Chiari type I malformation discovered through a glossopharyngeal neuralgia.

Glossopharyngeal neuralgia is a rare disease whose initial treatment is pharmacological. When medical therapy is not effective, different surgical options are available including stereotactic radiosurgery, microvascular decompression or nerve section. It is reported a case of a 26-year-old female with glossopharyngeal neuralgia and Chiari malformation. This rare type of neuralgia sometimes is associated with an abnormality of the cranio-cervical junction. It was performed a posterior fossa expansion with duraplasty and microvascular decompression. The patient showed a complete disappearance of the pain, with no need of tonsil resection.

[Bilateral chronic subdural haematoma: Analysis of a series of 190 patients]. / Hematoma subdural crónico bilateral: análisis de una serie de 190 pacientes.

OBJECTIVE: The aim of this study is to analyse the clinical findings and surgical results in a series of patients with bilateral chronic subdural haematoma (BCSDH), and compare the results with a series of patients treated for unilateral chronic subdural haematoma (UCSDH). PATIENTS AND METHODS: A retrospective study was performed on 1523 patients diagnosed and surgically treated for chronic subdural haematoma over a period of 30 years. Patients were divided into 2 groups: The study group consisting of 190 patients operated on for a BCSDH and the control group consisting of patients operated on for an UCSDH (1333 cases). RESULTS: The patient series included 126 males (66.3%) and 64 females (33.7%), with a mean age at diagnosis of 74.8±10.2. The control group consisted of 870 males (65.2%) and 463 women (34.8%), with a mean age of 73.2±12.1. The most common presenting symptoms was cognitive impairment in 63 patients (33.2%) with BCSDH and 416 (29.5%) with UCSDH. Recurrence rates were 9.4% (18 patients) and 5.7% (77 patients) in unilateral and bilateral haematomas, respectively. The mortality was 10 patients (5.2%) with BCSDH and 55(4%) with UCSDH. Factors significantly related to recurrence in the univariate analysis were being male (P=.040), anticoagulant/antiplatelet therapy (P=.032), and poor neurological status at admission (P=.039). CONCLUSIONS: This study indicates that BCSDH is more frequent in males, and the most common presentation is headache. The most important factors influencing recurrences are being male, intake of anticoagulant-antiaggregant drugs, and worse clinical status at admission.

La fenestración endoscópica como tratamiento de los quistes aracnoideos intracraneales / Endoscopic fenestration to treat intracranial arachnoid cysts

Los quistes aracnoideos son lesiones quísticas con un contenido similar al líquido cefalorraquídeo. Representan alrededor del 1% de todas las lesiones expansivas intracraneales y son característicos de las dos primeras décadas de la vida, aunque en ocasiones se diagnostican en adultos. Presentamos una revisión sobre nuestra experiencia en el tratamiento quirúrgico de quistes aracnoideos intracraneales. Material y métodos: Realizamos una revisión de 103 niños menores de 16 años intervenidos quirúrgicamente por un quiste aracnoideo intracraneal en los que se empleó una derivación cistoperitoneal en 53 casos; una craneotomía con fenestración del quiste, en 44 niños, y 11 casos con fenestración por vía endoscópica. Resultados: En todos los pacientes se consiguió alivio de la sintomatología y reducción o desaparición del quiste. Se presentaron 21 complicaciones quirúrgicas: 12 en los pacientes tratados con válvula (22.6%) y 9 en los sometidos a craneotomía (20.4%). La mortalidad de la serie fue de dos casos (1.95%). Discusión y conclusiones: El tratamiento de los quistes aracnoideos intracraneales debe reservarse exclusivamente para los casos sintomáticos. La craneotomía con fenestración de las membranas y la derivación cistoperitoneal son buenas opciones de tratamiento, ya que consiguen un buen control, tanto del tamaño del quiste como en la resolución de la sintomatología. La mejor opción terapéutica es en la actualidad la fenestración endoscópica, ya que se trata de una técnica poco invasiva, que no requiere la implantación de materiales extraños y cuyo índice de complicaciones y recidivas es relativamente bajo...

