نتایج جستجو برای: chondroblastic osteosarcoma

تعداد نتایج: 11710  

Journal: :Journal of pediatric hematology/oncology 2003
Ana Patiño-García Elena Sotillo Piñeiro Marta Zalacaín Díez Leire Gárate Iturriagagoitia Federico Antillón Klüssmann Luis Sierrasesúmaga Ariznabarreta

PURPOSE To analyze the genetic and epigenetic alterations affecting the RB1, TP53, p16INK4, and p21WAF1 tumor suppressor genes, loss of heterozygosity (LOH) at 3q and 18q, and the clinical variables of a series of Spanish children with osteosarcoma. These genetic changes were tested for an association with prognosis. METHODS Peripheral blood samples and clinical data were available from 76 pa...

Journal: :Anticancer research 2005
M Jäger A Schultheis B Westhoff R Krauspe

BACKGROUND Since the first trial of chemotherapy in patients with osteosarcoma the survival rate has gradually improved. For more than two decades, most osteosarcoma patients from Germany, Austria and Switzerland have been treated according to the protocols of the Cooperative Osteosarcoma Study Group (COSS). The uniform treatment concept of a high-dose polychemotherapy pre- and postoperatively ...

2016
Gaia Palmini Roberto Zonefrati Cecilia Romagnoli Alessandra Aldinucci Carmelo Mavilia Gigliola Leoncini Alessandro Franchi Rodolfo Capanna Maria Luisa Brandi

Osteosarcoma (OSA) is the most common primary malignant bone tumor, usually arising in the long bones of children and young adults. There are different subtypes of OSA, among which we find the conventional OS (also called medullary or central osteosarcoma) which has a high grade of malignancy and an incidence of 80%. There are different subtypes of high grade OS like chondroblastic, fibroblasti...

Journal: :Respiratory medicine 1998
M J Doherty A P Campbell M E Cowan M A Greenstone

The first descriptions of disease currently recognized as sarcoidosis were documented at the end of the 19th century and concerned skin eruptions (1). Since that time, it has been realized that it is a systemic disease characterized histologically by non-caseating granulomata. An aetiological agent eludes characterization. A number of recognizable patterns of disease at presentation are documen...

Journal: :Journal of neurosurgery 1995
P A Forsyth P J Kelly T L Cascino B W Scheithauer E G Shaw R P Dinapoli E J Atkinson

Fifty-one patients with supratentorial glioma treated with external beam radiotherapy (median dose 59.5 Gy) who then demonstrated clinical or radiographic evidence of disease progression underwent stereotactic biopsy to differentiate tumor recurrence from radiation necrosis. The original tumor histological type was diffuse or fibrillary astrocytoma in 21 patients (41%), oligodendroglioma in 13 ...

Journal: :Journal of clinical pathology 2003
K Okada T Hasegawa R Yokoyama Y Beppu E Itoi

AIMS To clarify the clinicopathological profile of osteosarcomas showing an intensely positive immunoreaction for cytokeratin. METHODS Clinicopathological and immunohistochemical features were analysed in 131 patients with non-metastatic, conventional osteosarcoma, treated in Akita University and National Cancer Centre in Tokyo between 1972 and 1999. RESULTS Six patients (4.5%; mean age, 32...

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