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[Clinical and epidemiological features of tuberculosis ostitis in BCG-vaccinated children]
Insights
Pediatric osteitis cases have risen since 2001. Molecular methods confirmed Bacillus Calmette-Guérin (BCG) as the cause in nearly half of the osteitis bone samples, verifying its etiology.
Area of Science:
- Pediatric Infectious Diseases
- Molecular Diagnostics
- Skeletal Tuberculosis
Background:
- Osteitis incidence in children has significantly increased since 2001.
- Tuberculous osteitis presents distinct clinical and epidemiological features compared to primary pulmonary tuberculosis in infants.
Purpose of the Study:
- To investigate the etiology of pediatric osteitis, particularly focusing on the role of Mycobacterium bovis (BCG).
- To differentiate BCG-related osteitis from other forms of childhood tuberculosis.
Main Methods:
- Comparative analysis of clinical and epidemiological data for tuberculous osteitis (n=70) and primary pulmonary tuberculosis (n=60) in infants.
- Molecular genetic analysis using polymerase chain reaction (PCR) to detect BCG M. bovis strain DNA in intraoperative bone samples and bone destruction foci cultures.
Main Results:
- BCG M. bovis strain DNA was identified in 13 (46.4%) intraoperative samples.
- BCG M. bovis DNA was also detected in 4 samples from bone destruction foci cultures.
- Isolation of BCG cultures confirmed the findings in bone lesions.
Conclusions:
- The detection of BCG M. bovis DNA or isolation of BCG cultures from bone lesions is a key criterion for diagnosing BCG etiology of osteitis.
- This finding is particularly relevant for pediatric osteitis exhibiting a productive necrotic tuberculosis morphology.
- Molecular methods provide significant diagnostic value in identifying BCG as the causative agent of pediatric osteitis.
Abstract:
There has been a drastic increase in the incidence of ostitis in children since 2001. Comparison of current tuberculous ostitis (n = 70) and primary pulmonary tuberculosis (n = 60) in infants revealed significant clinical and epidemiological differences. Molecular genetic methods identified BCG M. bovis strain DNA in 13 (46.4%) intraoperative samples and 4 samples of obtained cultures from bone destruction foci. Isolation of BCG cultures and/or verification of BCG M. ovis DNA from the bone lesion focus by polymerase chain reaction is a significant criterion for verification of the BCG etiology of ostitis having a morphological pattern of productive necrotic tuberculosis in children.
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