| 作成者 |
|
|
|
|
|
|
|
|
|
| 本文言語 |
|
| 出版者 |
|
|
|
| 発行日 |
|
| 収録物名 |
|
| 巻 |
|
| 開始ページ |
|
| 終了ページ |
|
| 出版タイプ |
|
| アクセス権 |
|
| JaLC DOI |
|
| 関連DOI |
|
|
|
|
|
| 関連URI |
|
|
|
|
|
| 関連情報 |
|
|
|
|
|
| 概要 |
Acromegaly is the clinical condition which results from prolonged, excessive circulating levels of growth hormone (GH) in adults, which occurs in the young before epiphyseal fusion, is called pituitar...y giantism. Acromegaly was first described in 1886 by Pierre Marie, who noted “a striking non-congenital hypertrophy of the extremities". Benign pituitary tumors are by far the most common cause of acromegaly. Whether the tumor results from a hypothalamic disturbance or a primary pituitary tumor is unknown at present. Acromegaly is a desease of the whole organism where everything but the central nervous system enlarges. Although the diagnosis is often made accidentally, the patient usually presents complaining of a change in appearance of the face, hands or whole body, headaches, sweating, goiter or secondary symptoms of pituitary enlargement. In this report, we presented typical cases with acromegaly. Early diagnosis is important but this depends upon a high index of suspicion. It often helps to look at old photographs as shown by ours.続きを見る
|
Mendeley出力
