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11. |
Human Acoustic Neuromas Secrete Interleukin‐6 in Cell CulturePossible Autocrine Regulation of Cell Proliferation |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 434-438
Eric Adams,
Brian Rafferty,
Jennifer Mower,
Helen Ward,
Beate Petersen,
Rudolf Fahlbusch,
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摘要:
INTERLEUKIN-6 (IL-6) SECRETION by cell cultures of human acoustic neuromas was examined. Secretory rates varied from 0.02 to 5.4 ng/105cells per 4 days, depending on the tumor. The IL-6 immunoreactivity eluted from a Sephadex G-100 column in a major peak corresponding to anMrof 30,000 and a lesser peak corresponding to anMrof 50,000. Western blot analysis revealed three IL-6 immunoreactive bands withMrs corresponding to 53,000, 29,000, and 24,000. Tumor necrosis factor-α, interleukin-1-ß, and cholera toxin all stimulated IL-6 secretion. An antisense phosphorothioate oligonucleotide against IL-6 messenger RNA inhibited both [3H]thymidine uptake and IL-6 secretion by acoustic neuroma cells in culture. In addition, [3H]thymidine uptake was inhibited by a specific polyclonal antibody against IL-6. We conclude that human acoustic neuroma cells produce and secrete IL-6, which may act in an autocrine manner to stimulate cellular proliferation.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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12. |
Detection and Quantification of Vascular Endothelial Growth Factor/Vascular Permeability Factor in Brain Tumor Tissue and Cyst FluidThe Key to Angiogenesis? |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 439-449
Karin Weindel,
Jean Moringlane,
Dieter Marmé,
Herbert Weich,
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摘要:
IN PRIMARY MALIGNANT brain tumors increased vascularity and marked edema strongly suggest a possible role of the vascular endothelial growth factor/vascular permeability factor (VEGF/VPF). This was confirmed by earlier in situ hybridization studies, by analysis of the expression of the mitogen in different subsets of glioblastoma cells, and by the fact that the VEGF/VPF receptorflt-1 (fms-like tyrosine kinase) is up-regulated in tumor cells in vivo. To assess and quantify the expression of the VEGF/VPF gene and of the receptor gene, 26 surgical specimens of brain tumor tissue from 24 patients were analyzed. In most malignant gliomas, the expression level of the VEGF/VPF gene is elevated and can be increased up to 20- to 50-fold in comparison with low-grade tumors. Using polymerase chain reaction-based amplification, it could be shown that the messenger RNAs of three different VEGF/VPF forms are synthesized in tumor tissue samples. Northern blot studies revealed that in some samples a significant expression of the gene coding for placenta growth factor, a growth factor closely related to VEGF/VPF, was observed. In addition, using a radioreceptor assay it was possible to detect high VEGF/VPF-like activity in the cyst fluids of brain tumors, indicating the accumulation of the mitogen and permeability factor in brain tumor cysts. Further investigations revealed that astrocytoma and glioblastoma cells in culture express the VEGF/VPF gene and secrete the VEGF/VPF protein, whereas gene expression of the two known VEGF/VPF receptors, kinase insert domain-containing receptor andflt-1, could not be detected. These data support previous reports, which stated that VEGF/VPF acts as a paracrine growth and permeability factor in brain tumors and may contribute to tumor growth by initiating tumor angiogenesis.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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13. |
T Cell‐mediated Cytotoxicity of Human GliomasA Tumor Necrosis Factor‐independent Mechanism |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 450-456
Gordon Baltuch,
Jean-Guy Villemure,
Ellie McCrea,
Jack Antel,
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摘要:
CELLULAR IMMUNE EFFECTOR mechanisms are implicated as potential therapies for malignant gliomas. We have examined the potential for anti-CD3-activated human peripheral blood-derived CD4+and CD8+T cells to induce lysis of human glioma cell lines in vitro, the mechanism of action of these cells, and the capacity of the glioma to inhibit the effect. We found that activated CD4+and CD8+T cell preparations containing less than 5% natural killer cells could induce significant lysis of the glioma cell line U251, as measured by an 18-hour, but not 5-hour, chromium-51 or lactate dehydrogenase release assay. This effect was not reproduced using recombinant tumor necrosis factor or inhibited with antitumor necrosis factor antibody. Anti-lymphocyte functional antigen-1 and anti-intercellular adhesion molecule antibodies also did not inhibit the effect. Glioma-derived supernatant could inhibit the proliferation of the T cells but not the cytotoxic effect. Human fetal astrocytes were also susceptible to the cytotoxic effect of the activated T cells. These results indicate that activated T cells can induce glioma cytotoxicity via a mechanism independent of tumor necrosis factor. The therapeutic potential of this effector mechanism will depend on its capacity to deliver these cells or their specific effector molecules to the tumor site or to augment the activity of such cells, which accumulate naturally in gliomas.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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14. |
Experimentally‐induced Autonomic NeuropathyBeneficial Effect of a Topical ACTH4–9Analogue on Oculomotor Nerve Regeneration |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 457-462
William Vandertop,
Willem de Vries,
Nicolette Notermans,
Cees Tulleken,
Willem Gispen,
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摘要:
