Management of Severe Hypercalcemia with Continuous Venovenous Hemodialysis and Regional Citrate Anticoagulation: A Case Report [0.03%]
连续静脉-静脉血液透析联合局部枸橼酸盐抗凝治疗重度高钙血症一例
Ruben M F Hendriks,Charlotte van Noord,Marjolein F Looije
Ruben M F Hendriks
Introduction: Severe hypercalcemia is a potentially life-threatening condition that often requires urgent medical intervention, especially when refractory to conventional treatments. Continuous renal replacement therapy (...
A Case of Chronic Active T-Cell-Mediated Rejection Caused by Plasma Cell-Rich Acute Rejection 12 Years after Kidney Transplantation [0.03%]
一例移植肾丰富浆细胞急性排斥反应后慢性活化T细胞介导排斥反应的病例报告
Ayaka Hayashi,Izumi Yamamoto,Mayuko Kawabe et al.
Ayaka Hayashi et al.
Introduction: Plasma cell rich-acute rejection (PCAR) is a variant of T-cell-mediated rejection in kidney transplantation. Its pathogenesis remains unknown and it is often refractory to standard immunosuppression strategi...
Immune Checkpoint Inhibitor - Associated Renal Tubular Acidosis and Nephrogenic Diabetes Insipidus: A Case Report [0.03%]
免疫检查点抑制剂相关肾小管酸中毒和继发性尿崩症：1例报告
Ido Cohen,Loaa Qormata,Orit Erman et al.
Ido Cohen et al.
Introduction: Immunotherapy has significantly changed the landscape of cancer treatment, yet it can lead to immune-related adverse events, including renal complications. This report highlights a unique case of tubular inj...
A Complement Factor B Mutation in a Chinese Family with Atypical Hemolytic Uremic Syndrome: A Case Report and Systematic Review [0.03%]
补体因子B突变导致中国儿童非典型溶血尿毒综合征1例及文献复习
Wan Peng,Xicui Long,Haoran Lei et al.
Wan Peng et al.
Introduction: Atypical hemolytic uremic syndrome (aHUS) is a rare and potentially life-threatening condition, often linked to dysregulation of the complement system. ...
Novel OFD1 Mutation Results in Unusually Early-Onset Polycystic Kidney Disease [0.03%]
新的OFD1突变导致常染色体隐性遗传性婴儿多囊肾病
Nicholas Jones,Matthew Nguyen,Dao Le et al.
Nicholas Jones et al.
Introduction: Mutations of the OFD1 gene cause oral-facial-digital syndrome type 1 (OFD 1) and variations of the related ciliopathies Joubert syndrome and primary ciliary dyskinesia. OFD 1 manifests with skeletal, CNS, an...
Nephritis-Associated Plasmin Receptor-Positive Post-Streptococcal Acute Glomerulonephritis Showing Full-House Pattern: A Case Report [0.03%]
抗链球菌阳性、肾炎相关纤溶酶受体阳性、全房型急性肾小球肾炎一例报告
Yusuke Takahashi,Naoto Kawata,Hiroki Nishiwaki et al.
Yusuke Takahashi et al.
Introduction: Post-streptococcal acute glomerulonephritis (PSAGN) is a disease in which patients develop hematuria and leg edema following streptococcal infection, which may lead to acute nephritic syndrome and nephrotic ...
Acute Interstitial Nephritis Associated to Pertussis Infection: A Case Report and Review of the Literature [0.03%]
百日咳感染相关急性间质性肾炎的病例报告及文献复习
Gabriel Sartori Pacini,Renata Asnis Schuchmann,Luis Henrique Vizioli et al.
Gabriel Sartori Pacini et al.
Introduction: Whooping cough (pertussis) is an acute respiratory infection primarily caused by Bordetella pertussis, which predominantly affects children. While the disease commonly presents with upper respiratory symptom...
The Diagnostic Challenge of Potassium-Wasting and Hypertension in Pregnancy: Lessons from a Geller Syndrome Workup [0.03%]
妊娠期钾丢失和高血压的诊断挑战：一个Geller综合征检查的经验教训
Justin David Tse,Ryan Lin,Jackson Wang
Justin David Tse
Introduction: Hypokalemia in pregnancy is usually attributed to benign causes, yet persistent hypokalemia with hypertension raises concerns for rare renal potassium-wasting disorders. Among these, Geller syndrome, a rare ...
Dent Disease 1 Presented Early with Bartter-Like Syndrome Features and Rickets: A Case Report [0.03%]
低磷血症型肾小管酸中毒合并原发性肾囊肿病一例报告
Cahyani Gita Ambarsari,Habibah Azzahra Putri Agianda,Meilania Saraswati et al.
Cahyani Gita Ambarsari et al.
Introduction: Dent disease (DD) is characterized by a triad of low-molecular-weight proteinuria, hypercalciuria, and nephrocalcinosis/nephrolithiasis. However, some cases were confounded by other clinical symptoms and sig...
A Relapsing Acute Tubulointerstitial Nephritis as an Expression of a Kappa Light Chain Multiple Myeloma: A Case Report [0.03%]
一例κ轻链型多发性骨髓瘤所致复发性急性间质性肾炎：病例报告
Andrea Angioi,Nicola Lepori,Matteo Floris et al.
Andrea Angioi et al.
Introduction: Light chain-mediated acute tubulointerstitial nephritis (LCTIN) is a rare and underrecognized renal manifestation of plasma cell dyscrasias, including multiple myeloma. It presents as a dense interstitial in...