Global Neurosurgery: An Overview.

In the following article, we define the practice of global neurosurgery and review the major historical events defining this movement within the larger context of global surgery. The current state of the neurosurgical workforce, disease burden, and ongoing collaborative efforts are highlighted. Ethical practice leading the sustainability is discussed, as well as future targets for the global community as we look beyond the next decade of opportunities to affect the neurosurgical burden of disease.

Jugular Foramen Paragangliomas.

Paragangliomas are the most common tumors at jugular foramen and pose a great surgical challenge. Careful clinical history and physical examination must be performed to adequately evaluate neurological deficits and its chronologic evolution, also to delineate an overview of the patient performance status. Complete imaging evaluation including MRI and CT scans should be performed, and angiography is a must to depict tumor blood supply and sigmoid sinus/internal jugular vein patency. Screening for multifocal paragangliomas is advisable, with a whole-body imaging. Laboratory investigation of endocrine function of the tumor is necessary, and adrenergic tumors may be associated with synchronous lesions. Preoperative prepare with alpha-blockage is advisable in norepinephrine/epinephrine-secreting tumors; however, it is not advisable in exclusively dopamine-secreting neoplasms. Best surgical candidates are young otherwise healthy patients with smaller lesions; however, treatment should be individualized each case. Variations of infratemporal fossa approach are employed depending on extensions of the mass. Regarding facial nerve management, we avoid to expose or reroute it if there is preoperative function preservation and prefer to work around facial canal in way of a fallopian bridge technique. If there is preoperative facial nerve compromise, the mastoid segment of the nerve is exposed, and it may be grafted if invaded or just decompressed. A key point is to preserve the anteromedial wall of internal jugular vein if there is preoperative preservation of lower cranial nerves. Careful multilayer closure is essential to avoid at most cerebrospinal fluid leakage. Residual tumors may be reoperated if growing and presenting mass effect or be candidate for adjuvant stereotactic radiosurgery.

Cranioplasty with Direct Revascularization in Hemorrhagic Moyamoya Disease: 2-Dimensional Operative Video.

Moyamoya disease is a progressive nonatherosclerotic stenosis of the terminal segments of the arteries of the Circle of Willis. Hemorrhagic presentation is a life-threatening condition, associated with an increased risk of rebleeding and ischemic events.1-7 We present the case of a 65-year-old woman with a right intracerebral hemorrhage who underwent emergency hematoma evacuation without bone flap replacement (Video 1). The investigation confirmed the diagnosis of Moyamoya disease and demonstrated hypoperfusion of the right cerebral hemisphere. Late angiography depicted no transdural collaterals through the bone defect and demonstrated preservation of the superficial temporal artery (STA). Next, it was chosen to perform 1-stage cranioplasty with direct revascularization. We detached the temporal fascia from the muscle and created a window through the fascia to give STA passage in a corridor through the temporal muscle until the brain's surface. Vascular anastomosis was performed with an interrupted suture line employing a 10-0 nylon thread. Flow within the right middle cerebral artery was retrograde, coming from branches of the posterior cerebral artery, and the end-to-side anastomosis was placed to orientate the STA flow in the same direction as in the middle cerebral artery. We used a custom-made titanium plate for the cranioplasty and gave enough room inferiorly for the course of STA. In the end, we sutured the temporal fascia to the titanium plate for a better cosmetic result. To avoid additional unnecessary procedures, the performance of direct revascularization during the cranioplasty is feasible and deserves additional investigation as a tool to prevent new hemorrhagic or ischemic events. Informed consent was obtained from the patient for the procedure and publication of this operative video.

Bipolar, high-voltage, long-duration pulsed radiofrequency ablation of the Gasserian ganglion for the treatment of trigeminal neuralgia in a patient with a cardiac implantable electronic device: illustrative case.

BACKGROUND: One of the common methods of treating trigeminal neuralgia (TN) nowadays is radiofrequency therapy. However, it has serious limitations in patients with a cardiac pacemaker because of electromagnetic interference. Therefore, it is crucial to select optimal radiofrequency ablation parameters to make this procedure safe with favorable outcomes for such patients. OBSERVATIONS: In this study, the authors present a case of a 70-year-old man with a history of cardiac pacemaker dependency and previous microvascular decompression with complaints of severe, constant facial pain. After reprogramming the cardiac implantable electronic device (CIED), the authors performed bipolar, high-voltage, long-duration pulsed radiofrequency therapy (PRFT) of the Gasserian ganglion under electrocardiography and pulse rate control in the pre-, intra-, and postoperative periods. There were no cardiovascular or neurological complications after PRFT. The patient reported relief of pain after the procedure, and at the 9-month follow-up, he was pain-free. LESSONS: This clinical case demonstrates that the use of bipolar, high-voltage PRFT for TN treatment in patients with a CIED can be safe and effective, provided that the rules and pacemaker instructions are followed. It is necessary to use ablative treatment with caution and to guide the patient in collaboration with a cardiac surgeon and an anesthesiologist resuscitator.

