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Childhood Tuberculosis Presenting with Haemophagocytic Syndrome

Haemophagocytic syndrome is a life threatening complication of systemic infection resulting from an exaggerated immune response to a triggering agent. Prompt recognition and treatment of this disorder can abrogate otherwise high fatality associated with this disorder. A 2 year old girl presented wit...

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Detalles Bibliográficos
Autores principales: Verma, Tarun, Aggarwal, Sameer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422387/
https://www.ncbi.nlm.nih.gov/pubmed/23997456
http://dx.doi.org/10.1007/s12288-011-0114-y
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author Verma, Tarun
Aggarwal, Sameer
author_facet Verma, Tarun
Aggarwal, Sameer
author_sort Verma, Tarun
collection PubMed
description Haemophagocytic syndrome is a life threatening complication of systemic infection resulting from an exaggerated immune response to a triggering agent. Prompt recognition and treatment of this disorder can abrogate otherwise high fatality associated with this disorder. A 2 year old girl presented with acute enteritis, developed prolonged fever and organomegaly complicated by multi-organ failure. She fulfilled the diagnostic criteria for haemophagocytic lymphohistiocytosis including bone marrow evidence of haemophagocytosis. In addition she had serological evidence of tubercular infection as well as a positive family history of tuberculosis. She responded rapidly to immunosuppressive therapy and anti-tubercular therapy. Our case illustrates the association of haemophagocytic syndrome with tuberculosis as well as the favourable response obtained with prompt diagnosis and treatment.
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spelling pubmed-34223872013-09-01 Childhood Tuberculosis Presenting with Haemophagocytic Syndrome Verma, Tarun Aggarwal, Sameer Indian J Hematol Blood Transfus Case Report Haemophagocytic syndrome is a life threatening complication of systemic infection resulting from an exaggerated immune response to a triggering agent. Prompt recognition and treatment of this disorder can abrogate otherwise high fatality associated with this disorder. A 2 year old girl presented with acute enteritis, developed prolonged fever and organomegaly complicated by multi-organ failure. She fulfilled the diagnostic criteria for haemophagocytic lymphohistiocytosis including bone marrow evidence of haemophagocytosis. In addition she had serological evidence of tubercular infection as well as a positive family history of tuberculosis. She responded rapidly to immunosuppressive therapy and anti-tubercular therapy. Our case illustrates the association of haemophagocytic syndrome with tuberculosis as well as the favourable response obtained with prompt diagnosis and treatment. Springer-Verlag 2011-10-08 2012-09 /pmc/articles/PMC3422387/ /pubmed/23997456 http://dx.doi.org/10.1007/s12288-011-0114-y Text en © Indian Society of Haematology & Transfusion Medicine 2011
spellingShingle Case Report
Verma, Tarun
Aggarwal, Sameer
Childhood Tuberculosis Presenting with Haemophagocytic Syndrome
title Childhood Tuberculosis Presenting with Haemophagocytic Syndrome
title_full Childhood Tuberculosis Presenting with Haemophagocytic Syndrome
title_fullStr Childhood Tuberculosis Presenting with Haemophagocytic Syndrome
title_full_unstemmed Childhood Tuberculosis Presenting with Haemophagocytic Syndrome
title_short Childhood Tuberculosis Presenting with Haemophagocytic Syndrome
title_sort childhood tuberculosis presenting with haemophagocytic syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422387/
https://www.ncbi.nlm.nih.gov/pubmed/23997456
http://dx.doi.org/10.1007/s12288-011-0114-y
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