著作: Yamashia Y/Akiyama T/[水澤 典子]/[吉本 勝彦]/Goto M/A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone/[International Journal of Oral and Maxillofacial Surgery]
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種別 | 必須 | 学術論文(審査論文) | |||
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言語 | 必須 | 英語 | |||
招待 | 推奨 | ||||
審査 | 推奨 | Peer Review | |||
カテゴリ | 推奨 | ||||
共著種別 | 推奨 | ||||
学究種別 | 推奨 | ||||
組織 | 推奨 |
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著者 | 必須 | ||||
題名 | 必須 |
(英) A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone |
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副題 | 任意 | ||||
要約 | 任意 |
(英) Hyperparathyroidism-jaw tumour (HPT-JT) syndrome is characterized by parathyroid tumours as well as by ossifying fibromas of the mandible and maxilla, renal cysts, or Wilms' tumours. Recently, the gene responsible for HPT-JT syndrome has been identified as the HRPT2 tumour suppressor gene. In an 18-year-old male, a tumour in the maxilla was first diagnosed as an ossifying fibroma. During biochemical screening before surgery, the patient received a diagnosis of primary hyperparathyroidism. Neck computed tomography scanning showed a parathyroid tumour. Surgical excisions to remove the jaw tumour and parathyroid adenoma were performed. The postoperative course has been uneventful and a follow up at 2 years revealed no evidence of recurrence. The HRPT2 germline mutation of 39delC was detected in the proband, but not in his unaffected parents. These results suggested that the germline mutation occurred de novo. |
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キーワード | 推奨 |
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発行所 | 推奨 | ||||
誌名 | 必須 |
International Journal of Oral and Maxillofacial Surgery(International Association of Oral and Maxillofacial Surgeons)
(pISSN: 0901-5027, eISSN: 1399-0020)
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巻 | 必須 | 36 | |||
号 | 必須 | 4 | |||
頁 | 必須 | 365 369 | |||
都市 | 任意 | ||||
年月日 | 必須 | 2007年 4月 初日 | |||
URL | 任意 | ||||
DOI | 任意 | 10.1016/j.ijom.2006.08.007 (→Scopusで検索) | |||
PMID | 任意 | 17052894 (→Scopusで検索) | |||
CRID | 任意 | ||||
WOS | 任意 | ||||
Scopus | 任意 | ||||
評価値 | 任意 | ||||
被引用数 | 任意 | ||||
指導教員 | 推奨 | ||||
備考 | 任意 |
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