首页 > 最新文献

Neurochirurgia最新文献

英文 中文
[Chronic subdural hematoma as a cause for blindness]. [导致失明的慢性硬膜下血肿]。
Pub Date : 1992-11-01 DOI: 10.1055/s-2008-1052280
L Russegger, J J Langmayr, K Twerdy

The uncommon complication of bilateral blindness resulting from a decompressive neurosurgical procedure is presented by the case of a 51-year old patient suffering from a traumatic chronic subdural haematoma. A breakdown of the altered vasoregulation of the optic nerves due to papilledema at the time of intracranial pressure drop is supposed to be the etiological background of optic atrophy and consequent amaurosis. The causal relationship of accident trauma and blindness in the presented case is pointed out.

摘要本文报告一位51岁病患,因外伤性慢性硬膜下血肿而接受减压神经外科手术,导致双侧失明的罕见并发症。在颅内压下降时,视神经因乳头水肿而改变的血管调节功能被破坏,这被认为是视神经萎缩和随后的黑朦的病因背景。指出了事故创伤与致盲的因果关系。
{"title":"[Chronic subdural hematoma as a cause for blindness].","authors":"L Russegger,&nbsp;J J Langmayr,&nbsp;K Twerdy","doi":"10.1055/s-2008-1052280","DOIUrl":"https://doi.org/10.1055/s-2008-1052280","url":null,"abstract":"<p><p>The uncommon complication of bilateral blindness resulting from a decompressive neurosurgical procedure is presented by the case of a 51-year old patient suffering from a traumatic chronic subdural haematoma. A breakdown of the altered vasoregulation of the optic nerves due to papilledema at the time of intracranial pressure drop is supposed to be the etiological background of optic atrophy and consequent amaurosis. The causal relationship of accident trauma and blindness in the presented case is pointed out.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 6","pages":"207-9"},"PeriodicalIF":0.0,"publicationDate":"1992-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052280","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12663714","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Supratentorial arachnoidal cyst with intracystic and subdural haematoma. 幕上蛛网膜囊肿伴囊内及硬膜下血肿。
Pub Date : 1992-11-01 DOI: 10.1055/s-2008-1052278
M M van Burken, A C Sarioglu, H D O'Donnell

A case of a arachnoidal cyst with intracystic bleeding and subdural haematoma is reported. The association of an arachnoidal cyst in the middle cranial fossa with a subdural haematoma or intracystic bleeding is emphasised. The diagnosis of such lesions, the nature of the pathology and therapy are discussed.

本文报告一例蛛网膜囊肿合并囊内出血及硬膜下血肿。强调中颅窝蛛网膜囊肿与硬膜下血肿或囊内出血的关系。讨论了这种病变的诊断、病理性质和治疗方法。
{"title":"Supratentorial arachnoidal cyst with intracystic and subdural haematoma.","authors":"M M van Burken,&nbsp;A C Sarioglu,&nbsp;H D O'Donnell","doi":"10.1055/s-2008-1052278","DOIUrl":"https://doi.org/10.1055/s-2008-1052278","url":null,"abstract":"<p><p>A case of a arachnoidal cyst with intracystic bleeding and subdural haematoma is reported. The association of an arachnoidal cyst in the middle cranial fossa with a subdural haematoma or intracystic bleeding is emphasised. The diagnosis of such lesions, the nature of the pathology and therapy are discussed.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 6","pages":"199-203"},"PeriodicalIF":0.0,"publicationDate":"1992-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052278","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12663712","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 23
Arachnoid cysts of the middle cranial fossa. 中颅窝蛛网膜囊肿。
Pub Date : 1992-11-01 DOI: 10.1055/s-2008-1052274
K von Wild

In 18 cases of temporal arachnoid cysts the etiology, clinical and radiographic findings, surgical treatment, and outcome are reviewed. Cysts of the middle cranial fossa are susceptible to trauma, which may cause bleeding either into the cyst or into the subdural space. CT or MRI scans are diagnostic in arachnoid cysts. In cases of intracranial mass lesion with displacement of the midline structures and increasing ICP, osteoplastic craniotomy is performed and the medial wall of the cyst is resected down to the tentorial notch, with opening into the basal cisterns. There were no operative or postoperative complications in 18 consecutive cases. However, one boy required a cystoperitoneal shunt 3 months later as a result of hydrocephalus following subdural hematoma and two other patients were also subsequently shunted. Asymptomatic arachnoid cysts are discussed with the respect to brain function and potential risks.

