Unilateral emboli in a patient with thrombotic thrombocytopenic purpura

Thrombotic 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 month...

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Published inJournal of the American Academy of Dermatology Vol. 29; no. 5; pp. 838 - 840
Main Authors Burruss, Jyoti B., Cohen, Lisa M., Thomas, Hollis A., Callen, Jeffrey P.
Format Journal Article
LanguageEnglish
Published New York, NY Mosby, Inc 01.11.1993
Elsevier
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Summary:Thrombotic 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.
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ISSN:0190-9622
1097-6787
DOI:10.1016/0190-9622(93)70250-W