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A child diagnosed with severe hemophilia A presenting with nephrotic syndrome: a case report
BACKGROUND: Nephrotic syndrome occurring as a complication of immune tolerance therapy for inhibitors in hemophilia B is well recognized. It is also known to occur in association with factor borne infections, especially hepatitis C. This is the first case report of nephrotic syndrome occurring in a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199537/ https://www.ncbi.nlm.nih.gov/pubmed/37208723 http://dx.doi.org/10.1186/s13256-023-03941-x |
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author | Chandrakumara, Janith Wijesundara, Madushika Amarakoon, Givani |
author_facet | Chandrakumara, Janith Wijesundara, Madushika Amarakoon, Givani |
author_sort | Chandrakumara, Janith |
collection | PubMed |
description | BACKGROUND: Nephrotic syndrome occurring as a complication of immune tolerance therapy for inhibitors in hemophilia B is well recognized. It is also known to occur in association with factor borne infections, especially hepatitis C. This is the first case report of nephrotic syndrome occurring in a child receiving prophylactic factor VIII in the absence of inhibitors of hepatitis infection. However, the pathophysiology of this phenomenon is poorly understood. CASE PRESENTATION: A 7-year Sri Lankan boy diagnosed with severe hemophilia A on weekly factor VIII prophylaxis was diagnosed with three episodes of nephrotic syndrome, a condition in which there is leakage of plasma protein into urine. He had three episodes of nephrotic syndrome, all of which responded well to 60 mg/m(2) daily dose of oral steroids, achieving remission within 2 weeks of starting daily prednisolone. He has not developed inhibitors for factor VIII. His hepatitis screening remained negative. CONCLUSIONS: There is a possible link between factor therapy for hemophilia A and nephrotic syndrome, which can be a T-cell-mediated immune response. This case also highlights the importance of monitoring for renal involvement in patients treated with factor replacement. |
format | Online Article Text |
id | pubmed-10199537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101995372023-05-21 A child diagnosed with severe hemophilia A presenting with nephrotic syndrome: a case report Chandrakumara, Janith Wijesundara, Madushika Amarakoon, Givani J Med Case Rep Case Report BACKGROUND: Nephrotic syndrome occurring as a complication of immune tolerance therapy for inhibitors in hemophilia B is well recognized. It is also known to occur in association with factor borne infections, especially hepatitis C. This is the first case report of nephrotic syndrome occurring in a child receiving prophylactic factor VIII in the absence of inhibitors of hepatitis infection. However, the pathophysiology of this phenomenon is poorly understood. CASE PRESENTATION: A 7-year Sri Lankan boy diagnosed with severe hemophilia A on weekly factor VIII prophylaxis was diagnosed with three episodes of nephrotic syndrome, a condition in which there is leakage of plasma protein into urine. He had three episodes of nephrotic syndrome, all of which responded well to 60 mg/m(2) daily dose of oral steroids, achieving remission within 2 weeks of starting daily prednisolone. He has not developed inhibitors for factor VIII. His hepatitis screening remained negative. CONCLUSIONS: There is a possible link between factor therapy for hemophilia A and nephrotic syndrome, which can be a T-cell-mediated immune response. This case also highlights the importance of monitoring for renal involvement in patients treated with factor replacement. BioMed Central 2023-05-20 /pmc/articles/PMC10199537/ /pubmed/37208723 http://dx.doi.org/10.1186/s13256-023-03941-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Chandrakumara, Janith Wijesundara, Madushika Amarakoon, Givani A child diagnosed with severe hemophilia A presenting with nephrotic syndrome: a case report |
title | A child diagnosed with severe hemophilia A presenting with nephrotic syndrome: a case report |
title_full | A child diagnosed with severe hemophilia A presenting with nephrotic syndrome: a case report |
title_fullStr | A child diagnosed with severe hemophilia A presenting with nephrotic syndrome: a case report |
title_full_unstemmed | A child diagnosed with severe hemophilia A presenting with nephrotic syndrome: a case report |
title_short | A child diagnosed with severe hemophilia A presenting with nephrotic syndrome: a case report |
title_sort | child diagnosed with severe hemophilia a presenting with nephrotic syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199537/ https://www.ncbi.nlm.nih.gov/pubmed/37208723 http://dx.doi.org/10.1186/s13256-023-03941-x |
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