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Biomedical subjects

D Katenkamp

Publications and source records attributed to D Katenkamp.

At least 163 records · Page 9Linked to original sources

[Investigations on the ultrastructural cytology of branchiomeric paragangliomas (author's transl)].

The paragangliomas of the jugular and carotid bodies are growth processes which show varying histological and cytological patterns. The real nature of these lesions is still a matter of discussion. In this study 6 jugular and 3 carotid body tumours were investigated using the electron microscope. The main components were irregular cells with short and long cytoplasmic processes closely packed and mostly arranged in complexes. The ultrastructural cytology of the jugular and carotid bodies showed no striking differences. The great majority of the cells exhibits a clear similarity to the cells of normal paraganglia, especially to chief cells of carotid bodies (type I cells). But there were some modifications in the cellular structure including the abnormal structure of mitochondria and a greater variation in the morphology of the dense cored granules. The cytoplasm was dominated by differing populations of mitochondria comprising such of the crista type and such showing tubulus-like structures with a dense matrix and very often intramitochondrial bodies. The characteristic feature was the occurrence of randomly distributed dense cored granules measuring 700-800 A in diameter. These granules display a homogeneous electron dense or moderately dense somewhat granular core which is separated from limiting membrane by a clear electron lucent halo. A further population of granules was of a greater dimension (3,000-4,000 A) revealing an oval or cigar-like shape. In contrast to the former type the homogeneous dense cores of these granules showed a smooth contour and the lucent halo was very narrow. In general, singular exocytotic phenomena could be supposed. More frequently, however, signs of granulolysis were encountered. Free ribosomes, arranged often as polysomes, sparse, disorderly distributed microfilaments of 60-80 A diameter, few 240 A-microtubules and some lysosomal structures are also observed. Usually the cell clusters abutted directly upon the vascular connective tissue. In other cases cytoplasmic processes are intercalated resembling sustentacular cells. Fenestrated capillaries known to be typical for the paraganglionic tissues were only seldom detected. In the interstitial tissue typical collagen fibres are found showing a periodicity of 600-700 A, but occasionally fibres with a periodicity of about 1,200 A could be seen resembling fibrous-long-spacing collagen. Synaptic junctions and nerves or axons were always lacking.

Carotid Body Tumor↗

Experimental tumors with features of malignant fibrous histiocytomas. Light microscopic and electron microscopic investigations on tumors produced by cell transplantation of an established fibrosarcoma cell line.

An established fibrosarcoma cell line (RFS) derived from a cadmium induced fibrosarcoma of rat and RFS-cells in different subcultures produced tumors in nude mice and baby rats which showed characteristics of fibrosarcoma, malignant fibrous histiocytoma and completely undifferentiated sarcoma. After thorough examination of cells in culture and in experimental tumors by light microscopic and electron microscopic methods that conclusion has been drawn that malignant fibrous histiocytoma can develop from fibrosarcoma. By this the assumption that malignant fibrous histiocytomas derive from tissue histiocytes is questioned. After the discussion of the general unspecifity of the storiform growth pattern and the cytology of malignant fibrous histiocytomas the idea is presented that many defined malignant soft tissue tumors inclusively fibrosarcomas may pass a phase which should morphologically be diagnosed as malignant fibrous histiocytoma. Conceding the practical value of this diagnosis we emphasize that the concept of the entity "malignant fibrous histiocytoma" should be critically reevaluated because of the probable heterogeneity of this tumor group.

Animals↗

[Differential diagnosis and therapy of plasmocytoma of the head and neck (author's transl)].

The differential diagnosis, therapy, and prognosis of extramedullary plasmocytoma of the mucosa in the head and neck region are discussed on the example of 10 own cases observed between 1965 and 1981. They are subdivided into three types: 1. The apparent solitary (or multiple) extramedullary plasmocytoma. However, after thorough clinical and paraclinical examination or after observation of the course of the disease the exact diagnosis of medullary plasmocytoma is established. For the therapy, cytostatics must be employed, and prognosis is unfavourable. 2. The genuine plasmocytoma of the mucosa. It has to be distinguished from the immunocytic lymphoma and corresponds to a Non-Hodgkin's-Lymphoma. The therapy is partly surgical and partly radiological; as a rule, prognosis is good. 3. The tumour-like granuloma of plasma cells which is of reactive inflammatory nature. Treatment is surgical only.

Adult↗

Malignant fibrous histiocytoma of bone. Light microscopic and electron microscopic examination of four cases.

Malignant fibrous histiocytoma (MFH) of bone is a well-defined tumor by light microscopy but no agreement has been achieved concerning its histogenesis. We present the light and electron microscopic findings of four cases of MFH of bone. In case 1 multiple bone tumors were observed and in case 4 the tumor developed after irradiation. It was our aim to document the cytological variability and to arrange the findings in a histogenetic concept of primary intraosseous MFH. We observed some undifferentiated cells but mainly histiocyte- and fibroblast-like cells including intermediate forms, and several types of giant cells. We should emphasize the fact that there were also some large cells with a light microscopic resemblance to rhabdomyoblasts and with electron microscopic characteristics of myoblastic differentiation. From the ultrastructural point of view, therefore, MFHs seem to derive from a primitive mesenchymal stem cell rather than from the ordinary histiocyte. It is suggested that osteosarcoma and MFH of bone may have a common progenitor cell but it is important to make a clear clinico-pathological distinction between the tumors because of differing biological behavior.

