Academic literature on the topic 'Meningoencephalocele'

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Journal articles on the topic "Meningoencephalocele"

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Wohon, Erfprinsi, Bambang Harijono, and Siti Chasnak Saleh. "Manajemen Anestesia pada Anak dengan Nasofrontal Meningoencephalocele dan Hydrocephalus Non-Communicant." Jurnal Neuroanestesi Indonesia 1, no. 1 (January 28, 2012): 39–43. http://dx.doi.org/10.24244/10.24244/jni.v1i1.85.

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Meningoencephalocele adalah defek kongenital yang sangat jarang, tapi insidennya tinggi di Asia Tenggara, termasuk di Indonesia. Penderita dengan nasofrontal meningoencephalocele memerlukan koreksi pembedahan sedini mungkin karena adanya kelainan bentuk wajah, gangguan pandangan, bertambahnya ukuran meningoencephalocele disebabkan bertambahnya prolaps cerebri dan risiko infeksi. Dalam laporan ini kami presentasikan kasus seorang bayi 9 bulan dengan meningoencephalocele naso-orbital dan hydrocephalus non communican yang menjalani operasi VP shunt dan eksisi cele. Adanya massa tersebut, baik meningoencephalocele nasofrontal atau frontoethmoidal maupun occipital, menimbulkan kesulitan bagi ahli anestesi mulai saat induksi, pemeliharaan anestesi dan pasca operasinya. Menjadi tantangan bagi ahli anestesi dalam pengelolaan meningoencephalocele, dimana sebagian besar penderitanya adalah anak-anak yang mempunyai kesulitan tersendiri, termasuk mengamankan jalan nafas dengan intubasi dan adanya massa yang akan mempersulit ventilasi saat induksi, adanya massa pada nasofrontal serta nasoethmoidal yang berhubungan dengan komplikasinya dan penilaian yang tepat terhadap perdarahan dan hipotermia.Anesthesia Management for A child with Nasofrontal Meningoencephalocele and Hydrocephalus Non CommunicantMeningoencephaloceles are very rare congenital malformations in the world that have a high incidence in the population of Southeast Asia, include in Indonesia. Children with nasofrontal meningoencephaloceles should have surgical correction as early as possible because of the facial dysmorphia, impairment of binocular vision, increasing size of the meningoencephalocele caused by increasing brain prolapse, and risk of infection of the central nervous system. In this report, we presented a case of a 9 months-old baby girl with nasofrontal meningoencephalocele and hydrocephalus non communican, posted for VP shunt (ventriculo-peritoneal shunt) and cele excision. Because of the mass, nasofrontal or frontoethmoidal and occipital meningoencephalocele leads the anaesthetist to problems since the preoperative visit, time of induction, maintenance of anaesthesia during the operation until post operative care. Anaesthetic challenges in management of meningoencephalocele, which most of the patients are children, include ventilation, intubation and securing the airway with intubation with the mass in nasofrontal and nasoethmoidal with its associated complications and accurate assessment of bloodloss and prevention of hypothermia.
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Jenner, Zachary B., Nuruddin Husein, Roy Riascos, and Yoshua Esquenazi. "Orbital and nasal meningoencephaloceles secondary to chronic hydrocephalus: A rare cause of bilateral proptosis." Neuroradiology Journal 31, no. 4 (June 8, 2018): 420–25. http://dx.doi.org/10.1177/1971400918778145.

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Introduction Orbital meningoencephalocele formation is primarily a result of congenital defects in the pediatric population and trauma of the anterior cranial fossa in adults. We present a unique case of nontraumatic nasal and orbital meningoencephaloceles presenting as bilateral proptosis with exotropia secondary to chronic hydrocephalus. Clinical presentation A 20-year-old male with a history of tuberous sclerosis, X-linked intellectual disability, and epilepsy presented to the emergency department with two days of nausea, emesis, seizures, and two months of progressive proptosis. Initial radiographs of the skull showed a “copper beaten” appearance, indicating chronically elevated intracranial pressure. Computed tomography imaging of the head demonstrated bilateral defects in the cribriform plate and anterior cranial fossa. Magnetic resonance imaging of the brain revealed triventricular hydrocephalus with meningoencephalocele extension into the nasal cavity and frontal horn herniation into the extraconal space of the orbits. The hydrocephalus was managed with ventriculoperitoneal shunt placement with rapid and complete resolution of the proptosis. Conclusion No reports have described bilateral proptosis as the presenting finding of orbital and nasal meningoencephaloceles in the absence of trauma or congenital defect. This case study demonstrates the management of meningoencephalocele formation secondary to chronic hydrocephalus.
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Khan, Maroof Aziz, and Iftikhar Salahuddin. "Intranasal Meningoencephalocele and the Use of Fibrin Glue." Ear, Nose & Throat Journal 76, no. 7 (July 1997): 464–67. http://dx.doi.org/10.1177/014556139707600710.

