Enxaqueca é uma cefaleia primária caracterizada por dores de cabeça recorrentes, de moderadas a graves. Geralmente a dor de cabeça afeta apenas um dos lados, é de natureza pulsátil e dura entre 2 e 72 horas. Os principais sintomas associados são náuseas, vómitos e sensibilidade à luz, ao som e ao odor. A dor geralmente agrava-se com a atividade física. Cerca de um terço das pessoas com enxaqueca veem uma aura – uma perturbação transitória visual, sensorial, motora ou na linguagem, que antecede a ocorrência de uma enxaqueca. Em alguns casos, a aura pode ocorrer sem ser seguida por enxaqueca.
Introdução
O que você precisa saber de cara
Neoplasias que afetam nervos cranianos e espinhais, manifestando-se com sintomas neurológicos agudos, fraqueza muscular, alterações visuais e, em alguns casos, puberdade precoce e escoliose.
Escala de raridade
<1/50kMuito rara
1/20kRara
1/10kPouco freq.
1/5kIncomum
1/2k
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Sinais e sintomas
O que aparece no corpo e com que frequência cada sintoma acontece
Partes do corpo afetadas
+ 38 sintomas em outras categorias
Características mais comuns
Os sintomas variam de pessoa para pessoa. Abaixo estão as 92 características clínicas mais associadas, ordenadas por frequência.
Linha do tempo da pesquisa
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Genética e causas
O que está alterado no DNA e como passa nas famílias
Genes associados
6 genes identificados com associação a esta condição.
Serine protease with a variety of targets, including extracellular matrix proteins such as fibronectin. HTRA1-generated fibronectin fragments further induce synovial cells to up-regulate MMP1 and MMP3 production. May also degrade proteoglycans, such as aggrecan, decorin and fibromodulin. Through cleavage of proteoglycans, may release soluble FGF-glycosaminoglycan complexes that promote the range and intensity of FGF signals in the extracellular space. Regulates the availability of insulin-like g
Cell membraneSecretedCytoplasm, cytosol
Probable regulator of the Hippo/SWH (Sav/Wts/Hpo) signaling pathway, a signaling pathway that plays a pivotal role in tumor suppression by restricting proliferation and promoting apoptosis. Along with WWC1 can synergistically induce the phosphorylation of LATS1 and LATS2 and can probably function in the regulation of the Hippo/SWH (Sav/Wts/Hpo) signaling pathway. May act as a membrane stabilizing protein. May inhibit PI3 kinase by binding to AGAP2 and impairing its stimulating activity. Suppress
Cell projection, filopodium membraneCell projection, ruffle membraneNucleusCytoplasm, perinuclear regionCytoplasmic granuleCytoplasm, cytoskeleton
Schwannomatosis, vestibular
An autosomal dominant neoplasia syndrome characterized by the development of multiple benign nerve sheath tumors called schwannomas, particularly affecting the vestibular nerve. Affected individuals usually present with bilateral vestibular schwannomas but can have schwannomas on other cranial, spinal, and peripheral/cutaneous nerves. Meningiomas are common, whereas 20 to 35% of affected individuals develop intramedullary spinal cord tumors called ependymomas. The condition is also characterized by several ophthalmic features such as lenticular opacities, retinal hamartoma, epiretinal membranes.
Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex that mediates ubiquitination of Ras (K-Ras/KRAS, N-Ras/NRAS and H-Ras/HRAS) (PubMed:30442762, PubMed:30442766, PubMed:30481304). Is a negative regulator of RAS-MAPK signaling that acts by controlling Ras levels and decreasing Ras association with membranes (PubMed:30442762, PubMed:30442766, PubMed:30481304)
Endomembrane systemRecycling endosomeGolgi apparatus
Glioma
Gliomas are benign or malignant central nervous system neoplasms derived from glial cells. They comprise astrocytomas and glioblastoma multiforme that are derived from astrocytes, oligodendrogliomas derived from oligodendrocytes and ependymomas derived from ependymocytes.
