Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/25698
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dc.contributor.authorWanninayake, L.-
dc.contributor.authorde Abrew, G.-
dc.contributor.authorLogeshwaran, D.-
dc.contributor.authorWeerasinghe, C.-
dc.contributor.authorGowinna, P.-
dc.contributor.authorMettananda, S.-
dc.contributor.authorPremaratna, R.-
dc.date.accessioned2022-12-20T05:13:30Z-
dc.date.available2022-12-20T05:13:30Z-
dc.date.issued2022-
dc.identifier.citationBMC Infectious Diseases.2022;22(1):946.en_US
dc.identifier.issn1471-2334-
dc.identifier.urihttp://repository.kln.ac.lk/handle/123456789/25698-
dc.descriptionindexed in MEDLINE.en_US
dc.description.abstractBackground: Post-COVID-19 multisystem inflammatory syndrome (MIS) has been increasingly recognized but fever with isolated tender cervical lymphadenitis as the initial presentation has been rarely reported. We present 2 female patients one a child and the other an adolescent. Case presentation: Case 1 was a 13-year-old girl who presented with tender cervical lymphadenopathy and fever 3-weeks post-COVID-19, and then developed features of MIS 5 days later. Case 2, also female, was 18 years old. She had no history of COVID-19 infection or immunization but had a serologic diagnosis of COVID-19. She similarly presented with fever and tender cervical lymphadenopathy, and then progressed rapidly to develop features of MIS. Both patients responded well to treatment with immunosuppressants and intravenous immunoglobulin. Conclusion: Tender cervical lymphadenopathy could be the herald of multi-system inflammatory syndrome following COVID-19 infection among children and adolescents, which the clinicians must have a good suspicion about.en_US
dc.language.isoenen_US
dc.publisherBioMed Central, Londonen_US
dc.subjectCOVID 19en_US
dc.subjectCase reporten_US
dc.subjectCervical lymphadenitisen_US
dc.subjectMultisystem inflammatory syndrome.en_US
dc.titleTender cervical lymphadenitis as a herald of multi-system inflammatory syndrome in COVID-19 infection of children and adolescents: a report of two casesen_US
dc.typeArticleen_US
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