Non-catheter-adherent right atrial mural thrombus in a patient with systemic sclerosis undergoing hemodialysis: a case report [0.03%]
系统性硬化病透析患者的非导管粘附右房壁血栓1例报告
Masato Habuka,Sahoko Otsuka,Ryohei Kobayashi et al.
Masato Habuka et al.
Catheter-related right atrial thrombosis is a rare, potentially fatal complication of central venous catheterization. While most reported cases involve thrombi attached to the catheter tip or mobile intracardiac masses, systemic sclerosis (...
Case Reports
CEN case reports. 2026 Jul 7;15(4):116. DOI:10.1007/s13730-026-01157-8 2026
Immunoglobulin A nephropathy with superimposed minimal change disease complicated by acute kidney injury requiring temporary hemodialysis [0.03%]
伴有急性肾损伤（需要临时血液透析）的最小病变性疾病并免疫球蛋白A肾病
Yuki Nagaike,Akifumi Tabei,Yu Shimizu et al.
Yuki Nagaike et al.
Immunoglobulin A (IgA) nephropathy (IgAN) with superimposed minimal change disease (MCD) is a rare but increasingly recognized clinicopathological phenotype that is generally associated with a favorable renal prognosis. We present a case of...
Case Reports
CEN case reports. 2026 Jul 4;15(4):115. DOI:10.1007/s13730-026-01155-w 2026
Denosumab increased bone mineral density but caused marked serum calcium fluctuations in a patient undergoing peritoneal dialysis [0.03%]
一例腹膜透析患者接受地诺单抗治疗后骨密度增加及血钙波动明显
Shunsuke Yamada,Soma Enomoto,Kana Matsuo et al.
Shunsuke Yamada et al.
Denosumab is increasingly used to treat osteoporosis in patients with advanced kidney disease, but clinically significant disturbances in calcium homeostasis remain a major concern. We report a peritoneal dialysis (PD) case in which denosum...
Case Reports
CEN case reports. 2026 Jun 30;15(4):114. DOI:10.1007/s13730-026-01142-1 2026
Postpartum TMA requiring dialysis with discordant complement tests: a case report [0.03%]
补体检测不一致的产后TMA并透析一例报告
Hikari Fujimura,Shun Minatoguchi,Riku Takeuchi et al.
Hikari Fujimura et al.
Pregnancy induces vascular, coagulation, and immune alterations that predispose to thrombotic microangiopathy (TMA). Within this spectrum-preeclampsia/ hemolysis, elevated liver enzymes, and low platelets syndrome (HELLP) and complement-med...
Case Reports
CEN case reports. 2026 Jun 29;15(4):110. DOI:10.1007/s13730-026-01138-x 2026
Late-onset oligomeganephronia in a young adult born extremely preterm with lifestyle-related hyperfiltration stress [0.03%]
极早早产导致年轻成人晚期寡肾单位和生活因素相关的高滤过压力损伤肾脏大小及结构
Satoko Abe,Wako Yumura,Ayano Izawa et al.
Satoko Abe et al.
Oligomeganephronia (OMN) is a rare congenital renal hypoplasia characterized by markedly reduced nephron number with compensatory glomerular hypertrophy. Although typically diagnosed in childhood, adult-onset OMN is uncommon and often under...
Case Reports
CEN case reports. 2026 Jun 29;15(4):111. DOI:10.1007/s13730-026-01150-1 2026
Pediatric case of anti-neutrophil cytoplasmic antibody-associated glomerulonephritis with immunoglobulin a deposition diagnosed early through school urinary screening [0.03%]
通过学校尿筛查早期诊断的儿童抗中性粒细胞胞浆抗体相关伴免疫球蛋白A沉积性肾小球肾炎病例
Takuto Kawamura,Yuko Kajiho,Keiichi Takizawa et al.
Takuto Kawamura et al.
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a rare but severe condition in children, and renal involvement in the form of ANCA-associated glomerulonephritis (AAGN) usually determines prognosis. Although AAGN i...
Case Reports
CEN case reports. 2026 Jun 29;15(4):109. DOI:10.1007/s13730-026-01152-z 2026
A case of lipoprotein glomerulopathy in which complete remission was achieved by pemafibrate therapy [0.03%]
佩玛法ibrate治疗脂蛋白肾小球病1例并获得完全缓解
Chika Tomita,Taichi Sato,Yuki Suzuki et al.
Chika Tomita et al.
Lipoprotein glomerulopathy (LPG) is a rare hereditary glomerular disease characterized by lipoprotein thrombi within dilated glomerular capillaries for which effective treatments remain limited. This report concerns a 25-year-old Japanese w...
Case Reports
CEN case reports. 2026 Jun 29;15(4):112. DOI:10.1007/s13730-026-01148-9 2026
Purtscher-like retinopathy presenting as acute vision loss in childhood nephrotic syndrome: case report with review of literature [0.03%]
儿童肾病综合征急性视力下降的Purtscher样视网膜病变一例报告及文献复习
Deepthika Sadasivam,Simar Rajan Singh,Sushmitha Poojary et al.
Deepthika Sadasivam et al.
Purtscher-like retinopathy is a rare occlusive microvasculopathy that causes acute, painless visual loss and characteristic retinal lesions. Although typically trauma-related, it can occur in systemic conditions such as nephrotic syndrome (...
Nephrin-IgG co-localization expression in pediatric steroid-resistant nephrotic syndrome: a case series from Indonesia [0.03%]
印尼儿童糖皮质激素抵抗性肾病综合征患者 Nephrin-IgG 共定位表达的病例系列研究
Rini Rossanti,Ahmedz Widiasta,Nana Sakakibara et al.
Rini Rossanti et al.
Steroid-resistant nephrotic syndrome (SRNS) remains a major clinical challenge due to its heterogeneous etiologies and poor response to conventional immunosuppressive therapy. Anti-nephrin IgG has been associated with podocyte injury and pr...
Case Reports
CEN case reports. 2026 Jun 29;15(4):113. DOI:10.1007/s13730-026-01144-z 2026
Correction: A pediatric case of membranous-like glomerulopathy with masked IgG kappa deposits [0.03%]
纠正：IgGκ轻链沉积物掩盖的类似膜性肾病的儿科病例
Yuichi Uno,Hiroshi Kitamura,Katsuyoshi Kanemoto et al.
Yuichi Uno et al.
Published Erratum
CEN case reports. 2026 Jun 29;15(4):106. DOI:10.1007/s13730-026-01136-z 2026