Core component of the BAF (hSWI/SNF) complex. This ATP-dependent chromatin-remodeling complex plays important roles in cell proliferation and differentiation, in cellular antiviral activities and inhibition of tumor formation. The BAF complex is able to create a stable, altered form of chromatin that constrains fewer negative supercoils than normal. This change in supercoiling would be due to the conversion of up to one-half of the nucleosomes on polynucleosomal arrays into asymmetric structures
Nucleus
Rhabdoid tumor predisposition syndrome 1
A familial cancer syndrome predisposing to renal or extrarenal malignant rhabdoid tumors and to a variety of tumors of the central nervous system, including choroid plexus carcinoma, medulloblastoma, and central primitive neuroectodermal tumors. Rhabdoid tumors are the most aggressive and lethal malignancies occurring in early childhood.
FAD-dependent monooxygenase required for two non-consecutive steps during ubiquinone biosynthesis (PubMed:26260787, PubMed:38425362). Required for the C5-ring hydroxylation during ubiquinone biosynthesis by catalyzing the hydroxylation of 4-hydroxy-3-(all-trans-decaprenyl)benzoic acid to 3,4-dihydroxy-5-(all-trans-decaprenyl)benzoic acid (PubMed:26260787, PubMed:38425362). Also acts downstream of COQ4, for the C1-hydroxylation during ubiquinone biosynthesis by catalyzing the hydroxylation of 2-m
Mitochondrion inner membraneGolgi apparatusCell projection
Coenzyme Q10 deficiency, primary, 6
An autosomal recessive disorder characterized by onset in infancy of severe progressive nephrotic syndrome resulting in end-stage renal failure and sensorineural deafness. Renal biopsy usually shows focal segmental glomerulosclerosis.
Adapter protein involved in invadopodia and podosome formation, extracellular matrix degradation and invasiveness of some cancer cells (PubMed:27789576). Binds matrix metalloproteinases (ADAMs), NADPH oxidases (NOXs) and phosphoinositides. Acts as an organizer protein that allows NOX1- or NOX3-dependent reactive oxygen species (ROS) generation and ROS localization. In association with ADAM12, mediates the neurotoxic effect of amyloid-beta peptide
CytoplasmCell projection, podosome
Medicamentos aprovados (FDA)
2 medicamentos encontrados nos registros da FDA americana.
Variantes genéticas (ClinVar)
2,315 variantes patogênicas registradas no ClinVar.
Vias biológicas (Reactome)
14 vias biológicas associadas aos genes desta condição.
Diagnóstico
Os sinais que médicos procuram e os exames que confirmam
Tratamento e manejo
Remédios, cuidados de apoio e o que precisa acompanhar
Onde tratar no SUS
Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)
🇧🇷 Atendimento SUS — Tumor dos nervos cranianos e espinhais
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Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.
Pesquisa ativa
Ensaios clínicos abertos e novidades científicas recentes
Pesquisa e ensaios clínicos
Nenhum ensaio clínico registrado para esta condição.
Publicações mais relevantes
Telovelar Approach for Fourth-Ventricular Epidermoid Cyst: Anatomical Respect, Functional Recovery, and Long-Term Stability.
Background and Clinical Significance: Fourth-ventricular epidermoid cysts are rare intracranial lesions. They account for fewer than 1% of all primary brain tumors. Fourth-ventricular epidermoid cysts grow slowly because they are closely related to brainstem, cerebellum, and major blood vessels, so their treatment requires special caution. Because the cyst capsule attaches to functionally sensitive locations, complete removal is usually not possible without compromising some aspect of brain or spinal cord function. Surgical decision-making always involves weighing the need to remove the entire cyst against the potential loss of function of the affected area. The following case study describes how a patient was treated with a focus on the relationship between the cyst and surrounding anatomy, allowing for successful decompression with minimal risk to the patient's neurologic status. Case Presentation: A young adult female patient was hospitalized with progressive truncal ataxia, disequilibrium and occipital headache accompanied by papilledema. Her physical examination disclosed significant dysfunction of the midline cerebellar region (SARA score = 18/40, ICARS score = 42/100), gaze-evoked nystagmus and bilaterally elevated grade II papilledema. MRI and MRA demonstrated a large, lobulated, nonenhancing, avascular mass located within the fourth ventricle, encroaching upon the dorsal medulla and obstructing both the foramen of Magendie and foramina of Luschka-findings typical of an epidermoid cyst. Microsurgical resection was accomplished via a median