{"title":"肾炎相关纤溶酶受体阳性链球菌感染后急性肾小球肾炎呈满屋型:1例报告。","authors":"Yusuke Takahashi, Naoto Kawata, Hiroki Nishiwaki, Yoshinori Sato, Toshiharu Ueno, Takashi Oda, Fumihiko Koiwa","doi":"10.1159/000546484","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Post-streptococcal acute glomerulonephritis (PSAGN) is a disease in which patients develop hematuria and leg edema following streptococcal infection, which may lead to acute nephritic syndrome and nephrotic syndrome. We present a case involving acute kidney injury and nephrotic syndrome with nonspecific pathological findings for PSAGN, which posed diagnostic challenges.</p><p><strong>Case presentation: </strong>A 25-year-old man presented with leg edema, cough, nephrotic syndrome, severe kidney dysfunction, and hematuria. Blood tests showed elevated antistreptolysin O levels and decreased complement C3 levels; therefore, PSAGN was suspected. Light microscopy revealed membranoproliferative glomerulonephritis, immunofluorescence staining revealed a full-house pattern, and electron microscopy revealed subendothelial deposition. The diagnosis was difficult, however, positive glomerular staining for nephritis-associated plasmin receptor and plasmin activity strongly suggested an infection-related etiology of glomerulonephritis. Treatment included the administration of 500 mg of methylprednisolone for 3 days, followed by 4 weeks of treatment with 50 mg of prednisolone. Subsequently, the dosage was reduced to 40 mg, and the patient was discharged. Urinary findings revealed resolution of hematuria 1 year after discharge.</p><p><strong>Conclusion: </strong>When PSAGN is suspected and other diseases are difficult to exclude, nephritis-associated plasmin receptor staining should be considered.</p>","PeriodicalId":9599,"journal":{"name":"Case Reports in Nephrology and Dialysis","volume":"15 1","pages":"198-205"},"PeriodicalIF":0.9000,"publicationDate":"2025-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12503611/pdf/","citationCount":"0","resultStr":"{\"title\":\"Nephritis-Associated Plasmin Receptor-Positive Post-Streptococcal Acute Glomerulonephritis Showing Full-House Pattern: A Case Report.\",\"authors\":\"Yusuke Takahashi, Naoto Kawata, Hiroki Nishiwaki, Yoshinori Sato, Toshiharu Ueno, Takashi Oda, Fumihiko Koiwa\",\"doi\":\"10.1159/000546484\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Post-streptococcal acute glomerulonephritis (PSAGN) is a disease in which patients develop hematuria and leg edema following streptococcal infection, which may lead to acute nephritic syndrome and nephrotic syndrome. We present a case involving acute kidney injury and nephrotic syndrome with nonspecific pathological findings for PSAGN, which posed diagnostic challenges.</p><p><strong>Case presentation: </strong>A 25-year-old man presented with leg edema, cough, nephrotic syndrome, severe kidney dysfunction, and hematuria. Blood tests showed elevated antistreptolysin O levels and decreased complement C3 levels; therefore, PSAGN was suspected. Light microscopy revealed membranoproliferative glomerulonephritis, immunofluorescence staining revealed a full-house pattern, and electron microscopy revealed subendothelial deposition. The diagnosis was difficult, however, positive glomerular staining for nephritis-associated plasmin receptor and plasmin activity strongly suggested an infection-related etiology of glomerulonephritis. Treatment included the administration of 500 mg of methylprednisolone for 3 days, followed by 4 weeks of treatment with 50 mg of prednisolone. Subsequently, the dosage was reduced to 40 mg, and the patient was discharged. Urinary findings revealed resolution of hematuria 1 year after discharge.</p><p><strong>Conclusion: </strong>When PSAGN is suspected and other diseases are difficult to exclude, nephritis-associated plasmin receptor staining should be considered.</p>\",\"PeriodicalId\":9599,\"journal\":{\"name\":\"Case Reports in Nephrology and Dialysis\",\"volume\":\"15 1\",\"pages\":\"198-205\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-07-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12503611/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Case Reports in Nephrology and Dialysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000546484\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Nephrology and Dialysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000546484","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Nephritis-Associated Plasmin Receptor-Positive Post-Streptococcal Acute Glomerulonephritis Showing Full-House Pattern: A Case Report.
Introduction: Post-streptococcal acute glomerulonephritis (PSAGN) is a disease in which patients develop hematuria and leg edema following streptococcal infection, which may lead to acute nephritic syndrome and nephrotic syndrome. We present a case involving acute kidney injury and nephrotic syndrome with nonspecific pathological findings for PSAGN, which posed diagnostic challenges.
Case presentation: A 25-year-old man presented with leg edema, cough, nephrotic syndrome, severe kidney dysfunction, and hematuria. Blood tests showed elevated antistreptolysin O levels and decreased complement C3 levels; therefore, PSAGN was suspected. Light microscopy revealed membranoproliferative glomerulonephritis, immunofluorescence staining revealed a full-house pattern, and electron microscopy revealed subendothelial deposition. The diagnosis was difficult, however, positive glomerular staining for nephritis-associated plasmin receptor and plasmin activity strongly suggested an infection-related etiology of glomerulonephritis. Treatment included the administration of 500 mg of methylprednisolone for 3 days, followed by 4 weeks of treatment with 50 mg of prednisolone. Subsequently, the dosage was reduced to 40 mg, and the patient was discharged. Urinary findings revealed resolution of hematuria 1 year after discharge.
Conclusion: When PSAGN is suspected and other diseases are difficult to exclude, nephritis-associated plasmin receptor staining should be considered.
期刊介绍:
This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.