Lesiones de cráneo en el mieloma múltiple / Skull Lesions in Multiple Myeloma

Fig A) Radiografía de cráneo en proyección lateral: se observan múltiples lesiones radiolúcidas distribuidas en todo el cráneo. B) Acercamiento donde se evidencian múltiples lesiones en sacabocado, compatibles con mieloma múltiple(AU)

Epidemiological Profile of 96 Intracranial Tumors Treated in a Single Reference Center

Objectives The present study aims to categorize the prevalence of intracranial tumors surgically treated at the neurosurgery service of Hospital Universitário Evangélico Mackenzie (HUEM) between 2016 and 2018. Material and Methods This survey included patients surgically treated due to primary or metastatic intracranial neoplasia between 2016 and 2018 at a referral center in the city of Curitiba. These patients were analyzed for epidemiological, histopathological, and topographic data, and they underwent an assessment of the outcome at the time of hospital discharge. Results Atotal of 96patientsmet the inclusion criteria. Themost prevalent tumorwas the glioma, with 39.6% of the sample, with glioblastoma being themost prevalent histological type. Brainmetastases andmeningiomas represented, respectively, 21.9%and 18.8%of the total. There was a predominance of supratentorial and intra-axial tumors in our sample. Conclusion Glioma was the most commonly found tumor, directly associated with high morbidity and mortality. The development of new and more effective drugs with action directed at themolecular level of intracranial tumorsmay be the path to a longer survival and improvement in the quality of life of these patients.

Giant Cell tumor of the Zygomatic Arch in a Pediatric Patient: Rare Case Report / Tumor de Células Gigantes do Arco Zigomático em um Paciente Pediátrico: Relato de Caso Raro / Tumor de Células Gigantes del Arco Cigomático en un Paciente Pediátrico: Informe de un Caso Raro

Introduction: A giant cell tumor (GCT) is a rare tumor, usually benign, which can be locally aggressive, with an almost unknown incidence in the skull. Case report: Case report of a pediatric patient diagnosed with Ewing's sarcoma (ES) and later GCT when sought medical care for an increased volume in the zygomatic arch and the right preauricular region. Imaging exams showed an expansive lesion in the zygomatic and squamous portion of the right temporal bone, with an extradural intracranial component in the middle fossa, with no evidence of infiltration. From the anatomopathological view, fusocelullar neoplasia was seen. The CD68 marker was positive and the S100 marker was negative. Tumor resection by microsurgery was performed. The patient remains in follow-up, with imaging exams at neurosurgery and orthopedics, the latest magnetic resonances of the skull showing a reduction in the size of the lesion. In addition, the patient did not submit to adjuvant therapy and is currently without complaints. Conclusion: This is an important case due to its rarity and clinical data that contributes for the understanding of the pathologies presented, allowing that, in the future, new studies are able to optimize the treatment, and the prognosis for these patients

Introdução: O tumor de células gigantes (TCG) é raro, geralmente benigno, e pode ser localmente agressivo, com incidência quase desconhecida no crânio. Relato do caso: Paciente pediátrico com diagnóstico de sarcoma de Ewing (SE) e posteriormente de TCG, quando procurou atendimento médico por conta do aumento de volume em arco zigomático e região préauricular à direita. Os exames de imagem evidenciaram lesão expansiva em porção zigomática e escamosa do osso temporal à direita, com componente intracraniano extradural em fossa média, sem evidências de infiltração. Do ponto de vista anatomopatológico, observou-se neoplasia fusocelular. O marcador CD68 foi positivo e o marcador S100, negativo. Realizouse microcirurgia para ressecção do tumor. O paciente permanece em acompanhamento com exames de imagem nos serviços de neurocirurgia e ortopedia, com as últimas ressonâncias magnéticas de crânio mostrando redução no tamanho da lesão. Além disso, não realiza terapia adjuvante e atualmente não apresenta queixas. Conclusão: Este é um caso importante em razão da sua raridade e dos dados clínicos que agregam informações sobre as patologias apresentadas, permitindo que, no futuro, novas pesquisas possam otimizar o tratamento da referida neoplasia e o prognóstico desses pacientes

