Results 1 to 10 of about 51,236 (315)

A rare case of non-functional Paraganglioma of urinary bladder with No LUTS [PDF]

open access: yesUrology Case Reports
Paraganglioma originates from chromaffin cells of the sympathetic nervous system. Paraganglioma of urinary bladder are very rare tumors that arise from the ganglion cells and usually mistakenly have been diagnosed and treated because of its rarity and ...
Mohammad Poury   +3 more
doaj   +2 more sources

Paraganglioma of the thyroid gland: A case report [PDF]

open access: yesVojnosanitetski Pregled, 2014
Introduction. Thyroid paraganglioma is a very rare malignant neuroendocrine tumor. Immunohistochemical features of thyroid paraganglioma are helpful for the diagnosis. Case report.
Filipović Aleksandar   +2 more
doaj   +3 more sources

Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports

open access: yesJournal of Medical Case Reports, 2021
Background Pheochromocytoma and paraganglioma caused by succinate dehydrogenase gene mutations is called hereditary pheochromocytoma/paraganglioma syndrome.
Rei Hirose   +12 more
doaj   +1 more source

A case report of primary colonic paraganglioma with lymph node metastasis

open access: yesFrontiers in Surgery, 2022
BackgroundParaganglioma is a kind of neuroendocrine tumor that originates from paraganglia outside the adrenal gland. Gastrointestinal tract paraganglioma is very rare and only four cases of paraganglioma originating in the colon have been reported.Case ...
Xinyi Zhu   +4 more
doaj   +1 more source

A patient with paraganglioma undergoing laparoscopic resection: A case report

open access: yesClinical Case Reports, 2021
Paraganglioma is a very rare extraadrenal nonepithelial tumor. The number of cases of laparoscopic surgery in Paraganglioma is small and controversial.
Hisamichi Yoshii   +5 more
doaj   +1 more source

Natural History and Management of Familial Paraganglioma Syndrome Type 1: Long-Term Data from a Large Family [PDF]

open access: yes, 2020
Head and neck paragangliomas are the most common clinical features of familial paraganglioma syndrome type 1 caused by succinate dehydrogenase complex subunit D (SDHD) mutation. The clinical management of this syndrome is still unclear.
Cantisani, Vito   +12 more
core   +1 more source

Differential diagnosis and unusual diffuse cytokeratin expression in renal paraganglioma: A case report

open access: yesIndian Journal of Pathology and Microbiology, 2020
Paraganglioma is a rare neuroendocrine tumor arising from undifferentiated cells of the primitive neural crest. We report a case of renal paraganglioma in a 67-year-old patient.
Junying Wang, Lin Zhong
doaj   +1 more source

Non-Functional Paraganglioma of the Urinary Bladder Treated by Transurethral Resection: Report of Two Cases [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Paraganglioma of the urinary bladder is a rare tumour derived from chromaffin tissue of the sympathetic nervous system. Paraganglioma of the urinary bladder especially the non-functional type is often misdiagnosed as urothelial cancer.
RICHA KATIYAR   +4 more
doaj   +1 more source

Abdominal nonfunctional paraganglioma in which succinate dehydrogenase subunit B (SDHB) immunostaining was performed: a case report

open access: yesJournal of Medical Case Reports, 2023
Background Abdominal nonfunctional paraganglioma is rare. Malignant potential of paraganglioma is assessed by Grading of Adrenal Pheochromocytoma and Paraganglioma score and genetic testing, but genetic testing is not common.
Takazo Tanaka   +8 more
doaj   +1 more source

A case of an unexpected posterior mediastinal functional paraganglioma: case report and literature review

open access: yesBMC Anesthesiology, 2020
Background Paraganglioma can be found in a wide range of locations. However, paraganglioma in the posterior mediastinum is rare. An unexpected paraganglioma located in the posterior mediastinum was found during surgery.
Zhuqing Yang, Qinye Shi, Fangping Bao
doaj   +1 more source

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