Pitfalls in the differential diagnosis of diarrhea after kidney transplantation: challenges in identifying Yersinia enterocolitica infection [0.03%]
肾移植后腹泻鉴别诊断的陷阱——耶尔森菌感染的识别困难
Asako Hayashi,Takayuki Okamoto,Toshiyuki Takahashi et al.
Asako Hayashi et al.
We present the case of a 14-year-old boy with a history of kidney transplantation due to focal segmental glomerulosclerosis who developed severe diarrhea and abdominal pain following an episode of antibody-mediated rejection. Despite stable...
Case Reports
CEN case reports. 2026 Jan 20;15(1):25. DOI:10.1007/s13730-025-01062-6 2026
Coincidence of autosomal dominant polycystic kidney disease and Alport syndrome: a case report and literature review [0.03%]
常染色体显性多囊肾病与Alport综合征并发1例及文献复习
Rui Liu,Fei Liu
Rui Liu
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic kidney disease, accounting for approximately 5% of kidney failure worldwide. While Alport syndrome (AS) is an inherited progressive disease that typically prese...
Post-transplant pelvic arteriovenous malformation in a living kidney transplant recipient [0.03%]
一名活体肾脏移植受者的术后盆腔动静脉畸形
Masatomo Ogata,Fumiya Kitano,Masahiko Yazawa et al.
Masatomo Ogata et al.
Arteriovenous malformations are rare vascular anomalies that may be congenital or occur secondary to trauma or surgery. Here, we report a rare case of a pelvic arteriovenous malformation that gradually enlarged after living-donor kidney tra...
Case Reports
CEN case reports. 2026 Jan 20;15(1):26. DOI:10.1007/s13730-025-01045-7 2026
Repeat kidney biopsy reveals new-onset IgA nephropathy in a patient with ANCA-associated vasculitis [0.03%]
ANCA相关性血管炎患者重复肾活检发现新发IgA肾病
Seina Iwami,Masahiro Eriguchi,Takaaki Kosugi et al.
Seina Iwami et al.
Microscopic polyangiitis (MPA) is a subtype of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). Although relapse during maintenance therapy is relatively common, the coexistence or subsequent development of other glom...
Case Reports
CEN case reports. 2026 Jan 20;15(1):23. DOI:10.1007/s13730-025-01056-4 2026
Tips of family history taking in diagnosing Alport syndrome: a report of six cases [0.03%]
问诊中的家庭史采集在Alport综合征诊断中的重要性——6例患者报告
Tatsuhiko Mori
Tatsuhiko Mori
Alport syndrome (AS) is a hereditary kidney disease characterized by progressive renal dysfunction, sensorineural hearing loss, and ocular abnormalities. This report describes six AS cases diagnosed by a single physician, focusing on diagno...
Minocycline infusion sclerotherapy for infected hepatic cysts in a patient with autosomal dominant polycystic kidney disease: a case report and literature review [0.03%]
成人型多囊肾病继发肝囊肿感染的米诺环素静脉注入硬化疗法：1例报告及文献复习
Yumeka Inamura,Shohei Fukunaga,Nanae Matsuo et al.
Yumeka Inamura et al.
We report the case of a Japanese man in his 60 s undergoing hemodialysis for end-stage renal disease due to autosomal dominant polycystic kidney disease, who had experienced repeated hepatic cyst infections. Despite treatment with oral anti...
Dual MPO-ANCA and PLA2R positivity in crescentic glomerulonephritis with MPO-associated membranous nephropathy: a case report with pathogenic insights [0.03%]
伴有MPO相关膜性肾病的新月体性肾小球肾炎的双阳性（MPO-ANCA和PLA2R）：具有致病见解的病例报告
Chikayuki Morimoto,Yoshihide Fujigaki,Hitoshi Anzai et al.
Chikayuki Morimoto et al.
Recent studies have suggested that myeloperoxidase (MPO) may serve as a target antigen in cases of MPO-associated membranous nephropathy (MN) occurring concurrently with MPO-antineutrophil cytoplasmic antibody (ANCA)-associated crescentic g...
Case Reports
CEN case reports. 2026 Jan 19;15(1):21. DOI:10.1007/s13730-025-01071-5 2026
Peritoneal dialysis associated peritonitis and Clostridioides difficile infection: Association or different entities? [0.03%]
腹膜透析相关性腹膜炎与难辨梭菌感染：有关还是无关？
Jesús Daniel Meléndez-Flores,Astrid Anahis Mendoza-Cardiel,Alan Iván Arreola-Sánchez et al.
Jesús Daniel Meléndez-Flores et al.
Peritoneal dialysis (PD) associated peritonitis is a common complication and main cause of PD failure among end-stage chronic kidney disease (CKD) patients, presenting with abdominal pain, diarrhea and cloudy dialysate. On the other side, t...
Case Reports
CEN case reports. 2026 Jan 19;15(1):20. DOI:10.1007/s13730-025-01040-y 2026
A case of chronic Campylobacter fetus infection-related glomerulonephritis, mimicking systemic autoimmune diseases [0.03%]
一例慢性胎儿弯曲菌感染相关性肾小球肾炎病例，临床表现及检查结果类似系统性自身免疫性疾病
Minami Matsumoto,Yuichiro Kitai,Shinya Yamamoto et al.
Minami Matsumoto et al.
Herein, we present the first case of chronic Campylobacter fetus infection-related glomerulonephritis (IRGN) in a 69-year-old man with a permanent cardiac pacemaker. The patient had a prior episode of fever and glomerulonephritis of undeter...
Case Reports
CEN case reports. 2026 Jan 13;15(1):18. DOI:10.1007/s13730-025-01065-3 2026
Keiichiro Kinoshita,Kenichi Koga,Kensei Yahata
Keiichiro Kinoshita
An 82-year-old man was admitted to our hospital with edema on the upper and lower extremities that had worsened over the past 5 months. He was diagnosed with nephrotic syndrome and acute renal failure. A computed tomography evaluation revea...
Case Reports
CEN case reports. 2026 Jan 8;15(1):17. DOI:10.1007/s13730-025-01061-7 2026