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  • 1
    ISSN: 1432-0533
    Keywords: Glioma ; Neovascularization ; Endothelium ; Vascular smooth muscle ; Immunohistochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Since the origin of cells contributing to microvascular proliferation (MVP) in glial neoplasms is unsettled, a light microscopic and immunohistochemical study for vascular smooth muscle cells and endothelial cells was performed in formalin-fixed, routinely processed brain tumor biopsy material. MVP in glial neoplasms was compared with that in intracerebral metastatic carcinomas and in intracranial granulation tissue. On the basis of the degree of hyperplasia of hypertrophic cells in the microvascular wall, MVP was subjectively divided into mild, moderate, and glomeruloid (marked) proliferation. The relative contribution of vascular smooth muscle cells and endothelial cells to different degrees of MVP was estimated immunohistochemically using antibodies against α-smooth muscle actin and von Willebrand factor, respectively. Glomeruloid MVP occurred in 50% of the malignant glial neoplasms. Moderate MVP was found in most malignant gliomas and in some pilocytic astrocytomas. Glomeruloid MVP was present in peritumoral glial tissue in 4 out of 15 intracerebral metastatic carcinomas, while only mild to moderate MVP was found within these tumors. In granulation tissue MVP was mild. In glomeruloid and moderate MVP vascular smooth muscle cells were more hypertrophic and more numerous than endothelial cells. The contribution of hypertrophic vascular smooth muscle cells to mild MVP was variable. MVP in glial neoplasms was generally not accompanied by a matrix of fibrous stroma but was directly embedded in glial tissue. The architecture of this MVP suggested “in situ” proliferation of microvascular cells without migration of these cells into the surrounding tissue.
    Type of Medium: Electronic Resource
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  • 2
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    Philadelphia : Periodicals Archive Online (PAO)
    Hispanic Review. 51:4 (1983:Autumn) 393-408 
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  • 3
    ISSN: 1432-0533
    Keywords: Key words Alzheimer's disease ; Senile plaques ; Microglia ; Lysosomes ; Immunohistochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract One of the major histopathological lesions in brains of patients with dementia of the Alzheimer type (DAT) is the senile plaque. Although previous studies have shown that senile plaques are often accompanied by microglial cells, the role of these cells in DAT pathology is still unclear. In an immunohistochemical and immuno-electron microscopical analysis of DAT and control brain tissues we addressed this issue using two monoclonal antibodies (mAbs KP1 and 25F9) directed against lysosomal antigens in monocytes and macrophages. Whereas KP1 stained lysosomes in both resting and activated microglial cells, 25F9-staining was predominantly found in lysosomes of activated microglial cells in classic senile plaques. The number and size of 25F9-positive lysosomes in activated microglial cells was increased compared to 25F9-staining in unaffected areas in DAT and control sections. We conclude that mAb 25F9 is a unique and useful lysosomal marker, with a higher specificity than other known markers, for activated microglial cells associated with classic, but not with diffuse, senile plaques.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0533
    Keywords: Key words Alzheimer’s disease ; Cerebellum ; Intercellular adhesion molecule-1 ; Cerebrovascular ; Inflammation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Inflammatory processes have been implicated in the formation of senile plaques in the cerebral cortex of patients with dementia of the Alzheimer type (DAT), since several inflammation-induced proteins are present within these plaques. The relation between inflammatory components and other amyloid β protein (Aβ)-containing lesions of the DAT brain [cerebrovascular amyloidosis (CA) and cerebellar senile plaques] is unclear. We studied the distribution of the inflammation-inducible protein intercellular adhesion molecule-1 (ICAM-1) in CA and in senile plaques of the cerebellum, using an immunohistochemical approach. We observed striking differences in ICAM-1 reactivity between the different types of Aβ-containing lesions. ICAM-1 was only expressed in classic senile plaques in the granular and Purkinje cell layer of the cerebellum, and not in diffuse senile plaques of the molecular layer. Also, ICAM-1 was not associated with CA; only when the vascular amyloid extended into the neuropil (dyshoric angiopathy) was perivascular ICAM-1 reactivity observed. This is in contrast to the putative primary involvement of inflammation in the formation of cerebrocortical classic and diffuse senile plaques. Our findings indicate that ICAM-1 expression, which may be an indicator of an inflammatory reaction, is induced in the neuropil depending on the specific site of Aβ production.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-7373
    Keywords: glioblastoma multiforme ; neovascularization ; immunohistochemistry ; image analysis ; computer-assisted ; therapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Conclusions Elucidation of the pathogenesis and biological significance of MVP in GBMs is essential for developing a rational treatment directed at the abrogation of neovascularization in these neoplasms. The present quantitative study illustrates the striking heterogeneity of the microvasculature in GBMs such that the number of vessels in many tumor areas does not exceed that of normal white matter. Thus, many regions of GBMs may not be overtly angiogenesis dependent and may be difficult to treat by anti-angiogenic therapy alone. Even in areas with florid MVP the efficacy of anti-angiogenic therapy is questionable since the contribution of these aberrant blood vessels to the functional circulation and thus to the viability and growth of GBMs is unclear.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neuro-oncology 32 (1997), S. 253-265 
    ISSN: 1573-7373
    Keywords: brain neoplasms ; neovascularization ; astrocytoma ; glioblastoma multiforme ; meningioma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Angiogenesis is the outgrowth of new blood vessels from the preexistent vasculature. In 1971, Folkman hypothesized that solid tumors are dependent on angiogenesis for sustained growthand that anti-angiogenic treatment is a potential antineoplastictherapy. Because glioblastoma multiforma (GBM) frequently shows florid microvascular proliferation (MVP), this tumor has beenconsidered since then as a suitable candidate for such treatmentthat attempts to eradicate or control a neoplasm by interfering withits blood supply. Indeed, in animal models the growth of gliomaxenografts can be inhibited by targeting the angiogenic process.However, unlike many glioma xenografts, human infiltrating gliomassuch as GBMs have a diffuse infiltrative growth pattern, and preexistent vessels may suffice to provide many tumor cells with much of their blood supply, particularly in the critical peripheral infiltrative margins. Thus, while attractive in concept,anti-angiogenic therapy of GBM must address the anatomic vascularrealities of this neoplasm. Even if anti-angiogenic therapy ultimately has a role in infiltrative neoplasms, thereare a host of other intracranial neoplasms whose discrete architecture might make them attractive candidates for anti-angiogenic therapy. This review summarizes the angiogenic process in GBM and suggestsother types of tumors for which the efficacy of anti-angiogenic therapymight be studied.
    Type of Medium: Electronic Resource
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  • 7
    Book
    Book
    Berlin u.a. :Springer,
    Title: Principles of computational fluid dynamics; 29
    Author: Wesseling, Pieter
    Publisher: Berlin u.a. :Springer,
    Year of publication: 2001
    Pages: 644 S.
    Series Statement: Springer series in computational mathematics 29
    Type of Medium: Book
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  • 8
    Book
    Book
    New York u.a. :Wiley,
    Title: ¬An¬ introduction to multigrid methods
    Author: Wesseling, Pieter
    Publisher: New York u.a. :Wiley,
    Year of publication: 1992
    Pages: 284 S.
    Series Statement: Pure and applied mathematics
    Type of Medium: Book
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