Reversal of Gastric Bypass Resolves Hyperoxaluria and Improves Oxalate Nephropathy Secondary to Roux-en-Y Gastric Bypass [0.03%]
胃旁路逆转可治疗回肠瓣胃绕行术所致的高草酸尿和草酸肾病
Varun Agrawal,Jonathan B Wilfong,Christopher E Rich et al.
Varun Agrawal et al.
Hyperoxaluria after Roux-en-Y gastric bypass (RYGB) increases the risk for kidney injury. Medical therapies for hyperoxaluria have limited efficacy. A 65-year-old female was evaluated for acute kidney injury [AKI, serum creatinine (Cr) 2.1 ...
A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy [0.03%]
转化生长因子-β诱导基因相关眼肾综合征一例：颗粒状角膜营养不良2型合并特殊类型肾脏损害
Yoichi Iwafuchi,Tetsuo Morioka,Yuko Oyama et al.
Yoichi Iwafuchi et al.
Many types of inherited renal diseases have ocular features that occasionally support a diagnosis. The following study describes an unusual example of a 40-year-old woman with granular corneal dystrophy type II complicated by renal involvem...
A Unique Cause of Proteinuria in Pregnancy: Class II Lupus Nephritis with Concomitant Minimal Change Disease [0.03%]
妊娠期蛋白尿的特殊原因：II型狼疮性肾炎伴微小病变病
Ryan Kunjal,Rabie Adam-Eldien,Raafat Makary et al.
Ryan Kunjal et al.
We report the case of a 22-year-old African American female who presented to another facility for routine follow-up in the 34th week of pregnancy with lower extremity swelling and nephrotic-range proteinuria. Although she was normotensive, ...
Maintenance Hemodialysis Using Native Arteriovenous Fistula in a Patient with Severe Generalized Recessive Dystrophic Epidermolysis Bullosa [0.03%]
用于治疗严重全身性显性营养不良型大疱表皮松解症患者的维持性血液透析术中的原生动静脉造瘘术
Takayasu Ito,Eiji Ishikawa,Hiroshi Matsuo et al.
Takayasu Ito et al.
Renal failure and infectious disease are strongly associated with morbidity and mortality in patients with severe generalized recessive dystrophic epidermolysis bullosa (RDEB-sev gen). However, it is reportedly difficult to introduce hemodi...
Coexistence of Acute Crescent Glomerulonephritis and IgG4-Related Kidney Disease [0.03%]
急性新月体性肾小球肾炎与IgG4相关性疾病并存
Zeyuan Lu,Jianyong Yin,Hongda Bao et al.
Zeyuan Lu et al.
Introduction: IgG4-related disease (IgG4-RD) is a fibroinflammatory disorder that may involve almost each organ or system. IgG4-related kidney disease (IgG4-RKD) refers to renal lesions associated with IgG4-RD. The most f...
Phospholipase A2 Receptor-Positive Idiopathic Membranous Glomerulonephritis with Onset at 95 Years: Case Report [0.03%]
95岁起病的磷脂酶A₂受体阳性特发性膜性肾病1例报告
Keiichi Kubota,Junichi Hoshino,Toshiharu Ueno et al.
Keiichi Kubota et al.
A 95-year-old woman was admitted to our hospital for evaluation of bilateral lower-limb edema persisting for 3 months. Serum creatinine was 1.55 mg/dl, and urinary protein excretion was 9.1 g/day. Renal biopsy revealed stage 1 membranous gl...
Acute Respiratory Distress Syndrome and Posterior Reversible Encephalopathy Syndrome following Rituximab Therapy [0.03%]
利妥昔单抗治疗后的急性呼吸窘迫综合征和可逆性后部脑病综合征
Katrina E Wardrope,Lynn Manson,Wendy Metcalfe et al.
Katrina E Wardrope et al.
The anti-CD20 monoclonal antibody rituximab is associated with rare but significant adverse events, notably posterior reversible encephalopathy syndrome (PRES) and acute respiratory distress syndrome (ARDS). We report a case of concomitant ...
Protracted Clinical Course of Postinfectious Glomerulonephritis in a Previously Healthy Child [0.03%]
一个此前健康的儿童感染后肾小球肾炎的病程延长
Camilla Grøndahl,Søren Rittig,Johan Vestergaard Povlsen et al.
Camilla Grøndahl et al.
Acute postinfectious glomerulonephritis (PIGN) affects children typically after upper respiratory tract or skin infections with streptococci but can complicate the course of other infections. In children, it is generally a self-limiting dis...
Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2 [0.03%]
家族性paired box protein 2基因突变的肾脏表型多样性
Yoichi Iwafuchi,Tetsuo Morioka,Takashi Morita et al.
Yoichi Iwafuchi et al.
A common renal phenotype of paired box protein 2 (PAX2) mutations is renal coloboma syndrome. We report a single family with diverse renal phenotypes associated with PAX2 mutation. The proband presented steroid-resistant focal segmental glo...
Treatment of Focal Segmental Glomerulosclerosis Recurrence in the Renal Allograft: A Report of Two Cases [0.03%]
肾移植后复发性局灶节段性肾小球硬化两例的治疗报告
Minh-Ha Tran,Cynthia Chan,Whitney Pasch et al.
Minh-Ha Tran et al.
Focal segmental glomerulosclerosis (FSGS) causes glomerular lesions that can progress to end-stage renal disease. It is suspected to be caused by a circulating factor that is amenable to plasmapheresis removal and exhibits a risk for recurr...