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Tonsillectomy in Immunoglobulin A vasculitis with nephritis: case series
Tonsillectomy in Immunoglobulin A vasculitis with nephritis: case series
There is no consensus-based treatment for adult-onset immunoglobulin A vasculitis with nephritis (IgAV nephritis). Tonsill...
Peritoneal lymphomatosis as a rare entity of post-transplant lymphoproliferative disorder after kidney transplantation: a case report
Peritoneal lymphomatosis as a rare entity of post-transplant lymphoproliferative disorder after kidney transplantation: a case report
Post-transplant lymphoproliferative disorder (PTLD) is a severe complication of solid organ transplantation, and its manif...
IgA nephropathy and IgA vasculitis in a pediatric Crohn’s disease patient with early IgA deposition in vascular walls of intestines
IgA nephropathy and IgA vasculitis in a pediatric Crohn’s disease patient with early IgA deposition in vascular walls of intestines
Patients with inflammatory bowel disease may present with extraintestinal manifestations. Crohn’s disease complicate...
A case of IgG-type heavy chain amyloidosis with membranous nephropathy-like changes with long-term survival
A case of IgG-type heavy chain amyloidosis with membranous nephropathy-like changes with long-term survival
We performed a kidney biopsy on a 68-year-old man with 2.6 g/day proteinuria. Immunofluorescence (IF) study showe...
Successful outcome of a refractory IgA vasculitis nephritis in children treated with telitacicept
Successful outcome of a refractory IgA vasculitis nephritis in children treated with telitacicept
IgA vasculitis (IgAV) is the most prevalent form of vasculitis in children. While most cases of IgAV present with mild cli...
Early administration of caplacizumab combined with plasma exchange for thrombotic microangiopathy due to malignant hypertension: a case report
Early administration of caplacizumab combined with plasma exchange for thrombotic microangiopathy due to malignant hypertension: a case report
Both thrombotic thrombocytopenic purpura (TTP) and malignant hypertension (MHT) present with thrombotic microangiopathy (T...
Systemic AA amyloidosis with amyloid deposition in the peritoneum at the time of initiating peritoneal dialysis
Systemic AA amyloidosis with amyloid deposition in the peritoneum at the time of initiating peritoneal dialysis
Amyloidosis is characterized by the deposition of insoluble amyloid fibrils formed by disease-specific precursor proteins ...
A case of systemic contact dermatitis associated with a peritoneal dialysis catheter and treated with dupilumab
A case of systemic contact dermatitis associated with a peritoneal dialysis catheter and treated with dupilumab
Eosinophilia during the induction of peritoneal dialysis (PD) is frequently caused by icodextrin, but allergic reactions t...
Genetic and protein structure prediction analyses identify a rare pathogenic variant causing autosomal dominant polycystic kidney disease
Genetic and protein structure prediction analyses identify a rare pathogenic variant causing autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common monogenic kidney disorders. The diagnosis o...
Clinicopathological features of familial fibronectin glomerulopathy caused by a splice site variant in the Fibronectin 1 gene: a case report
Clinicopathological features of familial fibronectin glomerulopathy caused by a splice site variant in the Fibronectin 1 gene: a case report
Fibronectin glomerulopathy (FNG) is a rare autosomal dominant inherited disease characterized by extensive deposits of fib...
A case of acute appendicitis in a patient with minimal change disease
A case of acute appendicitis in a patient with minimal change disease
Minimal change disease (MCD) is a common cause of idiopathic nephrotic syndrome (NS). MCD patients are complicated by acut...
Tubular damage and SGLT2 expression in a patient with Beni-koji tablet-associated acute kidney injury and Fanconi syndrome
Tubular damage and SGLT2 expression in a patient with Beni-koji tablet-associated acute kidney injury and Fanconi syndrome
Since March 2024, many cases of renal dysfunction have been reported in Japan among individuals taking a supplement contai...
A case of lupus nephritis with masked polyclonal IgG presenting as severe AKI, successfully treated and withdrawn from hemodialysis: a case report
A case of lupus nephritis with masked polyclonal IgG presenting as severe AKI, successfully treated and withdrawn from hemodialysis: a case report
Lupus nephritis (LN) is well-known as an immune-mediated glomerulonephritis characterized by the full-house pattern of imm...
Successful treatment of MPO-ANCA positive crescentic IgA nephropathy/IgA vasculitis with nephritis potentially triggered by a COVID-19 vaccine in a young adult female using corticosteroids, rituximab, and avacopan
Successful treatment of MPO-ANCA positive crescentic IgA nephropathy/IgA vasculitis with nephritis potentially triggered by a COVID-19 vaccine in a young adult female using corticosteroids, rituximab, and avacopan
An 18-year-old female presented with palpable purpura nine months before her hospital admission, which first appeared 1&am...
Renoprotective effects of combination therapy with tolvaptan and dapagliflozin in autosomal dominant polycystic kidney disease: a four-case series
Renoprotective effects of combination therapy with tolvaptan and dapagliflozin in autosomal dominant polycystic kidney disease: a four-case series
Autosomal dominant polycystic kidney disease (ADPKD), the most prevalent inherited kidney disorder, progresses inexorably ...
