoma and Paraganglioma
Frontiers in Pediatrics, 2017 Pheochromocytoma (PCC) and paraganglioma (PGL) are rare chromaffin cell tumors which secrete catecholamines and form part of the family of neuroendocrine tumors.
R. Bholah, T. Bunchman
semanticscholar +1 more source
Experimental Physiology, EarlyView.Abstract Recent studies highlight the important roles of cuproptosis in cancer cells. However, the roles of the cuproptosis‐related genes (CRGs) in different cancers are still not fully understood. Comprehensive analysis was performed using open‐source bioinformatic platforms to disclose the expression profiles, prognostic significance, genomic and ...
Xinyu Ge +10 more
wiley +1 more source
A case report of bladder paraganglioma and literature review
Radiology Case Reports, 2022 Bladder paraganglioma is a rare tumor originated from the chromaffin cells of the bladder. We discuss a case of a 49-year-old male patient with bladder paraganglioma, including the clinical and ultrasonographic features, the histopathological and ...
Xiang Ji, MD, Xia Zhang, MD
doaj
Overexpression of the Insulin-like growth factor 1 receptor (IGF-1R) is associated with malignancy in familial pheochromocytomas and paragangliomas [PDF]
, 2013 CONTEXT: Pheochromocytomas and paragangliomas (pheo/pgl) are neuroendocrine tumours derived from chromaffin cells. Although mostly benign, up to 26% of pheo/pgl will undergo malignant transformation.
Baserga +36 more
core +1 more source
Changes in multi‐gene cancer panels for children: A 4‐year retrospective review
Journal of Genetic Counseling, Volume 34, Issue 4, August 2025.Abstract The multi‐gene panel is the most utilized genetic test to evaluate for germline cancer predisposition syndromes. However, the rate of change of commercial multigene panels is not well understood, and its value as a standalone test has also not been investigated.
Elise G. Williams +4 more
wiley +1 more source