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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 394 (1981), S. 133-141 
    ISSN: 1432-2307
    Keywords: Pulmonary benign tumors ; Leiomyoma ; Hamartoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die licht- und elektronenmikroskopischen Befunde an den Lungentumoren eines Falles mit multiplen pulmonalen Leiomyomen werden beschrieben. Die Differential-Diagnose der leiomyomatösen Lungentumoren und besonders die Abgrenzung von der pulmonalen Lymphangiomyomatose wird besprochen. Multiple pulmonale Leiomyome werden in der Literatur als Metastasen von “low grade” uterinen Leiomyomen oder aber als Hamartome der Lunge betrachtet. Letztere Annahme beruht auf der Tatsache, daß auf der Oberfläche der Tumoren und in ihrem Inneren sich kubisches, drüsenartiges Epithel befindet. Dieses weist jedoch nach unseren Beobachtungen Merkmale der granulären Pneumocyten (Typ II) auf, insbesondere lamelläre Körper im Zytoplasma und Microvilli an der Oberfläche. Die Ausbildung dieser epithelialen Bedeckung wird deshalb als Reaktion des Alveolarepithels auf das Tumorwachstum aufgefaßt. Als mögliches Muttergewebe der multiplen pulmonalen Leiomyome wird das kontraktile System der Lungenacini (kontraktile interstitielle Zellen) diskutiert.
    Notes: Summary The light and electron microscopical features of the lung tumors in a case of multiple pulmonary leiomyomas are described. The differential diagnosis of leiomyomatous tumors of the lung is discussed. They have to be differentiated from lymphangio-leiomyomatosis of the lungs. In the literature, multiple pulmonary leiomyomas are generally considered to be metastases from low grade uterine leiomyosarcoma or to be hamartomatous lung tumors. This is suggested by the glandular structures both within the tumor and on the surface. However, our ultrastructural observations showed these epithelia to have features of granular pneumocytes (type II), in particular they contain lamellar bodies and posess microvilli on their surface. Their formation is considered to be a secondary reaction of alveolar lining cells to tumor growth. A possible origin of multiple pulmonary leiomyomas from the contractile system of the lung acini (contractile interstitial cells) is discussed.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 409 (1986), S. 749-750 
    ISSN: 1432-2307
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 13
    ISSN: 1432-2307
    Keywords: Cystadenolymphoma ; Salivary gland ; Histogenesis ; Cytokeratin ; Vimentin ; Glial fibrillary protein (GFP) ; Co-expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The distribution of selective cytokeratin polypeptides, vimentin, and glial fibrillary protein (GFP) in 5 human cystadenolymphomas of the parotid gland was compared with normal human parotid (n=5) and submandibular (n=4) glands using a panel of monoclonal antibodies against diverse and selective cytokeratin polypeptides, vimentin and glial fibrillary protein (GFP). A biotin-streptavidin method was used on cryostat sections. The immunocytochemical finding of identical cytokeratin polypeptides Nos. 7, 8, 18 and 19 and basal cells selectively labeled by the monoclonal antibody KS 8.58, in both the epithelial part of the cystadenolymphomas and in the duct epithelium of the parotid gland, confirms the hypothesis that the epithelial compartment of cystadenolymphomas is derived from the duct system. The triple expression of cytokeratin, vimentin and GFP in myoepithelial cells of the parotid gland is discussed.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 416 (1990), S. 535-538 
    ISSN: 1432-2307
    Keywords: Pancreatic tumour ; Immunohistochemistry ; Flow cytometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Immunohistochemical studies and DNA flow-cytometric investigations were performed in a case of solid-cystic tumour of the pancreas in a 35-year-old woman. All tumour cells were immunoreactive for the neuroendocrine cell markers chromogranin A and neuron-specificγ-enolase. Moreover, about 10% of tumour cells were immunoreactive for insulin, while hypoglycaemia was absent. Few tumour cells (less than 1%) were immunoreactive for somatostatin, and no cells were found to be immunoreactive for pancreatic polypeptide or glucagon. No immunoreactivity was present for duct cell marker carcino-embryonic antigen and only individual cells were reactive forα 1-antitrypsin. Nuclear DNA content of the tumour cells was diploid and the proliferative activity was low. In confirmation of some reports on neuroendocrine markers in solid-cystic tumour of the pancreas, our findings support the theory that the lesion is a hormonally inactive neuroendocrine pancreatic tumour.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 425 (1994), S. 1-1 
    ISSN: 1432-2307
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 16
    ISSN: 1432-2307
    Keywords: Necrotizing fasciitis ; Endocarditis ; Myocarditis ; Epicarditis ; Aspergillus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A patient with Aspergillus endocarditis, myocarditis and pericarditis is described. A 55-year-old man developed necrotizing fasciitis of the lower abdominal wall, pelvis and right thigh. Despite aggressive surgical débridement and antibiotic coverage, the patient died of multisystem organ failure. Autopsy revealed Aspergillus thromboulcerative endocarditis, myocarditis and pericarditis, acute necrotizing fungal bronchopneumonia and mycotic dissemination to brain, kidney and thyroid gland. A review of the literature showed that in the absence of open-heart surgery Aspergillus endocarditis and myocarditis are very uncommon.