本文回顾了18例颞叶蛛网膜囊肿的病因、临床和影像学表现、手术治疗和结果。颅中窝囊肿易受创伤,可导致出血进入囊肿或进入硬膜下间隙。CT或MRI扫描可诊断蛛网膜囊肿。如果颅内肿块病变伴有中线结构移位和颅内压增高,则行骨成形术,切除囊肿内侧壁至幕状切迹,并向基底池开放。18例均无手术及术后并发症。然而,一名男孩在3个月后由于脑膜下血肿引起的脑积水需要进行囊腹膜分流术,另外两名患者随后也进行了分流术。本文讨论无症状蛛网膜囊肿对脑功能和潜在风险的影响。
{"title":"Arachnoid cysts of the middle cranial fossa.","authors":"K von Wild","doi":"10.1055/s-2008-1052274","DOIUrl":"https://doi.org/10.1055/s-2008-1052274","url":null,"abstract":"<p><p>In 18 cases of temporal arachnoid cysts the etiology, clinical and radiographic findings, surgical treatment, and outcome are reviewed. Cysts of the middle cranial fossa are susceptible to trauma, which may cause bleeding either into the cyst or into the subdural space. CT or MRI scans are diagnostic in arachnoid cysts. In cases of intracranial mass lesion with displacement of the midline structures and increasing ICP, osteoplastic craniotomy is performed and the medial wall of the cyst is resected down to the tentorial notch, with opening into the basal cisterns. There were no operative or postoperative complications in 18 consecutive cases. However, one boy required a cystoperitoneal shunt 3 months later as a result of hydrocephalus following subdural hematoma and two other patients were also subsequently shunted. Asymptomatic arachnoid cysts are discussed with the respect to brain function and potential risks.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 6","pages":"177-82"},"PeriodicalIF":0.0,"publicationDate":"1992-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052274","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12663708","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 46
[Initial experiences with a new cerebrospinal fluid collection system]. [使用新型脑脊液收集系统的初步经验]。
Pub Date : 1992-11-01 DOI: 10.1055/s-2008-1052277
M Lorenz, F Repschläger, H Dietz

Due to clinical requirements and to improve the handling of CSF drainage set we developed a new concept, consisting of an arrangement of constructions, which are already available. Besides other advantages, the set provides an ICP monitoring, a pump device and a protection of the air filter of the collecting tank for safer transport. Opening the system for the performance of diagnostic or therapeutic manoeuvres can therefore be avoided. This new equipment has been tested in 28 patients having a ventricular or lumbar CSF drainage with good results and has been quickly accepted by the medical staff. The construction is described in detail.

由于临床需要和改进脑脊液引流装置的处理,我们开发了一种新的概念,由一系列结构组成,这些结构已经可用。除其他优点外,该装置还提供ICP监测,泵装置和收集罐空气过滤器的保护,以确保更安全的运输。因此,可以避免打开系统进行诊断或治疗操作。这种新设备已在28例脑室或腰椎脑脊液引流患者中进行了试验,效果良好,并迅速被医务人员所接受。对其结构进行了详细的描述。
{"title":"[Initial experiences with a new cerebrospinal fluid collection system].","authors":"M Lorenz,&nbsp;F Repschläger,&nbsp;H Dietz","doi":"10.1055/s-2008-1052277","DOIUrl":"https://doi.org/10.1055/s-2008-1052277","url":null,"abstract":"<p><p>Due to clinical requirements and to improve the handling of CSF drainage set we developed a new concept, consisting of an arrangement of constructions, which are already available. Besides other advantages, the set provides an ICP monitoring, a pump device and a protection of the air filter of the collecting tank for safer transport. Opening the system for the performance of diagnostic or therapeutic manoeuvres can therefore be avoided. This new equipment has been tested in 28 patients having a ventricular or lumbar CSF drainage with good results and has been quickly accepted by the medical staff. The construction is described in detail.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 6","pages":"196-8"},"PeriodicalIF":0.0,"publicationDate":"1992-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052277","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12663711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Von Hippel-Lindau disease: analysis of two families. Von Hippel-Lindau病:两家系分析。
Pub Date : 1992-11-01 DOI: 10.1055/s-2008-1052279
T Bilge, F Ozveren, S Senol, S Bilge, S Barut, O Karakaslar, Y Aydin