suboccipital craniectomy using a telovelar approach along the embryonic cerebellomedullary fissure to protect the integrity of the vermis and brainstem. The cyst contained layers of keratin embedded in a thin, translucent capsule. The capsule was carefully dissected away from the floor of the fourth ventricle. A very narrow band of capsule attached to the rhomboid fossa was intentionally spared to avoid damaging the cranial nerves. The patient had normal cerebrospinal fluid circulation restored and normal ventricular pulsation observed during surgery. Histopathology confirmed a benign epidermoid cyst consisting of keratinizing stratified squamous epithelium containing cholesterol clefts and laminated keratin debris. After surgery, the patient exhibited continuous neurological improvement including restoration of balance, disappearance of her headaches, and normalization of ocular pursuit. Sequential imaging studies were conducted post-operatively at one week, one month, three months, five months, and seven months to document stable decompression of the fourth ventricle, re-expansion of the fourth ventricle, and no evidence of cyst recurrence. Post-operative course was uncomplicated and the patient has remained free of symptoms and fully independent functionally at most recent follow-up. Conclusions: This case illustrates that when anatomically oriented, "maximal safe resection" can result in long-lasting decompression and clinically meaningful improvement in neurological function in patients with fourth-ventricular epidermoid cysts. Restoration of the patient's natural cerebrospinal fluid pathway and preservation of neural interface relationships is more beneficial than pursuing aggressive removal of the cyst capsule. Although the risk of late recurrence is present even after nearly total removal, continuous radiologic monitoring is necessary to identify any recurrence. These experiences illustrate that with the principles of surgical restraint and anatomical guidance, there can be a balance between long-term stability and low operative risk. The spinal accessory nerve (SAN, 11th cranial nerve, CN XI) is essential for neck and shoulder movement, as it innervates the sternocleidomastoid (SCM) and trapezius muscles through its spinal root. CN XI also contributes indirectly to intrinsic laryngeal musculature function via its cranial component, which arises from the nucleus ambiguus and merges with the vagus nerve (CN X) to supply motor fibers to the larynx, pharynx, and soft palate. While the SAN is primarily a motor nerve, recent evidence suggests it contains minor sensory (nociceptive) fibers that may play a limited role in sensory afferents to the trapezius and SCM. However, these muscles receive most of their sensory innervation from cervical spinal nerves C2 to C4. Minor injury can occur with daily movements or behaviors that exceed the elastic capacity of the SAN, such as excessive stretching or carrying heavy weights. However, the nerve may be severely damaged during neck tumor mass removal, particularly when the blood supply is compromised or partial resection is performed. In certain cases, removal of this nerve is accomplished to compensate for a peripheral nerve lesion, transfer it where electrical activity is absent, and attempt to restore limb function. Understanding the anatomy and function of CN XI allows clinicians to prevent iatrogenic injury, accurately localize lesions, and implement targeted rehabilitation strategies to preserve or restore motor function.
Quadrangular space schwannoma affecting the axillary nerve.
Schwannomas are benign neural tumors originating primarily from Schwann cells associated with cranial and spinal nerves, which are a well-known medical entity. However, their occurrence in the extremities, particularly those involving the axillary nerve, is a rare phenomenon with limited literature documentation. We present a case of a 29-year-old male who complained of painful swelling in the posterior shoulder region. Further diagnostic investigations, including ultrasound and magnetic resonance imaging, unveiled the presence of a subdeltoid tumor situated in the quadrangular space, originating from the axillary nerve. This case report documents our experience in successfully surgically excising this rare benign axillary nerve tumor using an extracapsular approach. Intraoperative neural monitoring was employed to safeguard neural integrity. Our case highlights the importance of a high degree of suspicion, early diagnosis, and meticulous surgical techniques in managing such uncommon nerve sheath tumors while preserving neurological function.
Choroid plexus tumors in adults: a retrospective mono-institutional study.