Introducción: El tumor de células gigantes (TCG) es un tumor raro, generalmente benigno, que puede ser localmente agresivo, con una incidencia casi desconocida en el cráneo. Relato del caso: Paciente pediátrico diagnosticado con sarcoma de Ewing (SE) y posteriormente con TCG, cuando procuró atención médica por aumento de volumen en arco cigomático y región preauricular derecha. Los exámenes de imagen mostraron una lesión expansiva en la porción cigomática y escamosa del temporal derecho, con componente intracraneal extradural en la fosa media, sin evidencias de infiltración. Desde el punto de vista anatomopatológico, se observó neoplasia fusocelular. El marcador CD68 fue positivo y el marcador S100 negativo. Se realizó microcirugía para resecar el tumor. El paciente permanece en seguimiento con exámenes de imagen en los servicios de neurocirugía y ortopedia, con las últimas resonancias magnéticas de cráneo mostrando una reducción en el tamaño de la lesión. Además, no se somete a terapia adyuvante y actualmente no tiene quejas. Conclusión: Este es un caso importante por su rareza y datos clínicos que agregan informaciones sobre las patologías presentadas, permitiendo, en el futuro, nuevas investigaciones para optimizar el tratamiento de la neoplasia referida, y el pronóstico de estos pacientes

Endolymphatic Sac Tumour: A Case Report and Review of the Literature

Introduction Endolymphatic sac tumor (ELST) is a slow-growing, low-grade, locallyinfiltrative tumor arising from the endolymphatic sac/duct, which is located in the posterior part of the petrous temporal bone. It may be sporadic in origin, or may be associated with Von-Hippel Lindau (VHL) syndrome. Case description A 40-year-old female patient with an ELST without VHL syndrome who was treated successfully by microsurgical extirpation of the tumor. Discussion We discuss the radiological features and the histopathology of this rare tumor and review the relevant literature. Conclusion The case herein reported adds to the previously-reported cases of this rare tumor.

Cranial osteomyelitis as a complication of furuncular myiasis / Osteomielite craniana como complicação de miíase furuncular

ABSTRACT Objective: To report the case of an infant with infrequent cranial osteomyelitis as a complication of furuncular myiasis. Case description: The patient was a 4-month-old male who presented to the emergency department with a nodular skull lesion with edema, tenderness, pain, and purulent drainage, as well as progress of the ulcerated lesion and evidence of larvae inside. Antibiotic treatment was initiated, and the patient was taken to the operating room to remove the larvae, but he had no symptomatic improvement. A skull radiograph was taken to visualize the osteolytic lesion, and a 3D computed tomography scan showed osteomyelitis of the external parietal surface. Antibiotic management readjustment continued for a total of six weeks, and a skin flap was used with clinical improvement. Comments: Myiasis is defined as the infestation of vertebrates with fly larvae. In mammals, larvae can feed on host tissue and cause a wide range of infestations depending on their location in the body. The cranial osteomyelitis as a complication of myiasis described in this report seems to be an exceptional case.

RESUMO Objetivo: Relatar um caso de criança com osteomielite craniana infrequente como complicação da miíase furuncular. Descrição do caso: Paciente do sexo masculino, com quatro meses de idade, que se apresentou no pronto-socorro com lesão nodular no crânio com edema, sensibilidade, dor e drenagem purulenta, com evolução da lesão ulcerada e evidência de larva no interior. O tratamento com antibióticos foi iniciado e o paciente foi levado à sala de cirurgia para remover as larvas, mas não houve melhora. Uma radiografia do crânio foi realizada para visualizar a lesão osteolítica e uma tomografia computadorizada em 3D mostrou osteomielite da superfície parietal externa. O reajuste do tratamento com antibióticos foi mantido por um total de seis semanas e um retalho cutâneo foi realizado com melhora clínica. Comentários: Miíase é definida como a infestação de vertebrados com larvas de moscas. Nos mamíferos, as larvas podem se alimentar do tecido hospedeiro e causar uma ampla variedade de infestações, dependendo da sua localização no corpo. A osteomielite como complicação da miíase, apresentada nesse caso, parece ser uma forma não usual de complicação dessa doença.

