1.Spontaneous Hematomyelia: Case Report.
Jeong Hyun HWANG ; Joo Kyung SUNG ; Sung Kyoo HWANG ; In Suk HAMM ; Yeun Mook PARK ; Seung Lae KIM
Journal of Korean Neurosurgical Society 2000;29(3):411-419
No abstract available.
Spinal Cord Vascular Diseases*
2.Posterior Thoracic Spinal Cord Artery Infarction.
Sang Don HAN ; Ha Young SHIN ; Sook Keun SONG ; Hae Sun KO ; Seung Min KIM ; Il Nam SUNWOO
Journal of the Korean Neurological Association 2005;23(5):718-720
No abstract available.
Arteries*
;
Infarction*
;
Spinal Cord Vascular Diseases
;
Spinal Cord*
3.Intervention of Vascular Diseases of the Spine.
Neurointervention 2008;3(1):7-15
Spinal AVMs consist of various congenital and acquired vascular diseases which may result in spinal neurological deficit. The anigoarchitecture of these diseases are often difficult to analyze while the risk of treatment is high due to the eloquence of the spinal cord. Recently, the understanding of the anatomy of the spinal vessels, the characteristics of the spinal vascular diseases, and the efficacy of endovascular management has grown. The purpose of this review is to introduce the latest understanding of these diseases and its management strategies.
Arteriovenous Fistula
;
Embolization, Therapeutic
;
Spinal Cord
;
Spinal Cord Vascular Diseases
;
Spine*
;
Vascular Diseases*
;
Vascular Malformations
4.Posterior Spinal Artery Infarction Presenting as a Sensory Ataxia.
Jeewon SUH ; So Young PARK ; Sung Bae PARK ; Yong Seok LEE
Journal of the Korean Neurological Association 2016;34(5):412-414
No abstract available.
Arteries*
;
Ataxia*
;
Infarction*
;
Spinal Cord Vascular Diseases
5.Spontaneous Thoracic Hematomyelia A Case Report.
Dong Won KIM ; Tae Sung KIM ; Kwang Myung KIM ; Gook Ki KIM ; Bong Arm RHEE ; Won LEEM
Journal of Korean Neurosurgical Society 1983;12(4):721-724
Spontaneous hematomyelia is an acute expanding lesion by the hemorrhage within the substance of the located primarily in the gray matter. It is necessary to have urgent operation to preserve the remainding cord function. We are reporting a rare case of spontaneous hematomyelia extending from T-8 to T-10 of unknown cause of which transverse symptoms have largely subsided after surgical evacuation of the liquefied hematoma.
Hematoma
;
Hemorrhage
;
Spinal Cord Vascular Diseases*
6.A Case of Spontaneous Hematomyelia.
Sung Gyun PARK ; Keun Bae RHA ; Chul Koo JUNG ; Tae Hoon CHO ; Un Sung CHOI
Journal of Korean Neurosurgical Society 1982;11(3):347-351
This is a report of 23 year old soldier who developed sudden onset of flaccid paraplegia and loss of all sensory modalited below the level of T4. The clinical entities of hematomyelia were sudden onset of pain, repidly developing pyramidal signs and paraplegia. The mainly involving sites of this disease were cervical and thoracic regions. The causative factors were hemorrhagic diasthesis, vascular malformation and inflammatory process as well as trauma and neoplasms affecting the spinal cord. We experienced a case of hematomyelia which did not combine with vascular anomaly, inflammatory process, hemophilia or trauma history.
Hemophilia A
;
Humans
;
Military Personnel
;
Paraplegia
;
Spinal Cord
;
Spinal Cord Vascular Diseases*
;
Vascular Malformations
;
Vascular Neoplasms
;
Young Adult
7.Novalis Stereotactic Radiosurgery for Spinal Dural Arteriovenous Fistula.
