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Visualization of Pseudomonas aeruginosa within the Sputum of Cystic Fibrosis Patients
Published on: July 16, 2020
[Pertussis in a 4-month-old infant with unrecognized cystic fibrosis]
Lukáš Homola1, Alena Holčíková, Eliška Zárošská
1Clinic of Pediatric Infectious Diseases, The University Hospital Brno, Czech Republic. lhomola@fnbrno.cz
Insights
This case report details a young boy with cystic fibrosis who experienced severe pertussis and pneumothorax. Early diagnosis and comprehensive cystic fibrosis therapy led to his recovery and improved growth.
Area of Science:
- Pediatrics
- Infectious Diseases
- Genetics
Background:
- Cystic Fibrosis (CF) is a genetic disorder affecting multiple organs.
- Pertussis (whooping cough) is a highly contagious respiratory infection.
- Vaccination failure in infants with failure to thrive can increase infection risk.
Observation:
- A 4-month-old boy with failure to thrive, unvaccinated against pertussis, developed severe respiratory distress and pneumothorax.
- Prolonged illness and failure to thrive raised suspicion for underlying cystic fibrosis.
- Diagnostic workup confirmed Pseudomonas aeruginosa infection, anemia, pancreatic insufficiency, positive sweat test, and CFTR gene mutations.
Findings:
- The patient presented with a complex clinical picture involving pertussis and pneumothorax, superimposed on undiagnosed cystic fibrosis.
- Serological confirmation of pertussis and subsequent comprehensive CF diagnostics were crucial.
- Successful management involved integrated cystic fibrosis therapy.
Implications:
- This case highlights the importance of considering cystic fibrosis in infants with severe or prolonged infections, especially pertussis.
- Highlights the critical role of vaccination in preventing severe outcomes of infectious diseases in vulnerable populations.
- Emphasizes the need for thorough diagnostic evaluation in infants with failure to thrive and respiratory complications.
Abstract:
We present a case report of a small boy with cystic fibrosis complicated by pertussis and pneumothorax. The child had not been vaccinated against Bordetella pertussis due to the failure to thrive and was infected with the bacterium at the age of 4 months. The course of the disease was severe, with respiratory distress and spontaneous pneumothorax. The diagnosis of pertussis was serologically confirmed. A suspicion for cystic fibrosis increased after an unusually prolonged course of the disease and a history of the failure to thrive. A comprehensive diagnostic procedure revealed Pseudomonas aeruginosa respiratory infection, anemia, pancreatic insufficiency, a positive sweat test and the presence of two CFTR gene mutations. The patient, treated with comprehensive cystic fibrosis therapy, recovered from acute respiratory illness and started to thrive soon.
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