共查询到20条相似文献,搜索用时 46 毫秒
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目的 探讨颧颞入路对中颅底肿瘤的疗效。方法 对中颅窝脑膜瘤 ,颅咽管癌、离膜肉瘤及神经鞘瘤各1例,采用颧颞入路手术,取下颧弓以扩大中颅窝底视野,对肿瘤长入后颅窝者,切开小脑天幕,切除天幕下肿瘤,对向前颅底及眶内生长者,以扩大的颧颞眶入路手术。结果 中颅底肿瘤全切6例,次全切3例,大部切除3例,肿瘤残留与肿瘤侵犯海绵窦、包绕颈内动脉、脑干受浸润有关。结论 颧颞入路可有效地适用于中颅底肿瘤切除术。 相似文献
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目的 探讨颧颞入路对中颅底肿瘤的疗效。方法 对中颅窝脑膜瘤 9例 ,颅咽管瘤、脑膜肉瘤及神经鞘瘤各 1例 ,采用颧颞入路手术 ,取下颧弓以扩大中颅窝底视野。对肿瘤长入后颅窝者 ,切开小脑天幕 ,切除天幕下肿瘤 ,对向前颅底及眶内生长者 ,以扩大的颧颞眶入路手术。结果 中颅底肿瘤全切 6例 ,次全切 3例 ,大部切除 3例。肿瘤残留与肿瘤侵犯海绵窦、包绕颈内动脉、脑干受浸润有关。结论 颧颞入路可有效地适用于中颅底肿瘤切除术。 相似文献
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目的探讨前颅底大型脑膜瘤的手术入路、显微手术方法和治疗效果。方法对显微手术治疗的21例前颅底大型脑膜瘤患者的影像学资料、手术入路、显微手术切除肿瘤的方法及疗效进行回顾性分析。结果按照Simpson切除标准,本组21例中,Ⅰ级切除16例(76.19%);Ⅱ级切除3例(14.29%);Ⅳ级切除2例即行脑膜瘤次全切除(9.52%)。肿瘤全切除90.48%,次全切除9.52%。无手术死亡,随访6~24个月,无复发。结论充分的术前影像学检查及评估,采用显微手术切除前颅底大型脑膜瘤,术中保护重要神经与血管、处理好受累的颅底骨质和脑膜,能明显提高肿瘤的全切除率,减少并发症,提高临床疗效。 相似文献
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目的:介绍了采用手术新入路,以显微外科技术切除累及中颅窝及鞍上,鞍旁肿瘤10例的体会,方法:采用眶-翼点及眶-颧弓入路经中颅窝硬膜外等改良翼点新的手术入路,同时采用显微外科技术切除中颅底肿瘤。结果:新的手术入中扩大了肿瘤的暴露范围,有利于肿瘤的切除,本组全切除7例,次全切除2例,大部切除1例,9例恢复良好,死亡1例,结论:采用眶-翼点及眶-颧弓入路经中颅窝硬膜外等改良翼点新的手术入路,结合显微外科技术是切除中颅底肿瘤的有效方法,可提高手术切除率,减少手术并发症,降低手术死亡率。 相似文献
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目的 介绍46例颅底脑膜瘤的诊断和治疗,方法 分析46例颅底脑膜瘤的临床及影像学特征,手术方法,手术结果,术后并发症等。结果 颅底脑膜瘤全切除37例,次全切除9例,其中12例采用显微手术,疗效优于直视手术,术后死亡2例,5例术后颅神经症状加重,21例无任何神经损伤症状20例颅神经症状同术前,结论 颅底脑膜瘤的手术治疗,熟悉颅底解剖选择良好入路可提高疗效,利用显微技术可提高全切除率,降低术后并发症和 相似文献
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目的探讨嗅沟脑膜瘤显微外科手术治疗的临床疗效。方法回顾性分析显微手术治疗嗅沟脑膜瘤21例的临床治疗情况和随访资料,对嗅沟脑膜瘤的显微手术技巧和颅底重建方法进行探讨。结果 21例脑膜瘤显微手术,Simpson I级全切除19例(90.5%),SimpsonⅡ级全切除2例(9.5%)。术前视力变差的15例,术后视力改善14例,术后视力无改善1例;Simpson I级全切除的病例术后平均随访30个月未见肿瘤复发。结论应用显微外科手术全切除嗅沟脑膜瘤和严密的颅底重建,能够取得较好的临床疗效。 相似文献
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The skull in chronic sarcoidosis 总被引:1,自引:0,他引:1
A report of a 63 year old woman with giant osteolytic skull lesions simulating metastatic disease, and generalized cutaneous lesions is presented. Biopsy of a skin lesion revealed non-caseating granulomas compatible with sarcoidosis. The literature dealing with calvarial sarcoidosis is reviewed. 相似文献
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Recognition of the many benign and malignant tumors that occur in the skull base is now simple, given three-dimensional CT scanning and MRI with enhancement. Recent developments in surgical technique have allowed these tumors to be approached, but only in the past two to three years has radical surgery been possible. 相似文献
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A young rickshaw puller admitted in Neurosurgery ward of Mymensingh Medical College Hospital due to ugly looking skull swelling on right side and iatrogenic ulceration on the postero-superior surface of the swelling. He also mentioned that he was not socially well-excepted and facing difficulty in getting married for that ugly lesion and was very unhappy at that time. CT scan was suggestive of fibrous dysplasia of skull bone and no other abnormalities were present on other part of the body. Then complete excision of the mass was done and fibrous dysplasia was confirmed by histopathological study. Two months after surgery he got married and expressed his happiness. In fibrous dysplasia, normal bone is replaced by fibrous connective tissue with varying degrees of osseous metaplasia. It is a benign disorder of bone commonly seen from childhood to the third decade. Virtually any bone in the body can be affected. Regarding investigations, plain radiography in the first line study. CT may be required to assess complex region such as the spine, pelvis, chest and facial skeleton. Histologically, fibrous dysplasia appears as multiple areas of fibrous tissue contained within islands of bone with evidence of both blastic and clastic activity. 相似文献
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A median defect in the region of the root of the nose, in between the two orbits, was discovered in the dried skull of a 44-year-old female cadaver, during routine undergraduate teaching. The two small nasal bones articulated with each other and the cribriform plate of the ethmoid. The lacrimal bones and frontal processes of the maxillary bones were also deformed. We propose that the median defect was due to abnormality at the fonticulus frontalis, the prenasal space and the interorbitonasal part of the nasal capsule, as well as defects in the ossification of the maxilla, lacrimal and frontal bones. 相似文献
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Shifa Bidhan Subhash Chandra Shaw Ganesh Saravagi Rakesh Gupta 《Medical Journal Armed Forces India》2019,75(4):464-466
Congenital neonatal skull depression, not associated with trauma is a rare clinical entity, with an incidence of 1 in 10000. The depression is thought to be due to compression by foetal limbs or maternal pelvis. Though the condition is mostly self-resolving over the course of a few months, it causes tremendous parental anxiety. We report a case of non-traumatic, congenital depression of skull of a neonate at birth without any neurological deficit or intracranial abnormality noticed on imaging. 相似文献