59 results match your criteria: "Foix-Alajouanine Syndrome"
Ann Med Surg (Lond)
November 2024
Departemnt of Neurosurgery, Cairo University Hospital, Cairo, Egypt.
J Neurosurg Case Lessons
November 2024
Department of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Background: Venous hypertensive myelopathy (VHM), formerly known as "Foix-Alajouanine syndrome," is a spinal cord dysfunction caused by impaired perfusion of the spinal cord. Most cases are attributed to spinal dural arteriovenous fistulas (dAVFs), but there are scattered reports of VHM without concomitant dAVF. Furthermore, no cases of VHM associated with intracranial hemorrhage exist.
View Article and Find Full Text PDFZh Nevrol Psikhiatr Im S S Korsakova
August 2024
Federal Scientific and Educational Center of Medical and Social Expertise and Rehabilitation named after G.A. Albrecht, St. Petersburg, Russia.
The Foix-Alajouanine syndrome was originally reported by these authors in 1926, as rapidly progressive vasculitis on the background of a viral infection. The pathology was represented by the huge, more than 10 times, dilation either of the lumen, or the walls of the spinal vessels, either of the arteries, or the veins. There were no signs of thrombosis, no malformations.
View Article and Find Full Text PDFArq Neuropsiquiatr
September 2024
Universidade Federal de Pernambuco, Centro de Ciências Médicas, Divisão de Neuropsiquiatria, Recife PE, Brazil.
Eur Neurol
August 2024
Department of Neurology, Instituto de Neurologia de Curitiba, Curitiba, Brazil.
World Neurosurg
May 2024
Department of Neurosurgery, Medical University of South Carolina, Charleston, South Carolina, USA.
Foix-Alajouanine syndrome is a rare cause of spinal dural arteriovenous fistula that can cause irreversible myelopathy and paraplegia if not treated promptly. The complex nature of this pathology often leads to missed or delayed diagnosis regardless of broad workups executed. We present a symptomatically classic Foix-Alajouanine 68-year-old patient with an accelerated progression reaching stages of severe myelopathy in less than a year.
View Article and Find Full Text PDFCureus
March 2023
Department of Neurosurgery, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Mexico City, MEX.
Clin Pract Cases Emerg Med
February 2022
Harbor-UCLA Medical Center, Department of Emergency Medicine, Torrance, California.
Radiol Case Rep
August 2021
Department of Radiology, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Br J Neurosurg
October 2023
Department of Neurosurgery, Royal Sussex County Hospital, Brighton, UK.
Background: Spinal dural arteriovenous fistulas (SDAVF) are rare with an incidence of 5-10/million annually. They can be difficult to diagnose causing a delay in treatment with significant morbidity. We describe the first case in the literature of a symptomatic mirror lumbar SDAVF which may go unnoticed due to its unique vascular anatomy.
View Article and Find Full Text PDFEur J Case Rep Intern Med
November 2020
Department of Neurology, Henry Ford Health System, Detroit, Michigan, USA.
Unlabelled: Foix-Alajouanine syndrome is an arteriovenous malformation causing subacute congestive myelopathy that can lead to progressive paraplegia. It typically affects the lower thoracic and lumbosacral levels. Arteriovenous fistula (AVF) leads to increased venous pressure, decreasing the arteriovenous pressure gradient and leading to a decrease in spinal cord perfusion, oedema and necrosis.
View Article and Find Full Text PDFRev Assoc Med Bras (1992)
July 2017
Division of Neurosurgery, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil.
