1.The Clock Is Ticking – Brain Atrophy in Case of Acute Trauma?
Alexandrina S NIKOVA ; Georgios SIOUTAS ; Konstantinos KOTOPOULOS ; Dimitar GANCHEV ; Varvara CHATZIPAULOU ; Theodossios BIRBILIS
Korean Journal of Neurotrauma 2019;15(2):117-125
OBJECTIVE: Brain atrophy and brain herniation are gaining a lot of attention separately, but a limited amount of studies connected them together, and because of this, we are going to review and examine the subject in the current meta-analysis. METHODS: The authors collected data reporting brain atrophy of alcoholic and schizophrenic cause, as well as data on control patients, all of which was published on MEDLINE between 1996 and 2018. The included 11 articles were processed with a statistical program. RESULTS: We found that the pericerebral space is unequal among the groups, while the intracranial volume is strongly correlated to the biggest foramen of the body. The effect of this inequality, however, is expressed in emergency cases, where the patients with brain atrophy will have more time before the final stage of brain herniation CONCLUSION: The current study raises a controversial issue that requires careful investigation and high attention from the health care personnel.
Alcoholics
;
Atrophy
;
Brain
;
Delivery of Health Care
;
Emergencies
;
Foramen Magnum
;
Humans
;
Research Design
;
Socioeconomic Factors
;
Ticks
2.Arnold-Chiari Type 1 Malformation Mimicking Benign Paroxysmal Positional Vertigo
Young Chul KIM ; Chae Dong YIM ; Hyun Jin LEE ; Dong Gu HUR ; Seong Ki AHN
Journal of the Korean Balance Society 2019;18(3):87-90
Arnold-Chiari malformation type 1 is a congenital disease characterized by herniation of the cerebellar tonsils through the foramen magnum. Most common clinical symptom is pain, including occipital headache and neck pain, upper limb pain exacerbated by physical activity or valsalva maneuvers. Various otoneurological manifestations also occur in patients with the disease, which has usually associated with dizziness, vomiting, dysphagia, poor hand coordination, unsteady gait, numbness. Patients with Arnold-Chiari malformation may develop vertigo after spending some time with their head inclined on their trunk. Positional and down-beating nystagmus are common forms of nystagmus in them. We experienced a 12-year-old female who presented complaining of vertigo related to changes in head position which was initially misdiagnosed as a benign paroxysmal positional vertigo.
Arnold-Chiari Malformation
;
Benign Paroxysmal Positional Vertigo
;
Child
;
Deglutition Disorders
;
Dizziness
;
Female
;
Foramen Magnum
;
Gait Disorders, Neurologic
;
Hand
;
Head
;
Headache
;
Humans
;
Hypesthesia
;
Motor Activity
;
Neck Pain
;
Palatine Tonsil
;
Upper Extremity
;
Valsalva Maneuver
;
Vertigo
;
Vomiting
3.A Rare Case of Subarachnoid Hemorrhage caused by Ruptured Venous Varix Due to Dural Arteriovenous Fistula at the Foramen Magnum Fed Solely by the Ascending Pharyngeal Artery.
Hyunjun KIM ; Yoon Soo LEE ; Ho Jun KANG ; Min Seok LEE ; Sang Jun SUH ; Jeong Ho LEE ; Dong Gee KANG
Journal of Cerebrovascular and Endovascular Neurosurgery 2018;20(2):120-126
Dural arteriovenous fistula (D-AVF) at the foramen magnum is an extremely rare disease entity. It produces venous hypertension, and can lead to progressive cervical myelopathy thereafter. On the other hand, the venous hypertension may lead to formation of a venous varix, and it can rarely result in an abrupt onset of subarachnoid hemorrhage (SAH) when the venous varix is ruptured. The diagnosis of D-AVF at the foramen magnum as a cause of SAH may be difficult due to its low incidence. Furthermore, when the D-AVF is fed solely by the ascending pharyngeal artery (APA), it may be missed if the external carotid angiography is not performed. The outcome could be fatal if the fistula is unrecognized. Herein, we report on a rare case of SAH caused by ruptured venous varix due to D-AVF at the foramen magnum fed solely by the APA. A review of relevant literatures is provided, and the treatment modalities and outcomes are also discussed.
Angiography
;
Arteries*
;
Central Nervous System Vascular Malformations*
;
Diagnosis
;
Fistula
;
Foramen Magnum*
;
Hand
;
Hypertension
;
Incidence
;
Rare Diseases
;
Spinal Cord Diseases
;
Subarachnoid Hemorrhage*
;
Varicose Veins*
4.Rotatory Vertebral Artery Syndrome in Foramen Magnum Stenosis
Ileok JUNG ; Jin Man JUNG ; Moon Ho PARK
Journal of the Korean Balance Society 2018;17(4):167-169
Rotatory vertebral artery syndrome (RVAS) is characterized by recurrent attacks of vertigo, nystagmus, and syncope induced by compression of the vertebral artery during head rotation. A 60-year-old man with atlas vertebrae fracture presented recurrent attacks of positional vertigo. Left-beat, upbeat and count clock-wise torsional nystagmus occurred after lying down and bilateral head roll (HR) showing no latency or fatigue. Magnetic resonance imaging revealed foramen magnum stenosis (FMS) and dominancy of right vertebral artery (VA). The flow of the right VA on transcranial Doppler decreased significantly during left HR. The slower the velocity was, the more the nystagmus was aggravated. RVAS can be evoked by FMS causing compression of the VA. And the nystagmus might be aggravated according to the blood flow insufficiency.
