Poststreptococcal glomerulonephritis (PSGN) is the most common cause of nephritic syndrome in children. PSGN typically occurs 1-3 weeks after a group A beta hemolytic streptococcal (GAS) pharyngitis or 3-6 weeks after a GAS skin infection. It is thought to be a glomerular immune complex disease leading to complement activation and triggered by specific nephrogenic strains of GAS.
The clinical features of PSGN are varied, with a majority of children presenting with asymptomatic microscopic hematuria. Common clinical features in symptomatic children include peripheral edema, hypertension, gross hematuria with characteristic tea- or cola-colored urine, acute kidney injury, and proteinuria, which at times reaches nephrotic levels.
Children typically have a good prognosis with normalization of creatinine. Adults may have residual effects of hypertension, recurrent proteinuria, and persistence of abnormal renal function.
Acute poststreptococcal glomerulonephritis
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Synopsis
![Acute poststreptococcal glomerulonephritis : Dark urine, Fatigue, Edema, Hematuria, Oliguria, BP increased](/visualdx/sympticonswm/1801.png?r=1fdb69a28)
Codes
ICD10CM:
N00.9 – Acute nephritic syndrome with unspecified morphologic changes
SNOMEDCT:
68544003 – Acute post-streptococcal glomerulonephritis
N00.9 – Acute nephritic syndrome with unspecified morphologic changes
SNOMEDCT:
68544003 – Acute post-streptococcal glomerulonephritis
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Last Reviewed:01/06/2019
Last Updated:10/09/2022
Last Updated:10/09/2022