Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemia
Systemic lupus erythematosus (SLE) is a multisystemic and chronic autoimmune disease with varying clinical manifestations. The role of various infectious agents in triggering the disease onset in genetically predisposed patients has been implicated in the pathogenesis of SLE. The severe acute respir...
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Format: | Article |
Language: | English |
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Wolters Kluwer Medknow Publications
2022-01-01
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Series: | Current Medicine Research and Practice |
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Online Access: | http://www.cmrpjournal.org/article.asp?issn=2352-0817;year=2022;volume=12;issue=5;spage=235;epage=237;aulast=Rauf |
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author | Abdul Rauf Shinto Francis Thekkudan Neena Mampilly Ajay Vijayan |
author_facet | Abdul Rauf Shinto Francis Thekkudan Neena Mampilly Ajay Vijayan |
author_sort | Abdul Rauf |
collection | DOAJ |
description | Systemic lupus erythematosus (SLE) is a multisystemic and chronic autoimmune disease with varying clinical manifestations. The role of various infectious agents in triggering the disease onset in genetically predisposed patients has been implicated in the pathogenesis of SLE. The severe acute respiratory syndrome coronavirus 2 has been reported to trigger various autoimmune diseases including SLE in few adults. Herein, we report the case of a previously well 12-year-old girl who presented with warm antibody Coombs-positive autoimmune haemolytic anaemia, 3 weeks after testing positive for COVID-19. COVID IgG antibody test was positive. During the hospital stay, she developed multisystem involvement in the form of neurological manifestations and arthritis. She was managed with steroids, intravenous (IV) immunoglobulins and supportive measures. Her anti-nuclear antibody and anti-dsDNA antibodies were positive and complement levels were low, confirming a diagnosis of SLE. Her clinical condition improved rapidly and remained neurologically normal, and serial haemoglobin showed an improving trend. IV steroids were changed to oral form, and hydroxychloroquine was also added. She remained well on 3-week follow-up. |
first_indexed | 2024-04-11T06:44:30Z |
format | Article |
id | doaj.art-452db8c97791438296efa4529ba1c6ac |
institution | Directory Open Access Journal |
issn | 2352-0817 2352-0825 |
language | English |
last_indexed | 2024-04-11T06:44:30Z |
publishDate | 2022-01-01 |
publisher | Wolters Kluwer Medknow Publications |
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series | Current Medicine Research and Practice |
spelling | doaj.art-452db8c97791438296efa4529ba1c6ac2022-12-22T04:39:23ZengWolters Kluwer Medknow PublicationsCurrent Medicine Research and Practice2352-08172352-08252022-01-0112523523710.4103/cmrp.cmrp_123_21Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemiaAbdul RaufShinto Francis ThekkudanNeena MampillyAjay VijayanSystemic lupus erythematosus (SLE) is a multisystemic and chronic autoimmune disease with varying clinical manifestations. The role of various infectious agents in triggering the disease onset in genetically predisposed patients has been implicated in the pathogenesis of SLE. The severe acute respiratory syndrome coronavirus 2 has been reported to trigger various autoimmune diseases including SLE in few adults. Herein, we report the case of a previously well 12-year-old girl who presented with warm antibody Coombs-positive autoimmune haemolytic anaemia, 3 weeks after testing positive for COVID-19. COVID IgG antibody test was positive. During the hospital stay, she developed multisystem involvement in the form of neurological manifestations and arthritis. She was managed with steroids, intravenous (IV) immunoglobulins and supportive measures. Her anti-nuclear antibody and anti-dsDNA antibodies were positive and complement levels were low, confirming a diagnosis of SLE. Her clinical condition improved rapidly and remained neurologically normal, and serial haemoglobin showed an improving trend. IV steroids were changed to oral form, and hydroxychloroquine was also added. She remained well on 3-week follow-up.http://www.cmrpjournal.org/article.asp?issn=2352-0817;year=2022;volume=12;issue=5;spage=235;epage=237;aulast=Raufautoimmune haemolytic anaemiachildrencovid-19severe acute respiratory syndrome coronavirus 2systemic lupus erythematosus |
spellingShingle | Abdul Rauf Shinto Francis Thekkudan Neena Mampilly Ajay Vijayan Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemia Current Medicine Research and Practice autoimmune haemolytic anaemia children covid-19 severe acute respiratory syndrome coronavirus 2 systemic lupus erythematosus |
title | Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemia |
title_full | Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemia |
title_fullStr | Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemia |
title_full_unstemmed | Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemia |
title_short | Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemia |
title_sort | childhood onset systemic lupus erythematosus probably triggered by severe acute respiratory syndrome coronavirus 2 infection presenting with autoimmune haemolytic anaemia |
topic | autoimmune haemolytic anaemia children covid-19 severe acute respiratory syndrome coronavirus 2 systemic lupus erythematosus |
url | http://www.cmrpjournal.org/article.asp?issn=2352-0817;year=2022;volume=12;issue=5;spage=235;epage=237;aulast=Rauf |
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