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Thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report
BACKGROUND: Antiphospholipid syndrome (APS) is a non-inflammatory autoimmune disorder induced by antiphospholipid antibodies, which occurs exceedingly rarely in pediatric population and even more rarely reported in HIV positive children. CASE SUMMARY: A case of 11 years old boy had a sudden onset of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992315/ https://www.ncbi.nlm.nih.gov/pubmed/33766024 http://dx.doi.org/10.1186/s12959-021-00273-y |
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author | Dong, Rong-Jing Lei, Su-Yun Li, Jun Yang, Xin-Ping Li, Yu-Ye Zhang, Yun-Gui |
author_facet | Dong, Rong-Jing Lei, Su-Yun Li, Jun Yang, Xin-Ping Li, Yu-Ye Zhang, Yun-Gui |
author_sort | Dong, Rong-Jing |
collection | PubMed |
description | BACKGROUND: Antiphospholipid syndrome (APS) is a non-inflammatory autoimmune disorder induced by antiphospholipid antibodies, which occurs exceedingly rarely in pediatric population and even more rarely reported in HIV positive children. CASE SUMMARY: A case of 11 years old boy had a sudden onset of swelling in his left lower leg along with pain which were worsening gradually. Initially, topical ointment was applied for 1 month which were ineffective in reducing pain and swelling. Instead, the symptoms were aggravated and suddenly spread to the proximal thigh, accompanied by dyskinesia of left lower leg. Both color doppler ultrasonography and vascular CT scan of left lower leg revealed deep venous thrombosis. His serum anti-phospholipid antibodies (aPLs) were tested positive. He was a known case of HIV virological failure with substantial HIV viral load (VL) despite receiving regular antiretroviral therapy (ART). His symptoms improved after giving aggressive antithrombotic and high dose corticosteroid treatments. CONCLUSION: When pediatric patients develop thrombotic disease, APS also needs to be ruled out. The autoantibodies levels should be routinely tested to look for recurrent thrombosis in children with HIV/AIDS. |
format | Online Article Text |
id | pubmed-7992315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79923152021-03-25 Thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report Dong, Rong-Jing Lei, Su-Yun Li, Jun Yang, Xin-Ping Li, Yu-Ye Zhang, Yun-Gui Thromb J Case Report BACKGROUND: Antiphospholipid syndrome (APS) is a non-inflammatory autoimmune disorder induced by antiphospholipid antibodies, which occurs exceedingly rarely in pediatric population and even more rarely reported in HIV positive children. CASE SUMMARY: A case of 11 years old boy had a sudden onset of swelling in his left lower leg along with pain which were worsening gradually. Initially, topical ointment was applied for 1 month which were ineffective in reducing pain and swelling. Instead, the symptoms were aggravated and suddenly spread to the proximal thigh, accompanied by dyskinesia of left lower leg. Both color doppler ultrasonography and vascular CT scan of left lower leg revealed deep venous thrombosis. His serum anti-phospholipid antibodies (aPLs) were tested positive. He was a known case of HIV virological failure with substantial HIV viral load (VL) despite receiving regular antiretroviral therapy (ART). His symptoms improved after giving aggressive antithrombotic and high dose corticosteroid treatments. CONCLUSION: When pediatric patients develop thrombotic disease, APS also needs to be ruled out. The autoantibodies levels should be routinely tested to look for recurrent thrombosis in children with HIV/AIDS. BioMed Central 2021-03-25 /pmc/articles/PMC7992315/ /pubmed/33766024 http://dx.doi.org/10.1186/s12959-021-00273-y Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Dong, Rong-Jing Lei, Su-Yun Li, Jun Yang, Xin-Ping Li, Yu-Ye Zhang, Yun-Gui Thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report |
title | Thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report |
title_full | Thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report |
title_fullStr | Thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report |
title_full_unstemmed | Thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report |
title_short | Thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report |
title_sort | thrombotic antiphospholipid syndrome in a child with human immunodeficiency virus: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992315/ https://www.ncbi.nlm.nih.gov/pubmed/33766024 http://dx.doi.org/10.1186/s12959-021-00273-y |
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