Search results for " sarcoma"

showing 10 items of 180 documents

Scanning electron microscopic evidence for neural differentiation in Ewing's sarcoma cell lines.

1990

A number of recent studies have suggested a relationship between Ewing's sarcoma (ES) and other small round cell tumours of childhood such as peripheral neuroepithelioma (PN). We report scanning electron microscopic studies on the character of induced neural differentiation in ES, neuroblastoma, PN, osteosarcoma and colon carcinoma. We found evidence of neural differentiation in both neural lines and in one of two Ewing's lines before treatment. After differentiation, both Ewing's and neural lines developed neuritic processes with varicosities and little arborization, except for the initially undifferentiated Ewing's line (A4573) which displayed extensive lateral sprouting from neuritic pro…

Pathologymedicine.medical_specialtyImmunocytochemistrySarcoma EwingBiologyAdenocarcinomaPathology and Forensic MedicineCell LineNeuroblastomamedicineHumansNeuroectodermal Tumors Primitive PeripheralMolecular BiologyOsteosarcomaNeural tubeEwing's sarcomaCell BiologyGeneral Medicinemedicine.diseasemedicine.anatomical_structureCell Transformation NeoplasticCell cultureColonic NeoplasmsMicroscopy Electron ScanningOsteosarcomaSarcomaFilopodiaVirchows Archiv. A, Pathological anatomy and histopathology
researchProduct

Ewing’s Sarcoma Family of Tumors

2020

Ewing’s sarcoma family of tumors (ESFT) is a family of small round cell sarcomas with specific molecular alterations showing a spectrum of neuroectodermal differentiation. There is a slightly greater incidence in males than females. The first two decades of life account for 80 % of patients (age at diagnosis ranges from 13 to 19 years), being more uncommon in adults and elderly patients and more frequent in white (Caucasian) people.

Pathologymedicine.medical_specialtyNeuroectodermal Differentiationbusiness.industryIncidence (epidemiology)Metastatic neuroblastomamedicineRound cellEwing's sarcomaAge at diagnosisSarcomamedicine.diseasebusiness
researchProduct

Oral Rhabdomyosarcoma: a review

2012

Rhabdomyosarcoma (RMS) is a rare malignant soft tissue neoplasm comprised of cells derived from the primitive mesen¬chyme. About 35% of RMS arises in the head and neck, are are classified as parameningeal and non-parameningeal forms. These are the most common soft tissue sarcoma of the children, adolescents and young adults. Their etiopathogenesis and its molecular relevance have been emphasized. The first line of treatment is radical excision and this is usually supplemented by radiotherapy. It is believed that adjunct combination chemotherapy may greatly improve the prognosis. Inadequately treated tumours grow in an infiltrative manner and recur in a high percentage of cases. Bone does no…

Pathologymedicine.medical_specialtyOral Medicine and Pathologybusiness.industryFirst linemedicine.medical_treatmentSoft tissue sarcomaCombination chemotherapyMalignant Soft Tissue NeoplasmParameningealOdontologíaReviewmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludRadiation therapyUNESCO::CIENCIAS MÉDICASMedicinebusinessHead and neckRhabdomyosarcomaGeneral Dentistry
researchProduct

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 ©…

Pathologymedicine.medical_specialtyUrinary bladder tumorAE1/AE3 cytokeratinmedicine.medical_treatmentUrologyVimentinSarcomatoid carcinomaCystectomyCytokeratinBiopsyHumansMedicineSarcomatoid carcinomaAgedUrinary bladderbiologymedicine.diagnostic_testAE1/AE3 cytokeratins; Human pancytokeratin; Sarcomatoid carcinoma; Urinary bladder tumors; Urologybusiness.industryCarcinomaSarcomamedicine.diseaseImmunohistochemistrymedicine.anatomical_structureUrinary Bladder NeoplasmsHuman pancytokeratinbiology.proteinKeratinsFemaleSarcomabusinessSpindle cell carcinoma
researchProduct

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…

Pathologymedicine.medical_specialtybiologybusiness.industryMelanomaEpithelioid sarcomaObstetrics and GynecologyVimentinmacromolecular substancesmedicine.diseaseVulvaCytokeratinmedicine.anatomical_structurebiology.proteinmedicineImmunohistochemistryAdenocarcinomaIntermediate filamentbusinessJournal of Obstetrics and Gynaecology
researchProduct

‘Pyogenic granuloma-like Kaposi's sarcoma’ on the hands: immunohistochemistry and human herpesvirus-8 detection

2009

Letter to Editor

Pathologymedicine.medical_specialtybusiness.industryPyogenic granulomapyogenic granulomaDermatologySettore MED/08 - Anatomia Patologicamedicine.diseaseKaposi’s sarcomaInfectious DiseasesMedicineImmunohistochemistrybusinessKaposi's sarcomaHHV-8Human herpesvirusJournal of the European Academy of Dermatology and Venereology
researchProduct

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…

Pathologymedicine.medical_specialtymedicine.diagnostic_testChemistrySoft tissue sarcomaSoft tissueCancerVeterinary oncologymedicine.diseaseMast cell tumorssymbols.namesakeOptical coherence tomographymedicinesymbolsRaman spectroscopyEx vivoOptical Biopsy XIX: Toward Real-Time Spectroscopic Imaging and Diagnosis
researchProduct

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…

Pathologymedicine.medical_specialtymedicine.diagnostic_testPAX3Small Cell SarcomaHistologyHistogenesisBiologymedicine.diseasePrimary NeoplasmPathology and Forensic MedicineBiopsymedicineNeoplasmSurgeryAnatomyRhabdomyosarcomaInternational Journal of Surgical Pathology
researchProduct

Detection of proteolytic (C 3-cleaving) activity on mouse mastocytoma (P815) cells and other mouse cell lines by formation of cell contact with C 3-c…

1979

Mouse mastocytoma cells (P 815) formed rosettes with normal mouse spleen lymphocytes which had been coated with uncleaved human C 3; this interaction was clearly dependent on the amount of C 3. Lymphocytes treated with C 3 b or buffer alone were ineffective. Formation of cell contact could be inhibited by the presence of protease inhibitors such as diisopropyl fluorophosphate, phenyl methyl sulfonyl fluoride and tosyllysyl chloromethyl ketone. Seve n out of 13 different cell lines behaved like P 815 cells. The results strongly suggested that a proteolytic activity on mouse tumor cells led to a cooperation with uncleaved C 3 on a carrier cell to connect these two cells. We interpreted these …

ProteasesRosette FormationImmunologyCellMast-Cell SarcomaCell CountBiologyCleavage (embryo)Cell LineCell membraneMicemedicineAnimalsImmunology and AllergyProtease InhibitorsLymphocytesCell MembraneMastocytomaComplement C3medicine.diseaseMolecular biologymedicine.anatomical_structureCell cultureMast cell sarcomaDiisopropyl fluorophosphateSpleenmedicine.drugEuropean Journal of Immunology
researchProduct

Pulmonary metastasectomy in soft tissue sarcomas: a systematic review

2021

Background Soft tissue sarcoma (STS) tend to metastasis to the lungs. Pulmonary metastasectomy seems to be a common practice always when plausible. The objective of this article was to review systematically the results of a literature search on pulmonary metastasectomy for STSs published in the last ten years and to offer a brief overview about the current practice as well. Methods Eight retrospective studies published in the period 2010-2020, which included patients with pulmonary metastases and metastasectomy were selected. Indication for surgery, survival rate and factors influencing survival were the primary outcomes, while further interesting findings in the studies were also collected…

Pulmonary and Respiratory MedicineLeiomyosarcomamedicine.medical_specialtybusiness.industrySoft tissue sarcomaOriginal Article on Pulmonary MetastasesSoft tissueRetrospective cohort studymedicine.diseaseSynovial sarcomaMetastasisMedicineRadiologyMetastasectomybusinessSurvival rateJournal of Thoracic Disease
researchProduct