Stenotrophomonas maltophilia‐associated odontogenic cerebral abscess in an immunocompetent patient: A case report

Author:

Scalia Gianluca1ORCID,Ponzo Giancarlo1,Giuffrida Massimiliano1,Patanè Domenico2,Riso Marcello Filippo3,Garozzo Adriana3,Chaurasia Bipin4ORCID,Umana Giuseppe Emmanuele56,Nicoletti Giovanni Federico1

Affiliation:

1. Neurosurgery Clinic, Department of Head and Neck Surgery Garibaldi Hospital Catania Italy

2. Department of Nursing Service Garibaldi Hospital Catania Italy

3. Microbiology Section, Department of Biomedical and Biotechnological Sciences University of Catania Catania Italy

4. Department of Neurosurgery Neurosurgery Clinic Birgunj Nepal

5. Department of Neurosurgery, Trauma and Gamma Knife Center Cannizzaro Hospital Catania Italy

6. Department of Medicine and Surgery Kore University of Enna Enna Italy

Abstract

Key Clinical MessageStenotrophomonas maltophilia can cause rare odontogenic brain abscesses in immunocompetent patients, highlighting the importance of considering uncommon pathogens in central nervous system infections. With only three reported cases of cerebral abscesses and one pituitary abscess caused by this microorganism, tailored diagnostic methods and individualized treatment regimens are crucial for accurate management.AbstractBrain abscesses present diagnostic and therapeutic challenges, with Stenotrophomonas maltophilia infections being exceptionally rare in the central nervous system. We present a case of odontogenic brain abscesses caused by S. maltophilia in an immunocompetent patient, highlighting the rarity and complexity of such infections. A 66‐year‐old male presented with spatial–temporal disorientation and left‐sided weakness. Radiological investigations revealed an expansive lesion in the right posterior frontal region. A craniotomy and drainage were performed, identifying S. maltophilia in the purulent material. The patient responded well to tailored antibiotic therapy. S. maltophilia‐related central nervous system infections are infrequent, emphasizing the need for a heightened clinical suspicion in atypical cases. This case contributes to the literature, emphasizing the importance of a multidisciplinary approach for successful diagnosis and management.

Publisher

Wiley

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