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pubmed-article:8408822pubmed:dateCreated1993-11-19lld:pubmed
pubmed-article:8408822pubmed:abstractTextThrombotic thrombocytopenic purpura is a rare disease most commonly associated with microangiopathic hemolytic anemia, thrombocytopenia, fever, neurologic disorders, and renal dysfunction. We describe a patient with a history of thrombotic thrombocytopenic purpura that had been quiescent for 4 months; he had a 3-week history of painful purpuric lesions on the left hand only. He also had mottling and a livedoid purpura of the distal fingertips, splinter hemorrhages of the left fingernails, and a decreased radial pulse. Findings of a biopsy specimen revealed multiple capillary and small vessel thromboses. Contrast aortography demonstrated a pseudoaneurysm of the proximal descending thoracic aorta with stenosis of the left subclavian artery at its origin and an associated thrombus.lld:pubmed
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pubmed-article:8408822pubmed:authorpubmed-author:CallenJ PJPlld:pubmed
pubmed-article:8408822pubmed:authorpubmed-author:ThomasH AHAlld:pubmed
pubmed-article:8408822pubmed:authorpubmed-author:CohenL MLMlld:pubmed
pubmed-article:8408822pubmed:authorpubmed-author:BurrussJ BJBlld:pubmed
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pubmed-article:8408822pubmed:volume29lld:pubmed
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pubmed-article:8408822pubmed:pagination838-40lld:pubmed
pubmed-article:8408822pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:8408822pubmed:year1993lld:pubmed
pubmed-article:8408822pubmed:articleTitleUnilateral emboli in a patient with thrombotic thrombocytopenic purpura.lld:pubmed
pubmed-article:8408822pubmed:affiliationDepartment of Medicine, University of Louisville School of Medicine, KY.lld:pubmed
pubmed-article:8408822pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8408822pubmed:publicationTypeCase Reportslld:pubmed