Growth hormone-secreting adenoma coexisted with gangliocytoma: a rare case

被引:0
作者
He, Min [1 ]
Zheng, Niandong [3 ]
Zhang, Jing [2 ]
Hu, Zhihong [4 ]
You, Guoliang [4 ]
Ren, Qingqing [2 ]
Liu, Hao [2 ]
Xu, Jianguo [2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Intens Care Unit, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Neurosurg, 37 Guoxue Alley, Chengdu 610041, Sichuan, Peoples R China
[3] Peoples Hosp Leshan, Dept Neurosurg, Leshan, Peoples R China
[4] Southwest Med Univ, Affiliated Hosp, Dept Neurosurg, Luzhou, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2018年 / 11卷 / 07期
关键词
Pituitary adenoma; gangliocytoma; growth hormone; PITUITARY-GLAND;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A gangliocytoma in the sellar region is extremely rare. We report a rare case of mixed gangliocytoma and growth hormone (GH)-secreting adenoma in a 50-year-old woman, who presented with acromegaly. Laboratory investigations revealed high levels of GH and insulinlike growth factor 1 (IGF-1). Sellar computed tomography scan and contrast enhanced magnetic resonance imaging (CE-MRI) showed a sellar mass. Based on clinical, biochemical, and radiologic evaluations, GH-secreting adenoma was diagnosed and operated by endonasal transsphenoidal approach achieving total removal of the tumor. After surgery, histopathological examination demonstrated mixed gangliocytoma and GH-secreting adenoma in the resected lesion. The clinical, radiological, and operative data are reviewed, as are the histological findings. To our knowledge, few cases of mixed gangliocytoma and GH-secreting adenoma have been reported.
引用
收藏
页码:3785 / 3788
页数:4
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