[Chronic calcified subdural haematoma: armoured brain]. / Hematoma subdural cronico calcificado: cerebro blindado.

TITLE: Hematoma subdural cronico calcificado: cerebro blindado.

[Cervical lymphatic metastasis of an intracranial meningioma]. / Metastasis linfatica cervical de un meningioma intracraneal.

INTRODUCTION: Meningioma is the most common primary intracranial tumor, accounting for around a third of all primary brain tumor. In most cases, they are benign neoplasms that start in the cells of the arachnoid mater. Meningiomas are typically slow growing; however they can metastasize in 0.1% of all patients. CASE REPORT: A 45-years-old woman was admitted with a four weeks history of a painless enlarging mass in the right side of his neck and present in a MRI recurrence of the frontal meningioma surgically removed four times over the last 18 years. The patient underwent a complete removal of lesions and the microscopic observation showed an anaplastic meningioma in both (grade III of the World Health Organization). CONCLUSIONS: Metastatic meningioma is a rare cause of neck mass, but should be considered in any patient with a history of meningioma, especially if the tumor has histological features of malignant behavior. The present case demonstrates the aggressive biologic potential of an intracranial meningioma, with potential for distant spread and lymphatic invasion.

[Spontaneous intracranial hypotension syndrome: two case reports]. / Sindrome de hipotension intracraneal espontanea: presentacion de dos casos.

INTRODUCTION. Spontaneous intracranial hypotension is caused by spontaneous spinal cerebrospinal fluid leaks and is known for causing orthostatic headaches, and a wide variety of associated symptoms have been reported. CASE REPORTS. We described two cases with spontaneous intracranial hypotension, treated in a short period of time, who presented with orthostatic headache and the neuroimaging studies showed subdural collections. Both patients were diagnosed of spinal cerebrospinal fluid leaks and treated with blood patches. CONCLUSIONS. Although intracranial hypotension is not an uncommon pathology, it usually presents diagnostic problems due to the diversity of symptoms that can occur. MRI is essential for the diagnosis by showing enhancement of the pachymeninges following administration of gadolinium and to prove the cerebrospinal fluid leak are useful spinal MRI, the computerized tomography myelography and the radionuclide cisternography. If conservative treatment falls, the epidural blood patch is the initial treatment of choice, reserving surgery for patients with persistent symptoms.

[Primary prophylaxis of early seizures after surgery of cerebral supratentorial tumors: Group for the Study of Functional-Sterotactic Neurosurgery of The Spain Society of Neurosurgery recommendations]. / Control de las crisis epilépticas durante el postoperatorio inmediato de los tumores cerebrales supratentoriales: recomendaciones del Grupo de Neurocirugía Funcional y Estereotáctica de la Sociedad Española de Neurocirugía.

Our review of the literature is basically focused on the primary prophylaxis of early seizures after surgery of cerebral supratentorial tumors, with the aim of suggesting several recommendations in medical antiepileptic treatment to avoid this kind of seizures which occur immediately after surgery. In conclusion, it is recommended to provide criteria for prophylaxis of early seizures after surgery of cerebral supratentorial tumors. It́s recommended a one week treatment with antiepileptic drugs in patients who didnt have seizures jet, starting immediately after the surgical treatment. If seizures appear during progress of the disease, a large period treatment will be needed. Preferred antiepileptic treatment is intravenous and with a low interactions profile. Levetiracetam, followed by valproic acid seem to be most appropriated drugs due to their properties and protective effects, particularly for our patients requirements. These recommendations are considered a general proposal to effective clinical management of early seizures after surgery, not taking into account the single circumstances of our patients. Always, clinical features of the patients could modify even significantly these guides in the benefit of each patient.