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Meningoencephaloceles are rarely seen in adults. This case report illustrates the management of a large intranasal meningoencephalocele in an adult man. Excision of this lesion resulted in a defect in the cribriform plate which was closed using tissue and fibrin glue.
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Marfatia, Hetal K., Kartik A. Parelkar, Adhara Chakraborty, and Shampa Mishra. "Pediatric Meningoencephaloceles Endoscopic Endonasal Repair: Our Experience." Allergy & Rhinology 9 (January 2018): 215265671880240. http://dx.doi.org/10.1177/2152656718802408.

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Background Pediatric patients presenting with a nasal mass is uncommon and a high index of suspicion for it to be a meningoencephalocele is essential. Majority of these are congenital and require early intervention owing to the risk of meningitis. Surgery in these cases is very challenging because of the risk of anesthesia and limited space. Objective This study aimed to describe our technique and experience in managing pediatric meningoencephaloceles. Methods A retrospective study of 19 pediatric patients (age ranging from 40-day-old infants to 11.5-year-old children) was conducted at our tertiary care center from January 2012 to February 2017. Patients presenting with an intranasal meningoencephalocele were treated by endoscopic approach, using otological microinstruments. After detailed imaging and clinical evaluation, a tailored repair, using fat/fascia/cartilage, a multilayer closure, was carried out in all cases. Results All patients had a successful repair and recovery, except for one death following an episode of convulsion. There was a minor circumferential narrowing of the nasal vestibule and synechia formation in 2 of our cases. Conclusion Transnasal endoscopic repair of meningoencephalocele is minimally invasive. It avoids permanent anosmia and is cosmetic. A combination of miniaturized instruments and a 4-mm 0° nasal endoscope gives excellent visual field and an adequate working space. Owing to the larger defects in congenital meningoencephaloceles, a multilayer repair provides excellent outcomes.
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Sakharkar, Kanchan, Sunil N. Mhaske, Liza Bulsara, and Sachin Vahadane. "Meningoencephalocele." Indian Journal of Trauma and Emergency Pediatrics 8, no. 2 (2016): 153–55. http://dx.doi.org/10.21088/ijtep.2348.9987.8216.21.

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Poutoglidis, Alexandros, Pavlos Pavlidis, Georgios Katsilis, and Gregory Alexander Schittek:. "Idiopathic temporal bone encephalocele: Diagnosed and treated during cochlear implantation." Medical Science and Discovery 7, no. 12 (December 27, 2020): 750–53. http://dx.doi.org/10.36472/msd.v7i12.454.

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Objective: Meningoencephaloceles of the temporal bone are rare entities. There are two main categories, congenital and acquired. Acquired meningoencephaloceles are more common due to iatrogenic injury to the tegmen tympani which is a common complication during mastoidectomy. Case Presentation: We present a case of an idiopathic meningoencephalocele that was diagnosed and treated successfully during cochlear implantation via transmastoid approach. Fascia lata graft was used to reconstruct the deficit of tegmen tympani. Audiological outcome has been improved. Conclusions: Idiopathic Meningoencephaloceles present without specific clinical symptomatology and as a result diagnosis delay significant. In literature, there are various surgical approaches with mixed results.
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Zuckerman, Jodi, James A. Stankiewicz, and James M. Chow. "Long-Term Outcomes of Endoscopic Repair of Cerebrospinal Fluid Leaks and Meningoencephaloceles." American Journal of Rhinology 19, no. 6 (November 2005): 582–87. http://dx.doi.org/10.1177/194589240501900609.