Constriction, Pathologic
;
Deception
;
Fatigue
;
Foramen Magnum
;
Head
;
Humans
;
Magnetic Resonance Imaging
;
Middle Aged
;
Spine
;
Syncope
;
Vertebral Artery
;
Vertigo
5.Extra-Axial Mass in the Foramen Magnum Causing Cervical Compressive Myelopathy as a Complication of Rosai-Dorfman Disease.
Sira CARRASCO-GARCÍA DE LEÓN ; José Manuel FLORES BARRAGÁN ; Fernanda RELEA CALATAYUD ; Osvaldo BALCAZAR ROJAS
Journal of Clinical Neurology 2017;13(3):312-314
No abstract available.
Foramen Magnum*
;
Histiocytosis, Sinus*
;
Spinal Cord Compression*
6.Surgical Outcome of Adult Idiopathic Chiari Malformation Type 1.
Woon Tak YUH ; Chi Heon KIM ; Chun Kee CHUNG ; Hyun Jib KIM ; Tae Ahn JAHNG ; Sung Bae PARK
Journal of Korean Neurosurgical Society 2016;59(5):512-517
OBJECTIVE: The pathophysiology of idiopathic Chiari malformation (CM) type 1 is disturbance of free cerebrospinal fluid (CSF) flow and restoration of normal CSF flow is the mainstay of treatment. Additional migration of the medulla oblongata in pediatric patients is referred to as CM type 1.5, but its significance in adult patients is unknown. This study is to compare surgical outcomes of adult idiopathic CM type 1.5 with that of type 1. METHODS: Thirty-eight consecutive adult patients (M : F=11 : 27; median, 33.5; range, 18–63) with syringomyelia due to idiopathic CM type 1 were reviewed. Migration of the medulla oblongata was noted in 13 patients. The modified McCormick scale (MMS) was used to evaluate functional status before and one year after surgery. All patients underwent foramen magnum decompression and duroplasty. Factors related to radiological success (≥50% decrease in the diameter of the syrinx) were investigated. The follow-up period was 72.7±55.6 months. RESULTS: Preoperative functional status were MMS I in 11 patients and MMS II in 14 of CM type 1 and MMS I in 8 and II in 5 of CM type 1.5. Of patients with MMS II, 5/14 patients in group A and 3/5 patients in group B showed improvement and there was no case of deterioration. Radiological success was achieved in 32 (84%) patients and restoration of the cisterna magna (p=0.01; OR, 46.5) was the only significant factor. CONCLUSION: Migration of the medulla oblongata did not make a difference in the surgical outcome when the cisterna magna was restored.
Adult*
;
Arachnoid
;
Cerebrospinal Fluid
;
Cisterna Magna
;
Decompression
;
Follow-Up Studies
;
Foramen Magnum
;
Humans
;
Medulla Oblongata
;
Rhombencephalon
;
Syringomyelia
7.Type I Chiari malformation presenting orthostatic syncope who treated with decompressive surgery.
Hyun Seung SHIN ; Jeong A KIM ; Dong Seok KIM ; Joon Soo LEE
Korean Journal of Pediatrics 2016;59(Suppl 1):S149-S151
Chiari malformations are a congenital anomaly of the hindbrain. The most common, Chiari malformation type I (CM-I), is characterized by herniation of the cerebellar tonsils extending at least 3 mm below the plane of the foramen magnum. Consequently, CM-I is associated with hydrocephalus and symptoms involving compression of the cervicomedullary junction by ectopic tonsils. Several studies have reported the clinical symptoms associated with CM-I, including suboccipital headache, weakness in the upper extremities, facial numbness, loss of temperature sensation, ataxia, diplopia, dysarthria, dysphagia, vomiting, vertigo, nystagmus, and tinnitus. Syncope is one of the rarest presentations in patients with CM-I. There are many hypotheses regarding the causes of syncope in patients with CM-I; however, the mechanisms are not clearly understood. Although surgical decompression for CM-I in patients with syncope has yielded good clinical results in some studies, such cases are rarely reported. We report a case of orthostatic syncope in a patient with CM-I who was treated with surgical intervention.
