Adult adrenal ganglioneuroblastoma: A rare case report

被引:5
作者
Ding, Xiaobo [1 ]
Hou, Yuchuan [2 ]
Ma, Xiaobo [3 ]
Zhang, Huipeng [2 ]
Wang, Chunxi [2 ]
Wang, Yanbo [2 ]
机构
[1] Jilin Univ, Hosp 1, Dept Radiol, Changchun 130023, Jilin Province, Peoples R China
[2] Jilin Univ, Hosp 1, Dept Urol, Changchun 130023, Jilin Province, Peoples R China
[3] Jilin Univ, Hosp 1, Dept Pathol, Changchun 130023, Jilin Province, Peoples R China
来源
CUAJ-CANADIAN UROLOGICAL ASSOCIATION JOURNAL | 2015年 / 9卷 / 1-2期
关键词
Adrenal gland; Case report; Ganglioneuroblastoma;
D O I
10.5489/cuaj.2410
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Ganglioneuroblastoma is an uncommon malignant tumour, and it is extremely rare in adults. A 27-year-old woman was admitted to hospital complaining of commitment left loin pain for 7 months accompanied with fever for 1 day. Computed tomography (CT) scan shows a huge cystic solid mass among the rear of the pancreatic body and tail, inside of the spleen, and the top of the left kidney. Hormone examinations showed that the serum levels of glucocorticoid, aldosterone, norepinephrine, and epinephrine were normal. However, neuron-specific enolase (NSE) was significantly higher (289.46 ng/mL, normal level <16.3 ng/mL). Adrenal mass resection was scheduled. However, intraoperative separation was very difficult and adrenal tumour resection, resection of the pancreatic body and tail, left nephrectomy, and splenectomy were carried out. Pathological diagnosis was ganglioneuroblastoma.
引用
收藏
页码:E75 / E77
页数:3
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