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Cryptogenic cervical intramedullary abscess with rapidly progressive myelopathy: illustrative case
Nebras M Warsi1, Ann Wilson1, Armaan K Malhotra1
11Division of Neurosurgery, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
Insights
This case report details a rare cervical intramedullary abscess caused by Eikenella and Gemella bacteria. Prompt diagnosis and surgical intervention led to significant recovery, highlighting the importance of early management.
Area of Science:
- Neurosurgery
- Infectious Disease
- Spinal Cord Pathology
Background:
- Presents a rare case of rapidly progressive myelopathy in a 68-year-old female.
- Highlights the diagnostic and therapeutic challenges of idiopathic cervical intramedullary abscess.
Observation:
- Surgical laminectomy and aspiration revealed purulent material with Eikenella corrodens and Gemella morbillorum.
- Postoperative antibiotics were administered; the patient showed significant recovery with residual hand dysesthesia at 6 months.
- Extensive infectious workup, including dental and cardiac assessments, did not identify the infection source.
Findings:
- First reported case of cryptogenic spinal intramedullary abscess due to coinfection with Eikenella spp. and Gemella spp.
- Intramedullary abscesses are rare, especially in adults without typical risk factors like immunosuppression or congenital malformations.
- The condition can be misdiagnosed as intramedullary neoplasms or demyelinating disease in adults.
Implications:
- Emphasizes the critical need for prompt diagnosis and management of rapidly progressive myelopathy.
- Highlights the importance of considering infectious etiologies, even in the absence of clear risk factors.
- Targeted imaging and thorough infectious workup are crucial to prevent severe neurological deficits from spinal cord abscesses.
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.
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