| Literature DB >> 27226920 |
Nawal Al-Maskari1, Ibrahim Hussain2, Suleiman Jumaa3, Essam A Al-Shail4.
Abstract
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 & 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.Entities:
Keywords: Antifungal Agents; Aspergillus flavus; Brain Abscess; Case Report; Fungus Disease; Immunocompetence; Saudi Arabia
Year: 2016 PMID: 27226920 PMCID: PMC4868528 DOI: 10.18295/squmj.2016.16.02.019
Source DB: PubMed Journal: Sultan Qaboos Univ Med J ISSN: 2075-051X