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Analysis of 18FDG PET/CT Imaging as a Tool for Studying Mycobacterium tuberculosis Infection and Treatment in Non-human Primates
Published on: September 5, 2017
Congenital tuberculosis in preterm infants in a high-burden setting in southwest China: a single-center
Xiaoling Zhuang1, Wanting Xu2, Wen Xu2
1Department of Pediatrics, The First People's Hospital of Liangshan Yi Autonomous Prefecture, Liangshan, China.
Insights
Congenital tuberculosis (CTB) in premature infants presents with non-specific symptoms and lab abnormalities. Early nucleic acid amplification testing is crucial for diagnosis in high-risk neonates.
Area of Science:
- Neonatology
- Infectious Diseases
- Pediatrics
Background:
- Congenital tuberculosis (CTB) is a rare, life-threatening infection in premature infants, often misdiagnosed.
- Characterization of CTB in preterm neonates is lacking, especially in high tuberculosis (TB) burden areas.
- This study focuses on CTB in a resource-limited NICU in southwest China.
Purpose of the Study:
- To thoroughly characterize congenital tuberculosis in premature infants.
- To identify clinical, laboratory, and microbiological features of CTB in preterm neonates.
- To evaluate treatment outcomes and prognosis for CTB in this vulnerable population.
Main Methods:
- Retrospective review of hospital records for premature infants diagnosed with CTB from January 2016 to December 2023.
- Data collection included demographics, maternal TB history, symptoms, laboratory markers, microbiological findings, imaging, treatment, and prognosis.
- Diagnosis was based on etiological and clinical evidence.
Main Results:
- Eleven premature infants with CTB were identified; 7 mothers had a history of TB, with 7 pregnancies resulting from in vitro fertilization and embryo transfer.
- Clinical manifestations were atypical and non-specific, including low fever, dyspnea, poor feeding, and coughing.
- Significant laboratory findings included elevated C-reactive protein, thrombocytopenia, hyponatremia, hypocalcemia, and hypomagnesemia. Nucleic acid amplification tests were 100% positive, and chest CT scans showed abnormalities in all patients.
Conclusions:
- Preterm infants with CTB often present with non-specific signs and reversible laboratory abnormalities.
- Maternal TB history and IVF/embryo transfer history are important risk factors.
- Early use of nucleic acid amplification testing is recommended for suspected CTB cases in preterm neonates.
Background:
Congenital tuberculosis (CTB) is an extremely rare and potentially life-threatening infection in premature infants that is frequently misdiagnosed. There is still a lack of thorough characterization of this condition in preterm neonates, particularly in high TB-burden settings.
Methods:
Premature infants with CTB were identified from hospital medical records from January 2016 to December 2023 in a high-burden, resource-limited neonatal intensive care unit (NICU) in southwest China. Diagnosis was based on etiology and clinical evidence. Data extracted included demographics, maternal history of tuberculosis (TB) exposure, symptoms, laboratory markers, microbiological findings, imaging findings, treatment regimens, and prognosis. These were evaluated during the pre-diagnosis, diagnosis, and posttreatment stages.
Results:
A total of 11 premature infants with CTB were included. Maternal TB was common in this cohort; 7 of the 11 mothers were diagnosed with TB following in vitro fertilization and embryo transfer. Clinical manifestations were atypical and consisted primarily of non-specific symptoms, including low fever, shortness of breath, poor reaction, less eating, and coughing. Laboratory findings during the active phase of CTB revealed statistically significant elevations in C-reactive protein levels (P = 0.001), thrombocytopenia (P = 0.007), hyponatremia (P = 0.040), hypocalcemia (P = 0.022), and hypomagnesemia (P = 0.025). Sputum acid-fast bacillus (AFB) smear was positive in 4 out of 11, while gastric juice AFB smear was positive in 6 out of 11. Mycobacterial liquid culture produced the highest positivity with 7 out of 11, followed by solid culture and interferon-gamma release assays with 5 out of 11. All nucleic acid amplification tests were positive, and chest CT scans showed abnormalities in each patient. Among the patients, five experienced liver function impairment after anti-TB treatment, as evidenced by elevated alanine aminotransferase levels.
Conclusions:
In this study, preterm infants with CTB frequently demonstrated non-specific clinical signs with a reversible pattern of inflammation, anemia, thrombocytopenia, and electrolyte disturbances that normalized after anti-TB therapy. These patterns, together with maternal TB risk or in vitro fertilization and embryo transfer history, may raise clinical suspicion and justify the early use of nucleic acid amplification testing, and generalizability outside this setting requires larger, controlled cohorts.
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