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  • 1
    ISSN: 1432-0568
    Keywords: Brainstem ; Mechanosensory system ; Otavolateral efferents ; Teleost ; Tract-tracing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The efferent neurons of the lateral line system of the euteleost Aplocheilus lineatus and the osteoglossomorph Pantodon buchholzi, both surface feeding fish, were examined by neuronal tract tracing. Besides horseradish peroxidase, fluorescent dextrans were used as tracers to allow simultaneus visualization of projections from different lateral line branches. Labeled efferent neurons were found in nuclei situated in the medulla ventral of ventricle IV. This position resembles the octavolateralis efferent nucleus of previous studies. The number of labeled cells in the efferent nucleus is low in both species. Most neurons were found ipsilaterally to the application site, some along the midline and only very few contralaterally. The size of efferent cells differs distinctly between Aplocheilus, possessing small cellbodies (length 16.5 μm), and Pantodon, which has very large efferent cells (length 47.0 μm). Efferent axon bundles course rostrally in both species, leaving the brain at the level of the anterior lateral line nerve. Only Aplocheilus has in addition lateral axon bundles leaving the brain at the level of the posterior lateral line nerve. After application of one fluorescent tracer to the lateral ramus and a different fluorescent tracer to the superficial ophtalmic ramus in a given animal, double-labeling of efferent cells hardly ever occurs. If the neuromasts I and IV of the dorsal skull of Pantodon are applied with one fluorescent tracer each, ∼10% of centrally labeled cells are double-labeled. Considering the results of double-labeling, the concept of a differential innervation of lateral line branches is supported and discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Langenbeck's archives of surgery 382 (1997), S. 226-230 
    ISSN: 1435-2451
    Keywords: Angiosarcoma ; Spleen ; Diagnosis ; Pathology ; Immunohistochemistry ; Surgery ; Angiosarkom ; Milz ; Diagnostik ; Pathologie ; Immunhistochemie ; Therapie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Mit ca. 140 publizierten Fällen stellt das Angiosarkom der Milz eine sehr seltene Erkrankung dar, die durch ihre hochmaligne Verlaufsform charakterisiert ist. Wir berichten über den Fall eines 42jährigen Patienten, dessen Befunde zunächst an eine disseminierte Echinokokkose denken ließen. Die richtige Diagnose konnte letztlich erst histologisch und immunhistochemisch nach Splenektomie gestellt werden. Der Patient verstarb 3 Monate nach Diagnosestellung bei ausgedehnter Lebermetastasierung. Anhand einer Literaturübersicht werden diagnostische und therapeutische Möglichkeiten diskutiert.
    Notes: Abstract Angiosarcoma of the spleen is a very rare but highly malignant vascular neoplasm. So far only 140 cases have been reported. A 42-year-old patient is presented in which the radiologic imaging misled to the diagnosis of infiltrating echinococcosis. After splenectomy histological and immunohistochemical staining gave proof of metastatic angiosarcoma. The patient died three months later as a consequence of multiple organ dysfunction syndrome. The literature is reviewed in regard to clinical features, diagnosis and therapy.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Langenbeck's archives of surgery 382 (1997), S. 226-230 
    ISSN: 1435-2451
    Keywords: Key words Angiosarcoma ; Spleen ; Diagnosis ; Pathology ; Immunohistochemistry ; Surgery ; Schlüsselwörter Angiosarkom ; Milz ; Diagnostik ; Pathologie ; Immunhistochemie ; Therapie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Mit ca. 140 publizierten Fällen stellt das Angiosarkom der Milz eine sehr seltene Erkrankung dar, die durch ihre hochmaligne Verlaufsform charakterisiert ist. Wir berichten über den Fall eines 42jährigen Patienten, dessen Befunde zunächst an eine disseminierte Echinokokkose denken ließen. Die richtige Diagnose konnte letztlich erst histologisch und immunhistochemisch nach Splenektomie gestellt werden. Der Patient verstarb 3 Monate nach Diagnosestellung bei ausgedehnter Lebermetastasierung. Anhand einer Literaturübersicht werden diagnostische und therapeutische Möglichkeiten diskutiert.
    Notes: Abstract Angiosarcoma of the spleen is a very rare but highly malignant vascular neoplasm. So far only 140 cases have been reported. A 42-year-old patient is presented in which the radiologic imaging misled to the diagnosis of infiltrating echinococcosis. After splenectomy histological and immunohistochemical staining gave proof of metastatic angiosarcoma. The patient died three months later as a consequence of multiple organ dysfunction syndrome. The literature is reviewed in regard to clinical features, diagnosis and therapy.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
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