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OBJECTIVE: Transcortical approaches using a spatula-based retraction system have traditionally been used for the microsurgical resection of deep-seated intraventricular and parenchymal brain tumors. Recently, transparent cylindrical or tubular retractors have been developed to provide a stable corridor to access deeper brain lesions and perform bimanual microsurgical resection. The flexible endoports minimize brain retraction injury during surgery and, along with the superior vision of endoscopes, offer several advantages over standard microsurgery. In this chapter, we describe the surgical technique of the endoport-guided endoscopic excision of deep-seated intraaxial brain tumors. METHODS: The endoscopic endoport technique that we use at our institution for the surgical management of intraventricular and intraparenchymal brain tumors has been described in detail with illustrative cases. RESULTS: Results from the literature review of intraventricular and intraparenchymal port surgery were analyzed, and the feasibility and safety of this technique were discussed. Surgical complication avoidance and management were highlighted. The port technique offers numerous potential advantages, including (1) reducing focal brain injury by distributing retraction forces homogenously, (2) minimizing white matter disruption and the risk of fascicle injury during cannulation, (3) ensuring the stability of the surgical corridor during the procedure, (4) preventing inadvertent expansion of the corticectomy and white fiber tract dissection throughout surgery, and (5) protecting the surrounding tissues against iatrogenic injuries caused by instrument entry and reentry. CONCLUSION: The endoport-assisted endoscopic technique is safe and offers an effective alternative option for the resection of intraventricular and intraparenchymal lesions.
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Neoplasias Encefálicas , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Neoplasias Encefálicas/cirugía , Neuroendoscopía/métodos , Neuroendoscopía/instrumentación , Procedimientos Neuroquirúrgicos/métodosRESUMEN
Background: Medical management is the first line of care for patients with trigeminal neuralgia (TN), and carbamazepine is the drug of choice used alone or in combination with other drugs. Gamma knife radiosurgery (GKRS) has been an established option in the management of refractory TN based on its noninvasiveness and robust safety profile. Our study aims to confirm the safety and assess the efficacy of GKRS in the management of TN. Material and Methods: A retrospective review of the patients with refractory TN treated with GKRS from 1997 to March 2019 by the senior author was carried out. Out of 194 eligible patients, detailed clinical information was not available in 41 patients. The remaining 153 patients' case files (post-GKRS cohort) were reviewed, and data obtained were collated, computed, and analyzed. An additional cross-sectional analysis was carried out telephonically in the post-GKRS cohort in January 2021 using Barrow Neurological Institute (BNI) pain scoring, to obtain the long-term efficacy of GKRS in TN. Results: The majority of the patients (96.1%) received a radiation dose of 80 Gy. At 6 months, 94.8% of patients had satisfactory response to GKRS. Follow-up ranged between 1 and 7.5 years. The recurrence rate was 9.2% and the complication rate was 4.6%. Facial numbness was the commonest complication. No mortality was reported. The cross-sectional arm of the study had a response rate of 39.2% (60 patients). Adequate pain relief (BNI I/II/IIIa/IIIb) was reported in 85% of patients. Conclusion: GKRS is a safe and effective modality of treatment for TN without any major complications. Both short-term and long-term efficacies are excellent.
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Radiocirugia , Neuralgia del Trigémino , Humanos , Estudios Retrospectivos , Neuralgia del Trigémino/radioterapia , Neuralgia del Trigémino/cirugía , Estudios Transversales , Resultado del Tratamiento , Radiocirugia/efectos adversos , Dolor/cirugía , Estudios de SeguimientoRESUMEN
Background: Endoscopic surgery has emerged in recent years as an alternative to conventional microsurgical approaches for removal of intraventricular tumors. Endoports have enhanced tumor access and visualization with a significant reduction in brain retraction. Objective: To evaluate the safety and efficacy of endoport-assisted endoscopic technique for the removal of tumors from the lateral ventricle. Methods: The surgical technique, complications, and postoperative clinical outcomes were analyzed with a review of the literature. Results: Tumors were primarily located in one lateral ventricular cavity in all 26 patients, and extension to the foramen Monro and the anterior third ventricle was observed in seven and five patients, respectively. Except for three patients with small colloid cysts, all other tumors were larger than 2.5 cm. A gross total resection was performed in 18 (69%), subtotal in five (19%), and partial removal in three (11.5%) patients. Transient postoperative complications were observed in eight patients. Two patients required postoperative CSF shunting for symptomatic hydrocephalus. All patients improved on KPS scoring at a mean follow-up of 4.6 months. Conclusions: Endoport-assisted endoscopic technique is a safe, simple, and minimally invasive method to remove intraventricular tumors. Excellent outcomes comparable to other surgical approaches can be achieved with acceptable complications.
