Thrombotic thrombocytopenic purpura and neurologic manifestations – Case report and integrative review
نویسندگان
چکیده
منابع مشابه
Thrombotic thrombocytopenic purpura, a case report.
We report a case of thrombotic thrombocytopenic purpura (TTP) in a 60 years-old woman with Sjogren's syndrome. Symptomatology on admission leads to evoke the diagnosis of TTP. Biological results allow to set the diagnosis. Actually, association of haemolytic anaemia, schizocytes and thrombocytopenia are in favour of TTP. Undetectable ADAMTS 13 activity (below 5%) confirms the diagnosis. In cong...
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Thrombotic Thrombocytopenic purpura (TTP) is a rare thrombotic microangiopathic disease, associated with thrombocytopenia and hemolytic anemia. It is caused by an enzymatic dysfunction responsible in cleavage of blood clotting factors. In this study we have tried to review the available approaches in diagnoses of the disease as well as treatment strategies. Based on the what the current review ...
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NEUROPSYCHIATRIC SYMPTOMS and signs are a prominent part of systemic lupus erythematosus (SLE) and thrombotic thrombocytopenic purpura (TTP). These disorders are similar also in that they frequently share such clinical manifestations as hemolytic anemia, thrombocytopenia, renal disease, and fever. Adding to the complexity of diagnosis is the fact that patients may occasionally have clinical and...
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Background: Posterior reversible leukoencephalopathy syndrome (PRLS) is a clinical and radiological syndrome of heterogeneous etiologies that are grouped because of the similar findings on neuroimaging studies which may occur at any age. The pathogenesis of RPLS remains unclear, but it appears to be related to disordered cerebral autoregulation and endothelial dysfunction. The syndrome is more ...
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BACKGROUND Thrombotic thrombocytopenic purpura is a very rare hereditary blood deficiency disorder of ADAMTS13 (von Willebrand factor-cleaving protease) and a life-threatening thrombotic microangiopathy characterized by thrombocytopenia and microangiopathic hemolytic anemia. The deficiency in ADAMTS13 metalloprotease, which cleaves the von Willebrand factor, may be congenital or acquired. The c...
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ژورنال
عنوان ژورنال: International Archives of Medicine
سال: 2016
ISSN: 1755-7682
DOI: 10.3823/2116