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How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome

Thrombotic thrombocytopenic purpura (TTP) and atypical haemolytic uraemic syndrome (aHUS) are acute, rare life‐threatening thrombotic microangiopathies that require rapid diagnosis and treatment. They are defined by microangiopathic haemolytic anaemia and thrombocytopenia, with renal involvement pri...

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Detalles Bibliográficos
Autores principales: Scully, Marie, Goodship, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley-Blackwell 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163720/
https://www.ncbi.nlm.nih.gov/pubmed/24387053
http://dx.doi.org/10.1111/bjh.12718
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author Scully, Marie
Goodship, Tim
author_facet Scully, Marie
Goodship, Tim
author_sort Scully, Marie
collection PubMed
description Thrombotic thrombocytopenic purpura (TTP) and atypical haemolytic uraemic syndrome (aHUS) are acute, rare life‐threatening thrombotic microangiopathies that require rapid diagnosis and treatment. They are defined by microangiopathic haemolytic anaemia and thrombocytopenia, with renal involvement primarily in aHUS and neurological and cardiological sequelae in TTP. Prompt treatment for most cases of both conditions is with plasma exchange initially and monoclonal therapy (rituximab in TTP and eculizumab in aHUS) as the mainstay of therapy. Here we discuss the diagnosis and therapy for both disorders.
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spelling pubmed-41637202014-09-22 How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome Scully, Marie Goodship, Tim Br J Haematol Reviews Thrombotic thrombocytopenic purpura (TTP) and atypical haemolytic uraemic syndrome (aHUS) are acute, rare life‐threatening thrombotic microangiopathies that require rapid diagnosis and treatment. They are defined by microangiopathic haemolytic anaemia and thrombocytopenia, with renal involvement primarily in aHUS and neurological and cardiological sequelae in TTP. Prompt treatment for most cases of both conditions is with plasma exchange initially and monoclonal therapy (rituximab in TTP and eculizumab in aHUS) as the mainstay of therapy. Here we discuss the diagnosis and therapy for both disorders. Wiley-Blackwell 2014-01-06 2014-03 /pmc/articles/PMC4163720/ /pubmed/24387053 http://dx.doi.org/10.1111/bjh.12718 Text en © 2014 The Authors. British Journal of Haematology Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Reviews
Scully, Marie
Goodship, Tim
How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome
title How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome
title_full How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome
title_fullStr How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome
title_full_unstemmed How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome
title_short How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome
title_sort how i treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163720/
https://www.ncbi.nlm.nih.gov/pubmed/24387053
http://dx.doi.org/10.1111/bjh.12718
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