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Neoplasias del Ventrículo Cerebral , Neuroendoscopía , Humanos , Neoplasias del Ventrículo Cerebral/cirugía , Ventrículos Laterales/cirugía , Neuroendoscopía/instrumentación , Neuroendoscopía/métodosRESUMEN
Segmental schwannomatosis involving a nerve in single limb is uncommon. Schwannomatosis is used to describe a distinct clinicopathological disease of multiple schwannomas without manifestations of neurofibromatosis, and it is termed segmental when a single extremity is involved. Surgery is indicated when there is progressive clinical deterioration or progressive increase in size of the tumors. We present a case series of segmental schwannomatosis involving the lower limb.
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Neurilemoma , Neurofibromatosis , Neoplasias Cutáneas , Humanos , Neurofibromatosis/cirugía , Neurofibromatosis/patología , Neurilemoma/diagnóstico , Neurilemoma/cirugía , Neurilemoma/patología , Neoplasias Cutáneas/cirugía , Extremidad InferiorRESUMEN
Skull-base chordomas (CD) and chondrosarcomas (CS) are locally-invasive tumors, have similar clinical presentations, while differing in their nature of growth and outcomes. In this study, we compare the long-term outcomes of Gamma Knife Radiosurgery (GKRS) as an adjunctive treatment modality for residual skull-base CD and CS. A retrospective analysis of clinico-radiological, pathological, radiotherapeutic and outcome data was carried out in patients who underwent adjunctive GKRS for residual skull-base CD and CS at P D Hinduja Hospital, Mumbai, between 1997 and 2020. All 27 patients included had either histopathologically proven CD (20 patients) or CS (7 patients). Brachyury immunohistochemistry in CD specimens gave 70.6% positivity. Total sessions of GKRS in CD and CS groups were 22 and 7, respectively. Mean tumor volume and mean margin dose in CD group were 6.53 ± 4.18 cm3 and 15.95 ± 1.49 Gy respectively, while for CS group, they were 4.16 ± 2.79 cm3 and 18.29 ± 3.15 Gy. With mean follow-up periods of 5.25 ± 4.73 years and 6 ± 2.07 years respectively, the CD and CS groups showed 5-year progression free survival (PFS) of 56.8% and 57.1%, and a 5-year overall survival (OS) of 82.1% and 100%. Sub-group analysis in both CD and CS groups revealed a better 5-year PFS with the following factors - CS histopathology, patient age < 45 years, margin dose > 16 Gy, tumor volume < 7 cm3 (p-value < 0.05), gross total resection, and brachyury positivity. Adjunctive radiotherapy for skull-base CD and CS holds promise.
