Primary renal carcinoid tumor: case report and review of the literature

被引：3
|
作者：
Li, Bin [1 ]
Cui, Tongyue [2 ]
Ban, Ziqin [3 ]
Luo, Lei [1 ]
Sun, Lijiang [1 ]
机构：
[1] Qingdao Univ, Affiliated Hosp, Dept Urol, Qingdao 266011, Shandong, Peoples R China
[2] Peoples Hosp Changle Cty, Dept Urol, Changle, Peoples R China
[3] Community Hlth Ctr, Qingdao, Shandong, Peoples R China
来源：
ONCOTARGETS AND THERAPY | 2016年 / 9卷
关键词：
renal; carcinoid tumors; parenchyma; KIDNEY;
D O I：
10.2147/OTT.S88730
中图分类号：
Q81 [生物工程学（生物技术）]; Q93 [微生物学];
学科分类号：
071005 ; 0836 ; 090102 ; 100705 ;
摘要：
Objective: The aim of this case report is to discuss the clinicopathological features of a patient with a primary renal carcinoid tumor. Methods: We report on the clinical and pathological information of one case of a patient with a primary renal carcinoid tumor as well as review relative literature. Results: The patient was diagnosed with a renal tumor when she received physical examination, and exhibited no positive symptoms. The diameter of tumor was 5 cm, the cross surface of the tumor was light yellow and firm, and the central part was soft with hemorrhage and necrosis. Immunohistochemical staining revealed strong and diffuse staining with synaptophysin, chromogranin A, and neuron-specific enolase. Conclusion: A primary renal carcinoid tumor is extremely rare. Surgical resection is a preferred therapeutic method.
引用
收藏
页码：741 / 743
页数：3
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