Choroid plexus tumors (CPT) are rare entities, and even rarer in adulthood. A retrospective consecutive series of 24 adult CPT patients was reviewed. We described 24 adult CPTs. Clinical onset included cerebellar signs (n = 11, 45.8%), intracranial hypertension signs (n = 8, 33.4%), cranial nerves impairment (n = 5, 20.8%), incidental findings (n = 4, 16.6%), seizures (n = 1, 4.2%), spinal signs (n = 1, 4.2%). At first diagnosis, CPT was mostly located in the ventricular system, but other locations can occur, including the spine (one case); meningeal involvement was present in one, pre-surgical hydrocephalus in one case only. CPT histological grade ranged from grade 1 (n = 17), grade 2 (n = 6), and grade 3 (n = 1). TERTp mutation was detected in 17.6% (n = 3/17). TP53 mutation in 5.9% (n = 1/17). Gross Total, Subtotal, Partial resection and Biopsy were achieved in 17 (70.8%), 3 (12.5%), 3 (12.5%) and 1 (4.2%) of patients, respectively. 76% of cases (n = 16/21) experienced clinical worsening suddenly after surgery for different reasons, and mostly gradually recovered. For three cases no data was available. Adjuvant therapy was performed only for grades 2 and 3. At recurrence, surgery, radiosurgery, radiotherapy and chemotherapy were considered. The median Overall Survival from surgery was 219.25 months (95% CI, 188.83-249.67). We confirm that CPT can occur in adults and are mostly grade 1 tumors located in the ventricular system. The surgical approach is the gold standard, although 76% of clinical worsening occurred, often transient. Adjuvant treatment was limited to higher grade CPT; however, no consensus has already been achieved about adjuvant therapy.
A rare diagnostic pitfall: Benign enhancing foramen magnum lesions mimicking perineural tumor spread along the spinal accessory nerves in a patient with sinonasal undifferentiated carcinoma.
Metastatic extra-axial medulloblastoma involving the trigeminal nerve: a rare prognostic entity with a comprehensive literature review.
Medulloblastomas (MB) are the most common malignant central nervous system tumors in children. They usually develop in the cerebellar vermis or the fourth ventricle, while in adults they typically originate from the paramedian region or the lateral cerebellar hemispheres. It's rare for MBs to originate outside the brain and spinal cord (extra-axial), such as in the skull, meninges, and nerves. Metastases of MB typically occur within the central nervous system, with metastases outside the nervous system (extra-neural) being uncommon at the time of diagnosis (1-2%), but can increase to 5-10% during advanced stages. Around 5-6% of MBs are associated with inherited cancer predisposition syndromes, with common genetic variants including PTCH1, SUFU, TP53, and SMO. This report describes the first pediatric patient harboring a CHEK2 germline variant of uncertain significance and developing a EA- MB localized at the trigeminal nerve and subsequent CNS and EN metastases.
Publicações recentes
Lumbosacral plexus and pudendal nerve magnetic resonance tractography: A systematic review of the clinical applications for pudendal neuralgia.
Primary cauda equina lymphoma confirmed by autopsy: A case report.
An Unusual Cause of Femoral Nerve Paresis in a Horse: Disseminated B Cell Lymphoma With Plasmacytoid Differentiation and Direct Neuronal Invasion.
Extracranial hypoglossal neurofibroma with a variant ansa cervicalis: a case report.
Plexal intraneural perineurioma: an analysis of the clinicoradiologic presentation of this rare variant.
📚 EuropePMCmostrando 190
Metastatic extra-axial medulloblastoma involving the trigeminal nerve: a rare prognostic entity with a comprehensive literature review.
Frontiers in oncologyCavernous hemangioma originating from the cervical vagus nerve masquerading as a schwannoma: a case report.
Frontiers in surgeryTelovelar Approach for Fourth-Ventricular Epidermoid Cyst: Anatomical Respect, Functional Recovery, and Long-Term Stability.
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World neurosurgeryLate-Onset Intracranial Melanotic Schwannoma of the Cerebellopontine Angle: Case Report and Review of the Literature.
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Journal of clinical neuroscience : official journal of the Neurosurgical Society of AustralasiaRisk of brain and other central nervous system tumors in Danish agricultural workers.
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Journal of neurological surgery. Part B, Skull baseSchwannoma of the Base of the Tongue: A Case Report of a Rare Disease and Review of Literatures.
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World neurosurgeryNot So Benign: A Rare Atypical Ectopic Choroid Plexus Papilloma.
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The Indian journal of radiology & imagingImaging Review of Paraneoplastic Neurologic Syndromes.
