Joseph Leena Dennis, Krishnamoorthy Sriram, Swaminathan Rajendiran, Kripesh Gokul, Sekar Hariharasudhan
Professor, Department of Pathology, Sri Ramachandra Medical College , Porur, Chennai, India .
Professor, Department of Urology, Sri Ramachandra Medical College , Porur, Chennai, India .
J Clin Diagn Res. 2016 Nov;10(11):PD12-PD14. doi: 10.7860/JCDR/2016/22057.8834. Epub 2016 Nov 1.
Primary epithelial tumour of the renal pelvis is a rare entity. So far, very few cases are reported in literature. Of these, mucin secreting adenocarcinomas are distinctly rare. However, mucinous cystadenocarcinoma, that too arising in a horse shoe kidney is extremely rare to be reported. Mucinous cystadenomas and carcinomas arising from the renal pelvis are regarded to be secondary to a metaplastic change in the urothelium. Here, we present a case of a 51-year-old male, who complained of abdominal pain, palpable abdominal mass, haematuria along with passage of mucoid material in the urine, with a very poorly functioning kidney. A pre-operative diagnosis of horse shoe kidney with pelvi ureteric junction obstruction and a poorly functioning kidney was made. Intraoperative findings and frozen section biopsy were suggestive of mucin secreting cystic mass and a right heminephrectomy was done. The final histopathology was suggestive of mucinous cystadenocarcinoma of the renal pelvis of the right moiety. This case is presented for its rarity, diagnostic challenges faced and the lessons learnt, stressing on the need for having a high index of clinical suspicion in making such diagnosis.
肾盂原发性上皮性肿瘤是一种罕见的疾病。到目前为止,文献中报道的病例非常少。其中,分泌黏液的腺癌极为罕见。然而,黏液性囊腺癌,尤其是发生在马蹄肾中的黏液性囊腺癌,更是极为罕见,鲜有报道。肾盂黏液性囊腺瘤和癌被认为是尿路上皮化生改变的继发结果。在此,我们报告一例51岁男性患者,其主诉为腹痛、可触及腹部肿块、血尿伴尿液中排出黏液样物质,且患侧肾功能极差。术前诊断为马蹄肾伴肾盂输尿管连接处梗阻及患侧肾功能差。术中发现及冰冻切片活检提示为分泌黏液的囊性肿块,遂行右半肾切除术。最终组织病理学检查提示右侧肾盂黏液性囊腺癌。本文报告此病例是因其罕见性、所面临的诊断挑战以及所吸取的经验教训,强调在做出此类诊断时需要高度的临床怀疑指数。