Resonancia magnética con secuencia HASTE de carcinoma epidermoide del hueso temporal / HASTE magnetic resonance imaging of a squamous cell temporal bone carcinoma

El carcinoma epidermoide del hueso temporal es una neoplasia derivada de células epidérmicas del estrato espinoso, y que dado su baja incidencia, y presentación clínica similar a un cuadro de otitis media crónica colesteatomatosa, su diagnóstico es habitualmente tardío. El estudio del carcinoma epidermoide del hueso temporal se realiza con tomografía computarizada, la que evidencia erosión ósea. Sin embargo, existen distintos diagnósticos diferenciales, tanto malignos como benignos, que pueden provocar hallazgos similares en la tomografía computarizada. La resonancia magnética (RM) es un método de exploración de gran valor complementario para el estudio del carcinoma de oído medio. La RM con secuencia de difusión HASTE ha surgido como herramienta de estudio en patología de hueso temporal, tales como colesteatomas y teratomas de oído medio, pese a esto, no existen reportes en la literatura de la presentación imagenológica del carcinoma epidermoide de hueso temporal utilizando este método. En este artículo se presenta un caso clínico de una paciente con carcinoma epidermoide de oído medio, cuyo estudio preoperatorio incluyó RM-HASTE. Aun cuando se requiere un mayor número de casos para establecer el patrón imagenológico, se concluye que esta técnica es de utilidad para diferenciar este tumor de otitis media crónica colesteatomatosa.

Squamous cell carcinoma of the temporal bone (SCC) is a malignancy originated from epidermis spinous cells. Its low incidence and similar presentation to cholesteatomas, contributes to its late diagnosis. The most widely used study for this tumor is computed tomography (CT), which mainly evidences erosion of the temporal bone. There are several other diagnoses, malignant and benign, that could provoke similar findings at the CT. Magnetic resonance imaging (MRI) is a method of great value to study SCC. MRI with HASTE diffusion sequence has recently emerged as an important tool in the study of temporal bone pathologies, such as cholesteatoma and middle ear teratoma, despite this, there are no reports in the literature of the imaging presentation of SCC using this method. This article presents a clinical case of a patient with SCC, in whose preoperative study was performed HASTE-MRI. Although a larger number of cases are required to establish an imaging pattern, it is concluded that this technique is useful to differentiate this tumor from middle ear cholesteatomas.

Malignant tumors of the temporal bone - our experience / Tumores malignos do osso temporal - a nossa experiência

ABSTRACT INTRODUCTION: Malignant tumors of the temporal bone are rare, with an estimated incidence of about 0.8-1.0 per 1,000,000 inhabitants per year. The vast majority of these tumors are squamous cell carcinomas and their treatment is eminently surgical. OBJECTIVE: This study is an attempt at systematizing the forms of clinical presentation, the therapeutic possibilities, and oncological outcomes of patients with malignant tumors of the temporal bone in a tertiary hospital in Portugal. METHODS: The authors present a retrospective study of temporal bone tumors treated and followed during otorhinolaryngology consultations between 2004 and 2014. A review of the literature is also included. RESULTS: Of the 18 patients included in the study, 16 had a primary tumor of the temporal bone, in most cases with squamous cell carcinoma histology. Of these, 13 patients were treated with curative intent that always included the surgical approach. Disease persistence was observed in one patient and local recurrence in five patients, on average 36.8 months after the initial treatment. CONCLUSIONS: The anatomical complexity of the temporal bone and the close associations with vital structures make it difficult to perform tumor resection with margins of safety and thus, tumor relapses are almost always local. A high level of suspicion is crucial for early diagnosis, and stringent and prolonged follow-up after treatment is essential for diagnosis and timely treatment of recurrances.

Resumo Introdução: Os tumores malignos do osso temporal são raros, com uma incidência estimada de cerca de 0,8-1 por milhão de habitantes por ano. A grande maioria são carcinomas espinocelulares e o seu tratamento é eminentemente cirúrgico. Objetivo: Este trabalho tem como objetivo tentar sistematizar as formas de apresentação clínica, as possibilidades terapêuticas e os resultados oncológicos de doentes com tumores malignos do osso temporal num hospital terciário em Portugal. Método: Os autores apresentam um estudo retrospectivo de tumores do osso temporal tratados e acompanhados em consultas de otorrinolaringologia entre 2004 e 2014. É também apresentada uma revisão da literatura. Resultados: Dos 18 doentes incluídos no estudo, 16 apresentavam um tumor primário do osso temporal, na maioria dos casos com histologia de carcinoma espinocelular. Destes, 13 doentes foram submetidos a tratamento com intuito curativo que incluiu sempre uma abordagem cirúrgica. Verificou-se persistência da doença em 1 doente e recidiva local em 5 doentes, em média 36,8 meses após o tratamento inicial. Conclusões: A complexidade anatómica do osso temporal e as estreitas relações com estruturas de importância vital tornam difícil a exérese tumoral com margens de segurança, pelo que as recidivas tumorais são quase sempre locais. Um nível de suspeição elevado é fundamental para um diagnóstico precoce e o seguimento rigoroso e prolongado após o tratamento é essencial para o diagnóstico e tratamento oportuno das recidivas.

