Spinal Arachnoid Web: A didactic report of two cases with clinical, radiological, surgical and pathological
S Bertholon1, S Grange1, R Grange1
1Department of Radiology, University Hospital of Saint-Etienne, 42055 Saint-Etienne cedex 2, France.
Background:
Arachnoid web (AW) is a rare but probably underestimated cause of spinal cord injury that is complex to diagnose due to subtle MRI findings and similarities to other better-known diseases such as arachnoid cyst (AC) or transdural spinal cord herniation (TSCH). Increased recognition of AW is mandatory since delay in diagnosis can lead to potentially serious neurological sequelae.
Case Presentations:
We report two additional cases of AW for didactic purposes, with special emphasis on the distinctive MRI and intraoperative findings. Both patients presented with progressively worsening neurological symptoms, including proprioceptive ataxia, motor weakness, numbness and neuropathic pain. The diagnosis of AW was suspected on the basis of specific MRI criteria, especially the so-called "scalpel sign". Formal confirmation of the diagnosis was obtained in two patients that were managed surgically. Postoperative follow-up demonstrated significant functional recovery.
Discussion:
There is a need for better recognition of AW by the medical community. Careful analysis of MRI semiology is crucial for the distinction between AW, AC and TSCH. Prompt and accurate diagnosis is mandatory to conserve functional prognosis, since appropriate surgical treatment with AW resection is curative, halting or even resolving the neurological symptoms.
Insights
Arachnoid webs (AW) are a rare cause of spinal cord injury, often missed due to subtle MRI findings. Early diagnosis and surgical resection of AW can halt or resolve neurological symptoms, improving patient outcomes.
Area of Science:
- Neurosurgery
- Neuroradiology
- Spinal Cord Imaging
Background:
- Arachnoid web (AW) is an underrecognized cause of spinal cord injury.
- Diagnostic challenges arise from subtle MRI findings and resemblance to arachnoid cysts (AC) or transdural spinal cord herniation (TSCH).
- Delayed diagnosis of AW can lead to severe neurological deficits.
Observation:
- Two cases of AW presenting with progressive neurological decline are presented.
- Symptoms included proprioceptive ataxia, motor weakness, numbness, and neuropathic pain.
- The "scalpel sign" on MRI was a key diagnostic indicator.
Findings:
- Specific MRI criteria, including the "scalpel sign", aided in suspecting AW.
- Surgical management confirmed the diagnosis in both patients.
- Postoperative follow-up revealed significant functional recovery after AW resection.
Implications:
- Enhanced recognition of AW by the medical community is crucial.
- Distinguishing AW from AC and TSCH requires meticulous MRI analysis.
- Prompt diagnosis and surgical intervention for AW are essential for preserving neurological function and achieving curative outcomes.
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