Search results for "sarcoma"
showing 10 items of 566 documents
Tissue microarrays analysis in chondrosarcomas: light microscopy, immunohistochemistry and xenograft study
2008
Abstract Background Chondrosarcoma (Chs) is the third most frequent primary malignant tumour of bone and can be primary or secondary, the latter results mainly from the malignant transformation of a benign pre-existing tumour. Methods All the cases diagnosed as Chs (primary tumours, recurrences and/or metastasis and xenotransplanted Chs) from the files of our Department were collected. Only cases with paraffin blocks available were selected (Total 32 cases). Six Tissue Microarrays (TMAs) were performed and all the cases and biopsies were distributed into the following groups: a) only paraffin block available from primary and/or metastatic tumours (3 TMAs), b) paraffin block available from p…
Sarcomatoid carcinoma of urinary bladder: Immunohistochemical study of an uncommon case
2002
A case of sarcomatoid carcinoma of the bladder is reported herein. Immunohistochemical staining with human pancytokeratin antibody was negative, while vimentin staining was strongly positive, suggesting a diagnosis of sarcoma of the bladder. Further immunohistochemical analysis revealed positivity for AE1/AE3 cytokeratins, permitting a correct diagnosis of sarcomatoid carcinoma of the bladder. It can be difficult to distinguish between sarcomatoid carcinoma, undifferentiated carcinoma and sarcoma, particularly if the biopsy specimens are of small size. In rare cases, sarcomatoid tumors may express epithelial markers different from those revealed by human pancytokeratin staining. Copyright ©…
Fibroblast and Myofibroblast Participation in Malignant Fibrous Histiocytoma (MFH) of Bone
1989
Eight malignant fibrous histiocytomas (MFH) of bone were studied with immunohistochemistry and electron microscopy. Ultrastructurally, fibroblasts and myofibroblasts were the main tumor cells in four cases and abundant in two other cases; these cells showed immunohistochemical positivity to alpha 1-antitrypsin, vimentin and anti-muscle antigen (HHF 35). Moreover, histiocytic-like tumor cells were electron-microscopically detected in four cases, being the main tumor cell type in two of the cases; immunohistochemically these cells expressed positivity to alpha-1-antichymotrypsin (A1ACT), alpha-1-antitrypsin (A1AT) and vimentin. Present results confirm the cellular heterogeneity of MFH of bone…
An immunohistochemical and biochemical study of cytokeratin polypeptides in a non-Paget type adenocarcinoma of the vulva
1988
SummaryThe intermediate filament composition was studied in a malignant neoplasm of the vulva in a 42 year old patient. The absence of vimentin excluded the diagnosis of malignant melanoma. Anaplastic squamous cell carcinoma could be excluded by the presence of glandular type cytokeratins numbers 7, 8, 18, 19 in the neoplastic cells. Intermediate filament typing did not support a diagnosis of epithelioid sarcoma. Since the typical epidermal involvement by tumour cells was lacking, Paget's disease was excluded. Metastatic adenocarcinoma was excluded by the lack of relevant clinical findings. It was concluded that the lesion represented an adenocarcinoma of the vulva of the non-Paget type mos…
‘Pyogenic granuloma-like Kaposi's sarcoma’ on the hands: immunohistochemistry and human herpesvirus-8 detection
2009
Letter to Editor
Malignant peripheral nerve sheath tumor of the maxila
2005
Summary We present a case of a malignant peripheral nerve sheath tumor [MPNST] of the maxilla corresponding to a 12 year old male who had a painful, ulcerated rapid growing tumor. Histology revealed the presence of a tumor consisting of fusiform cells with abundant mitosis, with negative cytokeratins, actin, desmin, myoglobin and factor VIII. In contrast, the protein S-100 was positive. MPNST was not associated with signs of Neurofibromatosis Type 1. The patient was surgically intervened and received radiotherapy, then died within 10 months posterior to surgical intervention after suffering recurrence.
Chirurgische Strategien bei Schilddrüsenerkrankungen im Kindes- und Jugendalter
1990
In the Department of Paediatric Surgery of the University Hospital of Mainz and the Department of Paediatric Surgery of the University Hospital of Frankfurt/M 90 children with thyroid gland lesions were operated on between 1970 and 1988. 78 patients had benign findings and 12 had malignant tumours. The most frequent operative indication for benign lesions was the euthyroid goitre (57 patients). We found nodular goitre in 45 patients, cystic goitre in 11 patients, and diffuse goitre in only 1 patient. 20 children were suffering from hyperthyroidism (11 with Basedow's disease, 9 with autonomy) and 1 from Hashimoto's thyroiditis. Among the malignant tumours, papillary carcinomas were the most …
Optical coherence tomography and Raman spectroscopy for ex vivo characterization of canine skin and subcutaneous tumors: preliminary results
2021
Cancer is one of the leading causes of companion animal mortality. Up to 30% of all canine and feline tumors appear on or directly under the skin. To date, only a limited number of studies applied biophotonics techniques for optical characterization and detection of tumors in pets. In this work, we acquired ex vivo optical coherence tomography (OCT) images and Raman spectra of native skin and the most common canine and feline skin and subcutaneous tumors; lipomas, mast cell tumors, and soft tissues sarcomas. Lipomas exhibited the most distinctive tissue morphology (i.e., honeycomb structure) and biochemistry (lipid-related Raman peaks of 1063, 1301, and 1652 cm-1). Moreover, lipomas had sig…
The intraclonal and interclonal phenotypic heterogeneity in a rhabdomyosarcoma cell line with abortive imitation of embryonic myogenesis
1988
Three distinct subpopulations (A, B, C) derived from a dimethylbenzanthracene-induced rat rhabdomyosarcoma were established as permanent cell lines. Although the clonal nature of each of these subpopulations was confirmed by repeated recloning procedures, a striking intraclonal phenotypic heterogeneity was observed. By means of immunofluorescence microscopy and transmission electron microscopy, it could be shown that these subpopulations closely recapitulate stages of embryonic rhabdomyogenesis both in vitro and in vivo, but differ in their particular range of maximum differentiation. Embryonic rhabdomyogenesis is imitated most perfectly by subpopulation C, in which multinuclear myotubes ar…
Primary Rhabdomyosarcoma Mimicking a Small Cell Sarcoma of Bone: A Nude Mice Xenograft, Cytogenetic, and Molecular Approach
1998
Small cell sarcomas of bone are difficult to classify and diagnose. The present case deals with such a tumor in which the original biopsy and the resected specimen, studied by histology before chemotherapy, provided no final information about its real nature. Thus several techniques were applied to discern its histogenesis and biology. Myogenin proved positive in isolated cells of the primary neoplasm but was extensively expressed in nude mice xenografts. Electron microscopy confirmed the existence of myofilaments. The cytogenetic analysis revealed a large number of chromo somal abnormalities, but not those found in the Ewing's/PNET (peripheral neuroectodermal tumor) family of tumors. This…