Reconstruções craniofaciais: ainda há espaço para os retalhos locorregionais? / Craniofacial reconstructions: is there still room for locoregional flaps?

Introdução: Os tumores avançados de cabeça e pescoço ainda têm elevada prevalência no Brasil. A reconstrução de um defeito resultante de ressecção craniofacial é um desafio para o cirurgião plástico. Os retalhos livres são a primeira escolha para essas reconstruções e os retalhos locorregionais têm sido utilizados em casos selecionados. O objetivo deste estudo é avaliar uma série de reconstruções com retalhos locorregionais em pacientes submetidos a ressecções oncológicas craniofaciais, demonstrando a aplicabilidade desses retalhos e o resultado final das reconstruções. Métodos: Foram avaliadas, retrospectivamente, quatro reconstruções craniofaciais com retalhos locorregionais de fronte e couro cabeludo. Os pacientes foram operados no Hospital das Clínicas da Universidade Federal de Pernambuco (HC-UFPE) e assinaram termo de consentimento permitindo a publicação científica de suas fotos e casos clínicos. Resultados: Todas as reconstruções foram bem sucedidas. Não ocorreram casos de infecção local ou meningite, necrose do retalho, fístulas liquóricas ou deiscências. As reconstruções com retalhos locorregionais apresentadas foram seguras e simples para reconstruir defeitos extensos em região craniofacial. Conclusões: Os cirurgiões plásticos podem realizar reconstruções complexas com estes retalhos, demonstrando que ainda há espaço para este tipo de reconstrução.

Introduction: Advanced tumors of the head and neck still have a high prevalence in Brazil. Reconstructing a defect resulting from a craniofacial resection is a challenge for the plastic surgeon. Free flaps are the first choice for these reconstructions, and locoregional flaps have been used in selected cases. The objective of this study was to evaluate a number of reconstructions with locoregional flaps in patients undergoing craniofacial oncologic resection, to demonstrate the applicability of these flaps and the end result of the reconstructions. Methods: We retrospectively studied four craniofacial reconstructions with locoregional flaps on the forehead and scalp. The patients were operated at the Clinical Hospital of the Federal University of Pernambuco. They signed a consent form allowing the scientific publication of their photographs and clinical case records. Results: All reconstructions were successful. There were no cases of local infection or meningitis, flap necrosis, liquor fistula, or dehiscence. Reconstructions with locoregional flaps were safe and simple to perform for extensive defects in the craniofacial region. Conclusions: Plastic surgeons can perform complex reconstructions with locoregional flaps, demonstrating that there is still room for this type of reconstruction.

Lesiones etmoidales con extensión secundaria: estrategia quirúrgica y complicaciones / Ethmoidal lesions with secondary extension: surgical strategies and complications

Introduction: The removal of ethmoidal tumors with secondary extension to the cranial base and/or facial region involves a high complexity and it is associated to a high morbility. Objective: To determine the results of craniofacial surgery in patient with ethmoid extended tumors. Methods: It was carried out a traverse retrospective descriptive study. The sample was conformed by the patients intervened surgically of anterior cranial base lesions by means of a combined craneofacial surgery during the period: January of the 2009 to January of the 2012 in the National Institute of Oncology and Radiobiology with a 2 year pursuit. Descriptive statistical variables were used. Results: 20 patients were intervened. The age average was of 44,8 years. It prevail the masculine sex (65 percent). Nasal obstruction constitutes the most frequent presentation. Adenocarcinoma and epidermoid carcinoma constituted the most frequent malignant lesions. Inside the benign lesions prevail the invertedpapiloma. The techniques more employees were the bilateral frontal craneotomy and total etmoidectomy. The most frequent complication was the cerebrospinal fluid leak. The 2 years overall survival in patients with malignant lesions was 35 percent. Conclusions: A high number of complications was identified but they didn’t affect the survival neither the quality of life. An acceptable rate of survival was achieved in malignant lesions.

