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Case Report
©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Apr 26, 2021; 9(12): 2862-2867
Published online Apr 26, 2021. doi: 10.12998/wjcc.v9.i12.2862
Successful endoscopic surgery for emphysematous pyelonephritis in a non-diabetic patient with autosomal dominant polycystic kidney disease: A case report
Yi Jiang, Richard Lo, Zhen-Quan Lu, Xiao-Bao Cheng, Lin Xiong, Bing-Feng Luo
Yi Jiang, Richard Lo, Zhen-Quan Lu, Xiao-Bao Cheng, Lin Xiong, Bing-Feng Luo, Department of Surgery, The University of Hong Kong-Shenzhen Hospital, Shenzhen 518053, Guangdong Province, China
Author contributions: Jiang Y contributed to the project development, data collection, surgery, data analysis, and manuscript composition; Lo R contributed to the supervision throughout the development of the work; Lu ZQ and Luo BF contributed to the data analysis; Cheng XB and Xiong L contributed to the data collection.
Informed consent statement: The informed written consent was waived by the Ethics Committee of the University of Hong Kong-Shenzhen Hospital. The Ethics Committee approval number is 2020144.
Conflict-of-interest statement: The authors declare that they have no competing interests to report.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Corresponding author: Yi Jiang, MM, Surgeon, Department of Surgery, The University of Hong Kong-Shenzhen Hospital, No. 1 Haiyuan Road, Futian District, Shenzhen 518053, Guangdong Province, China. jiangy8@hku-szh.org
Received: November 20, 2020
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
Core Tip

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.