Abstract

Rothia mucilaginosa is a Gram-positive coccus and an opportunistic pathogen in immunocompromised hosts. The microorganism has been implicated in serious infections, including bacteremia meningitis or endocarditis. However, there is a dearth of investigations on meningitis, especially in children. As this infection is rare and only a few cases have been recorded, evidence-based guidelines for adequate infection treatment are lacking. We herein report the case of a 12-year-old boy with myelodysplastic syndromes (MDS) presenting with a change in mental status who was diagnosed as having febrile neutropenia and bacterial meningitis caused by R. mucilaginosa at 23 days after unrelated cord blood transplant. In our case, the minimum inhibitory concentrations (MICs) of meropenem and vancomycin (VCM) were both ≤1 μg/mL, whereas the MIC of daptomycin (DAP) was 4 μg/mL. The patient was treated with intravenous antimicrobial therapy due to meropenem for 43 days because he had febrile neutropenia. During follow-up, the patient had no neurological complications. We retrospectively reviewed the antimicrobial susceptibility of all R. mucilaginosa isolates (n = 5) from blood or cerebrospinal fluid cultures at our hospital. The MIC of VCM was <0.5 μg/mL for all strains, whereas the MIC of DAP was ≥2 μg/mL for all strains. The MIC of MEPM was >1 μg/mL for one strain. We recommend choosing VCM as the primary treatment for invasive R. mucilaginosa infections until antimicrobial susceptibility results are known, especially in immunocompromised children.

Highlights

  • Previously known as Stomatococcus mucilaginosus, is a Gram-positive and coagulase-negative coccus occurring as a commensal organism in the oral cavity and respiratory tract [1]. e microorganism is an opportunistic pathogen in immunocompromised patients and has been implicated in several infections, including bacteremia, meningitis, pneumonia, arthritis, endocarditis, and/or osteomyelitis [2, 3]

  • We present the case of a 12-year-old boy diagnosed as having R. mucilaginosa meningitis, myelodysplastic syndromes (MDS), and febrile neutropenia

  • As R. mucilaginosa meningitis is rare and only a few cases have been reported, no guidelines have been established to assist in antibiotic selection for the treatment of invasive Rothia infections

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Summary

Rothia mucilaginosa Meningitis in a Child with Myelodysplastic Syndromes

Fumihiro Ochi ,1 Ryota Nakamura, Reiji Miyawaki, Kyoko Moritani, Shinobu Murakami, and Hisamichi Tauchi. There is a dearth of investigations on meningitis, especially in children. As this infection is rare and only a few cases have been recorded, evidencebased guidelines for adequate infection treatment are lacking. We report the case of a 12-year-old boy with myelodysplastic syndromes (MDS) presenting with a change in mental status who was diagnosed as having febrile neutropenia and bacterial meningitis caused by R. mucilaginosa at 23 days after unrelated cord blood transplant. E patient was treated with intravenous antimicrobial therapy due to meropenem for 43 days because he had febrile neutropenia. We recommend choosing VCM as the primary treatment for invasive R. mucilaginosa infections until antimicrobial susceptibility results are known, especially in immunocompromised children

Introduction
Case Reports in Pediatrics
Discussion
Vancomycin Teicoplanin Daptomycin Linezolid
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