Introducción: La remoción de lesiones etmoidales con extensión secundaria a la base cranealy/o región facial, entraña una elevada complejidad y se encuentra asociada a una elevada morbilidad. Objetivo: Determinar los resultados de la cirugía combinada craneofacial en pacientes con neoplasias etmoidales extendidas. Métodos: Se realizó un estudio descriptivo retrospectivo transversal. La muestra estuvo conformada por los pacientes intervenidos quirúrgicamente de lesiones de base craneal anterior mediante un abordaje combinado craneofacial durante el período: enero de 2009 a enero de 2012 en el Instituto Nacional de Oncología y Radiobiología con un seguimiento de 2 años. Se emplearon variables estadísticas descriptivas. Resultados: Fueron intervenidos 20 pacientes. El promedio de edad fue de 44,8 años. Predominó el sexo masculino (65 por ciento). La obstrucción nasal constituyó la presentación más frecuente. El adenocarcinoma y el carcinoma epidermoide constituyeron las lesiones malignas más frecuentes. Dentro de las lesiones benignas predominó el papiloma invertido. Las técnicas más empleadas fueron la craneotomía frontal bilateral y la etmoidectomía total. La complicación más frecuente fue la fístula de líquido cefalorraquídeo. La supervivencia global a los 2 años en los pacientes con lesiones malignas fue del 35 por ciento. Conclusiones: Se identificó un elevado número de complicaciones pero no afectaron la supervivencia ni la calidad de vida. Se logró una aceptable tasa de supervivencia en lesiones malignas.

Fortificación del arroz para corregir la deficiencia de micronutrientes en niños de 6 a 59 meses de edad / Rice fortification to correct micronutrient deficiency in children 6-59 months old

Objetivo. Realizar una revisión sistemática de la literatura sobre la eficacia del consumo de arroz fortificado en el incremento de los niveles de hierro y otros micronutrientes en niños de 6 a 59 meses de edad, con la finalidad de evaluar su utilidad como intervención de salud pública. Métodos. La búsqueda se realizó en las bases de datos Medline, Embase, The Cochrane Library y LILACS. Se incluyeron ensayos clínicos aleatorizados (ECA) que evaluaron el consumo de arroz fortificado comparado con placebo u otras formas de intervención sobre la mejora de los niveles de hierro y otros micronutrientes. Para evaluar la calidad metodológica, se utilizó la lista de verificación CONSORT®. El riesgo de sesgo de los estudios se evaluó según la metodología de la Colaboración Cochrane®. Resultados. Se incluyeron siete ECA en la revisión. Todos los estudios mostraron mejoras significativas en indicadores del estado nutricional de hierro en los grupos intervenidos, sin reportar efectos adversos. No se evidenció mejoría en los niveles de vitamina A, ni en los indicadores antropométricos de peso y talla como resultado secundario de la intervención. Los estudios incluidos mostraron calidad metodológica moderada. Conclusiones. La fortificación del arroz representó una estrategia de intervención eficaz para corregir la deficiencia de hierro en la población infantil menor de cinco años. Su implementación como medida de salud pública requiere estudios locales que evalúen su efectividad en intervenciones a largo plazo y en mayor escala.

Objective. To carry out a systematic review of the literature on the effectiveness of fortified rice consumption in terms of increasing levels of iron and other micro­nutrients in children aged 6-59 months, with a view to evaluating its usefulness as a public health intervention. Methods. A search was conducted in MEDLINE, Embase, Cochrane Library, and LILACS databases. The review included randomized clinical trials (RCTs) that assessed the consumption of fortified rice, compared with a placebo or other forms of intervention, in terms of enhanced levels of iron and other micronutrients. The CONSORT® checklist was used to assess methodological quality. The risk of bias in the studies was assessed using the Cochrane® Collaboration methodology. Results. Seven RCTs were included in the review. All the studies showed significant improvements in indicators of nutritional iron status in the intervention groups, without reporting adverse effects. There was no evidence of improvement in vitamin A levels or in anthropometric indicators of weight and height as a secondary result of the intervention. The included studies showed moderate methodological quality. Conclusions. Rice fortification was an effective intervention strategy to correct iron deficiency in children under age 5. For implementation as a public health measure, local studies are needed to assess its effectiveness in long-term and large-scale interventions.

