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Congestive Myelopathy due to Intradural Spinal AVM Supplied by Artery of Adamkiewicz: Case Report with Brief Literature Review and Analysis of the Foix-Alajouanine Syndrome Definition. | LitMetric

AI Article Synopsis

  • Spinal arteriovenous malformations (AVMs) can cause a condition called congestive myelopathy, also known as Foix-Alajouanine syndrome, which is rare and often misdiagnosed due to confusing definitions.
  • The case report discusses a 47-year-old male who had Foix-Alajouanine syndrome linked to an uncommon AVM from the artery of Adamkiewicz, treated with embolization, resulting in some symptom improvement.
  • The authors recommend that "Foix-Alajouanine syndrome" be specifically used for cases with chronic neurological symptoms due to spinal AVMs and suggest that CT angiography be used alongside other imaging techniques to aid diagnosis and treatment, which can include

Article Abstract

Background: Spinal arteriovenous malformations (AVMs) can lead to development of congestive myelopathy (Foix-Alajouanine syndrome). Spinal AVMs are rare and so is this syndrome. Diagnosis is often missed due to its rarity and confusing definitions of the Foix-Alajouanine syndrome.

Case Report: We report a case of a 47-year-old male patient suffering from this rare syndrome with an AVM arising from the artery of Adamkiewicz, which is another rarity. Our patient was treated by embolization of the lesion with 20% glue, after which he showed mild improvement of symptoms. We also present a brief review of literature on spinal AVMs and elucidate the evolution of the term Foix-Alajouanine syndrome.

Conclusions: Use of the term "Foix-Alajouanine syndrome" should be restricted to patients with progressive subacute to chronic neurological symptoms due to congestive myelopathy caused by intradural spinal AVMs. CT angiography should supplement DSA as preliminary Imaging modality. Patients may be treated with surgery or endovascular procedures.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492508PMC
http://dx.doi.org/10.12659/PJR.894304DOI Listing

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