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Clinical practice: The bleeding child. Part I: primary hemostatic disorders

Mucocutaneous bleeding is common in childhood and may be the result of primary hemostatic disorders such as vascular abnormalities, von Willebrand disease, thrombocytopenia, and platelet dysfunction. A detailed bleeding history and physical examination are essential to distinguish between normal and...

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Detalles Bibliográficos
Autores principales: van Ommen, C. Heleen, Peters, Marjolein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249149/
https://www.ncbi.nlm.nih.gov/pubmed/21800040
http://dx.doi.org/10.1007/s00431-011-1532-4
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author van Ommen, C. Heleen
Peters, Marjolein
author_facet van Ommen, C. Heleen
Peters, Marjolein
author_sort van Ommen, C. Heleen
collection PubMed
description Mucocutaneous bleeding is common in childhood and may be the result of primary hemostatic disorders such as vascular abnormalities, von Willebrand disease, thrombocytopenia, and platelet dysfunction. A detailed bleeding history and physical examination are essential to distinguish between normal and abnormal bleeding and to decide whether it is necessary to perform further laboratory evaluation. Initial laboratory tests include complete blood count, peripheral blood smear, mean platelet volume, von Willebrand factor (VWF) antigen assay, VWF ristocetin cofactor activity, and factor VIII activity. Once thrombocytopenia and von Willebrand disease have been excluded, platelet function should be tested by platelet aggregation. Additional specific diagnostic tests, such as platelet secretion tests and flow cytometry for the detection of platelet surface glycoprotein expression, are needed to confirm the raised hypothesis.
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spelling pubmed-32491492012-01-11 Clinical practice: The bleeding child. Part I: primary hemostatic disorders van Ommen, C. Heleen Peters, Marjolein Eur J Pediatr Review Mucocutaneous bleeding is common in childhood and may be the result of primary hemostatic disorders such as vascular abnormalities, von Willebrand disease, thrombocytopenia, and platelet dysfunction. A detailed bleeding history and physical examination are essential to distinguish between normal and abnormal bleeding and to decide whether it is necessary to perform further laboratory evaluation. Initial laboratory tests include complete blood count, peripheral blood smear, mean platelet volume, von Willebrand factor (VWF) antigen assay, VWF ristocetin cofactor activity, and factor VIII activity. Once thrombocytopenia and von Willebrand disease have been excluded, platelet function should be tested by platelet aggregation. Additional specific diagnostic tests, such as platelet secretion tests and flow cytometry for the detection of platelet surface glycoprotein expression, are needed to confirm the raised hypothesis. Springer-Verlag 2011-07-29 2012 /pmc/articles/PMC3249149/ /pubmed/21800040 http://dx.doi.org/10.1007/s00431-011-1532-4 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Review
van Ommen, C. Heleen
Peters, Marjolein
Clinical practice: The bleeding child. Part I: primary hemostatic disorders
title Clinical practice: The bleeding child. Part I: primary hemostatic disorders
title_full Clinical practice: The bleeding child. Part I: primary hemostatic disorders
title_fullStr Clinical practice: The bleeding child. Part I: primary hemostatic disorders
title_full_unstemmed Clinical practice: The bleeding child. Part I: primary hemostatic disorders
title_short Clinical practice: The bleeding child. Part I: primary hemostatic disorders
title_sort clinical practice: the bleeding child. part i: primary hemostatic disorders
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249149/
https://www.ncbi.nlm.nih.gov/pubmed/21800040
http://dx.doi.org/10.1007/s00431-011-1532-4
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