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Pulmonary mucormycosis: the last 30 years
F Y Lee1, S B Mossad, K A Adal
1Division of Internal Medicine, Cleveland Clinic Foundation, Ohio 44195, USA.
Archives of Internal Medicine
|July 1, 1999
Summary
Pulmonary mucormycosis, a rare fungal infection, primarily affects immunocompromised individuals. Early diagnosis and combined medical-surgical treatment improve survival rates for this potentially fatal condition.
Area of Science:
- Mycology
- Infectious Diseases
- Pulmonology
Background:
- Pulmonary mucormycosis is an uncommon opportunistic fungal infection.
- Literature on this condition is sparse, necessitating further clinical characterization.
Observation:
- A review of 87 cases identified key risk factors including diabetes mellitus, hematologic cancers, renal insufficiency, and organ transplantation.
- Pulmonary involvement often predilected upper lobes, and the air crescent sign on chest X-rays indicated a higher risk of pulmonary hemorrhage.
- Diagnosis was aided by fiberoptic bronchoscopy, with histopathology proving more sensitive than fungal cultures.
Findings:
- The overall survival rate for pulmonary mucormycosis was 44%.
- A combined medical-surgical approach was associated with better patient outcomes compared to medical management alone.
Implications:
- This rare but often fatal disease should be suspected in immunocompromised patients unresponsive to antibacterial therapy.
- Early recognition and aggressive management, including systemic antifungal therapy, surgical resection, and control of underlying conditions, are crucial for improving cure rates.
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