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DC Field | Value | Language |
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dc.contributor.author | Mettananda, C. | - |
dc.contributor.author | Williams, S. | - |
dc.date.accessioned | 2023-12-28T04:11:45Z | - |
dc.date.available | 2023-12-28T04:11:45Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | Case Reports in Infectious Diseases.2023;2023:3298520. | en_US |
dc.identifier.issn | 2090-6633 (Electronic) | - |
dc.identifier.uri | http://repository.kln.ac.lk/handle/123456789/27159 | - |
dc.description | Not Indexed in MEDLINE | en_US |
dc.description.abstract | Immune thrombocytopenic purpura (ITP) secondary to asymptomatic COVID-19 infection, especially in children, is not reported. Furthermore, persistent, treatment-resistant ITP secondary to COVID-19 is not reported. We report a previously healthy 14-year-old Asian boy who developed secondary ITP following an asymptomatic COVID-19 infection and is having a relapsing and remitting cause with poor response to immunosuppressants even after 21 months following the diagnosis. This case emphasizes the importance of testing for COVID-19 in newly diagnosed ITP patients and the need for follow-up platelet counts in patients who recover from COVID-19 as it may follow into developing secondary ITP yet being asymptomatic until you present with a bleeding complication of ITP. The poor response to standard immunosuppression warrants more understanding of the pathophysiology of persistently low platelets following COVID-19 infection. Long-term sequelae of the disease highlight the importance of getting vaccinated for COVID-19 despite COVID-19 being no longer a global emergency. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Hindawi | en_US |
dc.subject | immune | en_US |
dc.title | Persistent, poorly responsive immune thrombocytopenia secondary to asymptomatic COVID-19 infection in a child | en_US |
dc.type | Article | en_US |
Appears in Collections: | Journal/Magazine Articles |
Files in This Item:
File | Description | Size | Format | |
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CRIID2023-3298520.pdf | 942.54 kB | Adobe PDF | View/Open |
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