@article{10.11648/j.ajp.20210703.23,
  author = {Werdani Amina and Yahyaoui Omar and Jammeli Nesrine and Rassas Ahmed and Boussofara Raoudha and Khedher Mohamed and Mahjoub Bahri},
  title = {Kocuria Kristinae Meningitis and Cranial Nerve Palsies Secondary to Sphenoid Sinusitis: About a Case},
  journal = {American Journal of Pediatrics},
  volume = {7},
  number = {3},
  pages = {159-162},
  doi = {10.11648/j.ajp.20210703.23},
  url = {https://doi.org/10.11648/j.ajp.20210703.23},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajp.20210703.23},
  abstract = {Kocuria spp, previously classified as the members of Micrococcacae family, was rarely reported as a human pathogen. Kocuria Kristinae could cause invasive infections of large variety of tissues in patients of any age. We report the first case of meningitis with sixth and third nerve palsies secondary to sphenoid sinusitis caused by Kocuria Kristinae in a previously healthy 13 year-old boy. In effect, his cerebrospinal fluid (CSF) showed a cloudy appearance of the CSF, white blood cells count was 600 cells/µl (polymorphs 90% and 10% lymphocytes), red blood cells count was 200 cells/µl, protein level was elevated at 5.3 g/l and glucose level was low at 0.1 mmol/l. The direct examination showed positive-gram diplococci. The patient was initially treated with intravenous cefotaxim and vancomycin. The CSF culture was positive for gram-positive diplococci, which was identified as Kocuria kristinae. The meningitis was characterized by insidious evolution and persistent very low CSF glucose level. It was difficult to diagnose the sphenoid sinusitis because it is not accessible to direct clinical examination. It was diagnosed after the occurrence of a complication due to its anatomical location and proximity to the intracranial and orbital content. At day 5, the patient had remarkable resolution of symptoms. Complete recovery of cranial nerve palsy was noted at day 8. The aim of this case report is to present the first isolation of Kocuria Kristinae from cerebrospinal fluid sample and describe the clinical presentation and management outcomes.},
 year = {2021}
}

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TY  - JOUR
T1  - Kocuria Kristinae Meningitis and Cranial Nerve Palsies Secondary to Sphenoid Sinusitis: About a Case
AU  - Werdani Amina
AU  - Yahyaoui Omar
AU  - Jammeli Nesrine
AU  - Rassas Ahmed
AU  - Boussofara Raoudha
AU  - Khedher Mohamed
AU  - Mahjoub Bahri
Y1  - 2021/08/23
PY  - 2021
N1  - https://doi.org/10.11648/j.ajp.20210703.23
DO  - 10.11648/j.ajp.20210703.23
T2  - American Journal of Pediatrics
JF  - American Journal of Pediatrics
JO  - American Journal of Pediatrics
SP  - 159
EP  - 162
PB  - Science Publishing Group
SN  - 2472-0909
UR  - https://doi.org/10.11648/j.ajp.20210703.23
AB  - Kocuria spp, previously classified as the members of Micrococcacae family, was rarely reported as a human pathogen. Kocuria Kristinae could cause invasive infections of large variety of tissues in patients of any age. We report the first case of meningitis with sixth and third nerve palsies secondary to sphenoid sinusitis caused by Kocuria Kristinae in a previously healthy 13 year-old boy. In effect, his cerebrospinal fluid (CSF) showed a cloudy appearance of the CSF, white blood cells count was 600 cells/µl (polymorphs 90% and 10% lymphocytes), red blood cells count was 200 cells/µl, protein level was elevated at 5.3 g/l and glucose level was low at 0.1 mmol/l. The direct examination showed positive-gram diplococci. The patient was initially treated with intravenous cefotaxim and vancomycin. The CSF culture was positive for gram-positive diplococci, which was identified as Kocuria kristinae. The meningitis was characterized by insidious evolution and persistent very low CSF glucose level. It was difficult to diagnose the sphenoid sinusitis because it is not accessible to direct clinical examination. It was diagnosed after the occurrence of a complication due to its anatomical location and proximity to the intracranial and orbital content. At day 5, the patient had remarkable resolution of symptoms. Complete recovery of cranial nerve palsy was noted at day 8. The aim of this case report is to present the first isolation of Kocuria Kristinae from cerebrospinal fluid sample and describe the clinical presentation and management outcomes.
VL  - 7
IS  - 3
ER  - 

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