In this report we present two families with von Hippel-Lindau syndrome. We operated on haemangioblastomas in two members, one from each, in our clinic. In the first family we saw 17 lesions in 9 members. Although in the first family carcinoma of the kidney was often observed, in the second family retinal haemangioma was found to be predominant, namely, in eight out of nine patients. In both families there were 11 patients with retinal haemangioma; of these, 9 patients were blind (82%). In 6 patients with retinal haemangioblastoma blindness was unilateral and bilateral only in one. All the patients with renal carcinoma were male and died young. In one of our patients with renal carcinoma we found metastatic lesions in the distal and proximal parts of the femur, vertebral arch, cranium and the thoracic wall. In these two families 23 members had 32 lesions, from which eleven were retinal haemangiomas (3 + 8), nine haemangioblastomas of CNS (5 + 4), one a renal cyst (0 + 1), eight renal carcinomas (7 + 1), two pancreatic cysts (1 + 1) and one liver cyst (0 + 1).

在这个报告中,我们提出了两个家庭与冯希佩尔-林道综合征。在我们的诊所里,我们对两名成员的血管母细胞瘤进行了手术。在第一个家庭中,我们发现9名成员有17个病变。虽然在第一家族中经常观察到肾癌,但在第二家族中,视网膜血管瘤被发现是主要的,即在9名患者中有8名。两个家族均有11例视网膜血管瘤患者;其中9例失明(82%)。6例视网膜血管母细胞瘤患者单侧失明,双侧失明1例。所有肾癌患者均为男性,年轻时死亡。在我们的一个肾癌患者中,我们发现转移病灶位于股骨的远端和近端,椎弓,颅骨和胸壁。在这两个家族中,23名成员有32个病变,其中11个为视网膜血管瘤(3 + 8),9个为中枢神经系统血管母细胞瘤(5 + 4),1个肾囊肿(0 + 1),8个肾癌(7 + 1),2个胰腺囊肿(1 + 1)和1个肝囊肿(0 + 1)。
{"title":"Von Hippel-Lindau disease: analysis of two families.","authors":"T Bilge,&nbsp;F Ozveren,&nbsp;S Senol,&nbsp;S Bilge,&nbsp;S Barut,&nbsp;O Karakaslar,&nbsp;Y Aydin","doi":"10.1055/s-2008-1052279","DOIUrl":"https://doi.org/10.1055/s-2008-1052279","url":null,"abstract":"<p><p>In this report we present two families with von Hippel-Lindau syndrome. We operated on haemangioblastomas in two members, one from each, in our clinic. In the first family we saw 17 lesions in 9 members. Although in the first family carcinoma of the kidney was often observed, in the second family retinal haemangioma was found to be predominant, namely, in eight out of nine patients. In both families there were 11 patients with retinal haemangioma; of these, 9 patients were blind (82%). In 6 patients with retinal haemangioblastoma blindness was unilateral and bilateral only in one. All the patients with renal carcinoma were male and died young. In one of our patients with renal carcinoma we found metastatic lesions in the distal and proximal parts of the femur, vertebral arch, cranium and the thoracic wall. In these two families 23 members had 32 lesions, from which eleven were retinal haemangiomas (3 + 8), nine haemangioblastomas of CNS (5 + 4), one a renal cyst (0 + 1), eight renal carcinomas (7 + 1), two pancreatic cysts (1 + 1) and one liver cyst (0 + 1).</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 6","pages":"204-6"},"PeriodicalIF":0.0,"publicationDate":"1992-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052279","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12663713","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
[Legal evaluation of intervertebral disk surgery including post-discotomy syndrome]. [椎间盘手术包括椎间盘切开术后综合征的法律评价]。
Pub Date : 1992-09-01 DOI: 10.1055/s-2008-1052266
T Herter, H J König

