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Titlebook: Biological Characterization of Bone Tumors; A. Roessner (Prof. Dr.) Book 1989 Springer-Verlag Berlin Heidelberg 1989 Tumor.bone.cell.class

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楼主: exposulate
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Immunohistochemical Investigation of Chordomas: Histogenetic and Differential Diagnostic Aspects,
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Grundlagen der ovariellen Stimulation,gical appearance, they have presented a diagnostic challenge to pathologists. The age of the patient, radiographic appearance, and site of the tumor may help in some cases to distinguish between the different categories of lesions. Ewing’s sarcoma, for example, is a tumor more common in children and
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https://doi.org/10.1007/978-3-662-46014-6 is also found in nonmineralizing connective tissue of the skin, lung, liver, eyes, and tendons (C. 1981; G. and R. 1980; . M. 1981). Therefore the specific quality of bone matrix as a mineralizing connective tissue is probably due to its 10% noncollagenous protein content. Based on this assumption
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,Lebensführung und Konzeptionschancen,nd anaplastic, telangiectatic, and small cell areas are present. On the basis of their different morphology and histology D. and U. (1977) have introduced several subentities within osteosarcomas. Studies by G. etal. (1981) and R. (1984) have substantiated the value of a cytogenetic approach. During
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,Lebensführung und Konzeptionschancen, accepted principle of all current classifications. In bone tumor pathology, the spectrum of morphological criteria has been enlarged by roentgenological features; nevertheless, their Classification is often more difficult than that of carcinomatous neoplasms (S. etal. 1972; S. 1981). This is due no
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Grundlagen der ovariellen Stimulation,one tumors and tumor-like conditions, giant cell tumor of bone is a unique clinical-radiographic-pathological entity (Fig. 1) which is characterized by (1) female predominance, (2) peak incidence in the third and fourth decades of life, and (3) propensity to involve the long bones in the epiphyseal
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,Lebensführung und Konzeptionschancen,although lesions called chondroid chordoma clearly behave in a far more benign fashion than typical chordoma, the histogenesis of chondroid chordoma has been uncertain. Furthermore, the pathological features distinguishing it from related tumors have been blurred by its supposed bimorphic histology
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