Carcinoma de osso temporal sem foco metastático primário: relato de caso e revisão de literatura / Carcinoma temporal bone unfocused metastatic primary: case report and literature review

Os tumores do osso temporal são raros e geralmente apresentam sintomas como otorreia, otalgia e hipoacusia, por isso podem ser facilmente confundidos com um processo infeccioso, retardando o diagnóstico e piorando o prognóstico do paciente. KS, 7 anos, masculino. Estado geral: regular. Ao exame: consciente; linfonodos cervicais palpáveis, móveis; massa palpável, imóvel e indolor em topografia retroauricular esquerda; surdez à esquerda e paralisia facial esquerda. Tomografia computadorizada de crânio evidenciou lesão expansiva do osso temporal captante de contraste com extensão para fossa média e posterior do crânio. Realizada complementação radiológica com ressonância de encéfalo, a qual apresentou imagem hipercaptante em T1 contrastado. Nas incidências T2, observa-se edema lobotemporal adjacente à lesão. Exame angiográfico cerebral apresentou obstrução tumoral do seio sigmoide esquerdo. Paciente submetido à mastoidectomia radical esquerda com ligadura e ressecçãodo seio sigmoide esquerdo resultando em ressecção completa lesional. Anatomopatológico e exame imunoistoquímico compatíveis com adenocarcinoma. Encaminhado para terapia oncológica com quimioterapia e radioterapia. Óbito após quatro meses do tratamento neurocirúrgico. O diagnóstico precoce associado com a extensão do tumor acarreta melhor ou pior prognóstico para os pacientes acometidos por essa moléstia.

Tumors of the temporal bone are rare and usually have symptoms such as otorrhea, otalgia and hearing loss and, therefore, can be easily confused with an infectious process delaying diagnosis and worse prognosis. KS, age 7, male. General condition: regular. On examination: conscious, palpable cervical lymph nodes, mobile; palpable mass, painless and property surveying retroauricular left, left deafness and facial paralysis left. Cranial computed tomography showed a lesion of the temporal bone with extensionto the middle fossa and posterior skull that enhance with contrast. Performed complementation with radiological MRI brain image which showed uptake, in contrast T1. Incidences in T2, there is edema temporal lobe adjacent to the lesion. Cerebral angiography showed a tumor obstructing the left sigmoidsinus. Patient underwent left radical mastoidectomy with ligation and resection of the left sigmoid sinus resulting in complete lesional resection. Histopathological and immunohistochemical examination compatible with adenocarcinoma. Referred for cancer therapy with chemotherapy and radiation. Death within four months after neurosurgical treatment. Early diagnosis associated with tumor extension carries a better or worse prognosis for patients affected by this disease.

Costos económicos en craneotomía vigíl para la resección de tumores intracerebrales / Economic costs in a craniotomy monitor for the resection of intracerebral tumors

INTRODUCCIÓN: la técnica de craneotomía vigíl (CV) ha facilitado la extracción de lesiones intracerebrales cercanas a áreas elocuentes debido a la información inmediata que se puede obtener por vía de cortico-estimulación. OBJETIVO: describir los costos económicos comparativos entre CV y anestesia general (CAG). MÉTODO: se estudiaron los casos operados bajo CV, desde noviembre del 2007 a octubre del 2012, en el Hospital de Diagnóstico de El Salvador. Se operaron 63 pacientes bajo CV, de estos, 45 con patología oncológica fueron comparados contra 45 pacientes operados bajo CAG. Se analizan costos de CV versus CAG, los cuales se desglosan en: procedimiento, días de estancia intrahospitalaria y unidades intermedias. RESULTADOS: el costo promedio de CV fue de 6,540 USD (6,300 ­ 6,900) versus 8,550 USD (8,000 - 9,000) de CAG (p.0003). El tiempo en quirófano fue de 257.49 minutos en CV y de 247.51 minutos para CAG (p.0.63). El tiempo promedio hospitalización en CV fue de 2.1 días (1-4) y en CAG de 2.9 días (2-5) (p0.004). Tres (6.6%) pacientes de CV pasaron a unidad de cuidados intermedios (UCIM), de CAG 6 (13.3%) pacientes pasaron a UCIM (p.0.04). La tasa de resección volumétrica según RM control fue de 92% (40-100) en CV versus 95% (62-100) en CAG (p.0.5). CONCLUSIONES: la CV mostró ser más económica que la clásica CCAG e incurre en menor tiempo de hospitalización. Las series no fueron comparables en cuanto a cercanía de las lesiones a áreas elocuentes y a la existencia de complicaciones, ya que la mayoría de casos en dichas áreas fueron operados por CV