Although lumbar disc surgery (discectomy) definitely improves the overall situation of the patient in most cases, it does create problems of a hitherto absent kund in about 6% of the patients. Expertising of uncomplicated cases should not be too difficult. However, modulated by individual disposition, a syndrome may develop known as "failed back surgery syndrome" caused by intersegmental loosening, crumbling or fusing and scarification. The pain it causes is decisive for its assessment, not so much any motor or other neurological deficits. In mild cases the loss in capacity for gainful employment may be assessed at between 20% to at the most 30%, but the severely handicapped are unable to cope with their daily life without assistance, their incapacitation amounting to as much as 100%. If the patient concerned is on a job that places stress on this spine, he may be unfit for work even if the affliction is relatively mild.

虽然在大多数情况下,腰椎间盘手术(椎间盘切除术)确实改善了患者的整体情况,但在约6%的患者中,它确实产生了迄今为止没有的kund问题。对不复杂的病例进行鉴定不应该太难。然而,受个人倾向的影响,可能会出现一种综合征,称为“背部手术失败综合征”,由节段间松动、碎裂或融合和划伤引起。它引起的疼痛是对其评估的决定性因素,而不是任何运动或其他神经缺陷。在轻微的情况下,估计有收入就业能力的丧失在20%至最多30%之间,但严重残疾者在没有帮助的情况下无法应付日常生活,其丧失能力的比例高达100%。如果病人的工作对脊柱有压力,即使疼痛相对轻微,他也可能不适合工作。
{"title":"[Legal evaluation of intervertebral disk surgery including post-discotomy syndrome].","authors":"T Herter,&nbsp;H J König","doi":"10.1055/s-2008-1052266","DOIUrl":"https://doi.org/10.1055/s-2008-1052266","url":null,"abstract":"<p><p>Although lumbar disc surgery (discectomy) definitely improves the overall situation of the patient in most cases, it does create problems of a hitherto absent kund in about 6% of the patients. Expertising of uncomplicated cases should not be too difficult. However, modulated by individual disposition, a syndrome may develop known as \"failed back surgery syndrome\" caused by intersegmental loosening, crumbling or fusing and scarification. The pain it causes is decisive for its assessment, not so much any motor or other neurological deficits. In mild cases the loss in capacity for gainful employment may be assessed at between 20% to at the most 30%, but the severely handicapped are unable to cope with their daily life without assistance, their incapacitation amounting to as much as 100%. If the patient concerned is on a job that places stress on this spine, he may be unfit for work even if the affliction is relatively mild.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 5","pages":"137-44"},"PeriodicalIF":0.0,"publicationDate":"1992-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052266","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12607036","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
A giant hyperostosing meningioma in a child 儿童巨大的肥厚性脑膜瘤
Pub Date : 1992-09-01 DOI: 10.1055/s-2008-1052273
O. Cataltepe, O. Özcan, S. Sagmanli, B. Onol
A case of 15-year-old boy with a giant hyperostotic meningioma is presented. The patient had a huge prominence at the posterior parietal region. The CT scan showed a giant intracranial tumor in the left parieto-occipital region under the hyperostotic bone. The tumor and hyperostotic bone were totally resected with the involved portion of the sagittal sinus. Histological study revealed a meningioma. The presence of such a huge hyperostosis and some peculiarities of childhood meningiomas are discussed.
我们报告一个15岁的男孩患巨大的肥厚性脑膜瘤。患者在后顶叶区有一个巨大的突起。CT扫描显示一个巨大的颅内肿瘤在左顶骨至枕骨区域下骨质增生。肿瘤和肥厚骨连同矢状窦受累部分全部切除。组织学检查显示为脑膜瘤。我们讨论了这种巨大骨肥大的存在和儿童脑膜瘤的一些特点。
{"title":"A giant hyperostosing meningioma in a child","authors":"O. Cataltepe, O. Özcan, S. Sagmanli, B. Onol","doi":"10.1055/s-2008-1052273","DOIUrl":"https://doi.org/10.1055/s-2008-1052273","url":null,"abstract":"A case of 15-year-old boy with a giant hyperostotic meningioma is presented. The patient had a huge prominence at the posterior parietal region. The CT scan showed a giant intracranial tumor in the left parieto-occipital region under the hyperostotic bone. The tumor and hyperostotic bone were totally resected with the involved portion of the sagittal sinus. Histological study revealed a meningioma. The presence of such a huge hyperostosis and some peculiarities of childhood meningiomas are discussed.","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 1","pages":"171 - 175"},"PeriodicalIF":0.0,"publicationDate":"1992-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052273","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"58083016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
A giant hyperostosing meningioma in a child. 儿童巨大的肥厚性脑膜瘤。
Pub Date : 1992-09-01
O Cataltepe, O Ekin Ozcan, S Sagmanli, B Onol