AJNR. American journal of neuroradiology[Isolated lesion of the optic nerve and retina as a relapse of MALT lymphoma transforming into diffuse B-large cell lymphoma].
Vestnik oftalmologiiMicrosurgical resection of giant T11/T12 conus cauda equina schwannoma.
Bosnian journal of basic medical sciencesA rare case of malignant vagus nerve sheath tumor presenting with multiple cranial nerve dysfunction in a dog.
The Canadian veterinary journal = La revue veterinaire canadienne[Complex treatment of a patient with neurofibromatosis type 2].
Zhurnal nevrologii i psikhiatrii imeni S.S. KorsakovaOversized primary intrapulmonary schwannoma: A case report and a review of the literature.
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Journal of comparative pathology[Neurosarcoidosis (Brain)].
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Journal of neurosurgery. SpineForamen magnum meningiomas.
Handbook of clinical neurology[Successful Total Resection with Preceding Arterial Coil Embolization of Intradural Extramedullary Tumor at Craniovertebral Junction Encasing Dominant-side Vertebral Artery].
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World neurosurgeryPrimary Central Nervous System Lymphoma With Diffuse Neurolymphomatosis Involving Multiple Cranial and Spinal Nerve Roots.
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The Journal of craniofacial surgeryCranial nerve palsies in patients with hematological malignancies: a case series.
The International journal of neuroscience[Coexistence of Schwannomatosis from Vagal Nerve and Intercostal Nerve;Report of a Case].
Kyobu geka. The Japanese journal of thoracic surgeryPrimary Central Nervous System Lymphoma with Peripheral Nerve Involvement: Case Report.
CureusGiant paravertebral schwannoma near the lumbar nerve roots with bone destruction: A case report.
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Medical hypothesesClinical Reasoning: A misdiagnosis of atypical trigeminal neuralgia.
NeurologyA Rare Presentation of Axial Chordoma and the Approach to Management.
The American journal of case reportsMicrosurgical Resection of the Epidermoid Tumor in the Cerebellopontine Angle.
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BMJ case reportsSchwannomatosis of the Spinal Accessory Nerve: A Case Report.
Journal of brachial plexus and peripheral nerve injuryGlobal, regional, and national burden of brain and other CNS cancer, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016.
The Lancet. NeurologyClinical features of hypertrophic pachymeningitis in a center survey.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical NeurophysiologyThe link between idiopathic intracranial hypertension, fibromyalgia, and chronic fatigue syndrome: exploration of a shared pathophysiology.
Journal of pain researchElective neurosurgical humanitarian care in a deployed setting.
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Cancer gene therapyThe implications of intradural extension in paraspinal malignant peripheral nerve sheath tumors: effects on central nervous system metastases and overall survival.
Journal of neurosurgery. SpineOne burr-hole craniotomy: Upper retrosigmoid approach in helsinki neurosurgery.
Surgical neurology internationalPrimary histiocytic sarcoma of the central nervous system: a case report with platelet derived growth factor receptor mutation and PD-L1/PD-L2 expression and literature review.
Radiation oncology (London, England)Immediate selective laryngeal reinnervation in vagal paraganglioma patients.
The Journal of laryngology and otologyElectrical stimulation-based nerve location prediction for cranial nerve VII localization in acoustic neuroma surgery.
Brain and behaviorEndoscopic Endonasal Transclival Approach to Tumors of the Clivus and Anterior Region of the Posterior Cranial Fossa: An Anatomic Study.
World neurosurgeryMetastatic cardiophrenic lymph node resection following full-thickness resection of right diaphragm for advanced ovarian carcinoma.
Gynecologic oncologySchwannomatosis: a genetic and epidemiological study.
Journal of neurology, neurosurgery, and psychiatryExtensive Cranial Nerves Involvement in Neurofibromatosis: A Rare Presentation.
Journal of pediatric neurosciencesGuiding Device for Precision Grafting of Peripheral Nerves in Complete Thoracic Spinal Cord Injury: Design and Sizing for Clinical Trial.
Frontiers in neurologySIOPE - Brain tumor group consensus guideline on craniospinal target volume delineation for high-precision radiotherapy.
Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and OncologySyringobulbia in pediatric patients with Chiari malformation type I.
Journal of neurosurgery. PediatricsNeurolymphomatosis in non-Hodgkin lymphoma with cranial multineuritis: A case report.
