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Thrombotic microangiopathy.
Mörtzell, M; Berlin, G; Nilsson, T; Axelsson, C G; Efvergren, M; Audzijoni, J; Griskevicius, A; Ptak, J; Blaha, M; Tomsova, H; Liumbruno, G M; Centoni, P; Newman, E; Eloot, S; Dhondt, A; Tomaz, J; Witt, V; Rock, G; Stegmayr, B.
Affiliation
  • Mörtzell M; Department of Public Health and Medicine, Umeå University, Umea, Sweden. monika.mortzell@vll.se
Transfus Apher Sci ; 45(2): 119-23, 2011 Oct.
Article in En | MEDLINE | ID: mdl-21885345
ABSTRACT
Thrombotic microangiopathy (TMA) is a histopathological feature of various diseases including thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS). There are many secondary causes of TMA, many of them could mimic TTP or HUS. This article presents a short overview on TMA. In conclusion TMA is the result of various etiology reasons and pathologic reactions with various clinical entities. It is important to focus on a thorough history including family history when deciding on a diagnosis. Analysis of ADAMTS 13 and ADAMTS 13-antibodies may help to decide continued therapy.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombotic Microangiopathies Limits: Female / Humans / Male Language: En Journal: Transfus Apher Sci Journal subject: HEMATOLOGIA Year: 2011 Document type: Article Affiliation country: Sweden

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombotic Microangiopathies Limits: Female / Humans / Male Language: En Journal: Transfus Apher Sci Journal subject: HEMATOLOGIA Year: 2011 Document type: Article Affiliation country: Sweden