A case of 15-year-old boy with a giant hyperostotic meningioma is presented. The patient had a huge prominence at the posterior parietal region. The CT scan showed a giant intracranial tumor in the left parieto-occipital region under the hyperostotic bone. The tumor and hyperostotic bone were totally resected with the involved portion of the sagittal sinus. Histological study revealed a meningioma. The presence of such a huge hyperostosis and some peculiarities of childhood meningiomas are discussed.

我们报告一个15岁的男孩患巨大的肥厚性脑膜瘤。患者在后顶叶区有一个巨大的突起。CT扫描显示一个巨大的颅内肿瘤在左顶骨至枕骨区域下骨质增生。肿瘤和肥厚骨连同矢状窦受累部分全部切除。组织学检查显示为脑膜瘤。我们讨论了这种巨大骨肥大的存在和儿童脑膜瘤的一些特点。
{"title":"A giant hyperostosing meningioma in a child.","authors":"O Cataltepe,&nbsp;O Ekin Ozcan,&nbsp;S Sagmanli,&nbsp;B Onol","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>A case of 15-year-old boy with a giant hyperostotic meningioma is presented. The patient had a huge prominence at the posterior parietal region. The CT scan showed a giant intracranial tumor in the left parieto-occipital region under the hyperostotic bone. The tumor and hyperostotic bone were totally resected with the involved portion of the sagittal sinus. Histological study revealed a meningioma. The presence of such a huge hyperostosis and some peculiarities of childhood meningiomas are discussed.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 5","pages":"171-5"},"PeriodicalIF":0.0,"publicationDate":"1992-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12608434","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Management of missile wounds of the cerebral dura mater: experience with 69 cases. 脑硬脑膜飞弹伤69例治疗体会。
Pub Date : 1992-09-01 DOI: 10.1055/s-2008-1052268
D Vranković, I Hećimović, B Splavski, B Dmitrović

Over the period of seven months: from July 1991 to January 1992 sixty-nine patients with penetrating head war-injuries, were admitted in our hospital. Missile wounds of the dura mater require in most cases urgent operative management: watertight closure of the dura defects. However, a dilemma still exists as to the best material to be used to restore the missile dural defects. There are several possibilities: an autologous substitute as periosteum (pericranium) from surrounding, fascia of the temporalis muscle, fascia lata, or allograft transplant as lyophilised cerebral dura mater (lyodura). In the group of 69 patients, 7 were treated conservatively, 13 were treated surgically, but without closing the dural wounds because of their critical condition, and in 45 surgically treated patients the dural defects were covered with 53 transplants: with periosteum in 22 patients but 24 coverings, with fascia of temporalis muscle in 2 patients, with lyodura in 6 patients, with fascia lata in 15 patients but 21 coverings. In 4 patients the dura wounds were sutured by interrupted sutures. The best results were obtained in the fascia lata group.

