Acute Post-Streptococcal Glomerulonephritis in a Known Nephrotic Syndrome Patient: A Case Report. | ||||
| GEGET | ||||
| Volume 17, Issue 2, December 2022, Page 60-66 PDF (247.21 K) | ||||
| Document Type: Case Report | ||||
| DOI: 10.21608/geget.2022.287768 | ||||
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| Authors | ||||
Nancy Abdel-Salam   ; Moustafa Mahmoud Marei; Youmna El-Beltagi
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| Department of of Pediatrics, Faculty of Medicine, Alexandria University, Egypt. | ||||
| Abstract | ||||
| Nephrotic syndrome (NS) is one of the most common childhood kidney diseases. Idiopathic NS (INS) can affect children of any age from infancy to adolescence and predominantly occurs in those aged 1–6 years. Acute glomerulonephritis (AGN) is a disease characterized by edema, oliguria, hematuria, and hypertension. It characterized by inflammation of the glomerulus with proliferation of cellular elements secondary to an immunologic mechanism. Acute post-streptococcal glomerulonephritis (APSGN) results from an antecedent infection of the skin (impetigo) or throat (pharyngitis) caused by nephritogenic strains of group A beta-hemolytic streptococci. Here we present a case of APSGN in a patient with known steroid dependent INS. | ||||
| Keywords | ||||
| Minimal change disease; Nephrotic syndrome; Post Streptococcal Glomerulonephritis | ||||
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