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Background The management and surgical approach to cerebrospinal fluid (CSF) leaks and meningoencephaloceles have undergone transformation throughout the last 10 years. It is our interest to examine the long-term surgical outcome and reoccurrence rates of CSF leaks or meningoencephaloceles in patients having endoscopic surgical repair. Methods We performed a retrospective evaluation of 50 patients that underwent endoscopic surgical repair of a CSF leak, meningoencephalocele, or both, between September 1985 and October 2003. Results Cumulatively, reoccurrence rates were 15% (7/47) among the CSF leak patients with an average time frame for reoccurrence ranging from 1 to 25 months (average, 7 months). Patients with meningoencephaloceles had an overall reoccurrence rate of 8% (1/13). In addition, a Medline search on CSF leaks and meningoencephaloceles provided the names of 32 authors that have studied outcomes of endoscopic surgical repair. Of the 151 patients still followed in the 5- to 10-year postoperative group, there were 37 recurrences of CSF leaks and 5 reoccurrences of the meningoencephaloceles with a total recurrence rate of 27% (37 + 5/151). Of the 19 patients still followed in the >10-year postoperative group, there were three reoccurrences of CSF leaks and no reoccurrences of meningoencephaloceles, giving a reoccurrence rate of 16% (3 + 0/19). Conclusion Based on our cumulative results, a reoccurrence of a CSF leak or meningoencephalocele after endoscopic repair will occur within the first 2 years postoperatively. Once patients pass these postoperative time frames they are relatively free of reoccurrence from this very effective surgical management. Endoscopic repair results are better than craniotomy with much less morbidity.
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Tabaee, Abtin, Vijay K. Anand, Paolo Cappabianca, Aldo Stamm, Felice Esposito, and Theodore H. Schwartz. "Endoscopic management of spontaneous meningoencephalocele of the lateral sphenoid sinus." Journal of Neurosurgery 112, no. 5 (May 2010): 1070–77. http://dx.doi.org/10.3171/2009.7.jns0842.

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Object Spontaneous meningoencephaloceles of the lateral sphenoid sinus are rare lesions that are hypothesized to result from persistence of the lateral craniopharyngeal canal. Prior reports of the management of this lesion have been limited by its relative rarity. The objective of this paper is to report the theoretical etiology, surgical technique, and outcomes in patients undergoing endoscopic repair of spontaneous meningoencephalocele of the sphenoid sinus. Methods The authors conducted a retrospective review of a multiinstitutional series of 13 cases involving patients who underwent endoscopic repair of spontaneous meningoencephalocele of the lateral sphenoid sinus. The surgical technique and pathophysiological considerations are discussed. Results The clinical manifestations included CSF rhinorrhea (85%), chronic headache (77%), and a history of meningitis (15%). The endoscopic approaches to the lateral sphenoid sinus were transnasal (39%), transpterygoid (23%), and transethmoid (39%). Two patients (8%) had postoperative CSF leaks, one of which closed spontaneously and one of which required revision endoscopic closure. All patients were free of leak at most recent follow-up. One patient experienced postoperative meningitis in the early postoperative period. Conclusions Endoscopic endonasal closure is an effective modality in the treatment of spontaneous meningoencephaloceles of the lateral sphenoid sinus. If the sphenoid sinus has extensive lateral pneumatization, adequate exposure may require a transpterygoid approach.
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Mohindra, Satyawati, Sandeep Mohindra, and Sourabha Kumar Patro. "Successful Endoscopic Endonasal Repair of Nasal Meningoencephalocele in a 21-Day-Old Neonate." Allergy & Rhinology 6, no. 2 (January 2015): ar.2015.6.0121. http://dx.doi.org/10.2500/ar.2015.6.0121.

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Introduction Indications of surgical intervention in congenital nasal meningoencephaloceles includes presence of cerebro spinal fluid rhinorrhea having a risk of causing meningitis, episodes of prior meningitis and bilateral nasal obstruction causing respiratory difficulty in these obligate nasal breathers. Many authors would like to wait till the patient attains the age of 2 to 3 years for repair of the defect due to surgical feasibility. However, early intervention prevents further episodes of meningitis in the future. We present the youngest patient of nasal meningoencephalocele successfully repaired via endoscopic approach. Case Report A 21 days old neonate was referred to us with a nasal meningoencephalocele with active cerebrospinal fluid rhinorrhoea. Radiological investigation showed a cribriform plate defect on the right side. Repair was done by endoscopic route by multi-layered closure of the defect which was augmented with a mucoperichondrial flap from the septum. Patient was asymptomatic in the post-operative follow up period and did not have any episode of meningitis till date. Conclusion Early repair by transnasal endoscopic route is a feasible surgical option for congenital anterior skull base defects with meningoencephaloceles to prevent further episodes of meningitis. This is feasible even in the neonatal period due to improved technique and instrumentation now available for endoscopic nasal surgeries.
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Budu, Vlad, Tatiana Decuseara, Andreea Nicoleta Costache, Loredana Ghiuzan, Monica Hodor, Gabriel Dascalu, Mihai Tusaliu, and Ioan Bulescu. "Endoscopic endonasal resection of a nasal meningoencephalocele - Case report." Romanian Journal of Rhinology 7, no. 28 (December 1, 2017): 235–39. http://dx.doi.org/10.1515/rjr-2017-0025.