World Neurosurg
December 2017
Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA. Electronic address:
World Neurosurg
October 2017
Department of Neurosurgery, Ronald Reagan UCLA Medical Center, Los Angeles, California, USA; Department of Radiation Oncology, Ronald Reagan UCLA Medical Center, Los Angeles, California, USA; Department of Head and Neck Surgery, Ronald Reagan UCLA Medical Center, Los Angeles, California, USA; Jonsson Comprehensive Cancer Center, Ronald Reagan UCLA Medical Center, Los Angeles, California, USA; Department of Neurosurgery, Harbor-UCLA Medical Center, Torrance, California, USA; Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center, Torrance, California, USA. Electronic address:
World Neurosurg
January 2017
Division of Neurosurgery, Department of Clinical Neurological Sciences, London Health Sciences Centre, University Hospital, London, Ontario, Canada.
No Shinkei Geka
August 2015
Department of Neurosurgery, Kashiwa Hospital, Jikei University School of Medicine.
Foix-Alajouanine syndrome (FAS), also known as congestive myelopathy due to spinal vascular malformations, presents with paraplegia, sensory disturbance of lower limbs, and dysfunction of the bladder and rectum. Although FAS is characterized by a subacute onset of neurological symptoms that may wax and wane over a few years, the progression mechanism remains unclear. We report a case of FAS due to an angiographically occult arteriovenous fistula (AVF) that was diagnosed by an open surgical biopsy and intraoperative indocyanine green (ICG) angiography.
View Article and Find Full Text PDFPol J Radiol
July 2015
Department of Physiology, Baroda Medical College, Vadodara, India.
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.
View Article and Find Full Text PDFGlobal Spine J
December 2014
Department of Radiology, Khoula Hospital, Mina al Fahal, Muscat, Sultanate of Oman.
Spine J
June 2015
Department of Physical Medicine and Rehabilitation, PO Box 24035, Hadassah Hebrew-University Medical Center, Jerusalem, Israel. Electronic address:
Background Context: Spinal dural arteriovenous fistula (SDAVF) is a slow-flow extramedullary vascular lesion affecting primarily the lower thoracic and lumbar spine. The clinical sequela of these vascular changes is progressive myelopathy and severe lower-extremity weakness. Although surgical or embolic treatment of SDAVFs has improved significantly in the last years, the ambiguity of the symptoms may complicate and delay the diagnosis.
View Article and Find Full Text PDFAnn Indian Acad Neurol
July 2013
Department of Neurosurgery, National Neurosciences Centre, Peerless Hospital Complex, II Floor, 360 Panchasayar, Kolkata, West Bengal, India.
Spinal arteriovenous fistulas are rare entities. They often present with congestive myelopathy but are infrequently diagnosed as the cause of the patients' symptoms. Only one such case has been described previously in Indian literature.
View Article and Find Full Text PDFBrain Behav
May 2013
Department of Neurosurgery, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York Buffalo, New York.
We present what is to our knowledge the first reported case of thoracic disc herniation leading to venous congestive myelopathy (VCM), which was clinically and radiographically suggestive of Foix-Alajouanine syndrome (angiodysgenetic necrotizing myelopathy). In addition, we review current concepts in evaluating the etiology of VCM and discuss indications for surgery.
View Article and Find Full Text PDFSurg Neurol Int
July 2013
Department of Neurosurgery, Institute of Clinical Medicine, University of Tsukuba, Ibaraki, Japan.
Background: Venous congestive myelopathy is a progressive myelopathy that is generally caused by a spinal dural arteriovenous fistula.
Case Description: We report a patient with histologically confirmed venous congestive myelopathy without concurrent vascular malformations in radiological and intraoperative findings.
Conclusions: The definitive underlying etiology of this congestive myelopathy was unclear.
Coll Antropol
January 2011
University of Zagreb, Zagreb University Hospital Center, Department of Neurology, Zagreb, Croatia.
Spinal arteriovenous malformations (AVM) have been devided into dural (Type I), intramedullary glomus (Type II), juvenile (Type III), and perimedullary direct arteriovenous fistulae (Type IV). AVMs are usually associated with subacute myelopathy in what has been known as Foix-Alajouanine syndrome. We presented two patients with two intradural spinal arteriovenous malformations associated in what we call Foix-Alajouanine syndrome.
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