A rare case of concurrent pneumonia, rib osteomyelitis, spondylodiscitis, paravertebral and epidural abscesses in a patient with chronic granulomatous disease.
Nahid TavakolizadehAmir Mahmoud AhmadzadeBehnam BeizaeiMostafa IzanluFarzaneh KhoroushiBehzad AminzadehPublished in: Clinical case reports (2023)
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder that is characterized by deficiencies in the phagocytes capacity to eliminate ingested microorganisms, which frequently causes bacterial and fungal infections. The extensive involvement of the lungs, ribs, and vertebrae that is complicated by multiple abscesses from aspergillosis is rare. in this study, we report a 13-year-old boy with CGD who experienced concurrent pneumonia, rib osteomyelitis, spondylodiscitis, paravertebral, and epidural abscesses as a result of Aspergillus flavus infection with associated computed tomography scan and magnetic resonance imaging findings. Patients with CGD are susceptible to Aspergillus infection. Correct diagnosis based on clinical and paraclinical findings as well as choosing the best treatment regimen is essential for achieving a favorable outcome.
Keyphrases
- computed tomography
- magnetic resonance imaging
- rare case
- spinal cord
- positron emission tomography
- ultrasound guided
- locally advanced
- cell wall
- contrast enhanced
- interstitial lung disease
- case report
- thoracic surgery
- radiation therapy
- drug induced
- respiratory failure
- image quality
- combination therapy
- postoperative pain
- rheumatoid arthritis
- systemic sclerosis
- extracorporeal membrane oxygenation