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Cryptogenic cervical intramedullary abscess with rapidly progressive myelopathy: illustrative case.
Warsi, Nebras M; Wilson, Ann; Malhotra, Armaan K; Ku, Jerry C; Najjar, Ahmed A; Bui, Esther; Baker, Michael; Bartlett, Eric; Hodaie, Mojgan.
Affiliation
  • Warsi NM; 1Division of Neurosurgery, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
  • Wilson A; 1Division of Neurosurgery, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
  • Malhotra AK; 1Division of Neurosurgery, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
  • Ku JC; 1Division of Neurosurgery, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
  • Najjar AA; 2Division of Neurosurgery, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.
  • Bui E; 3Department of Medicine, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada; and.
  • Baker M; 3Department of Medicine, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada; and.
  • Bartlett E; 4Division of Neuroradiology, Department of Medical Imaging, Toronto Western Hospital, Toronto, Ontario, Canada.
  • Hodaie M; 1Division of Neurosurgery, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
J Neurosurg Case Lessons ; 1(4)2021 Jan 25.
Article in En | MEDLINE | ID: mdl-36131588
ABSTRACT

BACKGROUND:

The purpose of the present case report is to highlight the presentation, workup, clinical decision making, and operative intervention for a 68-year-old woman who developed rapidly progressive myelopathy secondary to idiopathic cervical intramedullary abscess. OBSERVATIONS The patient underwent laminectomy and aspiration/biopsy of the lesion. Intraoperatively, division of the posterior median sulcus released a large volume of purulent material growing the oral pathogens Eikenella corrodens and Gemella morbillorum. Broad-spectrum antibiotics were initiated postoperatively. At the 6-month follow-up, the patient had almost completely recovered with some persistent hand dysesthesia. Complete infectious workup, including full dental assessment and an echocardiogram, failed to reveal the source of her infection. LESSONS The authors report the first case of cryptogenic spinal intramedullary abscess secondary to Eikenella spp. and Gemella spp. coinfection. Intramedullary abscesses are exceptionally rare and most commonly develop in children with dermal sinus malformations or in the context of immunosuppression. In adults without risk factors, they can readily be mistaken for more common pathologies in this age group, such as intramedullary neoplasms or demyelinating disease. Prompt diagnosis and management based on rapidly progressive myelopathy, assessment of infectious risk factors and/or symptoms, and targeted imaging are critical to avoid potentially devastating neurological sequelae.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: J Neurosurg Case Lessons Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: J Neurosurg Case Lessons Year: 2021 Document type: Article Affiliation country: