Results 171 to 180 of about 40,129 (195)
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2006
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of children. Whereas adult sarcomas are mostly extremity tumors and rarely spread to regional nodes, RMS is ubiquitous, occurring almost everywhere in the body (most commonly in the head, neck, and genitourinary area), and frequently spreads to regional nodes (40% in extremity RMS). Survival
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Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of children. Whereas adult sarcomas are mostly extremity tumors and rarely spread to regional nodes, RMS is ubiquitous, occurring almost everywhere in the body (most commonly in the head, neck, and genitourinary area), and frequently spreads to regional nodes (40% in extremity RMS). Survival
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The American Journal of Surgery, 1969
The care of patients with rhabdomyosarcoma has undergone significant change in the past decade. Careful staging and multidisciplinary treatment have improved the prognosis for patients with this neoplasm. A review of the medical literature of the past decade documents these changes in staging, therapy and prognosis.
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The care of patients with rhabdomyosarcoma has undergone significant change in the past decade. Careful staging and multidisciplinary treatment have improved the prognosis for patients with this neoplasm. A review of the medical literature of the past decade documents these changes in staging, therapy and prognosis.
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Pediatric Hematology and Oncology, 2007
A 15-year-old boy was admitted with acute progressive dysphagia. On physical examination, the uvula was swollen and red, which did not respond to corticosteroid treatment.
Corapcioglu, Funda +2 more
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A 15-year-old boy was admitted with acute progressive dysphagia. On physical examination, the uvula was swollen and red, which did not respond to corticosteroid treatment.
Corapcioglu, Funda +2 more
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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.
Edwin R. Fisher +2 more
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Clinical Orthopaedics and Related Research, 1993
In children and young adults, rhabdomyosarcoma occurs with a frequency that is equal to or greater than that of all the other forms of soft-tissue sarcoma combined. Although the responsiveness of rhabdomyosarcoma to chemotherapy varies greatly among tumors with different primary sites and with different histologic features, the overall results of ...
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In children and young adults, rhabdomyosarcoma occurs with a frequency that is equal to or greater than that of all the other forms of soft-tissue sarcoma combined. Although the responsiveness of rhabdomyosarcoma to chemotherapy varies greatly among tumors with different primary sites and with different histologic features, the overall results of ...
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Cancer, 1972
A case of rhabdomyosarcoma of the heart diagnosed through biopsy material and confirmed by autopsy is reported because of the few recorded instances and the unusually diffuse nature of the neoplasm. The heart with tumor weighed 1450 g. There was a single metastasis to a mediastinal lymph node.
Arthur Lurie +2 more
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A case of rhabdomyosarcoma of the heart diagnosed through biopsy material and confirmed by autopsy is reported because of the few recorded instances and the unusually diffuse nature of the neoplasm. The heart with tumor weighed 1450 g. There was a single metastasis to a mediastinal lymph node.
Arthur Lurie +2 more
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Rhabdomyosarcoma of the tongue
British Journal of Oral and Maxillofacial Surgery, 1994Although rhabdomyosarcoma (RMS) has a predilection for the head and neck region its occurrence in the tongue is uncommon. We report 2 cases of RMS of the tongue, 1 paediatric and 1 adult patient. The child who had RMS of the alveolar type involving anterior two-thirds of the tongue was treated with surgery and chemotherapy and is disease-free at 84 ...
G Mukherjee +5 more
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Archives of Ophthalmology, 1969
That embryonal rhabdomyosarcoma is the most frequently encountered primary malignant neoplasm of the orbit in childhood is now a well-recognized fact. 1-5 Typically the unfortunate patient is an otherwise healthy child who has had no previous history of cancer.
Lorenz E. Zimmerman, Robert C. Kirk
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That embryonal rhabdomyosarcoma is the most frequently encountered primary malignant neoplasm of the orbit in childhood is now a well-recognized fact. 1-5 Typically the unfortunate patient is an otherwise healthy child who has had no previous history of cancer.
Lorenz E. Zimmerman, Robert C. Kirk
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Rhabdomyosarcoma of the Nasopharynx
Radiology, 1955Rhabdomyosarcoma of the nasal cavity often begins as a polypoid growth and may easily be mistaken for nasal polyps. For this reason, it is important that polypoid growths in the nasal cavity occurring in childhood be biopsied. Weber (17) described the first case of rhabdomyosarcoma in 1854, in the tongue of a twenty-one-year-old man. It was excised but
Elmer G. St. John, Zung-Pah Woo
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