[Morphogenesis and significance of epithelial metaplasia in the human prostate gland. An electron-microscopic study (author's transl)]
- PMID: 804744
- DOI: 10.1007/BF00432385
[Morphogenesis and significance of epithelial metaplasia in the human prostate gland. An electron-microscopic study (author's transl)]
Abstract
Electron-microscopic studies were done to point out the morphogenesis of transitional and squamous epithelial metaplasia in the human prostate gland. The basis of epithelial metaplasia is a multi-layered proliferation of the basal cells and subsequent divergent differentiation. Transitional metaplasia can be viewed under the light microscope; the electron microscope on the other hand does not show all structural features of the transitional epithelium, such as: The cover cells of the metaplastic epithelium, which do not reach the basement membrane; the surface cells, which are always mononuclear and show signs of beginning adenoid differentiation. Extreme twisting of the lateral cell membranes as a morphological equivalent of deformability was not observed. Squamous epithelial metaplasia, contrary to transitional epithelial metaplasia, shows the criterions true characteristics of squamous epithelium at both the light and electron microscopic levels: The metaplastic cells have an abundant cytoplasm containing the characteristic structures with numerous tonofibrils and broad desmosomes. Microvilli-like processes of the cytoplasm project into the lacunar interfacial canals. In addition aggregates of glycogen granules and deposits of osmiophilic material can be seen, representing the first step of keratinization. Epithelial metaplasias in the prostate occur not only in the central area near the urethra, but also in the peripheral ducts and glandular acini. An estrogen-androgen imbalance is suggested to be an essential factor in the etiology of prostatic epithelial metaplasia. A reversibility of squamous epithelial metaplasia is unlikely. To our knowledge, the epithelial metaplasias in the prostate do not represent a precancerous lesion.
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