Kyoung Su SUNG ; Young Jin SONG ; Ki Uk KIM
Journal of Korean Neurosurgical Society 2016;59(4):420-424
The spinal dural arteriovenous fistula (SDAVF) is rare, presenting with progressive, insidious symptoms, and inducing spinal cord ischemia and myelopathy, resulting in severe neurological deficits. If physicians have accurate and enough information about vascular anatomy and hemodynamics, they achieve the good results though the surgery or endovascular embolization. However, when selective spinal angiography is unsuccessful due to neurological deficits, surgery and endovascular embolization might be failed because of inadequate information. We describe a patient with a history of vasospasm during spinal angiography, who was successfully treated by spinal stereotactic radiosurgery using Novalis system.
Angiography
;
Central Nervous System Vascular Malformations*
;
Hemodynamics
;
Humans
;
Radiosurgery*
;
Spinal Cord Diseases
;
Spinal Cord Ischemia
8.Recurrent Myelopathy in a Patient with Klippel-Trenaunay Syndrome.
Yue Kyung KIM ; Young In EOM ; In Soo JOO
Korean Journal of Clinical Neurophysiology 2015;17(2):76-79
Klippel-Trenaunay syndrome (KTS) is a rare congenital malformation syndrome involving blood and lymph vessels, which is characterized by triad of cutaneous hemangioma, venous varicosities, and overgrowth of the affected limbs. Because vascular malformation in KTS can be located anywhere except the face and brain, the clinical presentation could be extremely variable. But there are only rare case reports that KTS is associated with spinal cord lesion. We report a case of recurrent myelopathy in a patient with KTS.
Brain
;
Extremities
;
Hemangioma
;
Humans
;
Klippel-Trenaunay-Weber Syndrome*
;
Spinal Cord
;
Spinal Cord Diseases*
;
Vascular Malformations
9.A case Report of a Spontaneous cervical Hematomyelia.
Dong Jo LEE ; Young Jin YUN ; Duk Hong MOON ; Eun Hi SA ; Seon Chool HWANG ; Seong Uk HONG
Journal of the Korean Neurological Association 1995;13(2):383-386
The spontaneous hematomyelia is an uncommon event and its predisposing conditions are vascular malformation, syringomyelia, pregnancy and delivery, angioma, hemophilia, anticoagulant therapy, etc. We have recently experienced the patient with spontaneous onset and resolving hematomyelia in the cervical spinal cord. A 30-year-old male patient with non-traumatic spinal shock was evaluated. On MRI, a hematomyelia along cervical spi-nal cord was revealed. A suspicious AV malformation was noticed at C3-4 level. Fol-low-up MRIs showed spontaneous resolution of the hematoma.
Adult
;
Hemangioma
;
Hematoma
;
Hemophilia A
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Pregnancy
;
Shock
;
Spinal Cord
;
Spinal Cord Vascular Diseases*
;
Syringomyelia
;
Vascular Malformations
10.Giant Thoracic Spinal Arteriovenous Fistula with Cord Compression: A Case Report.
Seung Rim PARK ; Kyu Jung CHO ; Young Hyun YUN ; Moon LEE ; Seok Bong KANG ; Hae Wook PYUN ; Se Jin JUNG
The Journal of the Korean Orthopaedic Association 2009;44(2):261-265
A spinal arteriovenous fistula is a rare vascular disease that is characterized by abnormal connections between the vertebral artery or its branches and the neighboring veins. Bruit and back pain are common symptoms related to the fistula. Spinal cord dysfunction can also occur as a result of blood flow steal, venous hypertension, or mechanical compression of the nerve roots and spinal cord. We report a huge arteriovenous fistula in the spinal canal at the thoracic vertebra, which was characterized by a large azygous vein connected to the epidural vein causing osteolysis on the vertebral body and spinal cord compression symptoms. Staged embolization was performed using 80 coils.
Arteriovenous Fistula
;
Back Pain
;
Fistula
;
Hypertension
;
Osteolysis
;
Spinal Canal
;
Spinal Cord
;
Spinal Cord Compression
;
Spine
;
Vascular Diseases
;
Veins
;
Vertebral Artery