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Published in: Clinical Reviews in Allergy & Immunology 2-3/2009

01-06-2009

Microthrombotic/Microangiopathic Manifestations of the Antiphospholipid Syndrome

Authors: Sonja Praprotnik, Dušan Ferluga, Alenka Vizjak, Anastazija Hvala, Tadej Avčin, Blaž Rozman

Published in: Clinical Reviews in Allergy & Immunology | Issue 2-3/2009

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Abstract

The paper presents an overview of clinical manifestations and histopathologic findings in different organs in microvascular thrombotic and microangiopathic antiphospholipid syndrome (MAPS). Subsets of antiphospholipid syndrome (APS) are presented and defined. Clinico-pathologic correlations seem insufficient so far, because of a lack of detailed systematic studies of the histopathology in different organs. Based on their own autopsy and biopsy studies, the authors propose a novel categorization of histopathologic lesions that occur in patients with classic and catastrophic APS. In addition to the already accepted category of a microvascular thrombotic type of lesions, microangiopathic lesions consistent with thrombotic microangiopathy are proposed to be included in new revised classification criteria for definite APS. Microvascular thrombotic and so far underestimated microangiopathic histopathologic lesions have been shown to appear in various combinations and of different ages in patients with both classic and catastrophic APS, which fits into the concept of MAPS. These preliminary findings of our studies are also in line with the most recent hypothesis of two main mechanisms in the pathogenesis of APS, emphasizing a key role of endothelial cell affection induced by aPL on the one hand and interference with coagulation cascade on the other side.
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Metadata
Title
Microthrombotic/Microangiopathic Manifestations of the Antiphospholipid Syndrome
Authors
Sonja Praprotnik
Dušan Ferluga
Alenka Vizjak
Anastazija Hvala
Tadej Avčin
Blaž Rozman
Publication date
01-06-2009
Publisher
Humana Press Inc
Published in
Clinical Reviews in Allergy & Immunology / Issue 2-3/2009
Print ISSN: 1080-0549
Electronic ISSN: 1559-0267
DOI
https://doi.org/10.1007/s12016-008-8104-z

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