Case of maternal uniparental isodisomy with autosomal recessive Alport syndrome combined with congenital myasthenia and Oguchi disease [0.03%]
一名以夏普塔-霍奇金综合征合并先天性肌无力及奥古契病为表现的母系单亲二体综合症患者的临床报道
Misaki Akiyama,Keiko Matsubara,Hiroshi Terashima et al.
Misaki Akiyama et al.
Uniparental isodisomy (UPiD) is a genetic condition in which an individual inherits two identical copies of a chromosome, or part of a chromosome, from one parent. UPiD can result in the development of autosomal recessive disorders if the c...
Successful use of avacopan in a case of ANCA-associated vasculitis with treatment-resistant medium-sized vessel involvement [0.03%]
阿瓦西普安在治疗难治性中等血管受累的ANCA相关性血管炎中的成功应用
Takaaki Tsuchiya,Yui Ohta,Masatoshi Oka et al.
Takaaki Tsuchiya et al.
We report the case of a 75-year-old woman who presented with fever, right back pain, paresthesia in the right extremities, erythema, purpura, and nodules. She had previously initiated dialysis due to rapidly progressive glomerulonephritis a...
An educational case of toluene intoxication: importance of kidney function and timing in diagnosis [0.03%]
甲苯中毒一例：肾脏功能及诊断时机的重要性
Masatomo Ogata,Naoto Tominaga,Satoru Morikubo et al.
Masatomo Ogata et al.
Metabolic acidosis (MA) is common in daily clinical settings and requires evaluation not only by serum anion gap (AG) but also by urine AG (UAG) and urine osmolal gap (UOG) to investigate potential causes and determine appropriate treatment...
A case of mucormycosis caused by Rhizopus microsporus in a renal transplant patient [0.03%]
一例移植肾患者感染微小根毛霉病病例报告
Miruzato Fukuda,Takayoshi Yokoyama,Morota Marie et al.
Miruzato Fukuda et al.
A 54-year-old man who had been on the kidney donor register for 32 years received a kidney from a 9-year-old boy who had died of fulminant myocarditis. The post-operative course was poor, and hemodialysis was still needed after surgery. A k...
Steroid-resistant nephrotic syndrome as paraneoplastic syndrome of Waldenström macroglobulinemia: a case report [0.03%]
Waldenstrom巨球蛋白血症的类癌性肾病综合征一例报告
Konosuke Hirano,Sayuri Shirai,Teppei Koyama et al.
Konosuke Hirano et al.
Reports of glomerulonephritis associated with lymphoproliferative disorders are common, but reports of minimal change disease (MCD) accompanying non-Hodgkin's lymphoma are rare. Here, we present a case of a 45-year-old woman diagnosed with ...
Successful treatment with bortezomib for refractory cryoglobulinemic vasculitis triggered by ischemic non-obstructive coronary artery disease [0.03%]
硼替佐米治疗由冠状动脉缺血性非梗阻性疾病诱发的难治性冷球蛋白血管炎反应良好
Yui Ohta,Takaaki Tsuchiya,Masatoshi Oka et al.
Yui Ohta et al.
Type I and mixed cryoglobulinemic vasculitis differ in pathophysiology, clinical presentation, and therapeutic response. We report a case of refractory cryoglobulinemic vasculitis diagnosed following ischemic non-obstructive coronary artery...
The application of omalizumab in children with atopic diseases complicated by nephrotic syndrome: a case report [0.03%]
奥马珠单抗治疗伴发肾病综合征的儿童过敏性疾病中的应用：1例报告
Yi Mao,Jialu Lu,Lei Yin et al.
Yi Mao et al.
Nephrotic syndrome (NS) and atopic diseases are linked through shared immunological pathways, with allergic triggers often contributing to NS relapses, particularly in immunoglobulin E (IgE)-mediated pathways. Omalizumab, a humanized monocl...
Effective combination of corticosteroid and cyclosporine A for immunoglobulin A nephropathy with membranoproliferative glomerulonephritis features: a case report [0.03%]
免疫抑制剂治疗以膜增生性肾小球肾炎为特征的IgA肾病一例报告
Saeko Hatanaka,Go Kanzaki,Kentaro Koike et al.
Saeko Hatanaka et al.
Immunoglobulin A nephropathy (IgAN) is the most common primary glomerulonephritis worldwide with heterogeneous histopathological phenotypes. Although IgAN with membranoproliferative glomerulonephritis (MPGN)-like features has been reported ...
A case of neuron-derived neurotrophic factor-positive, syphilis-related membranous nephropathy that achieved spontaneous remission [0.03%]
一例神经源神经营养因子阳性、与梅毒相关的膜性肾病自发缓解病例报告
Yuko Yoshida,Kenji Ueki,Yuta Matsukuma et al.
Yuko Yoshida et al.
Neuron-derived neurotrophic factor (NDNF) was discovered as a target antigen in membranous nephropathy (MN) caused by syphilis. However, there have been few reports of NDNF-positive MN in Japan. A 19-year-old female patient was admitted to ...
Granulomatosis with polyangiitis with rapidly progressive glomerulonephritis treated with a multipronged approach-a case based review [0.03%]
多管齐下治疗肉芽肿性多血管炎合并快速进展性肾小球肾炎一例及相关文献复习
Ujjwal Madan,Vishesh Goel,Jignesh Shah et al.
Ujjwal Madan et al.
Granulomatosis with polyangiitis is an ANCA-associated vasculitis that involves small to medium-sized vessels. The extent of renal involvement varies, which is also associated with disease prognosis, with aggressive renal involvement having...