| Literature DB >> 18344698 |
Ilhami Kiki1, Mehmet Gundogdu, Bulent Albayrak, Yilmaz Bilgiç.
Abstract
Thrombotic thrombocytopenic purpura (TTP) is characterized by disseminated thrombotic occlusions located in the microcirculation and a syndrome of microangiopathic hemolytic anemia (MAHA), thrombocytopenia, fever, and renal and neurologic abnormalities. Although several factors such as viral and bacterial pathogens, pancreatitis, drugs, collagen-vascular diseases, cancers, and pregnancy have been reported to be associated with TTP, brucellosis is an exceptional cause of this disorder. We represent a 19-year-old woman applying to our outpatient department with the complaints of headache, fever, sweat, malaise, and jaundice. Clinical signs and laboratory findings were consistent with TTP. Brucella agglutination was found to be 1/320 positive. After the administration of therapeutic plasma exchange, all symptoms and laboratory abnormalities improved dramatically. Antibiotic therapy directed to Brucella infection was initiated and no recurrence of TTP was seen.Entities:
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Year: 2008 PMID: 18344698 DOI: 10.1097/MAJ.0b013e3180d09f19
Source DB: PubMed Journal: Am J Med Sci ISSN: 0002-9629 Impact factor: 2.378