Aspergillus Flavus-induced brain abscess in an immunocompetent child : case report

• Published in: Sultan Qaboos University medical journal Vol. 16; no. 2; pp. 246 - 249
• Main Authors: Bin Husayn, Ibrahim, al-Suhayl, Isam A., Jumah, Sulayman, al-Maskari, Nawal
• Format: Journal Article
• Language: English
• Published: Muscat, Oman Sultan Qaboos University, College of Medicine and Health Sciences 01.05.2016; Sultan Qaboos University; Sultan Qaboos University Medical Journal, College of Medicine & Health Sciences
• Subjects: Abscess; antifungal agents; Aspergillus flavus; Blood; Brain; brain abscess; Case Report; Case reports; Edema; Fungal infections; fungus disease; Histopathology; Immunocompetence; Medical imaging; Mortality; Nervous system; Neutrophils; NMR; Nuclear magnetic resonance; Patients; saudi arabia; Tumors; الخراج; الدماغ; الطب; العقل; Brain Abscess; Saudi Arabia; Aspergillus flavus; Antifungal Agents; Immunocompetence; Fungus Disease; Case Report
• ISSN: 2075-051X; 2075-0528
• DOI: 10.18295/squmj.2016.16.02.019

Intracranial aspergillosis is an extremely rare manifestation of invasive aspergillosis in immunocompetent children and is associated with high morbidity and mortality. We report a 12-year-old immunocompetent male child who was referred to the King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia, in May 2010 after a sudden-onset headache and loss of consciousness. Brain imaging revealed a large right space-occupying occipital lesion and the patient underwent a craniotomy and resection. Histopathology of the lesion revealed necrotising granulomatous fungal encephalitis with many hyphae engulfed by multinucleated giant histiocytes. Two days later, a computed tomography scan showed debulking of the fungal mass and the patient was discharged on oral voriconazole. However, imaging at a six-week follow-up showed progression of the abnormality. A residual or persistent fungal brain lesion was suspected. Further neurosurgical resection of the lesion was performed and cultures showed growth of Aspergillus flavus. The patient was treated successfully with antifungal therapy over the following two years.