A5017080438- Meningioma and schwannoma management
- Vascular Malformations and Hemangiomas
- Vascular Malformations Diagnosis and Treatment
- Spinal Fractures and Fixation Techniques
- Botulinum Toxin and Related Neurological Disorders
- Intracranial Aneurysms: Treatment and Complications
- Pain Management and Treatment
- Glioma Diagnosis and Treatment
- Bone Tumor Diagnosis and Treatments
- Cerebrospinal fluid and hydrocephalus
- Spine and Intervertebral Disc Pathology
- Spinal Dysraphism and Malformations
- Temporomandibular Joint Disorders
- Advanced MRI Techniques and Applications
- Musculoskeletal pain and rehabilitation
- Gout, Hyperuricemia, Uric Acid
- Scoliosis diagnosis and treatment
- Protein Degradation and Inhibitors
- Sarcoma Diagnosis and Treatment
- Traumatic Brain Injury and Neurovascular Disturbances
- Teratomas and Epidermoid Cysts
- Facial Nerve Paralysis Treatment and Research
- Congenital Diaphragmatic Hernia Studies
- Oral and Maxillofacial Pathology
- Neurological disorders and treatments
Hospital Clínico San Carlos
2022-2025
Universidad Complutense de Madrid
2024-2025
Hospital Universitario de La Princesa
2015-2018
Cavernous hemangiomas are benign tumors that exceptionally affect the cranial bones. The first description of this type tumor was in 1845 by Toynbee. A review literature reveals less than 100 published cases and a growing trend every year. Total surgical excision is treatment choice, prognosis after complete excellent, with recurrence usually rare. We present case 57-year-old patient painless left frontal bone, slow growth osteolytic characteristics from neuro-radiological point view. lesion...
Abstract Background The differentiation by means of magnetic resonance between high-grade gliomas and intracranial solitary single metastasis is the utmost importance since they condition both surgical complementary treatment. Results Retrospective study that analyzes parameters advanced imaging: spectroscopy, diffusion perfusion, specifically focused on differences in coefficients metabolites Cho/Cr, Cho/NAA NAA/Cr peritumoral edema metastases. data have been statistically analyzed using...
Solitary intradural plasmacytomas are extremely rare. We present a case of patient with headache and diagnosis meningiomatosis. Onset symptoms were abrupt neurological deterioration paraparesis. The underwent surgery by craniotomy tumor resection, final pathological findings solitary extramedullary plasmacytoma without evidence multiple myeloma. Of note is the great similarity this infrequent pathology meningiomas need to differentiate it from dural involvement Treatment always includes...
Akinetic mutism is considered as an alteration of the motivational state person, which patient unable to initiate verbal or motor responses voluntary, even with preserved sensorimotor and surveillance functions.A 43 year-old male involved in a cerebellum arteriovenous fistula complicated hydrocephalus, who responded dramatically treatment bromocriptine.Typically, akinetic described transient surgeries posterior fossa. However, it can also occur after multiple valvular failure patients...
Chordoma is a malignant tumor that usually involves the axial skeleton, and its origin related to notochord remnants. In cervical spine they represent 5% of all chordomas. Cervical chordoma present high rate recurrence given their location growing in highly risky anatomical region with complex anatomy. We report young female chordoma, involving C7-D1 vertebrae discussing challenges this intervention. There currently controversy over type surgical modality: block resection versus...
Spine involvement in gout is an extremely uncommon complication. Dorsalgia and quadriplegia are some manifestations that may occur, although these symptoms seen more frequently other prevalent pathologies, such as spinal tumors.We present unusual case of thoracic cord compression at T10-T11 level caused by the extradural deposit tophaceous material a 52-year-old woman with uncontrolled chronic gout. In addition to intensive medical treatment, patient required surgery (hemilaminectomy...
Introduction: Intramedullary hemangioblastomas are usually accompanied by syringomyelia. However, a holocord syringomyelia is rare. The most common cause of continues to be Chiari disease, and only 10 cases with reported so far. Case report: We present case 35-year-old patient two-month history cervicobrachialgia at the C7-C8 root level, previously preceded pain D1-D2 level. Cervico-dorso-lumbar MRI revealed medullar tumor hyper-uptake mural nodule conus medullaris level an extensive...
Ring chromosome 20 syndrome is a rare genetic disorder, with late diagnosis.A 43-year-old woman who had refractory epilepsy since the age of six years, for which she was treated deep brain stimulation centromedian nucleus, and also ring 20.From findings study it can be concluded that nucleus ineffective in patients chromosome, but note must taken importance characterisation management epilepsy.Estimulacion del nucleo centromediano en la epilepsia farmacorresistente asociada al cromosoma...
Introduction: Temporomandibular joint syndrome is defined by a triad of intense pain together with restriction mouth opening and jaw clicking. The objective this study to evaluate the efficacy safety peripheral nerve stimulation for treatment pathology. Material Methods: A retrospective was conducted. All patients met selection criteria that include prior resistance medical or surgical completion series pre-surgical tests. An octopolar electrode implanted in affected preauricular region....
Introduction: Petrous Bone Cholesteatomas (PBCs) are epidermoid cysts, which have developed in the petrous portion of temporal bone and may be congenital or acquired.