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Updated: Jul 8, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Venous congestive myelopathy: three autopsy cases showing a variety of clinicopathologic features
Koushun Matsuo1, Akiyoshi Kakita, Nobutaka Ishizu
1Department of Pathology, Brain Research Institute, University of Niigata, Niigata, Japan. matsuo@pb4.so-net.ne.jp
Abstract:
We describe three patients with progressive myelopathy, in whom autopsy revealed spinal cord pathology compatible with that of venous congestive myelopathy (VCM) associated with dural arteriovenous fistula (AVF), formerly known as angiodysgenetic necrotizing myelopathy (Foix-Alajournine syndrome). In these three patients, common symptoms were gait disturbance and sensory disturbance of the extremities, and these symptoms slowly worsened. The clinical diagnoses varied and included spinal cord intramedullary tumor, cervical spondylosis and multiple sclerosis. At autopsy, all the patients showed enlarged, tortuous venous vessels on the dorsal surfaces of the spinal cord at the affected levels. In the affected spinal cord parenchyma, necrotic lesions manifested by various degrees of neuronal loss and gliosis, with increased numbers of hyalinized vessels, were evident. The presence or absence of associated spinal dural AVF could not be identified histopathologically. Even with the help of modern neurological examination methods, early and accurate clinical diagnosis of VCM is sometimes difficult. When encountering patients with progressive myelopathy, VCM, although recognized as rare, should be considered as an important differential diagnosis.
Insights
Venous congestive myelopathy (VCM), linked to dural arteriovenous fistulas, presents with progressive myelopathy. Early diagnosis is challenging, requiring consideration of VCM in differential diagnoses for myelopathy.
Area of Science:
- Neurology
- Pathology
Background:
- Progressive myelopathy can be challenging to diagnose.
- Venous congestive myelopathy (VCM) is a rare condition associated with dural arteriovenous fistulas (AVFs).
Observation:
- Three autopsy cases revealed spinal cord pathology consistent with VCM.
- Patients presented with slowly worsening gait and sensory disturbances.
- Clinical diagnoses included spinal cord tumors, cervical spondylosis, and multiple sclerosis.
Findings:
- Autopsies showed enlarged, tortuous dorsal spinal cord veins and necrotic lesions.
- Histopathology confirmed neuronal loss, gliosis, and hyalinized vessels.
- Associated spinal dural AVF presence was not definitively identified histopathologically.
Implications:
- VCM should be considered in the differential diagnosis of progressive myelopathy.
- Accurate early clinical diagnosis of VCM remains difficult despite modern neurological methods.
- Understanding VCM pathology aids in diagnosing rare myelopathies.
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