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Early-onset kidney failure in a girl with autosomal dominant tubulointerstitial kidney disease due to a de novo variant
Early-onset kidney failure in a girl with autosomal dominant tubulointerstitial kidney disease due to a de novo variant
Autosomal dominant tubulointerstitial kidney disease (ADTKD) is characterized by renal tubular and interstitial abnormalit...
Successful treatment of intractable edema with Goreisan in severe lupus nephritis with nephrotic syndrome: a case report
Successful treatment of intractable edema with Goreisan in severe lupus nephritis with nephrotic syndrome: a case report
Goreisan is an herbal medicine that regulates water metabolism, exerting a diuretic effect that does not alter urine volum...
Relapse of minimal change nephrotic syndrome after initiation of sulfamethoxazole–trimethoprim combination therapy: a case report
Relapse of minimal change nephrotic syndrome after initiation of sulfamethoxazole–trimethoprim combination therapy: a case report
Minimal change nephrotic syndrome (MCNS) is characterized by podocyte injury leading to severe proteinuria, mainly mediate...
A case of membranoproliferative glomerulonephritis-type IgA nephropathy modified by nintedanib
A case of membranoproliferative glomerulonephritis-type IgA nephropathy modified by nintedanib
A 73-year-old woman had been treated with nintedanib for 40 months for idiopathic pulmonary fibrosis. She present...
A case report of spontaneous remission and relapse in minimal change disease: a heterogeneous disease entity
A case report of spontaneous remission and relapse in minimal change disease: a heterogeneous disease entity
Minimal change disease (MCD) is a common cause of nephrotic syndrome and typically responds well to glucocorticoid therapy...
Kidney transplantation after chronic active Epstein-Barr virus infection remission
Kidney transplantation after chronic active Epstein-Barr virus infection remission
Chronic active Epstein-Barr virus is a rare but severe condition characterized by persistent Epstein-Barr virus activation...
Kidney Involvement in Sarcoidosis-Lymphoma Syndrome: A Report of Two Cases
Kidney Involvement in Sarcoidosis-Lymphoma Syndrome: A Report of Two Cases
Sarcoidosis-lymphoma syndrome, first described by Henrik Brincker in 1986, is defined by the association of sarcoidosis wi...
Recurrent obturator hernia in a patient with autosomal dominant polycystic kidney disease undergoing peritoneal dialysis: a case report
Recurrent obturator hernia in a patient with autosomal dominant polycystic kidney disease undergoing peritoneal dialysis: a case report
Obturator hernia, a rare condition that accounts for only 0.07–1% of all hernias, typically occurs in older adult, t...
A rare case of obstructive shock caused by a giant biloma with right heart compression in a patient undergoing hemodialysis
A rare case of obstructive shock caused by a giant biloma with right heart compression in a patient undergoing hemodialysis
A biloma is a localized bile collection caused by bile leakage that is usually resolved with percutaneous drainage. In mos...
An autopsy-proven case of normotensive scleroderma renal crisis with refractory pleuroperitoneal effusion
An autopsy-proven case of normotensive scleroderma renal crisis with refractory pleuroperitoneal effusion
Scleroderma renal crisis (SRC) is a serious complication of systemic sclerosis that typically presents with hypertension a...
Successful living kidney transplantation in a T-cell flow cytometry crossmatch-positive patient with atypical hemolytic uremic syndrome treated with an anti-C5 antibody: a case report
Successful living kidney transplantation in a T-cell flow cytometry crossmatch-positive patient with atypical hemolytic uremic syndrome treated with an anti-C5 antibody: a case report
Atypical hemolytic uremic syndrome (aHUS) is an intravascular hemolytic disorder caused by complement dysregulation. A 41-...
Multiple dyselectrolytemia in a patient with alcohol use disorder (AUD)
Multiple dyselectrolytemia in a patient with alcohol use disorder (AUD)
Alcohol use disorder (AUD) is a chronic disease characterized by an inability to limit alcohol use despite knowledge of th...
A case of autosomal dominant polycystic kidney disease with multiple bilateral spontaneous retroperitoneal hemorrhages
A case of autosomal dominant polycystic kidney disease with multiple bilateral spontaneous retroperitoneal hemorrhages
We experienced a 45-year-old male with ADPKD who developed spontaneous retroperitoneal hemorrhages with hypertension in th...
Relapse of subacute anti-glomerular basement membrane nephritis following self-discontinuation of steroid therapy
Relapse of subacute anti-glomerular basement membrane nephritis following self-discontinuation of steroid therapy
Anti-glomerular basement membrane (GBM) nephritis is an autoimmune disease which typically presents rapid progressive glom...
Olmesartan-associated enteropathy presenting with metabolic acidosis and acute kidney injury requiring hemodialysis: a rechallenge-confirmed case
Olmesartan-associated enteropathy presenting with metabolic acidosis and acute kidney injury requiring hemodialysis: a rechallenge-confirmed case
Olmesartan-associated enteropathy (OAE) is a delayed-onset drug-induced intestinal disorder that mimics celiac disease and...