INTRODUCTION: awake craniotomy (CV) technique made easier the resection of intracerebral lesions near eloquent cortex due to the immediate information that can be obtained via cortico-stimulation. OBJECTIVE: to investigate comparative costs at our center between CV and general anesthesia (CAG). METHOD: we analyzed the cases that were operated under CV from November 2007 to October 2012 at the Hospital de Diagnóstico de El Salvador. During this period 63 patients were operated using CV. 45 patients with oncological pathology were chosen that could be compared to 45 patients that were operated by the same team but under CAG. Comparative costs were studied and broken down in the direct cost of procedure, hospital stay in regular and intermediate care units. A brief description of the techniques used is provided and clinical results with regards to volumetric resection and neurologicalcomplications. RESULTS: the average cost of CV was 6,540 USD (6,300 ­ 6,900) versus 8,550 USD (8,000 - 9,000) of CAG (p.0003). Operating room time was 257.49 minutes in CV and 247.51 minutes for CAG p.0.63. The average hospitalization time was in CV 2.1 days (1-4) and 2.9 days in CAG (2-5) (p.0.004). Three (6.6%) patients of CV needed Intermediate Care (UCIM), in CAG 6 (13.3%) patients needed (UCIM p.0.04). The proportion of lesions next to or in eloquent cortex was CV (36) versus CAG (15) 2.4:1 (p.0.0031). Volumetric resection according MRI was 92% (40-100) in CV versus 95% (62-100) in CAG, (p.0.5). CONCLUSIONS: awake craniotomy showed to be less expensive than CAG and had less hospital stay. Both series were not comparable with regards to tumor resection in eloquent or near eloquent cortex and complications due to the fact that most of the complex cases were operated under CV

Nuances in the Treatment of Malignant Tumors of the Clival and Petroclival Region

Introduction: Malignancies of the clivus and petroclival region are mainly chordomas and chondrosarcomas. Although a spectrum of malignancies may present in this area, a finite group of commonly encountered malignant pathologies will be the focus of this review, as they are recognized to be formidable pathologies due to adjacent critical neurovascular structures and challenging surgical approaches. Objectives: The objective is to review the literature regarding medical and surgical management of malignant tumors of the clival and petroclival region with a focus on clinical presentation, diagnostic identification, and associated adjuvant therapies. We will also discuss our current treatment paradigm using endoscopic, open, and combined approaches to the skull base. Data Synthesis A literature review was conducted, searching for basic science and clinical evidence from PubMed, Medline, and the Cochrane Database. The selection criteria encompassed original articles including data from both basic science and clinical literature, case series, case reports, and review articles on the etiology, diagnosis, treatment, and management of skull base malignancies in the clival and petroclival region. Conclusions: The management of petroclival malignancies requires a multidisciplinary team to deliver the most complete surgical resection, with minimal morbidity, followed by appropriate adjuvant therapy. We advocate the combination of endoscopic and open approaches (traditional or minimally invasive) as required by the particular tumor followed by radiation therapy to optimize oncologic outcomes...

Advances in Computed Tomography Evaluation of Skull Base Diseases

Introduction: Computed tomography (CT) is a key component in the evaluation of skull base diseases. With its ability to clearly delineate the osseous anatomy, CT can provide not only important tips to diagnosis but also key information for surgical planning. Objectives: The purpose of this article is to describe some of the main CT imaging features that contribute to the diagnosis of skull base tumors, review recent knowledge related to bony manifestations of these conditions, and summarize recent technological advances in CT that contribute to image quality and improved diagnosis. Data Synthesis Recent advances in CT technology allow fine-detailed evaluation of the bony anatomy using submillimetric sections. Dual-energy CT material decomposition capabilities allow clear separation between contrast material, bone, and soft tissues with many clinical applications in the skull base. Dual-energy technology has also the ability to decrease image degradation from metallic hardwares using some techniques that can result in similar or even decreased radiation to patients. Conclusions: CT is very useful in the evaluation of skull base diseases, and recent technological advances can increase disease conspicuity resulting in improved diagnostic capabilities and enhanced surgical planning...

