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H Kastendieck

Publications and source records attributed to H Kastendieck.

50 records · Page 3Linked to original sources
PubMed1976

[Morphology and clinical significance of the meningeal hemangiopericytoma (author's transl)].

Hemangiopericytomas of the meninges are rare tumors. Three tumors of this type with a course over more than 10 years each are reported. All three tumors were primary diagnosed as meningiomas (one: vascular, two angioblastic). The diagnosis was changed to hemangiopericytoma only then when recurrences and extracranial metastases had occurred. Morphologically, "angioblastic meningioma" and "hemangiopericytoma of the meninges" show striking common features. The principal pattern bases on the blastomatous increase of capillary blood vessels lined by a normal endothelium, extracapillary proliferation of pericyte-like mesenchymal cells and an intercellular network of reticulin fibres. Light- and electron microsopic findings do not demonstrate the characteristics of a meningioma. Furthermore, clinical data and growth pattern of "angioblastic meningioma" and "hemangiopericytoma of the meninges" are well comparable. Therefore, it seems to be justified to interpret these tumors as a tumor entity with identical histogenesis. It is well known that hemangiopericytomas frequently recur and metastasise. On the other hand, meningiomas are usually benign. For those reasons we suggest that these tumors should be uniformly classified as "hemangiopericytoma of the meninges" in order to stress the significance of these particular tumors of the meninges regarding their treatment and behaviour.

Adult↗
PubMed1975

[Morphogenesis and significance of epithelial metaplasia in the human prostate gland. An electron-microscopic study (author's transl)].

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.

Basement Membrane↗
PubMed1975

[Ultrastructural findings in carcinoma of the prostate after combined endocrine and radiation treatment].

Carcinomas of the prostate treated by orchiectomy, 60Co-radiation, and hormonal drugs a relatively short time prior to the time of biopsy were studied with the electron microscope. The following degenerative changes of tumor cells and fibromuscular stroma were found: The nuclei of the tumor cells were intensely heterochromatic, irregularly shaped, and the perinuclear rim dilated; large atypical sizes, multiple segmentations and "nuclear invaginations" were observed. The tumor cell cytoplasm showed vacuolar degeneration, and the limiting membranes of the tumor cells were extensively destroyed. Remarkable changes were also found in the fibromuscular stroma: There was a proliferation of collagenous fibers as well as degenerative transformations ending in hyalinization. The smooth muscle cells were dissociated and fragmented, sometimes showing vacuolar degeneration of the cytoplasm. The endothelium of the blood vessels was swollen, and the vessel walls were thickened. In spite of these radiation-induced lesions it remains undecided as to what degree the other therapeutic measures take part in the total therapeutic effects as seen in the ultrastructural findings. However, these regressive changes are much more pronounced than those seen after orchiectomy alone and partly resemble the findings which are characteristic of radiation induced structural lesions. The morphological changes are not uniform throughout the tumor. It is not unusual to find intact tumor cells next to totally degenerated cells. They represent poorly differentiated tumor cells. It is discussed whether these "embryonic" tumor cell types are and remain resistant to treatment and if a tumor recurrance may originate in them later on.

Biopsy↗
PubMedDate not supplied

Immunocytochemical differential diagnosis of diffuse malignant pleural mesotheliomas--a clinicomorphological study of 158 cases.

Formalin-fixed paraffin-embedded material of 158 diffuse malignant pleural mesotheliomas (DMPMs) was used in order to determine the differential diagnostic value of immunocytochemical probes against 9 different antigens. While vimentin expression was found in only 50% of cases, regardless of their histological subtype all tumours were found to be cytokeratin-positive when an antibody with broad-spectrum cytokeratin reactivity was used. Conversely, none of the cases was immunostained by antisera against carcinoembryonic antigen (CEA), Leu-M1 antigen, chromogranin, S-100 protein, lysozyme and a T-cell associated antigen. The density of inflammatory cell infiltrates reactive with antisera against the three latter antigens was not associated with the clinical behaviour of the neoplasms examined. Eight DMPM cases showed immunoreactivity with HEA-antibodies against Egp 34, an antigen previously supposed only to be expressed by carcinomas. On the basis of these findings, the consistent cytokeratin reactivity, also of the sarcomatous type of DMPM, may help to exclude metastatic involvement of the pleura by a mesenchymal neoplasm of other origin. CEA and Leu-M1 staining of a given pleural tumour, on the other hand, is indicative of a carcinoma secondarily afflicting the pleura, thus making the diagnosis of primary DMPM unlikely.

Antigens, Differentiation, Myelomonocytic↗