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  • Ultrastructure  (3)
  • Amebic encephalitis  (1)
  • Asbestos  (1)
  • Cell & Developmental Biology  (1)
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  • 1
    ISSN: 1432-0533
    Keywords: Acanthamoeba ; Amebic encephalitis ; Corticosteroids ; Free-living amebas ; Immunosuppression ; Intracranial mass ; Naegleria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Clinical and brain biopsy or autopsy findings in six patients with Granulomatous Amebic Encephalitis (GAE) due toAcanthamoeba sp. were characterized by focal neurological symptoms, increased intracranial pressure, and focal neuroradiological findings. Craniotomies were performed because of the diagnostic possibility of a mass lesion such as a brain tumor or abscess. In four patients, frozen sections demonstrated free-living amebas. GAE may present as an acute or subacute intracerebral mass lesion with signs and symptoms of focal brain disease and should be differentiated from viral, bacterial, fungal, and other protozoal encephalitides.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 33 (1975), S. 173-177 
    ISSN: 1432-0533
    Keywords: Mesothelioma ; Pleura ; Metastases ; Brain ; Ultrastructure ; Asbestos
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A malignant fibrous mesothelioma in a 52 year old white man arising from the left parietal pleura associated with lupus erythematosus with metastases to brain and liver is reported. Asbestos bodies were found in digested pulmonary tissue but none in the primary or metastatic lesions. Light microscopic and ultrastructural studies suggest that this tumor contains mesothelial or endothelial cells, some of which revealed fibroblastic features while others disclosed epitheloid characteristics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 34 (1976), S. 237-253 
    ISSN: 1432-0533
    Keywords: Strabismus ; Extraocular muscles ; Hirano bodies ; Ultrastructure ; Luse bodies ; Leptomeres
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Thirty extraocular muscles (EOM) from 20 patients were evaluated by light microscopy (LM), electron microscopy (EM), and enzyme histochemistry (EZH). Twenty-one EOM were obtained from 13 patients with strabismus, 9 EOM from 4 patients undergoing eye surgery for other reasons and from 3 autopsy cases. One μm thick sections revealed marked variation in muscle fibre shape and size and in myofibrillar structure; also noted were small, hypertrophied, whorled, and ringbinden fibres. Dense and granular material in the central portion of some fibres and sarcomere disruption in 2–3 μm sections was observed. EZH revealed the absence of the classical mosaic pattern usually found in skeletal muscles. ATPase studies were inconsistent and did not correlate with the expected reciprocal activity of NAD-H diaphorase, particularly on the large fibres. Ultrastructural features consisted of vacuoles within myofilament bundles, “smearing” of Z bands, and “nemaline rods”. Occasional myelin figures and lipid-like droplets were observed in subsarcolemmal spaces, associated with scattered clusters of glycogen granules. Abnormal mitochondria and subsarcolemmal inclusions of dense and granular material were conspicuous. “Leptomeric” profiles, “Zebra bodies”, or “striated bodies” were noted in 8 EOM's, and an Hirano body was found in 1. The intramuscular nerves contained structures resembling “Luse bodies” in 7 cases. These observations suggest that EOM from individuals with and without strabismus possess unique structural characteristics suggestive of developmental and morphological disarrangement of contractile elements. Some of these changes might play a role in the pathogenesis of strabismus and in the development of clinical symptoms. These features are significantly different from striated skeletal muscle. Therefore the criteria used in the pathological evaluation and diagnosis of skeletal muscle disorders cannot be unequivocally applied to EOM investigations. These data establish the necessity to determine histological norms, ultrastructural patterns, and develop new enzyme histochemistry criteria for the evaluation of EOM. Only then can an acceptable comparison of EOM and skeletal muscle be made.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 29 (1974), S. 251-262 
    ISSN: 1432-0533
    Keywords: Polymyositis ; Ultrastructure ; Histiocytes ; Birbeck Granules ; Macrophages
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A fatal case of polymyositis in a young female is presented. Two muscle biopsies obtained before and after treatment with large doses of steroids, as well as autopsy tissue, demonstrated widespread degeneration of myofibres associated with cytoplasmic tuboreticular structures resembling paramyxovirus nucleocapsids in capillary endothelial cells and fibroblasts. Aggregates of spherical particles and “simple and granular” nuclear bodies suggested a virus-related or associated etiologic agent. In addition, interstitial cells of mesenchymal origin, probably related to macrophages or histiocytes were present. These contained numerous rodlike profiles or phagolysosomal bodies which resembled “Birbeck” granules. Inflammatory response was very scant. It would appear that polymyositis probably represents a primary reaction to antigemic substances and a morphologic manifestation of altered host macrophage response.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 149 (1977), S. 439-452 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Blood vessels of the human telencephalic germinal matrix during the tenth through the twenty-second week of gestation have been examined by light and electron microscopy. In all fetuses studied the ependymal and sub-ependymal zones of the germinal matrix have a prominent vascular network. During the tenth and twelfth weeks of gestation, the endothelial cells are plump and display numerous organelles, junctional complexes, conspicuous luminal microvilli and stub-like abluminal projections. Coated and micropinocytotic vesicles were found both in the cytoplasm and on luminal and abluminal surfaces. In endothelial cells intracytoplasmic, membrane-limited, rod-shaped bodies were frequently observed. These bodies have been linked to endothelial thromboplastic and clotting activities and related to abnormal clotting status. Their role in the pathogenesis of subependymal germinal matrix hemorrhage in premature infants remains unknown. Pericytes apposing the endothelial cells were recognized in all gestational periods. The endothelial basal lamina and astrocytic end-feet are ill defined, and the extracellular space is pronounced. By the fifteenth and seventeenth weeks of gestation the endothelial cells are still large and now possess more numerous luminal microvilli and abluminal projections. At this stage the pericytes, basal lamina and astrocytic end-feet are all well developed, resulting in a decrease in the surrounding extracellular space. By the twenty-second week the endothelial cells possess few luminal and abluminal projections and the associated basal lamina, glia, pericytes and extracellular compartment appear mature. The relationship of the germinal matrix vasculature to the pathogenesis of subependymal hemorrhage is discussed.
    Type of Medium: Electronic Resource
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