Fulminant Nocardiosis Due to a Multidrug-Resistant Isolate in a 12-Year-Old Immunocompetent Child
Olivia Senard1,2, Stéphane Blanot3, Gregory Jouvion4
1Department of General Pediatrics and Infectious Diseases, AP-HP, Necker-Enfants malades University Hospital, Sorbonne Paris Cité, Paris, France.
Insights
Nocardiosis, a rare infection, can be fatal in children, even those not immunocompromised. Early diagnosis and appropriate treatment are crucial due to multidrug-resistant Nocardia strains.
Area of Science:
- Medical Microbiology
- Pediatric Infectious Diseases
- Clinical Case Reports
Background:
- Nocardiosis is an opportunistic infection typically seen in immunocompromised adults.
- It is infrequently recognized in pediatric populations, especially in immunocompetent children.
- Prompt diagnosis and treatment are vital due to potential severity and antimicrobial resistance.
Observation:
- A previously healthy child presented with abdominal pain and altered general status, initially suspected as a renal malignancy.
- Clinical findings included lymphocytic meningitis, disseminated brain abscesses, and kidney cystic lesions.
- Despite broad-spectrum antibiotics and supportive care, the patient experienced a fatal outcome.
Findings:
- Cultures from renal biopsy and cerebrospinal fluid identified Nocardia species.
- Species identification revealed a multidrug-resistant strain within the Nocardia elegans/aobensis/africana complex.
- The case highlights diagnostic challenges in pediatric nocardiosis.
Implications:
- This case underscores the importance of considering Nocardia infection in children with unexplained disseminated disease.
- It emphasizes the need for awareness among pediatricians regarding Nocardia's varied presentations.
- The findings highlight challenges in treating Nocardia due to intrinsic antimicrobial resistance patterns.
Abstract:
Nocardiosis is a rare cause of infection that usually affects immunocompromised adult patients and might not be recognized by pediatricians. We report a fatal case of disseminated nocardiosis in a previously healthy child initially admitted for an abdominal mass with suspicion of a renal malignant tumor. The patient, originating from Mali without any medical history, displayed abdominal pain with progressive altered general status. Laboratory and imaging findings revealed lymphocytic meningitis and disseminated abscesses in the brain and the cerebellum and a large number of cystic lesions of the kidney. Despite being administered wide-spectrum antibiotics and antituberculous and antifungal therapies with an external ventricular drainage for intracranial hypertension, the patient died 6 days after his admission. Nocardia spp was cultured from a renal biopsy and the cerebrospinal fluid. Species identification and antibiotic susceptibility were obtained later, revealing a multidrug-resistant isolate of the Nocardia elegans/aobensis/africana complex. This case reveals the difficulties of diagnosing nocardiosis, in particular in children not known to be immunocompromised, because we face multiple differential diagnoses and the importance of treating nocardiosis appropriately because of intrinsic resistance issues.
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