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36_1309.pdf | 3.02 MB | Adobe PDF | 見る/開く |
タイトル: | Sipple症候群の1例 |
その他のタイトル: | Sipple's syndrome: a case report |
著者: | 高羽, 夏樹 ![]() 小林, 義幸 ![]() 高原, 史郎 ![]() 奥山, 明彦 ![]() 原田, 博 ![]() 佐藤, 文三 ![]() 吉田, 哲也 ![]() 高井, 新一郎 ![]() |
著者名の別形: | Takaha, Natsuki Kobayashi, Yoshiyuki Takahara, Shiro Okuyama, Akihiko Harada, Hiroshi Sato, Bunzo Yoshida, Tetsuya Takai, Shin-ichiro |
キーワード: | Sipple's syndrome Intrafamilial occurrence Medullary carcinoma of thyroid gland Pheochromocytoma |
発行日: | Nov-1990 |
出版者: | 泌尿器科紀要刊行会 |
誌名: | 泌尿器科紀要 |
巻: | 36 |
号: | 11 |
開始ページ: | 1309 |
終了ページ: | 1312 |
抄録: | A 41-year-old woman was hospitalized for evaluation of diabetes mellitus and hypertension. The hormonal and radiological examinations revealed that she had pheochromocytoma of bilateral adrenal gland and medullary carcinoma of thyroid gland. Therefore, she was diagnosed as having Sipple's syndrome. She had no definite familial history, but her two sisters, already dead, had been strongly suspected of having had pheochromocytoma. First, bilateral adrenalectomy was performed and secondly, total thyroidectomy, excision of parathyroid and cervical lymph node dissection were performed. Histopathological diagnosis was pheochromocytoma of bilateral adrenal gland, medullary carcinoma of thyroid gland and chief cell hyperplasia of parathyroid gland. We report a case of Sipple's syndrome, which probably is the 88th case in Japan, with the review of the previous Japanese literature. |
URI: | http://hdl.handle.net/2433/117042 |
PubMed ID: | 1981125 |
出現コレクション: | Vol.36 No.11 |

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