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Small-cell osteosarcoma

Devaney K, Vinh TN, Sweet DE. Small cell osteosarcoma of bone An immunohistochemical study with differential diagnostic considerations. Hum Pathol. 1993 24 1211-1225. [Pg.127]

Neuroblastomas are small, round, blue cell tumors that may arise in the adrenal gland and a variety of extra-adrenal sites. The differential diagnosis is wide and includes rhabdomyosarcoma, Ewing s sarcoma-primitive neuroectodermal tumor (ES-PNET), medulloblastoma, small cell osteosarcoma, lymphoblastic lymphoma, blastematous Wilms tumor, and small cell desmoplastic tumor. Numerous markers have been used for the diagnosis of neuroblastomas including NE markers, cytoskeletal proteins, catecholamine-synthesizing enzymes, and neuroblastoma-"specific antibodies (Eig. [Pg.318]

In addition to the small-cell tumors presented in the foregoing sections, others of a metastatic nature also may involve the mediastinum. These include small-cell osteosarcoma and Ewing s sarcoma/primitive neuroectodermal tumor (PNET) of bone, as well as small-cell malignant melanoma. Except for the last of these possibilities, the primary lesion in such cases is typically obvious and there is no question of whether the intra-thoracic neoplasm might have arisen there. Nonetheless, melanomas are certainly capable of producing distant metastasis in the absence of an obvious primary source. [Pg.350]

RB1 Codes for the pRB protein, a master brake of Retinoblastoma, osteosarcoma, and bladder, small cell... [Pg.1279]

Unlabeled Uses Adrenocortical, bladder, cervical, endometrial, prostatic, testicular carcinomas Ewing s sarcoma multiple sclerosis non-small cell, small cell lung cancer organ transplant rejection osteosarcoma ovarian germ cell, primary brain, trophoblastic tumors rheumatoid arthritis soft tissue sarcomas systemic dermato-myositis systemic lupus erythematosus Wilms tumor... [Pg.314]

Study of other rare hereditary cancers has led to the location of 20 or more additional probable tumor-suppressor genes. One of these, p53, is inactive in over 50% of all human cancers and over 90% of sqamous cell carcinomas of the skin.ee In small-cell lung cancers and osteosarcoma both RB and p53 are inactive.2 Protein p53 is a stronger tumor suppressor than protein Rb. Results of a variety of experiments have suggested that p53, a DNA-binding protein of known structure, plays a key role in checking DNA for damage at the C,... [Pg.574]

Malignant cartilage tumor Non-small-cell lung carcinoma Osteosarcoma Ovarian surface epithelial neoplasms Prostate cancer... [Pg.298]

Osteosarcoma Pancreatic cancer Small cell lung cancer ... [Pg.2290]

Osteosarcoma is highly unusual outside the skeletal system. Like their intraosseous counterparts, extraskeletal osteosarcomas have a variety of histologic patterns, including fibroblastic, chondroblastic, small-cell, and telangiectatic images. [Pg.122]

Clear cell sarcoma, adenoid cystic carcinoma, small cell lung carcinoma, Ewing sarcoma, synovial sarcoma, osteosarcoma, angiosarcoma, AML,... [Pg.63]


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See also in sourсe #XX -- [ Pg.103 ]




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