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First Case of Chryseobacterium gleum Post-COVID-19 in a Child with Recurrent Fever
Manuela Colosimo1, Filippo Luciani2, Maria Novella Pullano3
1Department of Microbiology and Virology, AO Dulbecco: Pugliese Hospital, 88100 Catanzaro, Italy.
Insights
This case study reports the first pediatric Chryseobacterium gleum infection following COVID-19. Early identification and treatment are crucial for preventing adverse outcomes in children with this emerging pathogen.
Area of Science:
- Pediatric Infectious Diseases
- Microbiology
- Emerging Pathogens
Background:
- Chryseobacterium gleum is an emerging Gram-negative opportunistic pathogen causing systemic infections in immunocompromised individuals.
- Limited data exists on Chryseobacterium gleum infections in pediatric populations.
- The post-COVID-19 era presents unique challenges for identifying and managing opportunistic infections in children.
Observation:
- A 2-year-old child presented with recurrent fever, lymphadenopathy, and rash post-COVID-19.
- Clinical findings included microcytic anemia, elevated C-reactive protein, conjunctivitis, and respiratory symptoms.
- Chryseobacterium gleum was identified in sputum and throat swabs using MALDI-TOF MS.
Findings:
- This represents the first documented case of Chryseobacterium gleum infection in a child following COVID-19.
- The bacterium was confirmed as the causative agent through microbiological analysis.
- The patient exhibited a range of systemic and localized symptoms.
Implications:
- Highlights the potential for Chryseobacterium gleum to cause severe infections in children, particularly post-COVID-19.
- Emphasizes the need for prompt microbiological identification and appropriate antimicrobial therapy.
- Suggests increased vigilance for opportunistic infections in pediatric patients recovering from COVID-19.
Abstract:
Background and Clinical Significance:Chryseobacterium gleum is a Gram-negative opportunistic and emerging pathogen able to induce systemic manifestations (e.g., peritonitis, pneumonia, urinary tract infections, meningitis) in immunocompromised patients. No data on children have been published. Case Presentation: A 2-year-old child presented in the pediatric ambulatory room with recurrent fever, submandibular lymphadenopathy, and skin rash. Laboratory findings revealed the presence of microcytic anemia with an increase in c-reactive protein. Chest X-ray reported mild accentuation of the bronchial structure, especially on the right side and middle-lower zone. In the peripheral blood smear, anisopoikilocytosis and elliptical red cells were evident. Clinical evaluation revealed the presence of conjunctivitis and polymorphic erythema, hyperemic pharynx and tonsils, SPO2 99%, auscultation of the chest, harsh vesicular murmur all over the area, and some wheezing. Microbiological analysis of sputum and throat swabs revealed the presence of numerous colonies of Chryseobacterium gleum confirmed using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS score > 2.2). Conclusions: This is the first case of Chryseobacterium gleum post-COVID in a child. We suggest that a quick identification and an appropriate treatment represent the critical factors able to prevent the adverse outcomes related to C. gleum infection.
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