| Item type |
☆紀要論文 / Departmental Bulletin Paper(1) |
| 公開日 |
2017-10-24 |
| タイトル |
|
|
タイトル |
<Case Reports> Growth hormone deficiency associated with short stature in a very low birth weight infant after treatment for suspected intracranial cavernous hemangioma |
|
言語 |
en |
| 著者 |
Wada, Norihisa
Minakata, Shunsuke
Konishi, Yuhei
Inoue, Tomohiro
Okada, Mitsuru
Takemura, Tsukasa
|
| 言語 |
|
|
言語 |
eng |
| キーワード |
|
|
主題 |
growth hormone deficiency, short stature, very low birth weight infant, intracranial cavernous hemangioma |
| 資源タイプ |
|
|
資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
|
資源タイプ |
departmental bulletin paper |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kindai University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kindai University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kindai University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kindai University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kindai University Faculty of Medicine |
| 著者 所属 |
|
|
値 |
Department of Pediatrics, Kindai University Faculty of Medicine |
| 版 |
|
|
出版タイプ |
NA |
|
出版タイプResource |
http://purl.org/coar/version/c_be7fb7dd8ff6fe43 |
| 出版者 名前 |
|
|
出版者 |
Kindai University Medical Association |
| 書誌情報 |
en : ACTA MEDICA KINDAI UNIVERSITY
巻 41,
号 2,
p. 57-62,
発行日 2016-12
|
| ISSN |
|
|
収録物識別子タイプ |
ISSN |
|
収録物識別子 |
03866092 |
| 抄録 |
|
|
内容記述タイプ |
Abstract |
|
内容記述 |
[Abstract] A female infant born at 30 weeks of gestation and weighing 1,276g developed a suspected intracranial cavernous hemangioma invading the sella turcica at the age of one month. She received high-dose steroid treatment with 5mg/ kg/ d of prednisolone, resulting in a reduction in the size of the hemangioma, and follow-up care began after discharge. At the age of six, it was noted that the girl’s growth in height was insufficient. Head magnetic resonance imaging (MRI) showed pituitary atrophy, and the results of a loading test led to a diagnosis of growth hormone deficiency resulting in a short stature. However, the administration of growth hormone brought her height up to the average by the age of 11.The patient’s intracranial lesion during the newborn period, which was suspected to be a cavernous hemangioma, may have contributed to her pituitary atrophy. The findings of this case suggest that infants who develop a space-occupying lesion in the sella turcica must be kept under long-term observation in view of the possible occurrence of a defective pituitary function. |
AA0050842X-20161200-0057.pdf (946.2 kB)
