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Invasive Aspergillosis Masquerading as Catastrophic Antiphospholipid Syndrome
Author(s) -
Kathryn S. Robinett,
Bethany Weiler,
Avelino C. Verceles
Publication year - 2013
Publication title -
american journal of critical care
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.592
H-Index - 81
eISSN - 1937-710X
pISSN - 1062-3264
DOI - 10.4037/ajcc2013659
Subject(s) - medicine , catastrophic antiphospholipid syndrome , aspergillosis , antiphospholipid syndrome , differential diagnosis , autopsy , lupus anticoagulant , catastrophic illness , dermatology , surgery , thrombosis , pathology , immunology
A 25-year-old woman with a history of systemic lupus erythematosus who was taking steroids came to the hospital because of vague signs and symptoms of weight loss, constipation, and oral ulcers. Multiorgan dysfunction developed, and catastrophic antiphospholipid syndrome was suspected. She was treated with an intravenous infusion of heparin, but she experienced a subdural hemorrhage and died on day 10 of the hospitalization. An autopsy revealed disseminated invasive aspergillosis. This case illustrates that invasive aspergillosis is a frequently missed diagnosis and should be part of the differential diagnosis for any patient who is immunosuppressed, including patients with autoimmune diseases such as systemic lupus erythematosus.

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