- 関
- paraganglia、paraganglion
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English Journal
- Pheochromocytoma-paraganglioma syndromes characterized by germline SDHB and SDHD mutations.
- Baysal B1, Maher E2.
- Endocrine-related cancer.Endocr Relat Cancer.2015 Jun 25. pii: ERC-15-0226. [Epub ahead of print]
- Pheochromocytomas and paragangliomas (PPGL) are rare neuroendocrine neoplasms that derive from small paraganglionic tissues which are located from skull base to the pelvic floor. Genetic predisposition plays an important role in development of PPGLs. Since the discovery of first mutations in the SDH
- PMID 26113606
- Endocrine Pathology: SY08-2 PARAGANGLIOMA.
- Lam AK1.
- Pathology.Pathology.2014 Oct;46 Suppl 2:S14. doi: 10.1097/01.PAT.0000454096.68373.ae.
- Paraganglioma normally occurs in sites that parallel the sympathetic and parasympathetic chain ganglions. Common locations of paraganglioma include tumours of paraganglionic system in head and neck region like carotid body paraganglioma and jugulotypmanic paraganglioma. There are also paragangliomas
- PMID 25188066
- Glomus jugulare tumours: a 15 year radiotherapy experience in South Australia.
- Wong BJ1, Roos DE2, Borg MF2.
- Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia.J Clin Neurosci.2014 Mar;21(3):456-61. doi: 10.1016/j.jocn.2013.05.020. Epub 2013 Aug 9.
- Glomus jugulare tumours (GJT) are one of a family of benign hypervascular neoplasms that arise from chief cells of the paraganglionic tissue from the dome of the jugular bulb. Historically, these tumours have primarily been managed surgically but radiation is an alternative treatment modality. The p
- PMID 24290904
Japanese Journal
- 後腹膜に発生した巨大Paragangliomaの1例
- 逢坂 公人,横西 哲広,伊藤 悠亮
- 泌尿器科紀要 56(7), 377-380, 2010-07
- … Paraganglioma is a rare neuroendocrine tumor which arises from extra adrenal paraganglionic cells of the autonomic nervous system. …
- NAID 120002381096
- Multiple minute nests of incidentally detected paraganglionic cells associated with urothelial carcinoma of the urinary bladder in a 73-year-old woman
- OHTSUKI Yuji,OCHI Kenji,OKADA Yuhei,LEE Gang-Hong,FURIHATA Mutsuo
- Medical molecular morphology : official journal of the Japanese Society for Clinical Molecular Morphology 41(1), 62-65, 2008-03-01
- NAID 10024380818
- Malignant Pheochromocytoma Lacking Clinical Features of Catecholamine Excess Until the Late Stage
- HONDA Munehiro,UESUGI Kazuto,YAMAZAKI Hiroyuki,DEZAWA Akira,MIZOGUCHI Kunio,YAMAJI Tohru,ISHIBASHI Miyuki
- Internal medicine 39(10), 820-825, 2000-10
- … Osseous metastases became manifest 12 years after successful removal of the primary tumor which originated in paraganglionic tissue near the right adrenal gland. …
- NAID 10006996705
Related Links
- Tumors of the paraganglionic tissues are known as paragangliomas, though this term tends to imply the nonchromaffin type, and can occur at a number of sites throughout the body. Chromaffin paragangliomas are issued from chromaffin cells, ...
- Most of the paraganglionic cells degenerate after birth. Of those that remain, some develop into a group of specialized chemoreceptors distributed throughout the body. In the head and neck, paraganglia can be found symmetrically distributed ...
Related Pictures
★リンクテーブル★
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- 英
- paraganglion、paraganglia、paraganglionic
- 同
- パラガングリオン、大動脈クロム親和体 aortic chromaffin body、ツッカーカンドル器官 organ of Zuckerkandl
- 関
- 大動脈傍体 paraaortic bodies
[★]
傍神経節、パラガングリオン
- 関
- paraganglion、paraganglionic
[★]
- 英
- paraganglion、paraganglia、paraganglionic
- 関
- 傍神経節
[★]
傍神経節、パラガングリオン
- 関
- paraganglia、paraganglionic