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Condrosarcoma , Cordoma , Radiocirugia , Neoplasias de la Base del Cráneo , Condrosarcoma/diagnóstico por imagen , Condrosarcoma/radioterapia , Condrosarcoma/cirugía , Cordoma/diagnóstico por imagen , Cordoma/radioterapia , Cordoma/cirugía , Estudios de Seguimiento , Humanos , Persona de Mediana Edad , Estudios Retrospectivos , Cráneo , Neoplasias de la Base del Cráneo/diagnóstico por imagen , Neoplasias de la Base del Cráneo/cirugía , Resultado del TratamientoRESUMEN
Background The effectiveness of open carpal tunnel release (OCTR) in treating carpal tunnel syndrome (CTS) is well known. However, the role of ancillary external neurolysis of the median nerve is not well-documented. The Boston carpal tunnel questionnaire (BCTQ) is a commonly used disease-specific outcome instrument for CTS, which is validated across major languages of the world. No such validated Hindi version of BCTQ exists. Objectives To analyze and compare the long-term outcome in patients who underwent OCTR alone and OCTR with external neurolysis of the median nerve, using BCTQ-Hindi version, while checking its validity. Materials and Methods A retrospective, cross-sectional study was conducted at a tertiary care institute. The BCTQ was translated into Hindi language by a language expert. Eighty-four consecutive patients who underwent either unilateral/bilateral OCTR, with or without external neurolysis of the median nerve, between 2009 and 2019 were included in the study. Outcome analysis was done using BCTQ-Hindi version and patient satisfaction scoring. BCTQ-Hindi version was examined for statistical validity. Subgroup analysis of the outcome based on surgical technique (OCTR vs. OCTR with external neurolysis) used was carried out. Results Response rate was 80.9%. Total hands evaluated were 108. BCTQ-Hindi version showed statistical validity. Overall symptom severity score (SSS) and functional severity score (FSS) were 1.14 ± 0.4 and 1.12 ± 0.35, respectively. Subgroup analysis of outcome revealed statistically significant results in favor of OCTR with external neurolysis of the median nerve. Conclusions BCTQ-Hindi version is statistically validated. OCTR with external neurolysis of the median nerve is a promising avenue in surgical management of CTS. Further prospective studies are warranted.
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Chondrosarcoma (CS) is a locally invasive, slow growing malignant neoplasm. Intracranial chondrosarcoma are extradural osseous lesions and intradural location with intratumoral hemorrhage is very rare. We report a rare case of 65-year-old male presenting with a small mass in left posterior skull base and later, suddenly deteriorating due to large cerebellar hemorrhage. A brief review of literature of such cases is also presented.
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Hemorragia Cerebral/diagnóstico por imagen , Hemorragia Cerebral/cirugía , Condrosarcoma/diagnóstico por imagen , Condrosarcoma/cirugía , Neoplasias de la Base del Cráneo/diagnóstico por imagen , Neoplasias de la Base del Cráneo/cirugía , Anciano , Hemorragia Cerebral/etiología , Condrosarcoma/complicaciones , Humanos , Imagen por Resonancia Magnética/métodos , Masculino , Base del Cráneo/diagnóstico por imagen , Base del Cráneo/cirugía , Neoplasias de la Base del Cráneo/complicacionesRESUMEN
BACKGROUND: Skull base chordoma (SBC) is relatively rare and data on its clinical outcome after surgical resection and adjuvant radiotherapy are still limited. OBJECTIVE: Analyzing the clinical postoperative outcome of SBC patients and defining prognostic factors regarding current treatment modalities. METHODS AND MATERIAL: In this study, 41 SBC patients from 2001 to 2017 were retrospectively analyzed in this single-center study. RESULTS: The most common clinical symptoms were headache (63%) and problems concerning vision (54%) like diplopia. The follow-up controls took place from 1 to 192 months. The mean survival time for the patients was 123.37 months (95% CI 90.89-155.86). The 5- and 10-year survival rates were 73.3 and 49%, respectively. Regarding the Karnofsky-Performance Scale (KPS), Cox regression showed a significant relationship between the survival rates in the overall study population and pre-surgery KPS (P = 0.004). This was further supported with a positive significant correlation between the pre-surgery KPS and the KPS at the last follow-up (P = 0.039). CONCLUSION: Statistical analysis showed that repeat surgical resection and radiotherapy could be prognostic factors. Furthermore, we were able to show that mortality decreased by 4.5% with each 10 points increase of pre-surgery KPS. This could be a major prognostic factor when deciding treatment modalities. Nevertheless, further standardized clinical studies with a larger patient population should be carried out to extrapolate prognostic factors and improve treatment modalities.
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Cordoma , Neoplasias de la Base del Cráneo , Cordoma/radioterapia , Cordoma/cirugía , Estudios de Seguimiento , Humanos , Pronóstico , Estudios Retrospectivos , Base del Cráneo , Neoplasias de la Base del Cráneo/cirugía , Resultado del TratamientoAsunto(s)
Tumores Neuroectodérmicos Periféricos Primitivos/patología , Sarcoma de Ewing/patología , Sarcoma de Ewing/radioterapia , Neoplasias de la Médula Espinal/patología , Adulto , Progresión de la Enfermedad , Femenino , Humanos , Tumores Neuroectodérmicos Periféricos Primitivos/diagnóstico , Tumores Neuroectodérmicos Periféricos Primitivos/radioterapia , Sarcoma de Ewing/diagnóstico , Neoplasias de la Médula Espinal/diagnóstico , Neoplasias de la Médula Espinal/radioterapia , Resultado del TratamientoRESUMEN
BACKGROUND: The most common cerebellopontine angle (CPA) tumor is a vestibular schwannoma. Schwannomas account for 8.5% of all intracranial tumors and more than 90% of the tumors originate from the eighth cranial nerve, but one in five CPA tumors are not vestibular schwannoma. These tumors may have different manifestations and require different management strategies. METHODS: We report 224 consecutive NVCPAT operated in the Department of Neurosurgery, P.D. Hinduja National Hospital and Medical Research Centre, Mumbai, by the senior author between 2001 and 2014 and discuss the different approaches and outcomes in NVCPAT. RESULTS: The age range was 20-60 years and there were 129 females and 95 male patients. The clinical material consisted of 81 cases of meningioma (36.1%), 44 cases of epidermoid (19.64%), 34 cases of trigeminal schwannoma (15.17%), 26 cases of jugular foramen schwannoma (11.60%), and 39 cases of other tumors (17.41%). In nonvestibular schwannoma (NVS), symptoms and signs from cranial nerve VIII are less frequent and other cranial nerves and cerebellar symptoms and signs predominate. CONCLUSION: Symptoms and signs are different in NVCPAT from those found in patients with vestibular schwannoma. Hearing loss is not the predominant symptoms. Cerebellar signs and trigeminal dysfunction are more common. The most common approach used in the current series was retrosigmoid craniotomy. Gamma knife radiosurgery was a useful adjunct in a subset of these patients.
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Radiation-induced brachial plexus neuropathy (RIBPN) is an uncommon problem. It is a delayed nontraumatic brachial plexus neuropathy following radiation treatment for carcinomas in the region of neck, axilla, and chest wall. The incidence is more commonly reported following radiation treatment for carcinoma of breast. The neurological features are characterized by severe neurogenic pain with progressive sensory-motor deficits in the affected upper limb. The incidence has increased following improved survival rate of patients with carcinomas of neck, axilla, and chest wall. The diagnosis of RIBPN is often confused with recurrence of the tumor in the neck and axilla. The management options are limited, and external neurolysis of the involved brachial plexus with excision of the perineural scar tissue is recommended in patients with severe clinical manifestations. We review our experience in the management of RIBPN from 2004 to 2017 and highlight the features of the 11 patients with this disorder whom we encountered during this period. The relevant clinical findings, natural history, pathophysiology, radiological characteristics, and various management options are briefly discussed.
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Neuropatías del Plexo Braquial/diagnóstico , Neuropatías del Plexo Braquial/cirugía , Neoplasias de la Mama/radioterapia , Traumatismos por Radiación/diagnóstico , Traumatismos por Radiación/cirugía , Neoplasias de la Mama/complicaciones , Humanos , Resultado del TratamientoRESUMEN
OBJECTIVE: A retrospective analysis of surgically treated 354 cases of injection-related iatrogenic peripheral nerve injuries was performed. The purpose of this clinical study was to present our experience in the management of various types of injection-related peripheral nerve injuries and discuss various issues that are associated with this subset of peripheral nerve injuries. METHODS: Over a 17-year period, 354 cases of injection-related iatrogenic peripheral nerve injuries were managed surgically at the Department of Neurosurgery at P.D. Hinduja Hospital and Seth G S Medical College, Mumbai. In our series, the injection-related iatrogenic nerve injuries were following intramuscular injections, brachial nerves block procedures, subclavian and jugular venous cannulation procedures for central line placements, and routine intravenous injections in the peripheral veins of the limbs. The age of the patients ranged from 5 years to 65 years. Pain, paresthesia, and sensory-motor deficits were the common presenting features in our series. The operative procedures performed in our series were external neurolysis and excision of neuroma/contused portion of the nerve and sural nerve cable grafting. The follow-up ranged from 6 months to 84 months. There were no major intraoperative complications in our series. RESULTS: In our series, functional improvement (power grade 3 or above) was noted in 190 (53.7%) patients following surgical intervention. In 164 (46.3%) patients, there was either a non-functional status or no recovery. Neurological deterioration in the form of motor weakness was noted in 9 (2.5%) patients in our series after the surgery. The best results (90.1%) were noted with radial nerve repair following surgical intervention. CONCLUSION: Injection-related iatrogenic nerve injuries are not an uncommon problem. Surgery should be the preferred treatment option when the injured nerve fails to recover following the insult. The results are rewarding in a significant percentage of patients following timely intervention. The problem of litigation attached with this type of injury is also highlighted.
