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1.
Comput Biol Med ; 169: 107807, 2024 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-38091727

RESUMEN

Chat Generative Pre-Trained Transformer (ChatGPT) is a sophisticated natural language model that employs advanced deep learning techniques and is trained on extensive datasets to produce responses akin to human conversation for user inputs. In this study, ChatGPT's success in the Turkish Neurosurgical Society Proficiency Board Exams (TNSPBE) is compared to the actual candidates who took the exam, along with identifying the types of questions it answered incorrectly, assessing the quality of its responses, and evaluating its performance based on the difficulty level of the questions. Scores of all 260 candidates were recalculated according to the exams they took and included questions in those exams for ranking purposes of this study. The average score of the candidates for a total of 523 questions is 62.02 ± 0.61 compared to ChatGPT, which was 78.77. We have concluded that in addition to ChatGPT's higher response rate, there was also a correlation with the increase in clarity regardless of the difficulty level of the questions with Clarity 1.5, 2.0, 2.5, and 3.0. In the participants, however, there is no such increase in parallel with the increase in clarity.


Asunto(s)
Inteligencia Artificial , Evaluación Educacional , Lenguaje , Neurocirugia , Neurocirugia/educación
2.
Neurosurg Rev ; 46(1): 62, 2023 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-36856827

RESUMEN

The suprafloccular transhorizontal fissure approach is a modified variant of the classical retrosigmoid approach option to be chosen for cerebellopontine angle lesions. In this study, we aimed to demonstrate a previously described but not widely used method, the suprafloccular transhorizontal fissure approach with anatomical dissection on the cadaver, accompanied by a case presentation with the largest clinical series in the literature. Klingler's protocol was used to prepare 8 silicone injected and 8 non-silicone injected human hemispheres. A total of 210 patients who underwent surgery in the cerebellopontine angle between 2019 and 2022 were evaluated in our clinic. Of these, the suprafloccular transhorizontal fissure approach was applied in 33 patient, and it was successful in 26 patient, but this approach could not be achieved in 7 patients. The transhorizontal fissure is a fissure in the cerebellum located between the superior semilunar lobule and the inferior semilunar lobule. In the 26 patients we operated with the suprafloccular transhorizontal fissure approach, there was no need for retraction and no complications developed. However, in 7 patients, this fissure could not be dissected due to adhesions. Suprafloccular approach is an alternative to the classical retrosigmoid approach in tumours smaller than 2 cm, medially localised with little cerebellar oedema and neurovascular compression syndrome. Because in this approach, no cerebellum retraction is required, vascular structures are better preserved and the surgical time is shortened. This approach can be applied in smaller tumours than 2 cm when the sulcal anatomy is appropriate.


Asunto(s)
Ángulo Pontocerebeloso , Disección , Humanos , Cadáver , Tempo Operativo , Siliconas
3.
Br J Neurosurg ; 37(3): 309-312, 2023 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-32915076

RESUMEN

OBJECTIVES: Hyperactive dysfunction syndrome (HDS) is defined as symptoms arising from overactivities in cranial nerves, like trigeminal neuralgia (TN), hemifacial spasm (HFS), and glossopharyngeal neuralgia (GPN). A combination of these cranial nerve neuralgias, that might or might not occur in one or both sides, either synchronously, or metachronously is called combined hyperactive dysfunction syndrome (CHDS). CASE PRESENTATION: We presented a 73 years-old male patient with CHDS presenting with GPN as the initial symptom, with total relief from GPN, TN, and HFS after microvascular decompression. Up to date, only nine patients have been reported in the literature with symptomatic. CONCLUSIONS: TN-HFS-GPN. Our case is the first case with GPN as the initial symptom. The combination of arterial and venous origin of the offending vessels makes the case picturesage.


Asunto(s)
Enfermedades del Nervio Glosofaríngeo , Espasmo Hemifacial , Cirugía para Descompresión Microvascular , Neuralgia , Neuralgia del Trigémino , Humanos , Masculino , Anciano , Enfermedades del Nervio Glosofaríngeo/diagnóstico , Enfermedades del Nervio Glosofaríngeo/etiología , Enfermedades del Nervio Glosofaríngeo/cirugía , Nervios Craneales/cirugía , Neuralgia del Trigémino/diagnóstico , Neuralgia del Trigémino/etiología , Neuralgia del Trigémino/cirugía , Neuralgia/cirugía , Espasmo Hemifacial/cirugía , Nervio Glosofaríngeo/cirugía
4.
BMC Pediatr ; 20(1): 183, 2020 04 24.
Artículo en Inglés | MEDLINE | ID: mdl-32331522

RESUMEN

BACKGROUND: Sotos syndrome is caused by a gene deletion with an autosomal dominant pattern of inheritance. The Sotos syndrome was first described by Juan Sotos. Cole and Hughes identified the clinical characteristics of this syndrome. This syndrome is characterized by macrocephaly, frontal bossing, ocular hypertelorism, overgrowth, subdural hygroma, ventricular dilatation, agenesis of the corpus callosum. This syndrome is associated with mutations in NSD 1 (nuclear receptor SET domain-containing protein 1) gene, protein insufficiency, and a 5q35 microdeletion. Sotos syndrome is reported to occur in approximately 1/10,000-15,000 births. CASE PRESENTATION: We present a patient with Sotos syndrome who is harboring a sacral lipoma and tethered cord syndrome and she had growth retardation, frontal bossing and hypertelorism. After a standard approach for tethered cord syndrome, the patient was discharged 3 days after without any additional neurodeficits. CONCLUSION: In the literature, sacral lipoma and tethered cord syndrome with Sotos syndrome have not been published yet.


Asunto(s)
Defectos del Tubo Neural , Síndrome de Sotos , Femenino , Humanos , Mutación , Síndrome de Sotos/complicaciones , Síndrome de Sotos/diagnóstico , Síndrome de Sotos/genética
5.
Childs Nerv Syst ; 36(5): 1075-1078, 2020 05.
Artículo en Inglés | MEDLINE | ID: mdl-31786630

RESUMEN

Intraparenchymal schwannomas of the brain are very rare, accounting for < 1% of intracranial schwannomas. We present a case of an 11-year-old boy with a left frontotemporal lobe schwannoma presented with seizure and neurogenic pulmonary edema. To our knowledge, this is the first case of intracerebral schwannoma with neurogenic pulmonary edema published to date and is the first case of an intracerebral schwannoma operated with fluorescein guidance.


Asunto(s)
Neoplasias Encefálicas , Neurilemoma , Edema Pulmonar , Neoplasias Encefálicas/complicaciones , Neoplasias Encefálicas/diagnóstico por imagen , Neoplasias Encefálicas/cirugía , Niño , Fluoresceína , Humanos , Masculino , Neurilemoma/complicaciones , Neurilemoma/diagnóstico por imagen , Neurilemoma/cirugía , Convulsiones/etiología , Convulsiones/cirugía
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