Multilocular Cystic Renal Neoplasm of Low Malignant Potential in a Patient with Chronic Pyelonephritis and End-Stage Renal Disease: A Rare Case Report

被引：0

作者：

Kaur, Rupinder ^{[1
]}

Nijhawan, Vijay Shrawan ^{[1
]}

Kediya, Ayushi ^{[1
]}

Dhawan, Vishesh ^{[1
]}

Singhal, Sahil ^{[1
]}

Joshi, Ashmita ^{[1
]}

机构：

[1] Maharishi Markandeshwar Deemed Univ, Maharishi Markandeshwar Inst Med Sci & Res, Dept Pathol, Ambala 133207, Haryana, India

来源：

JOURNAL OF LABORATORY PHYSICIANS | 2024年 / 16卷 / 01期

关键词：

Bosniak; cystic disease; end-stage renal disease; pyelonephritis; CELL CARCINOMA; TUMOR; EXPERIENCE; SERIES;

D O I：

10.1055/s-0043-1772850

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Multilocular cystic renal neoplasm of low malignant potential (MCNLMP) is a rare subtype of clear cell carcinoma having an excellent prognosis. These tumors exhibit distinct morphology and comprises of multiple cysts separated by thin septa lined by clear cells with no expansile growth. These cysts, though rare in a setting of chronic pyelonephritis and end-stage renal disease, are usually diagnosed on radiography using the Bosniak classification. But in certain situations where cysts are not visible radiologically, a final diagnosis is made with the help of histopathology and immunohistochemistry only. We, hereby, report such a rare incidental case of MCNLMP diagnosed on histopathology in a nephrectomy specimen of an elderly male with chronic pyelonephritis and end-stage renal disease.

引用

页码：130 / 133

页数：4

共 19 条

[1] Cystic renal cell carcinomas in adults. Is preoperative recognition of multilocular cystic renal cell carcinoma possible? [J].