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Association of a giant developmental venous anomaly and acute disseminated encephalomyelitis: A case report and
Louis Deprez1, Emilie Lommers2
1Departement of Radiology, CHU de Liège, Belgium.
Abstract:
We describe the first reported association between acute disseminated encephalomyelitis (ADEM) and giant developmental venous anomaly (DVA) in the context of myelin oligodendrocyte associated glycoprotein (MOG) associated disorder (MOGAD). Patient was a young woman presenting with headache, bradypsychia and tetrapyramidal syndrome. Imaging showed disseminated tumefactive inflammatory lesions in the brain and spinal cord, with a massive right frontal lobe lesion centred around a giant DVA. Demyelinating inflammatory lesions are known to occur in a perivenular pattern, and the association between some inflammatory diseases such as multiple sclerosis (MS) and DVA has already been described. Developmental venous anomalies are variant of the normal venous drainage of the brain, responsible of a local alteration of the venular network, and micro-perfusion anomalies as well as possible increased of blood-brain barrier permeability. As such, they might be responsible for a favourable environment for pathogenic auto-antibodies penetrance in such region, potentializing the inflammatory lesion size. Perfusion imaging showed a significant increase in regional blood volume and blood transit time in the DVA and the surrounding brain tissue, which regressed in the follow-up imaging studies after the acute stage. This case illustrates the potential role of DVA in the setting of demyelinating diseases, and its consequences on the local micro-perfusion of the brain, evolving between the acute and chronic phase of the illness.
Insights
This study reports the first association between acute disseminated encephalomyelitis (ADEM) and giant developmental venous anomaly (DVA) in myelin oligodendrocyte glycoprotein antibody-associated disorder (MOGAD). Giant DVAs may create a conducive environment for demyelinating lesions, impacting brain micro-perfusion.
Area of Science:
- Neuroimmunology
- Neuroradiology
- Vascular Neurology
Background:
- Acute disseminated encephalomyelitis (ADEM) is an immune-mediated demyelinating disease.
- Developmental venous anomalies (DVAs) are common cerebral vascular malformations.
- Myelin oligodendrocyte glycoprotein antibody-associated disorder (MOGAD) is a CNS demyelinating disease.
Purpose of the Study:
- To report the first association between ADEM and a giant DVA in a patient with MOGAD.
- To investigate the potential role of DVAs in the pathogenesis and imaging findings of MOGAD.
Main Methods:
- Case report of a young woman with MOGAD presenting with neurological symptoms.
- Neuroimaging including MRI and perfusion studies to characterize brain lesions and DVA.
- Follow-up imaging to assess lesion evolution and micro-perfusion changes.
Main Results:
- The patient presented with headache, bradypsychia, and tetrapyramidal syndrome.
- Imaging revealed disseminated tumefactive inflammatory lesions, with a large lesion centered on a giant right frontal DVA.
- Perfusion imaging showed increased blood volume and transit time in the DVA and surrounding tissue, which normalized post-treatment.
Conclusions:
- Giant DVAs may predispose to or potentiate demyelinating lesions in MOGAD.
- DVAs can alter local brain micro-perfusion, influencing the evolution of inflammatory demyelinating diseases.
- This case highlights the potential interaction between vascular anomalies and neuroinflammatory conditions.
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