An adolescent presenting with IgA nephropathy and persistent decreased kidney function after COVID-19 vaccination during follow-up for asymptomatic hematuria: a clinicopathological study
An adolescent presenting with IgA nephropathy and persistent decreased kidney function after COVID-19 vaccination during follow-up for asymptomatic hematuria: a clinicopathological study
Although the coronavirus disease 2019 (COVID-19) vaccine has been proven to be effective and safe in most adults and child...
Taurine supplementation improves physical activity level in a hemodialysis patient with mitochondrial disease: a case report
Taurine supplementation improves physical activity level in a hemodialysis patient with mitochondrial disease: a case report
Mitochondrial diseases (MDs) are inherited metabolic disorders that affect multiple organ systems, including the kidneys. ...
A case of rapidly progressive IgA nephropathy after SARS-CoV-2 vaccination, successfully treated with cyclophosphamide
A case of rapidly progressive IgA nephropathy after SARS-CoV-2 vaccination, successfully treated with cyclophosphamide
A 61-year-old woman with a 10-year history of type 1 diabetes mellitus was referred to our nephrology department due to ra...
Lupus-like membranous nephropathy during the postpartum period expressing glomerular antigens exostosin 1/exostosin 2 and phospholipase A2 receptor: a case report
Lupus-like membranous nephropathy during the postpartum period expressing glomerular antigens exostosin 1/exostosin 2 and phospholipase A2 receptor: a case report
Recently, several target antigens of membranous nephropathy (MN), such as phospholipase A2 receptor (PLA2R) and exostosin ...
Correction to: Two acute kidney injury episodes after ICI therapy: a case report
Correction to: Two acute kidney injury episodes after ICI therapy: a case report
Cite this articleIshiga, K., Kobayashi, R., Kanaoka, T. et al. Correction to: Two acute kidney injury episodes after ICI t...
Two acute kidney injury episodes after ICI therapy: a case report
Two acute kidney injury episodes after ICI therapy: a case report
A 74-year-old Japanese male with lung squamous cell carcinoma received his first dose of immune checkpoint inhibitors (ICI...
Hypereosinophilia-associated acute intradialytic hypotension: a report of three cases and literature review
Hypereosinophilia-associated acute intradialytic hypotension: a report of three cases and literature review
Occasionally, patients undergoing dialysis develop acute severe hypotension that requires interruption of dialysis within ...
Immunoglobulin A-dominant membranoproliferative glomerulonephritis-like pattern of injury as a possible paraneoplastic nephropathy in a breast cancer patient
Immunoglobulin A-dominant membranoproliferative glomerulonephritis-like pattern of injury as a possible paraneoplastic nephropathy in a breast cancer patient
A middle-aged woman was found to have proteinuria during a health check-up. About sixteen months later, she was diagnosed ...
Case of successful treatment with glucocorticoid for isolated anti-centromere antibody-positive acute interstitial nephritis
Case of successful treatment with glucocorticoid for isolated anti-centromere antibody-positive acute interstitial nephritis
Acute interstitial nephritis (AIN) is known to cause acute kidney injury and is characterized by immunocyte infiltration a...
A case of de novo glomerulonephritis following COVID-19 in a patient with preexistent IgA vasculitis
A case of de novo glomerulonephritis following COVID-19 in a patient with preexistent IgA vasculitis
During the unprecedented COVID-19 outbreak, new-onset or relapsing glomerulonephritis, such as ANCA-associated glomerulone...
Unusual late presentation of cryptococcal meningitis with simultaneous CMV antigenemia in a kidney transplant recipient
Unusual late presentation of cryptococcal meningitis with simultaneous CMV antigenemia in a kidney transplant recipient
Cryptococcosis is the third most common invasive fungal infection in solid-organ transplant (SOT) recipients after candidi...
Macroscopic hematuria-associated severe acute kidney injury triggered by kidney stone formation in a patient with thin basement membrane and no history of microscopic hematuria
Macroscopic hematuria-associated severe acute kidney injury triggered by kidney stone formation in a patient with thin basement membrane and no history of microscopic hematuria
Macroscopic hematuria (MH)-associated acute kidney injury (AKI) is a rare condition that causes acute tubular damage due t...
Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused by paired box protein 2 gene variant
Familial focal segmental glomerulosclerosis with Alport-like glomerular basement changes caused by paired box protein 2 gene variant
Paired box protein 2 (PAX2) gene variant causes renal coloboma syndrome (MIM#120330). Further, they are associated with fo...
Neural epidermal growth factor-like 1 protein (NELL1)-associated membranous nephropathy with heterogeneous underlying diseases: a case report
Neural epidermal growth factor-like 1 protein (NELL1)-associated membranous nephropathy with heterogeneous underlying diseases: a case report
Neural epidermal growth factor-like 1 protein (NELL1) is a target antigen of membranous nephropathy (MN). NELL1-associated...
A case of ifosfamide-induced acute kidney injury, Fanconi syndrome, and nephrogenic diabetes insipidus
A case of ifosfamide-induced acute kidney injury, Fanconi syndrome, and nephrogenic diabetes insipidus
Ifosfamide, a cytotoxic antineoplastic drug, can induce rare complications of Fanconi syndrome and nephrogenic diabetes in...
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