Adult↗

Granuloblastomas of the stomach (so-called eosinophilic granulomas)-- a variant of fibrous histiocytomas?

25 cases of focal connective tissue proliferations in the submucosa of the stomach are presented. These lesions are termed "granuloblastomas" and have many features in common with so-called eosinophilic granulomas of the stomach. We found that granuloblastomas may be subdivided into two groups: (1) 8 cases are considered to be the result of the proliferation of a peculiar granulation tissue with abundant eosionophilic granulocytes, and (2) 17 cases show a more or less marked storiform pattern and the cellularity is constituted by fibroblasts and histiocytes as well as differing amounts of eosinophilic granulocytes. After discussing the concept of "fibrous histiocytomas" it is concluded that at least the second group of granuloblastomas may be interpreted as a pseudotumorous variant of fibrous histiocytomas. It remains to be clarified in future if submucosal neurofibromas can show the histological features of lesions which we designate granuloblastomas.

Adult↗

[Clinical data and therapy of malignant non-Hodgkin's lymphoma of nasal cavity and paranasal sinuses (author's transl)].

From 1950 to 1979 276 malignant tumors of nasal cavity and paranasal sinuses were treated in the Clinic of Oto-Rhino-Laryngology of the University. 40 cases (14,5% of these tumors) were diagnosed as malignant non-Hodgkin's lymphoma, 18 cases of them could be classified according to the so-called Kiel classification. There were 11 highly malignant lymphomas (including 7 immunoblastic lymphomas) and 7 low malignant (immunocytic) lymphomas. Basing on the histologic types of lymphomas and the predominant localization in the inner nose and the anterior ethmoidal sinus a pathogenetic importance of a chronic immunologic inflammation for the development of the lymphomas is suggested. Highly malignant immunoblastic lymphomas have a poor prognosis, almost all tumors generalize and lead to death within one year. Therefore, after the initial staging procedure, after the primary therapeutic irradiation and the following operation a polychemotherapy must be performed. The prognosis of immunocytic lymphomas is somewhat better, they generalize more seldom than highly malignant lymph node tumors. From the findings presented here the conclusion can be drawn that in the region of nasal cavity and paranasal sinuses the regional lymphatic spread of lymphomas is of little importance only.

Female↗

Synovial sarcoma of the abdominal wall. Light microscopic, histochemical and electron microscopic investigations.

A synovial sarcoma of the abdominal wall in a 56-year old woman showed the typical features of this tumor type. Histologically a characteristic biphasic cellular pattern with epithelium-like cell complexes and sarcomatous spindle cell areas was found. The histochemical examination revealed that tumor cells synthesize glycoproteins and weakly acid glycosaminoglycans (mainly hyaluronic acid). Electron microscopically the tumor cells in epithelium-like cell islets were sometimes arranged in gland-like formations with microvilli at the luminal side, specialized intercellular junctions and a peripheral basement membrane-like condensation of the ground substance. There was no fundamental cytological difference between cells of epithelium-like and spindle cell areas. Generally the tumor cells imitated cells of the synovial membrane and we found no evidence for origin from cells of the nerve sheath. Because of the submicroscopic relationship and histochemical similarities of synovial sarcomas and mesotheliomas we suggest that they should be united in a group of sarcomas with possible biphasic cellular pattern, while preserving their clinicopathologic definition.

Abdominal Muscles↗

Unusual leiomyoma of vulva with fibroma-like pattern and pseudoelastin production.

A unique case of a 71-year old woman with an unusual fibroma-like leiomyoma of the vulva in the region of the left Bartholin's gland is reported. Light microscopically the tumor resembled a fibroma, but electron microscopically the cells corresponded to modified smooth muscle cells. The great number of vessels and their intimate relation to the tumor cells is remarkable. In the intercellular space granular and fibrillar pseudoelastic material was found and thus the presence of collagen type III in addition to type I is suggested. In the region of the right Bartholin's gland a mesenchymal proliferation with similar histological features was seen but there was more resemblance to a conventional leiomyoma. The histogenesis remains obscure so that the designation of these lesions should include light microscopic and electron microscopic appearances as well as localization.

Aged↗

Myofibroblasts in connective tissue capsules around implanted dental materials.

For testing the biocompatibility of dental materials in an experimental animal model the capsular tissues around the implanted dental materials were examined light and electron microscopically. The exudative inflammation and fibrosis at different times after implantation were thought to be the indicators of the degree of the compatibility. Starting from the knowledge of the occurrence of myofibroblasts in reparative granulation tissue we looked for such cells in the capsular tissues. Myofibroblasts were especially found at three weeks after onset of the experiments. Structural peculiarities of this fibroblast modulation are emphasized. Myofibroblasts are considered as an essential link between the early exudative reaction and the late fiber formation in tissue reactions after mechanical injury.

Animals↗