慢性肾盂肾炎和终末期肾病患者恶性潜能低的多室囊性肾肿瘤:一例罕见病例报告

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of Laboratory Physicians Pub Date : 2023-05-31 DOI:10.1055/s-0043-1772850
R. Kaur, V. Nijhawan, Ayushi Kediya, Vishesh Dhawan, Sahil Singhal, Ashmita Joshi
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引用次数: 0

摘要

摘要:低恶性潜能多房囊性肾肿瘤是一种罕见的透明细胞癌亚型,预后良好。这些肿瘤表现出独特的形态,包括由薄间隔隔开的多个囊肿,内衬透明细胞,无扩张生长。这些囊肿虽然在慢性肾盂肾炎和终末期肾脏疾病中很少见,但通常在x线摄影上使用Bosniak分类进行诊断。但在某些情况下,囊肿在放射学上不可见,最后的诊断只能在组织病理学和免疫组织化学的帮助下做出。我们在此报告一例罕见的MCNLMP偶然病例,该病例来自于一位患有慢性肾盂肾炎和终末期肾病的老年男性肾切除术标本。
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Multilocular Cystic Renal Neoplasm of Low Malignant Potential in a Patient with Chronic Pyelonephritis and End-Stage Renal Disease: A Rare Case Report
Abstract 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.
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来源期刊
Journal of Laboratory Physicians
Journal of Laboratory Physicians MEDICINE, GENERAL & INTERNAL-
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99
审稿时长
31 weeks
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