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Updated: Jul 12, 2026

Histological Quantification to Determine Lung Fungal Burden in Experimental Aspergillosis
Published on: March 9, 2018
[Pulmonary aspergillosis in a child with chronic granulomatous disease]
Mohamed Slim Abdelmoula1, Rim Abdelmalek, Kais Chleyfa
1Service de Pédiatrie, EPS la Rabta.
Insights
Chronic granulomatous disease (CGD) patients require prophylaxis against opportunistic infections. This case highlights successful management of invasive aspergillosis in a CGD patient with a complex presentation.
Area of Science:
- Immunology
- Infectious Diseases
- Pediatrics
Background:
- Chronic granulomatous disease (CGD) predisposes individuals to severe bacterial and fungal infections.
- Primary prophylaxis is crucial for preventing opportunistic infections like Pneumocystis and Aspergillus in CGD patients.
- Early and aggressive management is key to improving outcomes in CGD-related infections.
Observation:
- A 12-year-old boy with CGD presented with refractory pleuro-pneumonia at age 10, despite long-term prophylaxis.
- Aspergillus was identified as the causative agent through clinical, radiological, and serological evidence.
- The patient developed dorsal spondylodiscitis, with suspected vertebral aspergillosis or Pott's disease.
Findings:
- Amphotericin B treatment led to a positive clinical and radiological response for the pleuro-pulmonary infection.
- A combination therapy including antituberculous agents, antifungals, interferon (IFN), granulocyte transfusions, and granulocyte-macrophage colony-stimulating factor (GM-CSF) achieved clinical improvement and radiological stabilization for spondylodiscitis.
- Vertebral biopsy was inconclusive, necessitating a comprehensive treatment approach.
Implications:
- This case underscores the importance of considering invasive fungal infections, particularly Aspergillus, in CGD patients with refractory pneumonia.
- The successful management of complex vertebral aspergillosis highlights the potential benefit of multimodal adjuvant therapies in immunocompromised patients.
- Further research into optimal prophylaxis and treatment strategies for invasive fungal infections in CGD is warranted.
Abstract:
The chronic granulomatous disease is characterised by the occurence of multiple bacterial and fungal infections since the early childhood. This susceptibility to infections must be prevented by a primary prophlylaxis against the opportunistic germs like pneumocystis and aspergillus. Our case is about a twelve-year-old boy who had a prophylaxis since his fourth month of life. At 10 years he presented a pleuro-pneumonia refractory to a large spectrum antibiotherapy. The aspergillar etiology was established on clinical, radiological and serological arguments. An amphotericine B treatment allowed a good clinical and radiological outcome of this pleuro-pulmonary affection. However, a dorsal spondylodiscitis complicated the course of the disease. A secondary vertebral aspergillosis or a Pott's disease were suspected. The vertebral bipsy was'nt conclusive. The association of antituberculous and antifungal agents with adjuvant molecules (IFN, granulotic transfusions and GM-CSF) permitted a good clinical outcome and the stabilisation of the radiological lesions.
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