Abstract
OBJECTIVE: To investigate the outcomes of childhood diffuse endocapillary proliferation Henoch-Schönlein purpura nephritis (DEP-HSPN) in response to early diagnosis and prompt treatment. METHODS: Eleven cases of DEP-HSPN in children were investigated in comparison to HSPN without diffuse endocapillary proliferation (non-DEP-HSPN). RESULTS: DEP-HSPN had a higher prevalence of nephrotic syndrome but a lower prevalence of hematuria compared to non-DEP-HSPN. IgA, IgG and IgM antibody deposition was found in DEP-HSPN by histopatho- logical examination. Proteinuria cleared in all 11 cases through treatment with steroids and/or immuno- suppressive drugs. However, half of the DEP-HSPN patients continuously had hematuria after treatment. CONCLUSION: The early diagnosis and prompt initiation of immunosuppressive treatment based on renal biopsy are important for achieving favorable outcomes.
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Fu, H., Mao, J., Xu, Y., Gu, W., Zhu, X., & Liu, A. (2016). Clinical features and outcomes of diffuse endocapillary proliferation henoch-schönlein purpura nephritis in children. Clinics, 71(9), 550–554. https://doi.org/10.6061/clinics/2016(09)11
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