Results 101 to 110 of about 34,897 (270)
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
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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
Vertigo as the sole complaint of tympanomastoid paraganglioma
Journal of Otology, 2020 Background: Tympanomastoid paragangliomas are usually benign, slowly growing, painless tumors. The common presenting symptoms of this tumor are pulsatile tinnitus and conductive hearing loss.
Xi-Xing Li, Wei-Na Cui, Guo-Dong Gao
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A laboratóriumi diagnosztika eredményei az elmúlt 20 évben kórismézett 155 phaeochromocytoma/paraganglioma szindrómás beteg adatainak elemzése alapján. [PDF]
, 2015 INTRODUCTION: Laboratory diagnosis of pheochromocytoma-paraganglioma syndrome has been markedly improved during the past two decades. AIM: Retrospective assessment of diagnostic utility of urinary catecholamines and their metabolites as well as serum ...
Balog B +11 more
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IJU Case Reports, Volume 8, Issue 3, Page 202-205, May 2025.Introduction Well‐differentiated neuroendocrine tumors of the kidney are rare and generally less aggressive than renal cell carcinoma, although metastasis is still present at the time of diagnosis. Surgical resection remains the preferred treatment, even in cases with lymph node metastases.
Huy‐Hoang Nguyen +3 more
wiley +1 more source
SAGE Open Medical Case Reports, 2017 Neurofibromatosis type 1 is a complex, multi-system genetic disorder that is associated with an increased prevalence of pheochromocytoma and paraganglioma compared to the general population, 1.0%–5.7% versus 0.2%–0.6%, respectively.
Joshua M Tate +2 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
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In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in Paraganglioma [PDF]
, 2015 International audiencePurpose: Germline mutations in genes encoding mitochon-drial succinate dehydrogenase (SDH) are found in patients with paragangliomas, pheochromocytomas, gastrointestinal stromal tumors, and renal cancers. SDH inactivation leads to a
Amar, Laurence +20 more
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Ultrasound in Obstetrics &Gynecology, Volume 65, Issue 5, Page 552-559, May 2025.ABSTRACT Objective To critically review the literature and synthesize evidence on the incremental yield of prenatal exome sequencing (PES) in fetuses with an apparently normal phenotype with a normal G‐banded karyotype or chromosomal microarray (CMA).
A. Sotiriadis +5 more
wiley +1 more source
A Rare Case: Sporadic Bladder Paraganglioma
Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2013 Paraganglioma is a rare tumor which originates from paraganglia tissue from neural crest. Bladder paraganglioma is suggested to be from crommaffin cells by the remains of the embryological cells.
Hakan Ercil +5 more
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