Severe Clozapine Poisoning Treated by Extracorporeal Blood Purification Therapy [0.03%]
严重氯氮平中毒采用血液净化治疗急诊重症监护病房多学科协作救治1例报告
Andreas Hartjes,Matthäus Machnik,Christa Kubasta et al.
Andreas Hartjes et al.
Clozapine is a frequently used antipsychotic that, in case of overdose, can cause severe adverse side effects, such as hematological, cardiovascular, and neurological complications. As there is no specific antidote or reversal agent availab...
Campylobacter Colitis as a Trigger for Atypical Hemolytic Uremic Syndrome: About One Case [0.03%]
营亚利桑那菌结肠炎诱发非典型溶血性尿毒综合征1例报告
Thomas Quinaux,Zead Tubail,Isabelle Vrillon et al.
Thomas Quinaux et al.
We present the case of a 17-year-old Caucasian male whose condition featured acute renal failure, anemia, and deep thrombocytopenia after five consecutive days of diarrhea. Campylobacter coli was identified in stool cultures and, although t...
A Case Report of Kidney-Only Transplantation in Primary Hyperoxaluria Type 1: A Novel Approach with the Use of Nedosiran [0.03%]
一种新的治疗1型原发性高草酸尿症的肾脏移植个案报告：使用Nedosiran药物的方法
Matthew C Breeggemann,Stephen L Gluck,Marshall L Stoller et al.
Matthew C Breeggemann et al.
The primary hyperoxalurias (PHs) are a group of diseases characterized by kidney stones, nephrocalcinosis, and chronic kidney disease. At stages of advanced kidney disease, glomerular filtration of oxalate becomes insufficient, plasma level...
Low-Density Lipoprotein Adsorption by Centrifugal Plasma Separation Can Shorten Treatment Time [0.03%]
离心血浆分离法低密度脂蛋白吸附可缩短治疗时间
Atsushi Ohkubo,Takatoshi Sakurasawa,Shotaro Naito
Atsushi Ohkubo
Low-density lipoprotein (LDL) apheresis is effective for nephrotic syndrome in drug-resistant focal segmental glomerulosclerosis (FSGS). Dextran sulfate adsorption of LDL (DSAL) is widely used for this purpose. The Liposorber LA-15 system p...
Single-Dose Pharmacokinetics and Total Removal of Cyclophosphamide in a Patient with Acute Kidney Injury Undergoing Intermittent Haemodialysis and Prolonged Intermittent Kidney Replacement Therapy: A Case Report [0.03%]
间歇血液透析和延长间断性肾脏替代治疗下急性肾损伤患者环磷酰胺单次给药药代动力学及总清除率：病例报告
Catherina Lück,Gernot Beutel,W Nikolaus Kühn-Velten et al.
Catherina Lück et al.
The largest study on cyclophosphamide pharmacokinetics in dialysis patients comprises of 6 subjects. In the 2 decades since these data were obtained, dialyser membranes, treatment intensities, and treatment duration have changed considerabl...
Nephropathy in a Child with Severe Recessive Dystrophic Epidermolysis Bullosa Treated with Cyclophosphamide: A Case Report [0.03%]
环磷酰胺治疗的严重隐性营养不良型大疱性表皮松解症患儿肾病一例报告
Cahyani Gita Ambarsari,Retno Palupi-Baroto,Fira Alyssa Gabriella Sinuraya et al.
Cahyani Gita Ambarsari et al.
Long-term inflammation and recurrent skin infection in recessive dystrophic epidermolysis bullosa (RDEB) are associated with the presence of immunoglobulin A (IgA)-containing immune complexes in the glomerulus. Only eight pediatric RDEB cas...
A Case of Multicystic Dysplastic Kidney Presenting as a Single Midline Pelvic Cyst [0.03%]
中线盆腔囊肿型多囊性肾发育不良一例报告
Kristin M Ebert,Christina B Ching
Kristin M Ebert
We present an unusual case of a female neonate presenting with a single midline pelvic cyst. Prenatal imaging was suggestive of multicystic dysplastic kidney (MCDK), but postnatal imaging was atypical for this diagnosis given the location a...
Acquired Perforating Dermatosis as a Paraneoplastic Feature: A Case Report, Literature Review, and Novel Association [0.03%]
获得性穿通性皮肤病作为副肿瘤性特征的病例报告、文献综述及新关联
Nashat Imran
Nashat Imran
Kyrle's disease is an uncommon form of acquired transepidermal elimination dermatosis frequently associated with diabetes mellitus and chronic kidney disease. An association with malignancy has been sporadically reported in the literature. ...
Recurrent Hyponatremia in the Setting of Autoimmune Disease with Sicca Syndrome: A Case Report [0.03%]
自身免疫性疾病伴口干综合征反复出现低钠血症一例报告
Ahmad El-Moussa,Syed Umer Mohsin,Omer Alrawi et al.
Ahmad El-Moussa et al.
Sjogren's syndrome is an autoimmune disease associated with xerostomia and xerophthalmia. The association of Sjogren's with hyponatremia has rarely been reported and has been attributed to syndrome of inappropriate antidiuretic hormone secr...
Isolated Proteinuria Caused by CUBN Gene Mutations: A Case Report and Review of the Literature [0.03%]
由CUBN基因突变引起的孤立性蛋白尿：1例报告及文献复习
Jingyang Ran,Qingsong Chen,Yudong Hu et al.
Jingyang Ran et al.
Mutations in the cubilin (CUBN) gene commonly cause Imerslund-Gräsbeck syndrome, while isolated proteinuria as a result of CUBN variations is rarely reported. The clinical manifestation is mainly chronic isolated proteinuria in the non-nep...