1.Megalocytic Interstitial Nephritis Following Acute Pyelonephritis with Escherichia coli Bacteremia: A Case Report.
Hee Jin KWON ; Kwai Han YOO ; In Young KIM ; Seulkee LEE ; Hye Ryoun JANG ; Ghee Young KWON
Journal of Korean Medical Science 2015;30(1):110-114
Megalocytic interstitial nephritis is a rare form of kidney disease caused by chronic inflammation. We report a case of megalocytic interstitial nephritis occurring in a 45-yrold woman who presented with oliguric acute kidney injury and acute pyelonephritis accompanied by Escherichia coli bacteremia. Her renal function was not recovered despite adequate duration of susceptible antibiotic treatment, accompanied by negative conversion of bacteremia and bacteriuria. Kidney biopsy revealed an infiltration of numerous histiocytes without Michaelis-Gutmann bodies. The patient's renal function was markedly improved after short-term treatment with high-dose steroid.
Acute Disease
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Acute Kidney Injury/complications/*drug therapy/pathology
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Anti-Bacterial Agents/therapeutic use
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Azithromycin/therapeutic use
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Bacteremia/*drug therapy/microbiology/pathology
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Cefotaxime/therapeutic use
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Creatinine/blood
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Escherichia coli
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Escherichia coli Infections/*drug therapy/microbiology/pathology
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Female
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Humans
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Kidney/pathology
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Methylprednisolone/therapeutic use
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Middle Aged
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Nephritis, Interstitial/*drug therapy/immunology/pathology
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Pyelonephritis/complications/*drug therapy/pathology
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Renal Dialysis
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Shock, Septic/drug therapy/microbiology
2.Acute kidney injury in liver cirrhosis: new definition and application.
Clinical and Molecular Hepatology 2016;22(4):415-422
The traditional diagnostic criteria of renal dysfunction in cirrhosis are a 50% increase in serum creatinine (SCr) with a final value above 1.5 mg/dL. This means that patients with milder degrees of renal dysfunction are not being diagnosed, and therefore not offered timely treatment. The International Ascites Club in 2015 adapted the term acute kidney injury (AKI) to represent acute renal dysfunction in cirrhosis, and defined it by an increase in SCr of 0.3 mg/dL (26.4 µmoL/L) in <48 hours, or a 50% increase in SCr from a baseline within ≤3 months. The severity of AKI is described by stages, with stage 1 represented by these minimal changes, while stages 2 and 3 AKI by 2-fold and 3-fold increases in SCr respectively. Hepatorenal syndrome (HRS), renamed AKI-HRS, is defined by stage 2 or 3 AKI that fulfils all other diagnostic criteria of HRS. Various studies in the past few years have indicated that these new diagnostic criteria are valid in the prediction of prognosis for patients with cirrhosis and AKI. The future in AKI diagnosis may include further refinements such as inclusion of biomarkers that can identify susceptibility for AKI, differentiating the various prototypes of AKI, or track its progression.
Acute Kidney Injury/complications/*diagnosis/drug therapy/pathology
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Biomarkers/blood
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Creatinine/blood
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Humans
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Liver Cirrhosis/*complications
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Prognosis
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Serum Albumin/therapeutic use
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Severity of Illness Index
3.A Case of Severe Acute Hepatitis A Complicated with Pure Red Cell Aplasia.
Pyoung Suk LIM ; In Hee KIM ; Seong Hun KIM ; Seung Ok LEE ; Sang Wook KIM
The Korean Journal of Gastroenterology 2012;60(3):177-181
Hepatitis A is typically a self-limited acute illness that does not progress to chronic hepatitis. In rare cases, acute hepatitis A can be associated with serious complications (such as fulminant hepatitis or acute kidney injury) and may result in death or liver transplantation. Pure red cell aplasia (PRCA) is a rare hematologic disorder characterized by anemia, reticulocytopenia in the blood, and isolated erythroblastopenia with normal granulopoiesis and megakaryopoiesis in the bone marrow. PRCA is a rare hematopoietic complication of acute viral hepatitis, and few cases associated with hepatitis A virus infection have been reported. Recently, we experienced a case of severe hepatitis A complicated by fulminant hepatitis and acute kidney injury followed by PRCA which showed a favorable response to oral corticosteroids.
