Acute poststreptococcal glomerulonephritis APSGN is one of the most common causes of hematuria in childhood nbsp; The hematological changes are not typical in APSGN except anemia due to hemodilution and mild hemolysis The concurrent occurence of idiopathic nbsp;thrombocytopenic purpura ITP and APSGN has very rarely been reported In this article due to its rarity we report a 13 year old boy with APSGN who simultaneously developed ITP Turk Arch Ped 2011; 46: 171 3
📌 3 Key Takeaways
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Objective & Hypothesis:Acute poststreptococcal glomerulonephritis APSGN is one of the most common causes of hematuria in childhood nbsp; The hematological changes are not typical in APSGN except anemia due to hemodilution and mild hemolysis The concurrent occurence of idiopathic nbsp;thrombocytopenic purpura ITP and APSGN has very rarely been reported In this article due to its rarity we report a 13 year old boy with APSGN who simultaneously developed ITP Turk Arch Ped 2011; 46: 171 3
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Key Findings & Data:Acute poststreptococcal glomerulonephritis APSGN is one of the most common causes of hematuria in childhood nbsp; The hematological changes are not typical in APSGN except anemia due to hemodilution and mild hemolysis The concurrent occurence of idiopathic nbsp;thrombocytopenic purpura ITP and APSGN has very rarely been reported In this article due to its rarity we report a 13 year old boy with APSGN who simultaneously developed ITP Turk Arch Ped 2011; 46: 171 3
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Conclusion & Impact:Acute poststreptococcal glomerulonephritis APSGN is one of the most common causes of hematuria in childhood nbsp; The hematological changes are not typical in APSGN except anemia due to hemodilution and mild hemolysis The concurrent occurence of idiopathic nbsp;thrombocytopenic purpura ITP and APSGN has very rarely been reported In this article due to its rarity we report a 13 year old boy with APSGN who simultaneously developed ITP Turk Arch Ped 2011; 46: 171 3
Acute poststreptococcal glomerulonephritis APSGN is one of the most common causes of hematuria in childhood nbsp; The hematological changes are not typical in APSGN except anemia due to hemodilution and mild hemolysis The concurrent occurence of idiopathic nbsp;thrombocytopenic purpura ITP and APSGN has very rarely been reported In this article due to its rarity we report a 13 year old boy with APSGN who simultaneously developed ITP Turk Arch Ped 2011; 46: 171 3
Özet
Akut poststreptokoksik glomerülonefrit (APSGN) çocukluk ça¤›n›n en s›k hematüri nedenlerinden biridir. Akut poststreptokoksik glomerülonefritde hematolojik de¤ifliklikler hemodilüsyon ve hafif düzeyde hemoliz nedeniyle geliflebilen anemi d›fl›nda tipik de¤ildir. ‹diyopatik trombositopenik purpura (‹TP) ve APSGN birlikteli¤i ise nadiren bildirilmektedir. Bu makalede efl zamanl› APSGN ve ‹TP saptanan 13 yafl›nda bir hasta nadir görülmesi nedeniyle sunulmufltur.
Bal, A., Yurtseven, A., Şahbudak, Z., Anıl, M., Aksu, N. (2011). Idiopathic thrombocytopenic purpura in a child with acute poststreptococcal glomerulonephritis. Türk Pediatri Arşivi, Cilt: 46 Sayı: 2, 71–73. https://doi.org/10.4274/tpa.46.67
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