PLA2R-positive primary membranous nephropathy in an adolescent with type 1 diabetes mellitus and autoimmune hypothyroidism: a case report
PLA2R-positive primary membranous nephropathy in an adolescent with type 1 diabetes mellitus and autoimmune hypothyroidism: a case report
Membranous nephropathy (MN) is an uncommon cause of nephrotic syndrome in children, accounting for fewer than 5% of cases....
Early recognition of atypical hemolytic uremic syndrome to prevent irreversible kidney injury: cardiac failure and refractory hypertension as critical clues in young patients
Early recognition of atypical hemolytic uremic syndrome to prevent irreversible kidney injury: cardiac failure and refractory hypertension as critical clues in young patients
Atypical hemolytic uremic syndrome (aHUS) is a rare, life-threatening thrombotic microangiopathy that predominantly affect...
Renal and gastrointestinal complications following tosufloxacin therapy for suspected mycoplasma infection in a 10-year-old child
Renal and gastrointestinal complications following tosufloxacin therapy for suspected mycoplasma infection in a 10-year-old child
Tosufloxacin, a fluoroquinolone antibiotic, is increasingly prescribed for pediatric patients, particularly for macrolide-...
A case of acute tubulointerstitial nephritis with suspected Saikokaryukotsuboreito involvement responding to glucocorticoid therapy
A case of acute tubulointerstitial nephritis with suspected Saikokaryukotsuboreito involvement responding to glucocorticoid therapy
Drug-induced kidney injury is a major cause of acute tubulointerstitial nephritis (AIN). The standard treatment for AIN is...
A case of effective tocilizumab for arthropathy due to dialysis-related amyloidosis
A case of effective tocilizumab for arthropathy due to dialysis-related amyloidosis
A 79-year-old male patient on hemodialysis for 29 years was admitted to the hospital with unexplained fever (C-re...
Reduction of polycystic kidney and liver volumes in a patient with tolvaptan-resistant autosomal dominant polycystic kidney disease and acromegaly during lanreotide therapy
Reduction of polycystic kidney and liver volumes in a patient with tolvaptan-resistant autosomal dominant polycystic kidney disease and acromegaly during lanreotide therapy
A 35-year-old female was diagnosed with autosomal dominant polycystic kidney disease (ADPKD) in 2002 and referred to the N...
Efficacy of hemodialysis and importance of tonicity monitoring in mannitol-induced acute kidney injury with hyponatremia
Efficacy of hemodialysis and importance of tonicity monitoring in mannitol-induced acute kidney injury with hyponatremia
Mannitol is an osmotic diuretic that can induce acute kidney injury (AKI) and hypertonic hyponatremia. Rapid mannitol remo...
Early low-density lipoprotein apheresis for steroid-resistant minimal change disease with acute kidney injury: a case report
Early low-density lipoprotein apheresis for steroid-resistant minimal change disease with acute kidney injury: a case report
We report the case of a 75-year-old woman with steroid-resistant minimal change disease (MCD) whose refractory proteinuria...
Williams syndrome presenting as infantile hypercalcemia with acute kidney injury: a case report
Williams syndrome presenting as infantile hypercalcemia with acute kidney injury: a case report
Williams syndrome is an autosomal-dominant multisystem disorder. Infantile hypercalcemia has been documented in 15% of inf...
Nephrotic syndrome after switching from irinotecan, S-1, and bevacizumab combination to trifluridine/tipiracil
Nephrotic syndrome after switching from irinotecan, S-1, and bevacizumab combination to trifluridine/tipiracil
Trifluridine/tipiracil (FTD/TPI) has shown efficacy in treating advanced colorectal and gastric cancers. Although renal in...
Tubulointerstitial nephritis with predominant monotypic plasma cell infiltration in three cases of Sjögren's syndrome: case reports and literature review
Tubulointerstitial nephritis with predominant monotypic plasma cell infiltration in three cases of Sjögren's syndrome: case reports and literature review
Tubulointerstitial nephritis (TIN) is a common kidney manifestation of Sjögren's syndrome, typically characterize...
Long-term outcomes of kidney transplantation in a transfusion-dependent alpha-thalassemia patient
Long-term outcomes of kidney transplantation in a transfusion-dependent alpha-thalassemia patient
The improved survival rates of patients with thalassemia have led to the identification of new complications, including re...
Diagnosing apparent mineralocorticoid excess in a child with hypertension and nephrocalcinosis: from symptoms to genetics
Diagnosing apparent mineralocorticoid excess in a child with hypertension and nephrocalcinosis: from symptoms to genetics
Apparent mineralocorticoid excess (AME) is a rare genetic disorder caused by reduced activity of the 11β-hydroxystero...
A case of Frasier syndrome achieved complete remission by cyclosporine A for steroid-resistant nephrotic syndrome
A case of Frasier syndrome achieved complete remission by cyclosporine A for steroid-resistant nephrotic syndrome
In pediatric steroid-resistant nephrotic syndrome (SRNS), causative genetic abnormalities are now being identified. Immuno...
Sustained eGFR improvement after dapagliflozin in a patient with antiretroviral therapy-related chronic kidney disease
Sustained eGFR improvement after dapagliflozin in a patient with antiretroviral therapy-related chronic kidney disease
Chronic kidney disease (CKD) is an emerging concern in the aging population of people living with HIV, especially in those...
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