Results 211 to 220 of about 50,529 (255)
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Seminars in Pediatric Surgery, 2012
Rhabdomyosarcoma (RMS) is a malignant childhood tumor of mesenchymal origin that currently has a greater than 70% overall 5-year survival. Multimodality treatment is determined by risk stratification according to pretreatment stage, postoperative group, histology, and site of the primary tumor.
Roshni, Dasgupta, David A, Rodeberg
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Rhabdomyosarcoma (RMS) is a malignant childhood tumor of mesenchymal origin that currently has a greater than 70% overall 5-year survival. Multimodality treatment is determined by risk stratification according to pretreatment stage, postoperative group, histology, and site of the primary tumor.
Roshni, Dasgupta, David A, Rodeberg
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The Ultrastructure of Rhabdomyosarcoma
American Journal of Clinical Pathology, 1970The ultrastructural features of one embryonal and two pleomorphic rhabdomyosarcomas in adults are described. The presence of thick myofilaments in formations suggesting sarcomeres and a rare arrangement of mitochondria in tandem allow for identification of the spindle cells in embryonal rhabdomyosarcoma as skeletal muscle cells.
B L, Horvat, M, Caines, E R, Fisher
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Topics in Companion Animal Medicine
A geriatric Holland Lop rabbit presented for acute lameness. A pathologic fracture of the right distal femur associated with a pleomorphic rhabdomyosarcoma was diagnosed, and staging radiographs showed no overt metastasis upon initial presentation. The limb was amputated and submitted for microscopic examination. Immunohistochemical evaluation revealed
Logan Kopp, Michael Garner, Kara Priest
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A geriatric Holland Lop rabbit presented for acute lameness. A pathologic fracture of the right distal femur associated with a pleomorphic rhabdomyosarcoma was diagnosed, and staging radiographs showed no overt metastasis upon initial presentation. The limb was amputated and submitted for microscopic examination. Immunohistochemical evaluation revealed
Logan Kopp, Michael Garner, Kara Priest
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Rhabdomyosarcoma of the larynx
The Journal of Laryngology & Otology, 1975A case of rhabdomyosarcoma of the larynx in a 54-year-old man is reported. Patient presented dramatically with a large tumour mass obstructing his laryngeal inlet. The patient remains alive and well sixteen months after a total laryngectomy. Only seven previous reports of a rhabdomyosarcoma of the larynx could be found in the literature and these are ...
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Classification of Rhabdomyosarcoma
1995Lesions now classified as rhabdomyosarcoma (RMS) in children are as a rule comprised of very primitive cells which do not show obvious features of fully developed muscle. It is not surprising that the early attempts to classify this group of tumors focused upon tumors that showed some recognizable features of skeletal muscle such as cross-striations ...
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