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Retroperitoneal fibrosis (RPF) is an uncommon form of chronic interstitial nephritis, usually with an indolent clinical course. The etiology is unknown, but the most common cause is a known neoplasm of the retroperitoneum. With the commonly used criteria for RPF, small renal cell carcinomas, which are now discovered with increasing frequency, have a high risk of developing RPF; 10-20% of patients with RPF have concurrent renal cell carcinoma. Treatment is based on the underlying condition and its extent. Interventional radiology techniques, including catheter-guided biopsy, cystoscopy, and percutaneous renal puncture, may be used to establish a diagnosis, and percutaneous renal cryotherapy may be an alternative to nephrectomy. Large mediastinal masses or diffuse retroperitoneal lymphadenopathy are indications for surgical removal. Persistent or progressive urinary obstruction is a potential indication for nephrectomy, although surgery may fail to prevent relapse of nephritis. Extensive involvement of the posterior pararenal space and uncinate process is a poor prognostic sign, and these areas should be closely followed.Q:
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