Autosomal Dominant Polycystic Kidney Disease Patient Specified Bilateral Renal Mass: A Case Report

被引:0
作者
Ogreden, Ercan [1 ]
Guner, Bayram [1 ]
Benli, Erdal [2 ]
机构
[1] Ozel Giresun Ada Hastanesi Urol Klinig, Gazi Mustafa Kemal Bulvan 248, TR-28100 Giresun, Turkey
[2] Ordu Univ Tip Fak Urol Anabilim Dali, Ordu, Turkey
关键词
Polycystic Kidney; Renal Cell Carcinoma; Nephron-Sparing Surgery;
D O I
10.4328/JCAM.1873
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hereditary cystic lesions of the kidney cysts nonherediter lesion with a wide range. They may be the only finding in the form of extrarenal renal cysts may also be part of a clinical syndrome. For this reason, multi-disciplinary approach brings with cystic lesions in the different units. Autosomal dominant polycystic kidney disease, kidney different sizes and numbers of both systemic and hereditary disease that manifests itself in the form of cystic changes. Hereditary and acquired cystic lesions on the basis of some of the rare tumor association is determined in several studies. Here are diagnosed with autosomal dominant polycystic kidney disease, abdominal pain because of a mass in the last six months, physical examination, radiological and laboratory findings were diagnosed with bilateral renal tumors are uncommon and the right renal mass nephron-sparing surgery, the patients with left renal mass followed with active surveillance discussed in the current literature.
引用
收藏
页码:136 / 138
页数:3
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