Published online Apr 26, 2021. doi: 10.12998/wjcc.v9.i12.2862
Peer-review started: November 20, 2020
First decision: December 24, 2020
Revised: January 5, 2021
Accepted: February 19, 2021
Article in press: February 19, 2021
Published online: April 26, 2021
Processing time: 142 Days and 12.7 Hours
Emphysema pyelonephritis (EPN) is a very dangerous type of urinary tract infection. It is a lethal disease that develops rapidly and causes the patient to deteriorate rapidly, and it can easily lead to systemic infections and even sepsis. The incidence is extremely low, and it is prevalent in patients with diabetes. We here report a case of EPN in a non-diabetic patient with autosomal dominant polycystic kidney disease (ADPKD). We share the diagnosis and treatment procedure for this extremely rare condition to make this disease easier to identify and address early.
A 47-year-old woman presented to the emergency department of our hospital with a high fever and left back pain lasting 4 d. She had a history of autosomal dominant polycystic kidney and polycystic liver. She was diagnosed with left type I EPN and her vital signs deteriorated so quickly that she underwent an emergency operation in which a D-J tube was inserted into her left ureter on the second day after admission. Two months later, she underwent a second-stage flexible ureteroscopy and lithotripsy. Despite postoperative sepsis, she finally recovered after active symptomatic support treatment and effective anti-infective treatment.
Although EPN is more likely to occur in diabetic patients, for non-diabetic patients with ADPKD and upper urinary tract obstruction, the disease also causes rapid deterioration. Early and accurate diagnosis and timely removal of the obstruction by invasive means may be able to save the damaged kidney and the patient’s life.
Core Tip: Emphysematous pyelonephritis (EPN) is a rare but critical necrotizing infection. Most patients have diabetes, and the incidence of EPN in non-diabetic patients with autosomal dominant polycystic kidney disease (ADPKD) is extremely rare. There are very few published articles about conservative treatment and nephrectomy that are used to treat such patients. We present the clinical case of a 47-year woman who was diagnosed with EPN and multiple renal stones with ADPKD confirmed by a non-contrast computed tomography. The patient was treated successfully with insertion of a double “J” stent followed by a second-stage flexible ureteroscopy and lithotripsy. For non-diabetic patients diagnosed with EPN and ADPKD, it is critical to relieve the combined upper urinary tract obstruction by internal drainage.