    Type of Medium: Electronic Resource
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  • 17
    ISSN: 1432-2307
    Keywords: Mediastinal lymphoma ; Clear cell lymphoma ; Immunoglobulin-deficient B cell lymphoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary This is a report on 8 mediastinal tumours that occurred in young adults (19–43 years, mean: 29.4); predominantly in females (6/8). Initial symptoms consisted of thoracic pain and venectasia and in only one case in B symptoms. After surgical tumour reduction, radiation and/or chemotherapy, local recurrence was observed in each case under clinical care; abdominal spread is presently suspected in 3 patients; 3 died 11, 13 and 22 months after diagnosis. None developed leukaemia. The tumours are B-cell neoplasms with a characteristic immunophenotype: leucocyte common antigen+, common acute lymphoblastic leukaemia antigen−, B 1-antigen+, surface and cytoplasmic immunoglobulin−. Flow cytometry revealed DNA-diploidy in 7 cases and a moderately (3.2–3.8%) to extremely high (8.0–20.6%) S-phase component. The proliferation associated antigen Ki67 was detectable in 10–60% of the tumour cell nuclei, thus stressing the considerable or rapid growth. Histopathology is characterized by a diffuse growth pattern and a clearness and abundance of cytoplasm of the pleomorphic tumour cells, which vary in size and nuclear morphology from patient to patient. Apoptoses are more numerous than mitoses. Fibrosis and focal necrosis are common, sclerosis is present in 3 cases. We suggest that primary mediastinal lymphoma of B cell type is a novel B-lymphoma variant.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 429 (1996), S. 334-343 
    ISSN: 1432-2307
    Keywords: Whipple's disease ; Tropheryma whippelii ; SPC cells ; Pathology ; Endoscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Whipple's disease is an infectious disorder with intestinal and extra-intestinal manifestations. We reinvestigated the intestinal histology in a series of 48 patients (10 females, 38 males; mean age 56.5 years, standard deviation of the mean ± 11.2 years). A total of 126 biopsy samples, obtained prior to, during, and after therapy, were evaluated by light microscopy. In 43 patients (90%), histology was consistent with common descriptions, while it was uncommon in 3 patients (6%), and non-diagnostic in 2 patients (4%). During treatment, several alterations occurred. Apart from a continuous decrease in PAS-positive macrophages, the pattern of mucosal infiltration changed from diffuse to patchy. Moreover, the cytological aspects of PAS-positive macrophages changed substantially, and this change was used to propose four different subtypes. Initially, subtype 1 macrophages predominated (74%), but showed a gradual decrease within a few months of therapy. After 15 months, subtype 3 and subtype 4 macrophages predominated (〈80%). In 7 of 9 patients followed over long periods some subtype 3 or subtype 4 macrophages persisted. It is concluded that at diagnosis and during treatment the intestinal histology of Whipple's disease is heterogeneous. A few PAS-positive macrophages commonly persist at long-term follow-up. This and other features suggest the presence of a persistent immune defect.
    Type of Medium: Electronic Resource
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  • 19
    ISSN: 1432-2307
    Keywords: Epidermal growth factor receptor (EGFR) ; Breast carcinoma ; Fibroadenoma ; Myoepithelial cells ; Fibroblasts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Using the monoclonal antibody EGFR1, normal mammary gland and a series of 213 unselected primary breast tumours were investigated immunohistochemically for expression of epidermal growth factor receptor (EGFR). In normal breast EGFR was expressed in variable patterns in lobular, ductal, and myoepithelial cells. In fibroadenoma, EGFR was detectable in variable numbers of ductal and myoepithelial cells and in stromal fibroblasts. The myoepithelial compartment of 2 cystosarcomas phyllodes also expressed EGFR. Among the 197 carcinomas tested only 20.3% contained EGFR expressing tumour cells which represented a minority in 12.2%, the majority in 2.1%, and the entire neoplastic population in 6.1% of the cases. Again, non-neoplastic ductal remnants often contained EGFR positive myoepithelial and ductal cells whereas stromal fibro-blasts expressed EGFR only occasionally. We conclude that in contrast to the normal state, EGFR-expression is a rather rare phenomenon in breast carcinoma cells, positively correlated with a declining grade of differentiation (p〈0.025) and at least occasionally associated with squamous metaplasia within the tumour, that EGFR expression is not exclusively restricted to cells of the epithelial lineage, and that EGFR may have other functions not related to proliferation, since it is commonly detectable in myoepithelial cells.
    Type of Medium: Electronic Resource
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  • 20
    ISSN: 1432-1963
    Keywords: Schlüsselwörter Diastrophische Dysplasie ; Osteochondrodysplasie ; Key words Diastrophic dysplasia ; Osteochondrodysplasia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary The authors describe the histopathology of the resting cartilage and the growth plate in a case of diastrophic dysplasia and review the differential diagnosis with pseudodiastrophic dysplasia and atelosteogenesis type II.
    Notes: Zusammenfassung An einem eigenen Fall und anhand der Literatur besprechen die Autoren die histopathologischen Ergebnisse im Bereich des sog. ruhenden Knorpels und der Epiphysenfuge der selten auftretenden diastrophischen Dysplasie. Außerdem wird die Differentialdiagnose zum pseudodiastrophischem Kleinwuchs und zur Atelosteogenese Typ II tabellarisch dargestellt.
    Type of Medium: Electronic Resource
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