[Primary cranial vault lymphoma]. / Linfoma primario de la calota craneal.

INTRODUCTION: Primary bone lymphomas account for 3-7% of all malignant bone tumours and less than 2% of lymphomas in adults. Having the cranial vault as their primary location is very infrequent. CASE REPORT: A 59-year-old female who presented a painful tumour on the cranial vault which, following radical surgical removal, was found to be an ALK-negative primary large-cell lymphoma. CONCLUSIONS: After reviewing the literature we believe that this is the first case of cranial vault lymphoma in which the translocation of the ALK protein-producing gene has been studied.

[Tumours of the nerve root sheath in the spine]. / Tumores de la vaina de las raíces nerviosas espinales.

INTRODUCTION: Spinal schwannomas account for about 30% of intradural spinal cord tumors in adults. More are solitary tumors, which can occur throughout the spinal canal. The multiple form of neurofibromas is known as von Recklinghausen disease. AIM. To analyze clinical and radiologic characteristics, treatment and evolution of patients with spinal nerve sheath tumor. PATIENTS AND METHODS: This was a retrospective study in a series of patients treated surgically of spinal schwannomas during 25 years. The following variables were evaluated: gender, age, symptomatology, radiological findings, localization, surgical findings and results. RESULTS: We treated 35 male and 33 female with a mean age of 55 years (range: 12-76 years).The most common pre-surgical symptom was local or radicular pain in 55 patients (80.8%). In 49 cases (66.2%), the tumor was sited in the lumbosacral, in 15 cases (20.2%) in the dorsal tract, and in 10 cases (13.6%) in the cervical tract. Total removal was achieved in 70 cases (94.5%) and subtotal resection in 4 (5.5%). 66 tumors (89.1%) were schwannomas and the other 8 cases (10.9%) neurofibromas. CONCLUSIONS: Tumors of the spinal root sheaths can occur at any level of the spinal canal. Most patients present with local and/or radicular pain and in most cases total resection its possible with good functional recovery.

Lumbar synovial cyst in an adolescent: case report.

BACKGROUND: Spinal extradural cysts are a rare cause of spinal cord or nerve root compression which tends to occur in the elderly but rarely reported in the under 20s. HISTORY: A 14-year-old girl with a 9-month history of left radicular pain was found to have an intraspinal cystic lesion causing radicular compression. MRI showed a 1.1-cm extradural cystic lesion with a low signal on T1 and high signal on T2-weighted images lying in the spinal canal at the L4 vertebral body level. The patient underwent an L4 hemi-laminectomy and excision of a synovial cyst, and the radicular pain completely regressed. DISCUSSION: We discuss the pathogenesis, radiological techniques, and management of synovial cyst in a pediatric patient. CONCLUSION: Intraspinal ganglion cysts are extremely rare in children and only two other cases have been reported previously. They are benign lesions, frequently presenting radiculopathy, and should be considered in the differential diagnosis, in patients with low back pain and radiculopathy.

Lumbar synovial cyst in a adolescence: case report.

BACKGROUND: Spinal extradural cysts are a rare cause of spinal cord or nerve root compression which tends to occur in the elderly but rarely reported in the under 20s. HISTORY: A 14-year-old girl with a 9-month history of left radicular pain was found to have an intraspinal cystic lesion causing radicular compression. Magnetic resonance imaging showed a 1.1-cm extradural cystic lesion with a low signal on T1-weighted images and high signal on T2-weighted images lying in the spinal canal at the L4 vertebral body level. The patient underwent an L4 hemilaminectomy and excision of a synovial cyst, and the radicular pain completely regressed. DISCUSSION: We discuss the pathogenesis, radiological techniques and management of synovial cyst in a paediatric patient CONCLUSION: Intraspinal ganglion cysts are extremely rare in children and only two other cases have been reported previously. They are benign lesions, frequently presenting radiculopathy, and should be considered in the differential diagnosis in patients with low back pain and radiculopathy.