Mortality rate in patients with nosocomial Acinetobacter meningitis from a Brazilian hospital

BACKGROUND: The mortality rate due to Acinetobacter baumannii nosocomial meningitis (ANM) is high. OBJECTIVE: The aim of this study was to evaluate the factors that have influence over the outcomes in ANM patients. METHODS: A retrospective analysis of 22 cases of ANM was conducted in a hospital with high incidence of multidrug resistance. RESULTS: The mean age of patients was 43 years (21 to 91) and 54.5 percent were male. All ANM cases occurred within 60 days of admission and the mean duration of illness was of 18.2 days. All cases were associated with previous neurosurgical procedures: elective surgery (27.2 percent), external shunt (54.4 percent) and emergency surgery due to trauma (18.1 percent). Imipenem resistance was observed in 40.9 percent of cases, but ampicillin/sulbactam resistance was lower (27.2 percent). The mortality rate of ANM patients was of 72.7 percent. The only risk factor associated with mortality was inappropriate therapy within five days after CSF collection. All patients who survived the meningitis episode had received appropriate therapy, in contrast to only 69.2 percent of those who did not survive (OR = 5.15; IC = 0.45-54.01). CONCLUSIONS: The high mortality rate observed in our study suggests the need for aggressive empirical treatment with addition of drugs, including intrathecal therapy, where multi-resistant A. baumannii is endemic.

Meningiomas petroclivais: planejamento cirúrgico / Petroclival meningiomas: surgical planning

Objetivo: O tratamento cirúrgico dos tumores originários da região petroclival, ou com extensão para essa área, é um desafio para os neurocirurgiões. Aqui descrevemos duas abordagens de base de crânio a menigeomas petriclivais, definidos como tumores originários dos dois terços superiores do clivus, na junção petroclival, e medial ao nervo trigêmeo. Descrição: A abordagem cranio-orbito-zigomática (COZ) é descrita. para lesões localizadas no clivus superior, com e sem extensão ao seio cavernoso, e a abordagem petrosa posterior, usada para alcançar lesões no clivus médio com e sem extensão ao clivus superior ou inferior. Na abordagem COZ, o canal auditivo interno é uma extensão inferior. Conclusões: A remoção radical dos meningeomas (graus 1 e 2 da escala simpson) é bem estabelecida com o melhor tratamento. Abordagens à base do crânio são mais adequadas para a remoção radical de meningeomas petroclivais tumores moles como schawannomas trigemiais, cistos epidermóides ou meningeomas com extensão para a região petroclival, porém sem insersão, podem ser removidos pela abordagem retrosigmóidea.

Meningioma da região do forame magno / Foramen Magnum Meningiomas

Meningiomas do forame magno estão entre os tumores maisdifíceis de serem removidos. A abordagem cirúrgica, assimcomo a extensão da remoção óssea, são pontos de controvérsia.Neste trabalho os autores apresentam sua experiência com otratamento cirúrgico destes tumores, a forma de abordá-los,baseada na expansão tumoral e no local de origem são ospontos fundamentais que norteiam o planejamento cirúrgico. Asmanifestações clínicas, assim como a morbidade mais comumrelacionada com estes tumores serão apresentadas.

Primary melanoma of Meckel's cave: case report

Apresentamos um caso de neuralgia do trigêmeo com investigação radiológica de ressonância magnética (RM) e tomografia computadorizada apresentando resultado normal. A dor não apresentou alívio com carbamazepina, sendo indicado descompressão microvascular do trigêmio. Passados dois meses, o paciente queixava-se de dor com intensidade similar à do pré-operatório. Nova RM mostrou lesão expansiva no cavo de Meckel, a qual foi tratada cirurgicamente por abordagem extra-dural. O exame anatomopatológico foi compatível com melanoma primário. O seguimento radiológico, após seis meses da cirurgia, não apresentou anormalidades.

Trigeminal schwannoma. Classification and surgical approaches

This paper reviews and expands the Jefferson's Classification regarding the localization of trigeminal schwannomas. The authors present a series of specific surgical approaches best suited to remove these tumors. Using skull base neurosurgical techniques, the authors present the most direct, efficient and safety surgical approaches to remove each of five different types of trigeminal schwannomas. Three illustrative cases of their own are also presented.

Skull base chordomas

Chordomas are difficult and challenger tumors to treat. Despite of its pathological appearance that demonstrates an slow-growing behavior, their location and patterns of spread through the base of the skull make these tumors one of the most difficult diseases to treat at the base of the skull. The inadequate response to the conventional radiation therapy and the high incidence of recurrence, in cases treated with classical neurosurgical approaches, make mandatory a radical removal of the tumor mass and the surrounding pathological bone which can only be achieved with the use of skull base approaches associated with an extensive drilling of the bony tumor. In order to reach the goal of the surgical treatment of the skull base chordomas, the mastery of the skull base anatomy and the management of the drill are crucial points to obtain a successful results. In this report, we express our philosophy to treat these tumors which is based on the radical removal associated to a postoperative proton beam therapy. The main characteristic of the skull base chordomas is to spread through the base of the skull, which dictates the surgical approach that should be employed for each patient. In this article we will address the management of the skull base chordomas, with special emphasis to the role of the surgical and radiation treatment. The pathologic diagnosis and the radiological findings of chordomas of the skull base also will be discussed.