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Published on: March 9, 2018
Concomitant orbital aspergillosis and mucormycosis in a 17 months old immunocompetent child
Fatima A Habroosh1, Habibullah Eatamadi1, Rawia M Mohamed1
1Sheikh Khalifa Medical City, United Arab Emirates.
Abstract:
Isolated multiple orbital fungal infection (aspergillosis & mucormycosis) is extremely rare disease in immunocompetent individuals and especially in children. Placement of prosthetic device during the surgery could be one of the risk factors. The presentation is usually masquerading other entities which make early diagnosis a challengeable. This case presenting a 17 months old immunocompetent child who is diagnosed with isolated multiple orbital fungal infection: aspergillosis & mucormycosis. The presentation was mimicking orbital cellulitis and chronic dacryocystitis. The definitive diagnosis was made by tissue biopsy. The child was managed by surgical debridement and IV amphotericin B liposomal. High index of suspicion to fungal infection should be considered after surgical intervention with insertion prosthetic materials. To the best of our knowledge, orbital aspergillosis in immunocompetent young children is exceptionally rare.
Insights
This case study highlights a rare instance of multiple orbital fungal infections, including aspergillosis and mucormycosis, in an immunocompetent child. Early diagnosis is challenging due to symptoms mimicking other conditions.
Area of Science:
- Ophthalmology
- Mycology
- Pediatric Infectious Diseases
Background:
- Multiple orbital fungal infections (aspergillosis & mucormycosis) are exceptionally rare in immunocompetent children.
- Prosthetic device placement during surgery may be a risk factor.
- Orbital fungal infections often present with symptoms that mimic other orbital diseases, complicating diagnosis.
Purpose of the Study:
- To report a rare case of isolated multiple orbital fungal infection in an immunocompetent child.
- To emphasize the diagnostic challenges and management of such rare conditions.
Main Methods:
- A case presentation of a 17-month-old immunocompetent child with orbital fungal infection.
- Diagnosis confirmed via tissue biopsy.
- Management included surgical debridement and intravenous liposomal amphotericin B.
Main Results:
- The child was diagnosed with co-existing orbital aspergillosis and mucormycosis.
- The clinical presentation mimicked orbital cellulitis and chronic dacryocystitis.
- Successful treatment was achieved with surgical intervention and antifungal therapy.
Conclusions:
- A high index of suspicion for fungal infection is crucial after surgical interventions involving prosthetic materials.
- Orbital aspergillosis is exceptionally rare in immunocompetent young children.
- Prompt diagnosis and appropriate management are vital for favorable outcomes in pediatric orbital mycoses.
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