Simultaneous Suprasellar and Pineal Germ Cell Tumors in Five Late Stage Adolescents: Endocrinological Studies and Prolonged Follow-up

被引:0
|
作者
Vuillermet, P. [1 ]
Cauliez, B. [2 ]
Freger, P. [3 ]
Vannier, J. P. [4 ]
Pellerin, A. [5 ]
Kuhn, J. M. [1 ]
机构
[1] Univ Hosp, Dept Endocrinol, Rouen, France
[2] Univ Hosp, Inst Clin Biol, Rouen, France
[3] Univ Hosp, Dept Neurosurg, Rouen, France
[4] Univ Hosp, Dept Pediat Oncol, Rouen, France
[5] Univ Hosp, Dept Pathol, Rouen, France
来源
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | 2008年 / 21卷 / 12期
关键词
pineal germ cell tumor; suprasellar germ cell tumor; central nervous system; pituitary deficiency; diabetes insipidus;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary germ cell tumors (PGCT) of the central nervous system usually develop in the third ventricle area, and most frequently in the pineal region. The suprasellar region is the second preferential site for development of these tumors which are rarely simultaneously present in these two sites. We report five new cases of PGCT with pineal and suprasellar localizations, which appeared in late puberty in four boys and one girl aged 17-19 years. The clinical picture associated signs of intracranial hypertension, convergence and verticality palsies, diabetes insipidus and pituitary deficiency. Encephalic MRI revealed a double localization. Endocrine tests revealed a particular pattern associating central diabetes insipidus and a hypothalamic-pituitary disconnection syndrome. Following identification of the pathological type of lesions via a neurosurgical approach, treatment was based on a combined method using chemotherapy, radiotherapy and hormone replacement. Based on this treatment, prolonged remissions were obtained with a good quality of life.
引用
收藏
页码:1169 / 1178
页数:10
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