[Haemolytic uremic syndrome and thrombotic thrombocytopenic purpura: classification based on molecular etiology and

Zoltán Prohászka1

  • 1Semmelweis Egyetem, Altalános Orvostudományi Kar III. Belgyógyászati Klinika, Kutatólaboratórium Budapest. prohoz@kut.sote.hu

Orvosi Hetilap
|June 27, 2008
PubMed

Haemolytic uremic syndrome and thrombotic thrombocytopenic purpura are overlapping clinical entities based on historical classification. Recent developments in the unfolding of the pathomechanisms of these diseases resulted in the creation of a molecular etiology-based classification. Understanding of some causative relationships yielded detailed diagnostic approaches, novel therapeutic options and thorough prognostic assortment of the patients. Although haemolytic uremic syndrome and thrombotic thrombocytopenic purpura are rare diseases with poor prognosis, the precise molecular etiology-based diagnosis might properly direct the therapy of the affected patients. The current review focuses on the theoretical background and detailed description of the available diagnostic possibilities, and some practical information necessary for the interpretation of their results.

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