MedicineSyringobulbia: A delayed complication following spinal cord injury - case report.
The journal of spinal cord medicineNetrin-1 Confines Rhombic Lip-Derived Neurons to the CNS.
Cell reportsIntravenous Remifentanil Analgaesia for an Obstetric Patient with Type I Neurofibromatosis and a Factor V Leiden Mutation.
Sultan Qaboos University medical journalPerineural Spread of Melanoma to the Brachial Plexus: Identifying the Anatomic Pathway(s).
World neurosurgeryMultiple cranial nerve enhancement as a rare presentation of secondary brain lymphoma.
Neurology IndiaPlexus and peripheral nerve metastasis.
Handbook of clinical neurologyA clinical case of neosporosis in a 4-week-old holstein friesian calf which developed hindlimb paresis postnatally.
The Journal of veterinary medical scienceRecent advances in intradural spinal tumors.
Neuro-oncologyContralateral brachial plexus injury following retromastoid suboccipital craniotomy: A report and review of literature.
Neurology India[Anterior skull-base schwannoma].
Neurocirugia (Asturias, Spain)CNS Tumors in Neurofibromatosis.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology[Giant tumor from the nerve sheath].
Acta ortopedica mexicanaExtensive Involvement of Multiple Cranial and Spinal Nerves in Lymphomatous Meningitis.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiquesNeuro-Myelomatosis of the Brachial Plexus - An Unusual Site of Disease Visualized by FDG-PET/CT: A Case Report.
The American journal of case reportsSolid Freeform Techniques Application in Bone Tissue Engineering for Scaffold Fabrication.
Tissue engineering and regenerative medicineFamilial Schwannomatosis: A Diagnostic Challenge.
Journal of clinical and diagnostic research : JCDRSurgical Management of Mandibular Intraosseous Schwannomas.
The Journal of craniofacial surgeryAcute myeloid leukemia presenting with complete paraplegia and bilateral total blindness due to central nervous system involvement.
Spinal cord series and casesNeuropathic Pain Due to Iatrogenic Lingual Nerve Lesion: Nerve Grafting to Reduce Otherwise Untreatable Pain.
The Journal of craniofacial surgeryChildhood neurofibromatosis type 2 (NF2) and related disorders: from bench to bedside and biologically targeted therapies.
Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-faccialeThe inhibiting activity of meadowsweet extract on neurocarcinogenesis induced transplacentally in rats by ethylnitrosourea.
Journal of neuro-oncologyPaediatric Extracranial Spinal Accessory Nerve Schwannoma: An Extremely Rare Case Report.
Journal of clinical and diagnostic research : JCDRIsolating tape method is useful for an early judgment of curability during pancreaticoduodenectomy for pancreatic cancer.
Journal of hepato-biliary-pancreatic sciencesRole of tumor necrosis factor-alpha in zebrafish retinal neurogenesis and myelination.
International journal of ophthalmologyReirradiation of Recurrent Pediatric Brain Tumors after Initial Proton Therapy.
International journal of particle therapyIncidence of intraoperative seizures during motor evoked potential monitoring in a large cohort of patients undergoing different surgical procedures.
Journal of neurosurgeryAcute idiopathic polyradiculoneuritis concurrent with acquired myasthenia gravis in a West Highland white terrier dog.
BMC veterinary researchWhat are Head Cavities? - A History of Studies on Vertebrate Head Segmentation.
Zoological scienceExpanding the Horizon of the Suboccipital Retrosigmoid Approach to the Middle Incisural Space by Cutting the Tentorium Cerebelli: Anatomic Study and Illustration of 2 Cases.
World neurosurgeryVisualization of Cranial Nerves Using High-Definition Fiber Tractography.
NeurosurgerySchwannoma (Neurilemmoma) on the Base of the Tongue: A Rare Clinical Case.
The American journal of case reportsGanglioglioma arising from olfactory sheath: A rare site of an uncommon tumor.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of AustralasiaDiagnosis, Management, and New Therapeutic Options in Childhood Neurofibromatosis Type 2 and Related Forms.
Seminars in pediatric neurologyBilateral inferior alveolar nerve reconstruction with a vascularized sural nerve graft included in a free fibular osteocutaneous flap after segmental mandibulectomy.
