Cargando…

Dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report

BACKGROUND: Dengue is a common mosquito-borne infection in tropical countries. Dengue incidence in Sri Lanka is generally showing a rising trend. Both chronic immune thrombocytopenia purpura (ITP) children and chronic ITP triggered by dengue fever in the pediatric age group are rarely reported. This...

Descripción completa

Detalles Bibliográficos
Autores principales: Thadchanamoorthy, V., Dayasiri, Kavinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370471/
https://www.ncbi.nlm.nih.gov/pubmed/32699523
http://dx.doi.org/10.1186/s41182-020-00248-1
_version_ 1783560983670685696
author Thadchanamoorthy, V.
Dayasiri, Kavinda
author_facet Thadchanamoorthy, V.
Dayasiri, Kavinda
author_sort Thadchanamoorthy, V.
collection PubMed
description BACKGROUND: Dengue is a common mosquito-borne infection in tropical countries. Dengue incidence in Sri Lanka is generally showing a rising trend. Both chronic immune thrombocytopenia purpura (ITP) children and chronic ITP triggered by dengue fever in the pediatric age group are rarely reported. This unusual presentation is a diagnostic challenge to clinicians. The authors have reported a pediatric patient who presented with chronic ITP following recovery from dengue hemorrhagic fever. CASE PRESENTATION: A 14-year-old previously healthy boy was initially managed as for dengue hemorrhagic fever. Following initial detection of persistent thrombocytopenia at 2 weeks post-discharge, his parents defaulted follow-up for 1 year as he remained asymptomatic. However, 1 year after initial admission, the child re-presented with ecchymotic patches and a platelet count of 30 × 10(3)/cumm. Review of serial blood counts performed during previous hospital admission and by his parents themselves revealed persistent thrombocytopenia over preceding 12 months. Subsequently, the child had an in-depth evaluation. The diagnosis of ITP was confirmed by ruling out differential diagnosis and he was managed as for chronic ITP. His platelet counts showed good response to oral corticosteroids and he is currently being followed up at the pediatric hematology clinic. CONCLUSION: While reporting, a 14-year-old boy who developed chronic ITP following dengue hemorrhagic fever, this report highlights importance of frequent monitoring of blood counts to accurately detect and manage critical phase of dengue fever. The report also highlights the value of monitoring platelet counts in post-recovery phase to ensure they have normalized.
format Online
Article
Text
id pubmed-7370471
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-73704712020-07-21 Dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report Thadchanamoorthy, V. Dayasiri, Kavinda Trop Med Health Case Report BACKGROUND: Dengue is a common mosquito-borne infection in tropical countries. Dengue incidence in Sri Lanka is generally showing a rising trend. Both chronic immune thrombocytopenia purpura (ITP) children and chronic ITP triggered by dengue fever in the pediatric age group are rarely reported. This unusual presentation is a diagnostic challenge to clinicians. The authors have reported a pediatric patient who presented with chronic ITP following recovery from dengue hemorrhagic fever. CASE PRESENTATION: A 14-year-old previously healthy boy was initially managed as for dengue hemorrhagic fever. Following initial detection of persistent thrombocytopenia at 2 weeks post-discharge, his parents defaulted follow-up for 1 year as he remained asymptomatic. However, 1 year after initial admission, the child re-presented with ecchymotic patches and a platelet count of 30 × 10(3)/cumm. Review of serial blood counts performed during previous hospital admission and by his parents themselves revealed persistent thrombocytopenia over preceding 12 months. Subsequently, the child had an in-depth evaluation. The diagnosis of ITP was confirmed by ruling out differential diagnosis and he was managed as for chronic ITP. His platelet counts showed good response to oral corticosteroids and he is currently being followed up at the pediatric hematology clinic. CONCLUSION: While reporting, a 14-year-old boy who developed chronic ITP following dengue hemorrhagic fever, this report highlights importance of frequent monitoring of blood counts to accurately detect and manage critical phase of dengue fever. The report also highlights the value of monitoring platelet counts in post-recovery phase to ensure they have normalized. BioMed Central 2020-07-20 /pmc/articles/PMC7370471/ /pubmed/32699523 http://dx.doi.org/10.1186/s41182-020-00248-1 Text en © The Author(s) 2020 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/.
spellingShingle Case Report
Thadchanamoorthy, V.
Dayasiri, Kavinda
Dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report
title Dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report
title_full Dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report
title_fullStr Dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report
title_full_unstemmed Dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report
title_short Dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report
title_sort dengue hemorrhagic fever as a rare cause of chronic immune thrombocytopenic purpura—a pediatric case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370471/
https://www.ncbi.nlm.nih.gov/pubmed/32699523
http://dx.doi.org/10.1186/s41182-020-00248-1
work_keys_str_mv AT thadchanamoorthyv denguehemorrhagicfeverasararecauseofchronicimmunethrombocytopenicpurpuraapediatriccasereport
AT dayasirikavinda denguehemorrhagicfeverasararecauseofchronicimmunethrombocytopenicpurpuraapediatriccasereport