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Published on: August 18, 2015
Disseminated cerebral aspergillosis complicated by thrombotic microangiopathy
Robynn Lester1, Deirdre Church1,2, Anshula Ambasta1,3,4
1Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Abstract:
Invasive aspergillosis (IA) is a serious condition that can affect almost any organ. Cerebral aspergillosis itself is rapidly fatal without treatment. We report a case of disseminated cerebral IA in a patient exposed to cyclophosphamide, rituximab and prednisone. This case is unique because: 1) disseminated IA has not been described in anti-glomerular basement membrane glomerulonephritis; 2) IA led to thrombotic microangiopathy with normal ADAMTS13 and 3) voriconazole toxicity necessitated use of isavuconazole for IA treatment.
Insights
Disseminated cerebral invasive aspergillosis (IA) occurred in a patient with anti-glomerular basement membrane disease. This rare case highlights IA complications and treatment challenges, including drug toxicity.
Area of Science:
- Medical Mycology
- Immunology
- Nephrology
Background:
- Invasive aspergillosis (IA) is a severe fungal infection with high mortality, particularly cerebral IA.
- Immunosuppressive therapy, including cyclophosphamide, rituximab, and prednisone, increases susceptibility to IA.
- Anti-glomerular basement membrane glomerulonephritis is a rare autoimmune kidney disease.
Observation:
- A unique case of disseminated cerebral IA in a patient with anti-glomerular basement membrane glomerulonephritis is presented.
- The patient experienced IA despite immunosuppressive treatment, leading to neurological complications.
- Thrombotic microangiopathy developed secondary to IA, with normal ADAMTS13 levels.
Findings:
- Disseminated IA has not been previously reported in the context of anti-glomerular basement membrane glomerulonephritis.
- IA can precipitate thrombotic microangiopathy even with normal ADAMTS13 activity.
- Voriconazole toxicity required a switch to isavuconazole for effective IA treatment.
Implications:
- This case expands the understanding of IA manifestations in immunocompromised patients with autoimmune diseases.
- It underscores the importance of considering IA in patients with unexplained neurological symptoms and immunosuppression.
- The case highlights challenges in IA management, including drug toxicity and the need for alternative antifungal agents.
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