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Severe CD8 deficiency in a child with miliary tuberculosis
Faisal Nayel Kordy1, Sulaiman Al-Jumaah, Abdulaziz Al-Ghonaim
1Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Insights
A 6-month-old boy experienced severe CD8 deficiency secondary to miliary tuberculosis. His CD8 count normalized after treatment, ruling out primary immunodeficiency.
Area of Science:
- Immunology
- Pediatrics
- Infectious Diseases
Background:
- Severe CD8 deficiency can present in infants.
- Miliary tuberculosis is a disseminated form of TB.
- Primary immunodeficiencies require early diagnosis and management.
Observation:
- A 6-month-old boy presented with symptoms of miliary tuberculosis.
- The patient exhibited a severe deficiency in CD8+ T-cells upon initial presentation.
Findings:
- The CD8 deficiency was determined to be secondary to miliary tuberculosis.
- CD8+ T-cell counts returned to normal levels six months post-tuberculosis therapy.
- A genetic defect in ZAP-70, a cause of primary CD8 deficiency, was excluded.
Implications:
- This case highlights a potential complication of miliary tuberculosis in pediatric patients.
- It suggests that severe CD8 deficiency can be a transient, acquired condition in the context of active infection.
- Early identification and treatment of miliary TB may reverse acquired CD8 lymphopenia.
Abstract:
This report described a 6-month-old boy who presented with miliary tuberculosis and severe CD8 deficiency, which is most likely secondary to miliary tuberculosis since his CD8 was back to normal 6 month after therapy and primary CD8 deficiency, (ZAP 70 defect) was ruled out. To our knowledge this is the first paediatric case reported with severe CD8 deficiency secondary to miliary TB.
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