Arnold-Chiari Malformation
;
Ataxia
;
Decompression, Surgical
;
Deglutition Disorders
;
Diplopia
;
Dysarthria
;
Foramen Magnum
;
Headache
;
Humans
;
Hydrocephalus
;
Hypesthesia
;
Hypotension, Orthostatic
;
Palatine Tonsil
;
Rhombencephalon
;
Sensation
;
Syncope*
;
Tinnitus
;
Upper Extremity
;
Vertigo
;
Vomiting
8.Treatment of Syringomyelia due to Chiari Type I Malformation with Syringo-Subarachnoid-Peritoneal Shunt.
Akin AKAKIN ; Baran YILMAZ ; Murat Sakir EKSI ; Turker KILIC
Journal of Korean Neurosurgical Society 2015;57(4):311-313
Chiari type I malformation is a tonsillar herniation more than 3 mm from the level of foramen magnum, with or without concurrent syringomyelia. Different surgical treatments have been developed for syringomyelia secondary to Chiari's malformations: craniovertebral decompression with or without plugging of the obex, syringo-subarachnoid, syringo-peritoneal, and theco-peritoneal shunt placement. Shunt placement procedures are useful for neurologically symptomatic large-sized syrinx. In this paper, authors define the first successful treatment of a patient with syringomyelia due to Chiari type I malformation using a pre-defined new technique of syringo-subarachnoid-peritoneal shunt with T-tube system.
Decompression
;
Encephalocele
;
Foramen Magnum
;
Humans
;
Syringomyelia*
9.Foramen Magnum Decompression and Duraplasty is Superior to Only Foramen Magnum Decompression in Chiari Malformation Type 1 Associated with Syringomyelia in Adults.
Mehmet Sabri GURBUZ ; Mehmet Zafer BERKMAN ; Emre UNAL ; Elif AKPINAR ; Sevki GOK ; Metin ORAKDOGEN ; Salih AYDIN
Asian Spine Journal 2015;9(5):721-727
STUDY DESIGN: Retrospective cohort study. PURPOSE: To compare surgical results of foramen magnum decompression with and without duraplasty in Chiari malformation type 1 (CM-1) associated syringomyelia (SM). OVERVIEW OF LITERATURE: The optimal surgical treatment of CM-1 associated with SM is unclear. METHODS: Twenty-five cases of CM-1 with SM were included. There were 12 patients (48%) in the non-duraplasty group and 13 patients (52%) in the duraplasty group. The rate of improvement, state of postoperative SM size, amount of tonsillar herniation, preoperative symptom duration, complications and reoperation rates were analysed. RESULTS: The rate of clinical improvement was significantly higher with duraplasty (84.6%) than without (33.3%, p <0.05). The rate of postoperative syrinx regression was significantly higher in the duraplasty group (84.6%) than in the non-duraplasty group (33.3%, p <0.05). One case in the duraplasty group needed a reoperation compared with five cases in the non-duraplasty group (p =0.059). CONCLUSIONS: Duraplasty is superior to non-duraplasty in CM-1 associated with SM despite a slightly higher complication rate.
Adult*
;
Cohort Studies
;
Decompression*
;
Encephalocele
;
Foramen Magnum*
;
Humans
;
Reoperation
;
Retrospective Studies
;
Syringomyelia*
10.Foramen Magnum Meningioma: Some Anatomical and Surgical Remarks through Five Cases.
Asian Spine Journal 2015;9(1):54-58
STUDY DESIGN: Foramen magnum meningioma foramen magnum meningioma (FMM) represents 2% all of meningiomas. The clinical symptomatology is usually insidious and consists of headache, neck pain and hypoesthesia in C2 dermatome. Because of their location, the management is challenging. PURPOSE: The purpose of this paper is to present our experience in the surgery of FMM. OVERVIEW OF LITERATURE: Since 1938, numerous series have been published but they are very heterogeneous with high variability of location and surgical approaches. METHODS: During two years, we operated 5 patients with FMM. All the patients had magnetic resonance imaging (MRI) with angio-MRI to study the relationship between tumour and vertebral artery (VA). In all the cases, we used prone position. RESULTS: In one case, considering the tumour localization (posterior and pure intradural) the tumour was removed via a midline suboccipital approach with craniotomy and C1-C2 laminectomy. In all other cases, meningiomas were posterolateral (classification of George) with extradural extension in one case. In all cases, VA was surrounded by tumor. So, we opted for a modified postero-lateral approach with inverted L incision, craniotomy and C1-C2 laminectomy without resect occipital condyle. Epidural part of VA was identified and mobilized laterally. Once VA was identified we opened dura mater and began to remove the tumour. CONCLUSIONS: In this paper, we present five cases of operated FMM, describe our approaches, the reason of each approach and propose some surgical remarks.
Cranial Fossa, Posterior
;
Craniotomy
;
Dura Mater
;
Foramen Magnum*
;
Headache
;
Humans
;
Hypesthesia
;
Laminectomy
;
Magnetic Resonance Imaging
;
Meningioma*
;
Neck Pain
;
Neurosurgery
;
Prone Position
;
Vertebral Artery

Result Analysis
Print
Save
E-mail