Abstract
The increasing knowledge of the functional and phenotypic heterogeneity of epithelial cells and of the specific organization of cellular microenvironments for T cell maturation and regulation of self-tolerance in the normal thymus has substantially contributed to a better understanding of the complex morphology of thymic epithelial tumors and their relationship with paraneoplastic immune syndromes, of which the association to autoimmune myasthenia gravis (MG) is most frequent.1–3 Previous morphological typing of thymomas has been mainly descriptive distinguishing between epithelioid, epidermoid and spindle cell features of thymomatous epithelial cells as well as lymphocytic, mixed, and epithelial tumor types according to their lymphocytic component.4–6
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Kirchner, T., Müller-Hermelink, H.K. (1989). New Approaches to the Diagnosis of Thymic Epithelial Tumors. In: Cecilia Fenoglio-Preiser, M., Wolff, M., Rilke, F. (eds) Progress in Surgical Pathology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-12823-7_10
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DOI: https://doi.org/10.1007/978-3-662-12823-7_10
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