MELANOCORTINS, PEPTIDES RELATED to corticotropin (ACTH) and melanocyte-stimulating hormone, are known to exert beneficial neurotrophic effects in peripheral sensorimotor neuropathies. This has been demonstrated after both systemic and local administration of the peptides. By photographing the rat's pupil under standardized conditions, the authors have previously shown that systemic administration of a synthetic ACTH4–9analogue can also be beneficial in autonomic neuropathies. The present study demonstrates that topical application of a synthetic ACTH4–9analogue incorporated in a two-component fibrin glue enhances the speed of recovery of the parasympathetic nerve fibers in the oculomotor nerve after a crush lesion. This may have implications for future use in neurosurgery.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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15. |
Combined and Three‐dimensional Rendered Multimodal Data for Planning Cranial Base SurgeryA Prospective Evaluation |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 463-471
Advait Gandhe,
Derek Hill,
Colin Studholme,
David Hawkes,
Clifford Ruff,
Timothy Cox,
Michael Gleeson,
Anthony Strong,
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摘要:
MAGNETIC RESONANCE (MR), X-RAY computed tomography (CT), and angiographic images best depict soft tissue, bone, and blood vessels respectively. No one on its own is sufficient in the preoperative assessment of cranial base lesions. We have developed and evaluated a computational technique for the three-dimensional (3D) combination and display of multimodality images for planning cranial base surgery. This evaluation was prospective and performed in such a way that the results could be quantified. Eight patients (three acoustic neuromas, four subfrontal and suprasellar meningiomas, and one petrous apex meningioma) underwent MR, CT, and MR angiographic investigations. These images were registered with anatomical landmarks rather than an external frame. Two techniques were used to display the resulting combined images: multiple slices in which bone from CT was overlaid on soft tissue from registered MR and pseudo-3D-rendered movie sequences showing bone from CT, lesions and optic nerves from MR, and blood vessels from MR angiography. The advantages of the combined displays compared with those of conventional methods of viewing were assessed prospectively by the operating surgeon and by an independent surgeon, and the results were compared with operative findings. The preoperative assessment showed a significant improvement (P< 0.05, sign test) in the depiction of both individual structures (lesion and bone from overlaid slices and lesion and vasculature from 3D-rendered displays) and structural relationships (tumor-bone relationships from overlaid slices and of tumor-vasculature relationships from 3D-rendered displays). The operative findings indicated that a more accurate interpretation of this information was possible from the combined images.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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16. |
Cranial Base Approaches to Intracranial Aneurysms in the Subarachnoid Space |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 472-483
Laligam Sekhar,
Kamal Kalia,
Howard Yonas,
Donald Wright,
Henry Ching,
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摘要:
THE USE OF cranial base approaches to aneurysm surgery is illustrated by means of patient examples. Over a 9-year period, cranial base approaches were used to expose and treat 38 aneurysms involving the anterior communicating artery complex, proximal internal carotid artery, basilar artery, or vertebral artery. The approaches included orbital osteotomy, orbitozygomatic osteotomy, petrous apicectomy, presigmoid petrosectomy, and extreme lateral transcondylar methods. Complications related to the approaches included one partial ptosis and two cerebrospinal fluid leaks, which resolved with treatment. The technique of three-dimensional computed tomographic angiography was useful in delineating the vascular anatomy and its relation to the cranial base structures. This helped the surgeon plan the appropriate approach to the aneurysm. Cranial base approaches, used selectively, can provide improved exposure of deep-seated aneurysms and large or giant aneurysms, while minimizing brain retraction.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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17. |
Efficacy of Prophylactic Antibiotics for CraniotomyA Meta‐analysis |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 484-492
Fred Barker,
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摘要:
A META-ANALYSIS OF published randomized studies comparing prophylactic antibiotics to placebo in craniotomies was performed. Ten studies were examined; eight met criteria for inclusion into the meta-analysis. The analysis showed an advantage of antibiotics over placebo at theP< 10−8level. Tests for homogeneity of effect size between the individual studies showed similar effects of antibiotic treatment between trials, despite variation in the randomization methods and antibiotic regimens used. No statistically significant difference was detected between antibiotic regimens that did or did not cover gram-negative organisms or between single- and multiple-dose regimens. Cumulative meta-analyses showed that this conclusion could have been confidently drawn by 1988, after only four of the eight eligible trials had been published. Trials published since that time have reinforced these conclusions but have not significantly altered them. Future studies should compare proposed new antibiotic regimens with one of those already demonstrated to be effective, not with a placebo.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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18. |
Aggressive Papillary Middle Ear TumorsA Report of Two Cases with Review of the Literature |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 493-497
Michael Polinsky,
James Brunberg,
Paul McKeever,
Howard Sandler,
Steven Telian,
Donald Ross,
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摘要:
ADENOMATOUS TUMORS OF the middle ear are rare, with only approximately 100 cases reported. A distinct subclass of this tumor demonstrates microscopic papillary architecture and has a propensity to erode the petrous bone and extend intracranially. The term “aggressive papillary middle ear tumor” has recently been proposed to describe this more invasive type of middle ear tumor. Thirty-seven cases of aggressive papillary middle ear tumors have been reported. We present two additional cases and discuss the clinical, radiologic, histologic, and operative features of this locally aggressive neoplasm. The tumor affects adults of both sexes. The clinical prodrome is prolonged. Presenting signs and symptoms most often relate to the involvement of cranial nerves V-VIII. Imaging studies reveal large, enhancing, destructive tumors with a generous vascular supply. Intraoperatively, the tumors are bloody, fibrous, and adherent to surrounding structures. Various surgical approaches in combination or in series may be used. Preoperative embolization may be helpful. The role of adjunctive radiation is unclear. Aggressive papillary middle ear tumors are histologically benign tumors with clinically destructive behavior. However, it appears that aggressive surgical management affords prolonged survival with minimal worsening of cranial nerve deficits.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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19. |
Dural Cavernous Angiomas Outside the Middle Cranial FossaA Report of Two Cases |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 498-504
Adam Lewis,
John Tew,
Troy Payner,
Hwa-shain Yeh,
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摘要:
CAVERNOUS ANGIOMAS OF the dura mater are clinically and radiographically distinct from parenchymal cavernous angiomas. In this report, we present two cases of dural cavernous angiomas located outside the middle cranial fossa. The first patient is a 36-year-old woman with two dural cavernous angiomas, including one that enlarged during a 2-year period of observation. The second patient is a 33-year-old man with medically intractable seizures from a dural cavernous angioma of the convexity, which was discovered at autopsy. From our experience and a review of the literature, we have identified two groups of dural cavernous angiomas that differ in incidence, natural history, and surgical management. Most dural cavernous angiomas arise from the middle fossa; in contrast, only 15 cases of dural cavernous angiomas outside the middle fossa have been reported. Those in the middle fossa are more clinically aggressive and more difficult to resect surgically, because they grow toward the cavernous sinus and the parasellar region. Most patients with dural cavernous angiomas outside the middle fossa present with headaches, whereas those patients with dural cavernous angiomas in the middle fossa present with ocular signs, visual field defects, endocrinopathy, and trigeminal symptoms. Radiographically, both of the angiomas resemble meningiomas. Because of their intimate association with the cavernous sinus, surgical resection of middle fossa cavernous angiomas often is incomplete and may require postoperative radiosurgery to control growth. In contrast, angiomas in other locations are easily and successfully resected with little blood loss. The location of dural cavernous angiomas is an important factor in making the surgical decision and in predicting the outcome.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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20. |
Pseudotumoral Lymphocytic Hypophysitis Successfully Treated by Corticosteroid AloneFirst Case Report |
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Neurosurgery,
Volume 35,
Issue 3,
1994,
Page 505-508
Nathalie Beressi,
Régis Cohen,
Jean-Paul Beressi,
Jean-Luc Dumas,
Maggy Legrand,
Marie-Thérèse Iba-Zizen,
Elisabeth Modigliani,
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摘要:
WE REPORT THE first case of pseudotumoral lymphocytic hypophysitis successfully treated by corticosteroids without surgery. A 27-year-old woman had been monitored for chronic headache 13 months after giving birth, associated with amenorrhea and galactorrhea. Cranial magnetic resonance imaging revealed a markedly enlarged pituitary gland with a suprasellar extension; the only biochemical abnormality was a mild hyperprolactinemia. Because of a putative diagnosis of prolactinoma, bromocriptine was prescribed at a dose of 5 mg daily, soon followed by the transitory appearance of menstruation. Two years later, panhypopituitarism was present and was revealed by acute adrenal insufficiency. Magnetic resonance imaging revealed that the pituitary mass was the same as previously described, but hormonal investigation showed evidence of complete hypopituitarism and no hyperprolactinemia. Nuclear antibodies were negative as well as other autoantibodies. Human leukocyte antigen serological Class II typing was DR3/DR4. Lymphocytic hypophysitis was then suspected; in the absence of visual complication and because this patient refused surgery, corticosteroids were attempted at a daily dose of 60 mg of prednisone for 3 months, progressively decreased for the next 6 months. Under this treatment, a gradual recovery of all pituitary hormones was observed and magnetic resonance imaging showed a reduction of two-thirds in pituitary mass. Five months after the end of corticoid treatment, our patient relapsed with panhypopituitarism and an increase of pituitary volume. She underwent steroid treatment, and a biopsy was performed and confirmed the diagnosis of autoimmune hypophysitis. Such a case emphasizes the importance of clinical, biological, and radiological criteria leading one to suspect the diagnosis of lymphocytic hypophysitis: steroid treatment proved to be useful in our observation, both in the reduction in tumoral volume and in hormonal recovery.
ISSN:0148-396X
出版商:OVID
年代:1994
数据来源: OVID
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