Acute Disease
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Acute Kidney Injury/etiology
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Adult
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Anti-Inflammatory Agents/therapeutic use
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Bone Marrow/pathology
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Female
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Hepatitis A/complications/*diagnosis
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Humans
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Prednisone/therapeutic use
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Red-Cell Aplasia, Pure/complications/*diagnosis/drug therapy
4.Immunoglobulin A Nephropathy Associated with Plasmodium falciparum Malaria.
Dong Eun YOO ; Jeong Ho KIM ; Jeong Hae KIE ; Yoonseon PARK ; Tae Ik CHANG ; Hyung Jung OH ; Seung Jun KIM ; Tae Hyun YOO ; Kyu Hun CHOI ; Shin Wook KANG ; Seung Hyeok HAN
Journal of Korean Medical Science 2012;27(4):446-449
Glomerulonephritis occurs as a rare form of renal manifestation in Plasmodium falciparum malaria. Herein, we report a case of falciparum malaria-associated IgA nephropathy for the first time. A 49-yr old male who had been to East Africa was diagnosed with Plasmodium falciparum malaria. Microhematuria and proteinuria along with acute kidney injury developed during the course of the disease. Kidney biopsy showed mesangial proliferation and IgA deposits with tubulointerstitial inflammation. Laboratory tests after recovery from malaria showed disappearance of urinary abnormalities and normalization of kidney function. Our findings suggest that malaria infection might be associated with IgA nephropathy.
Acute Kidney Injury/etiology/pathology
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Antimalarials/therapeutic use
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Creatinine/blood
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Glomerulonephritis, IGA/*diagnosis/*etiology
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Hematuria/etiology
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Humans
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Immunoglobulin A/*metabolism
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Malaria/*complications/drug therapy/*pathology
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Male
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Middle Aged
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Plasmodium falciparum/*isolation & purification
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Proteinuria/etiology
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Quinine/therapeutic use
5.Drug rash with eosinophilia and systemic symptoms syndrome following cholestatic hepatitis A: a case report.
Jihyun AN ; Joo Ho LEE ; Hyojeong LEE ; Eunsil YU ; Dan Bi LEE ; Ju Hyun SHIM ; Sunyoung YOON ; Yumi LEE ; Soeun PARK ; Han Chu LEE
The Korean Journal of Hepatology 2012;18(1):84-88
Hepatitis A virus (HAV) infections occur predominantly in children, and are usually self-limiting. However, 75-95% of the infections in adults are symptomatic (mostly with jaundice), with the illness symptoms usually persisting for a few weeks. Atypical manifestations include relapsing hepatitis, prolonged cholestasis, and complications involving renal injury. Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome is a severe, drug-induced hypersensitivity reaction characterized by skin rash, fever, lymph-node enlargement, and internal organ involvement. We describe a 22-year-old male who presented with acute kidney injury and was diagnosed with prolonged cholestatic hepatitis A. The patient also developed DRESS syndrome due to antibiotic and/or antiviral treatment. To our knowledge, this is the first report of histopathologically confirmed DRESS syndrome due to antibiotic and/or antiviral treatment following HAV infection with cholestatic features and renal injury.
Acute Kidney Injury/diagnosis
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Anti-Bacterial Agents/*adverse effects/therapeutic use
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Cefotaxime/adverse effects/therapeutic use
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Cholestasis/complications/*diagnosis
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Cytomegalovirus/genetics
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Cytomegalovirus Infections/drug therapy/virology
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DNA, Viral/analysis
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Eosinophilia/etiology
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Exanthema/*chemically induced/pathology
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Ganciclovir/therapeutic use
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Hepatitis A/complications/*diagnosis/drug therapy
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Humans
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Hydrocortisone/therapeutic use
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Immunoglobulins/therapeutic use
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Male
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Syndrome
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Young Adult