在1991年7月至1992年1月的7个月期间,我们医院收治了69名头部穿透性战争伤患者。硬脑膜飞弹伤在大多数情况下需要紧急手术处理:对硬脑膜缺损进行水密封闭。然而,一个难题仍然存在,最好的材料,以用于恢复导弹硬脑膜缺陷。有几种可能性:自体替代物,如周围骨膜、颞肌筋膜、阔筋膜,或同种异体移植物,如冻干脑硬脑膜(硬脊膜)。在69例患者中,保守治疗7例,手术治疗13例,但由于病情危重,没有关闭硬膜伤口,手术治疗的45例患者中,53例移植覆盖硬膜缺损:骨膜22例,24例覆盖,颞肌筋膜2例,lyodura 6例,阔筋膜15例,21例覆盖。4例采用间断缝合线缝合硬脑膜伤口。阔筋膜组效果最好。
{"title":"Management of missile wounds of the cerebral dura mater: experience with 69 cases.","authors":"D Vranković,&nbsp;I Hećimović,&nbsp;B Splavski,&nbsp;B Dmitrović","doi":"10.1055/s-2008-1052268","DOIUrl":"https://doi.org/10.1055/s-2008-1052268","url":null,"abstract":"<p><p>Over the period of seven months: from July 1991 to January 1992 sixty-nine patients with penetrating head war-injuries, were admitted in our hospital. Missile wounds of the dura mater require in most cases urgent operative management: watertight closure of the dura defects. However, a dilemma still exists as to the best material to be used to restore the missile dural defects. There are several possibilities: an autologous substitute as periosteum (pericranium) from surrounding, fascia of the temporalis muscle, fascia lata, or allograft transplant as lyophilised cerebral dura mater (lyodura). In the group of 69 patients, 7 were treated conservatively, 13 were treated surgically, but without closing the dural wounds because of their critical condition, and in 45 surgically treated patients the dural defects were covered with 53 transplants: with periosteum in 22 patients but 24 coverings, with fascia of temporalis muscle in 2 patients, with lyodura in 6 patients, with fascia lata in 15 patients but 21 coverings. In 4 patients the dura wounds were sutured by interrupted sutures. The best results were obtained in the fascia lata group.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 5","pages":"150-5"},"PeriodicalIF":0.0,"publicationDate":"1992-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052268","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12608429","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 25
Unique complications of cerebrospinal fluid shunts in children--a report of two cases. 儿童脑脊液分流的独特并发症——附两例报告
Pub Date : 1992-09-01 DOI: 10.1055/s-2008-1052269
A Jamjoom, N Ur-Rahman, Z A Jamjoom, A Jawad, F Fadley

The authors report on two cases with unusual CSF shunt complications. The first case had a peritoneal catheter which migrated down a patent processus vaginalis into a hydrocoele. The second case had an atrial catheter which perforated the atrial wall and came to lie in the pericardium causing an effusion. Clinicians should be aware of the frequent and occasionally bizarre complications of CSF shunting.

作者报告了两例不寻常的脑脊液分流并发症。第一个病例有一个腹膜导管,它沿着阴道未闭进入积水。第二例心房导管穿过心房壁,进入心包引起积液。临床医生应该意识到脑脊液分流的频繁和偶尔奇怪的并发症。
{"title":"Unique complications of cerebrospinal fluid shunts in children--a report of two cases.","authors":"A Jamjoom,&nbsp;N Ur-Rahman,&nbsp;Z A Jamjoom,&nbsp;A Jawad,&nbsp;F Fadley","doi":"10.1055/s-2008-1052269","DOIUrl":"https://doi.org/10.1055/s-2008-1052269","url":null,"abstract":"<p><p>The authors report on two cases with unusual CSF shunt complications. The first case had a peritoneal catheter which migrated down a patent processus vaginalis into a hydrocoele. The second case had an atrial catheter which perforated the atrial wall and came to lie in the pericardium causing an effusion. Clinicians should be aware of the frequent and occasionally bizarre complications of CSF shunting.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"35 5","pages":"156-9"},"PeriodicalIF":0.0,"publicationDate":"1992-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052269","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12608430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 15
期刊
Neurochirurgia
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1