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AbstractNasal meningoencephaloceles are rare findings, represented by protrusions of intracranial contents into the nasal cavity. They present as unilateral masses, and commonly determine unilateral nasal obstruction, rhinorrhea and non-characteristic headaches.We present the case of a 34-year-old patient diagnosed with a posttraumatic transethmoidal meningoencephalocele. The patient presented with unilateral nasal obstruction, mild headache and episodic watery rhinorrhea. The treatment was endoscopic endonasal surgical excision and repair of the skull base defect, in a mixt ENT-neurosurgical team. Patient follow-up showed no remaining mass or symptoms and normal closure of the skull base defect.
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Dissertations / Theses on the topic "Meningoencephalocele"

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FALLON, PHILIPPE. "Meningo-encephalocele du lobe temporal prolabee dans la fosse pterygo-maxillaire." Lille 2, 1992. http://www.theses.fr/1992LIL2M162.

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Book chapters on the topic "Meningoencephalocele"

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David, David J., David C. Hemmy, and Rodney D. Cooter. "Meningoencephaloceles." In Craniofacial Deformities, 93–100. New York, NY: Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3232-2_6.

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Jones, Heidi, and Aristotelis Poulios. "Meningoencephalocoele." In Rhinology and Anterior Skull Base Surgery, 249–50. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-66865-5_51.

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Leung, Randal. "Temporal Bone Meningoencephaloceles." In Encyclopedia of Otolaryngology, Head and Neck Surgery, 2736–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-23499-6_200196.

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"Meningoencephalocele." In Encyclopedia of Otolaryngology, Head and Neck Surgery, 1645. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-23499-6_100609.

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"33 Surgery of Skull Base Meningoencephalocele." In Atlas of Pediatric Head and Neck and Skull Base Surgery, edited by Dan M. Fliss and Ari DeRowe. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/b-0041-180018.

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"18 Endoscopic Management of Anterior Skull Base Meningoencephalocele." In Transnasal Endoscopic Skull Base and Brain Surgery, edited by Aldo Cassol Stamm. Stuttgart: Georg Thieme Verlag, 2011. http://dx.doi.org/10.1055/b-0034-81695.

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Liatis, Theophanes, Alberta De Stefani, Panagiotis Mantis, and Giunio Bruto Cherubini. "Delayed forebrain syndrome due to traumatic intranasal meningoencephalocele in a cat." In BSAVA Congress Proceedings 2019, 541. British Small Animal Veterinary Association, 2019. http://dx.doi.org/10.22233/9781910443699.85.26.

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Rapastella, Sofia, Robert Brash, Heather Covey, and Mellora Sharman. "Intranasal meningoencephalocele in a one-year-old Staffordshire Bull Terrier with unilateral destructive rhinitis." In BSAVA Congress Proceedings 2020, 540–41. British Small Animal Veterinary Association, 2020. http://dx.doi.org/10.22233/9781910443774.89.2.

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Tabaee, Abtin, and Edward McCoul. "Management of Skull Base Defects: Cerebrospinal Fluid Rhinorrhea, Meningoencephalocele and Endoscopic Skull Base Surgery." In Sataloff’s Comprehensive Textbook of Otolaryngology: Head and Neck Surgery (Rhinology/Allergy and Immunology) -Volume 2, 871. Jaypee Brothers Medical Publishers (P) Ltd., 2016. http://dx.doi.org/10.5005/jp/books/12714_62.

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"12 Meningoencephaloceles." In Pediatric Endoscopic Endonasal Skull Base Surgery, edited by Harminder Singh, Jeffrey P. Greenfield, Vijay K. Anand, and Theodore H. Schwartz. Stuttgart: Georg Thieme Verlag, 2020. http://dx.doi.org/10.1055/b-0040-177068.

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Conference papers on the topic "Meningoencephalocele"

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Hernandez, Jesus Gimeno, Carla Fernandez Garcia, Melchor Saiz Pardo-sanz, Manuel Gomez Serrano, Ivan Muerte Moreno, Jose Roan Roan, Eduardo Castillo Serrano, and Andrea Lopez Salcedo. "Endoscopic Endonasal Treatment of Frontal Sinus Meningoencephalocele." In 30th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1702676.

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Basak, Hazan, Suha Beton, Gokmen Kahilogullari, and Cem Meco. "Endonasal Endoscopic Management of a Craniopharyngeal Canal Meningoencephalocele in a 6-Month-Old Patient." In 30th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1702618.

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