Patel Rashmi D, Vanikar Aruna V, Modi Pranjal R
Department of Pathology, Laboratory Medicine and Transfusion Services and Immunohematology, G. R. Doshi and K. M. Mehta Institute of Kidney Diseases and Research Center-Dr. H. L. Trivedi Institute of Transplantation Sciences, Civil Hospital Campus, Asarwa, Ahmedabad, Gujarat, India.
Saudi J Kidney Dis Transpl. 2014 May;25(3):647-50. doi: 10.4103/1319-2442.132224.
Mucinous cystadenocarcinoma of renal pelvis is a rare epithelial tumor with poor prognosis. It is postulated to arise from metaplastic glandular mucosa in response to chronic irritation, and comprises less than 0.3% of total renal pelvic tumors. We present this case of a tumor noted in a 45-year-old lady that was diagnosed as mucinous cystadenocarcinoma on histological examination after radical nephrectomy. The patient is remaining well over a follow-up of three months.
肾盂黏液性囊腺癌是一种预后较差的罕见上皮性肿瘤。据推测,它起源于化生的腺黏膜对慢性刺激的反应,占肾盂肿瘤总数的比例不到0.3%。我们报告了一例45岁女性患者的肿瘤病例,该肿瘤在根治性肾切除术后经组织学检查诊断为黏液性囊腺癌。在三个月的随访中,患者情况良好。