Head & neckAsymmetric margin setting at the cranial and caudal sides in respiratory gated and non-gated stereotactic body radiotherapy for lung cancer.
The British journal of radiologyAdult cervicomedullary pilocytic astrocytoma: A case report.
Experimental and therapeutic medicineCranial Nerve Palsies: A Rare, Long-Term Complication of Radiotherapy for Nasopharyngeal Carcinoma.
Connecticut medicineNeurofibromatosis type 2.
Handbook of clinical neurologyAnti-VEGF treatment improves neurological function and augments radiation response in NF2 schwannoma model.
Proceedings of the National Academy of Sciences of the United States of AmericaHSV-1 as a novel therapy for breast cancer meningeal metastases.
Cancer gene therapy[Radiotherapy for Alleviation of Paraparesis due to Leptomeningeal and Cauda Equina Metastasis of HER2-Positive Breast Cancer: A Case Report].
No shinkei geka. Neurological surgeryPrimary Dural Spinal Lymphoma Presentation of a Rare Spinal Tumor Case.
Case reports in surgeryPrimary multifocal myxopapillary ependymoma of the filum terminale.
Journal of neurosurgical sciencesAtypical teratoid/rhabdoid tumor (ATRT) arising from the 3rd cranial nerve in infants: a clinical-radiological entity?
Journal of neuro-oncologyEndotracheal Tube Electrodes to Assess Vocal Cord Motor Function During Surgery in the Cerebellopontine Angle.
NeurosurgerySurgical Treatment of Jugular Foramen Schwannoma: Surgical Treatment Based on a New Classification.
NeurosurgerySevere acute inflammatory demyelinating polyradiculoneuropathy with persistent weakness associated with tumor-like nerve root enlargement.
Journal of clinical neuromuscular diseaseParaneoplastic brainstem encephalomyelitis and atypical form of chronic inflammatory demyelinating polyneuropathy in patient with testicular germinal tumor-is this an overlap syndrome? a case report.
Neurologia i neurochirurgia polska[Cervico-sternotomy for thoracic inlet conditions in children].
Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia PediatricaDecision Making for Patients With Concomitant Pituitary Macroadenoma and Ophthalmologic Comorbidity: A Clinical Controversy.
World neurosurgeryNeurolymphomatosis: A report of 2 cases representing opposite ends of the clinical spectrum.
Muscle & nerveSpinal accessory nerve schwannomas masquerading as a fourth ventricular lesion.
Journal of neurosciences in rural practiceAssociações
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Referências e fontes
Bases de dados externas citadas neste artigo
Publicações científicas
Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.
- Telovelar Approach for Fourth-Ventricular Epidermoid Cyst: Anatomical Respect, Functional Recovery, and Long-Term Stability.
- Quadrangular space schwannoma affecting the axillary nerve.
- Choroid plexus tumors in adults: a retrospective mono-institutional study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology· 2025· PMID 39621171mais citado
- A rare diagnostic pitfall: Benign enhancing foramen magnum lesions mimicking perineural tumor spread along the spinal accessory nerves in a patient with sinonasal undifferentiated carcinoma.Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia· 2025· PMID 40663856mais citado
- Metastatic extra-axial medulloblastoma involving the trigeminal nerve: a rare prognostic entity with a comprehensive literature review.
- Lumbosacral plexus and pudendal nerve magnetic resonance tractography: A systematic review of the clinical applications for pudendal neuralgia.
- Primary cauda equina lymphoma confirmed by autopsy: A case report.
- An Unusual Cause of Femoral Nerve Paresis in a Horse: Disseminated B Cell Lymphoma With Plasmacytoid Differentiation and Direct Neuronal Invasion.
- Extracranial hypoglossal neurofibroma with a variant ansa cervicalis: a case report.
- Plexal intraneural perineurioma: an analysis of the clinicoradiologic presentation of this rare variant.
Bases de dados e fontes oficiais
Identificadores e referências canônicas usadas para montar este verbete.
- ORPHA:252057(Orphanet)
- MONDO:0016749(MONDO)
- GARD:12697(GARD (NIH))
- Variantes catalogadas(ClinVar)
- Busca completa no PubMed(PubMed)
- Q55786403(Wikidata)
Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.
Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar
