WordNet
- a benign epithelial tumor of glandular origin
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- 副甲状腺の,上皮小体の
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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/02/09 16:57:34」(JST)
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- 1. 原発性副甲状腺機能亢進症の診断および鑑別診断 diagnosis and differential diagnosis of primary hyperparathyroidism
- 2. 原発性副甲状腺機能亢進症のマネージメント management of primary hyperparathyroidism
- 3. 原発性副甲状腺機能亢進症の臨床症状 clinical manifestations of primary hyperparathyroidism
- 4. 原発性副甲状腺機能亢進症の発症機序および病因 pathogenesis and etiology of primary hyperparathyroidism
- 5. 原発性副甲状腺機能亢進症の副甲状腺診査 parathyroid exploration for primary hyperparathyroidism
English Journal
- Patient affected by neurofibromatosis type 1 and thyroid C-cell hyperplasia harboring pathogenic germ-line mutations in both NF1 and RET genes.
- Ercolino T1, Lai R2, Giachè V3, Melchionda S4, Carella M4, Delitala A2, Mannelli M5, Fanciulli G2.Author information 1Endocrinology Unit, Careggi Hospital, Azienda Ospedaliera Universitaria Careggi, Florence, Italy. Electronic address: tonino.ercolino@unifi.it.2Department of Clinical and Experimental Medicine, University of Sassari, Azienda Ospedaliera Universitaria, Sassari, Italy.3Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy.4Medical Genetic Unit, IRCCS Ospedale Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.5Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy; Istituto Toscano Tumori, Florence, Italy.AbstractNeurofibromatosis type 1 (NF1) is a rare autosomal dominant disease with an estimated incidence of 1 in 3000/3500 live births. NF1 is caused by a mutation in a gene which encodes a protein known as neurofibromin. In up to 5% of cases, NF1 is associated with pheochromocytomas. RET proto-oncogene encodes a member of the receptor tyrosine kinase family involved in the normal development or the neoplastic growth of neural crest cell lineages. Germ-line RET mutations account for cases of Multiple Endocrine Neoplasia type 2 (MEN2), an autosomal dominant genetic syndrome where medullary thyroid carcinoma (MTC) is the major and more clinically severe feature, with nearly complete penetrance. C-cell hyperplasia (CCH) is described in MEN2 patients, and it has been implicated as the precursor of in situ MTC. Patients with RET mutations develop pheochromocytomas in 50% of cases. Rarely, patients with NF1 have been found to present, in addition to the NF1 clinical picture, other lesions, such as parathyroid hyperplasia/adenoma and/or medullary thyroid carcinoma. In spite of the presence of these MEN2 lesions, in none of these patients mutations of gene RET have been found so far. In this report, we describe the first case of a patient affected by a germ-line mutation in both NF1 and RET genes.
- Gene.Gene.2014 Feb 25;536(2):332-5. doi: 10.1016/j.gene.2013.12.003. Epub 2013 Dec 21.
- Neurofibromatosis type 1 (NF1) is a rare autosomal dominant disease with an estimated incidence of 1 in 3000/3500 live births. NF1 is caused by a mutation in a gene which encodes a protein known as neurofibromin. In up to 5% of cases, NF1 is associated with pheochromocytomas. RET proto-oncogene enco
- PMID 24361808
- Acute pancreatitis and hyperparathyroidism: A case series.
- Chowdhury SD, Kurien RT, Pal S, Jeyaraj V, Joseph AJ, Dutta AK, Chandramohan A, Abraham D, Augustine J, Hephzibah J, Simon EG.Author information Department of Gastrointestinal Sciences, Christian Medical College, Vellore, 632 004, India, sudipto.d.c@gmail.com.AbstractPrimary hyperparathyroidism is a rare cause of acute pancreatitis. Five consecutive patients with acute or recurrent acute pancreatitis and primary hyperparathyroidism were included. All patients had elevated serum calcium on admission and high levels of circulating parathyroid hormone. Both ultrasonography and Sestamibi scan was used to localize parathyroid adenoma. Except for one, all patients underwent parathyroidectomy and postoperative histology was consistent with parathyroid adenoma. One patient died while on treatment. Metabolic causes of acute pancreatitits, though uncommon, are important as early recognition helps management and prevents recurrence.
- Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology.Indian J Gastroenterol.2014 Jan 14. [Epub ahead of print]
- Primary hyperparathyroidism is a rare cause of acute pancreatitis. Five consecutive patients with acute or recurrent acute pancreatitis and primary hyperparathyroidism were included. All patients had elevated serum calcium on admission and high levels of circulating parathyroid hormone. Both ultraso
- PMID 24419705
Japanese Journal
- The role of colour Doppler ultrasonography in the preoperative localization of parathyroid adenomas
- MOHAMMADI Afshin,MOLOUDI Farzad,GHASEMI-RAD Mohammad
- Endocrine journal 59(5), 375-382, 2012-05-01
- NAID 10030816296
- 症例 甲状腺内副甲状腺腺腫による原発性副甲状腺機能亢進症の1例
- 黒川 貴則,室田 千晶,金井 基錫 [他]
- 外科 74(5), 551-554, 2012-05
- NAID 40019307217
Related Pictures
★リンクテーブル★
| リンク元 | 「parathyroid neoplasm」「副甲状腺腫」 |
| 関連記事 | 「parathyroid」「adeno」 |
「parathyroid neoplasm」
「副甲状腺腫」
- 英
- parathyroid adenoma
- 同
- 上皮小体腺腫、副甲状腺腺腫
「parathyroid」
- adj.
- 副甲状腺の、上皮小体の
「adeno」
- comb form.
- アデノ、腺の