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Enfermedad Iatrogénica , Procedimientos Neuroquirúrgicos/efectos adversos , Traumatismos de los Nervios Periféricos/cirugía , Adolescente , Adulto , Anciano , Niño , Preescolar , Femenino , Humanos , Inyecciones Intramusculares/efectos adversos , Masculino , Persona de Mediana Edad , Bloqueo Nervioso/efectos adversos , Traumatismos de los Nervios Periféricos/etiología , Estudios Retrospectivos , Resultado del Tratamiento , Adulto JovenAsunto(s)
Aspergilosis/diagnóstico por imagen , Espacio Epidural/diagnóstico por imagen , Granuloma/diagnóstico por imagen , Enfermedades de la Médula Espinal/diagnóstico por imagen , Antifúngicos/uso terapéutico , Aspergilosis/tratamiento farmacológico , Espacio Epidural/microbiología , Granuloma/microbiología , Humanos , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Enfermedades de la Médula Espinal/tratamiento farmacológico , Enfermedades de la Médula Espinal/microbiología , Resultado del TratamientoAsunto(s)
Infecciones por VIH/complicaciones , Leiomiosarcoma/etiología , Leiomiosarcoma/virología , Neoplasias de la Columna Vertebral/etiología , Neoplasias de la Columna Vertebral/virología , Actinas/metabolismo , Adulto , Proteínas de Unión a Calmodulina/metabolismo , Desmina/metabolismo , Femenino , VIH/patogenicidad , Infecciones por VIH/diagnóstico por imagen , Infecciones por VIH/cirugía , Herpesvirus Humano 4/patogenicidad , Humanos , Leiomiosarcoma/diagnóstico por imagen , Imagen por Resonancia Magnética , Tomografía de Emisión de Positrones , ARN Viral/metabolismo , Neoplasias de la Columna Vertebral/diagnóstico por imagen , Neoplasias de la Columna Vertebral/cirugíaRESUMEN
INTRODUCTION: Contralateral ear hearing loss (CHL) is an extremely rare but a potentially devastating complication in a patient with already compromised hearing due to a Vestibular schwannoma (VS). Our patient had CHL accompanied by contralateral facial palsy. Our case is only the second case reported in literature to the best of our knowledge. PRESENTATION OF CASE: A 55-year elderly male presented with right sided sensorineural hearing loss, cerebellar signs and Grade II House & Brackmann (H&B) facial nerve weakness for last1-year. Magnetic resonance imaging (MRI) scan revealed a large right sided vestibular schwannoma (VS) with severe compression of the ipsilateral pons. The pre-operative pure tone audiometry (PTA) documented severe sensory neural hearing loss (SNHL) on the right side along with mild SNHL on the left side. A right retromastoid suboccipital craniotomy was performed and VS was completely excised. The ipsilateral facial nerve was preserved anatomically. On the 4th post-operative day he developed severe pain and tinnitus in left ear. In the next 24-h there were hearing loss and grade II facial nerve paresis. The PTA done on the 5th post-operative day revealed severe SNHL on both sides. He was managed conservatively with steroids and vasodilators. At 6-months of follow-up the left side hearing loss and facial weakness had significantly recovered. The PTA showed significant improvement in the left side SNHL DISCUSSION: Contralateral hearing disturbance with contralateral facial palsy after acoustic neuroma surgery is extremely rare. The exact etiopathogenesis of this unusual phenomenon is not clear and various theories have been proposed. There is no standard recommendation for treatment of these rare complications and the etiology remains obscure. CONCLUSION: Hearing loss and facial palsy on the contralateral side after VS surgery is extremely rare. It is imperative that this rare complication should be considered following VS surgery.