Advances in Magnetic Resonance Imaging of the Skull Base

Introduction: Over the past 20 years, magnetic resonance imaging (MRI) has advanced due to new techniques involving increased magnetic field strength and developments in coils and pulse sequences. These advances allow increased opportunity to delineate the complex skull base anatomy and may guide the diagnosis and treatment of the myriad of pathologies that can affect the skull base. Objectives: The objective of this article is to provide a brief background of the development of MRI and illustrate advances in skull base imaging, including techniques that allow improved conspicuity, characterization, and correlative physiologic assessment of skull base pathologies. Data Synthesis Specific radiographic illustrations of increased skull base conspicuity including the lower cranial nerves, vessels, foramina, cerebrospinal fluid (CSF) leaks, and effacement of endolymph are provided. In addition, MRIs demonstrating characterization of skull base lesions, such as recurrent cholesteatoma versus granulation tissue or abscess versus tumor, are also provided as well as correlative clinical findings in CSF flow studies in a patient pre- and post-suboccipital decompression for a Chiari I malformation. Conclusions: This article illustrates MRI radiographic advances over the past 20 years, which have improved clinicians' ability to diagnose, define, and hopefully improve the treatment and outcomes of patients with underlying skull base pathologies...

Implantes extraorais em pacientes irradiados / Extraoral implants in irradiated pacients

O objetivo deste trabalho foi avaliar o resultado da osseointegração de implantes extraorais lemento de suporte e retenção de próteses nas reabilitações de deformidades faciais. MÉTODO: Estudo retrospectivo de prontuários de 59 indivíduos operados de câncer, submetidos a 164 implantes para retenção de prótese facial. RESULTADOS: Dos 59 indivíduos, 14 foram previamente irradiados e receberam 42 implantes. Quarenta e cinco indivíduos não foram irradiados e receberam 122 implantes. Do total de 164 implantes, oito não osseointegraram, dos quais dois foram instalados em osso previamente irradiados. O resultado representou o sucesso de 116 (95,1%) implantes osseointegrados nos indivíduos não irradiados. E sucesso de 40 (95,3%) implantes osseointegrados em ossos irradiados. CONCLUSÃO: Concluiu-se que o uso de implantes extraorais é uma técnica segura e eficaz como suporte e retenção para próteses faciais em indivíduos com deformidades nessa região. A radioterapia não impede a osseointegração.

The aim of this study is to analyze the success of extraoral osseointegrated implants used to support designed to rehabilitate craniofacial deformities. METHOD: This study was based on the retrospective assessment of charts from 59 patients submitted to cancer surgery and who received 164 extraoral implants to contain facial prosthesis. RESULTS: Among 164 implants, 42 were fixed in previously irradiated regions. Eight of the implants did not have osseointegration; and from these, two were fixed in irradiated bone. The result show 116 (95.1%) successfully osseointegrated implants in non-irradiated sites. The success rate among 42 implants fixed in previously irradiated bones was 40 (95.3%) osseointegrated implants. CONCLUSION: The use of extraoral craniofacial implants represents a safe and effective approach to treat facial deformities as a support for the rehabilitation prosthesis. Radiotherapy treatment does not prevent osseointegration.

Vestibular schwannoma: 825 cases from a 25-year experience

Introduction: Acoustic nerve tumors have been recognized as a clinico-pathologic entity for at least 200 years, and they represent 90% of cerebellopontine angle diseases. Histologically, the tumors are derived from Schwann cells of the myelin sheath, with smaller tumors consisting of elongated palisade cells, while in large tumors, cystic degeneration can be found in the central areas, possibly due to deficient vascularization. We retrospectively reviewed 825 cases of vestibular schwannomas, reported between January 1984 and August 2006, in which the patients underwent surgery to remove the tumor. Objective: To evaluate signs, symptoms, aspects of clinical diagnosis, including the results of audiological and imaging studies, and surgical techniques and complications. Methods: A retrospective chart review. The medical records of all patients undergoing surgical treatment for schwannoma during the period indicated were reviewed. Results and Conclusion: Hearing loss was the first symptom reported in almost all cases, and tumor size was not proportional to the impairment of the auditory threshold. The surgical techniques allowed safe preservation of facial function. In particular, the retrolabyrinthine route proved useful in small tumors, with 50% preservation of hearing...