Results 201 to 210 of about 50,529 (255)
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The Indian Journal of Pediatrics, 2004
Rhabdomyosarcoma, the most common soft tissue sarcoma of children, carried a 10-15% survival rate in the late 1960s. Since then, better understanding of biology and pathology of the tumor and the judicious use of chemotherapy and radiation has improved the prognosis drastically.
Andrea, Stuart, Jayant, Radhakrishnan
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Rhabdomyosarcoma, the most common soft tissue sarcoma of children, carried a 10-15% survival rate in the late 1960s. Since then, better understanding of biology and pathology of the tumor and the judicious use of chemotherapy and radiation has improved the prognosis drastically.
Andrea, Stuart, Jayant, Radhakrishnan
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Seminars in Pediatric Surgery, 2016
A malignant tumor of striated muscle origin, rhabdomyosarcoma (RMS) is a childhood tumor that has benefited from nearly 30 years of multimodality therapy, culminating in a >70% overall 5-year survival. Prognosis for RMS is dependent on primary tumor site, age, completeness of resection, presence and number of metastatic sites, histology, and biology of
Roshni, Dasgupta +2 more
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A malignant tumor of striated muscle origin, rhabdomyosarcoma (RMS) is a childhood tumor that has benefited from nearly 30 years of multimodality therapy, culminating in a >70% overall 5-year survival. Prognosis for RMS is dependent on primary tumor site, age, completeness of resection, presence and number of metastatic sites, histology, and biology of
Roshni, Dasgupta +2 more
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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.
Aydin, Omer +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.
Aydin, Omer +2 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.
R C, Kirk, L E, Zimmerman
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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.
R C, Kirk, L E, Zimmerman
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Seminars in Pediatric Surgery, 2016
Pediatric non-rhabdomyosarcoma soft tissue sarcomas (NRSTS) are a heterogeneous group encompassing more than 50 different histological diagnoses arising from primitive mesenchymal tissue. Together, they comprise about half the soft tissue sarcomas diagnosed in children and young adults.
Roshni, Dasgupta, David, Rodeberg
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Pediatric non-rhabdomyosarcoma soft tissue sarcomas (NRSTS) are a heterogeneous group encompassing more than 50 different histological diagnoses arising from primitive mesenchymal tissue. Together, they comprise about half the soft tissue sarcomas diagnosed in children and young adults.
Roshni, Dasgupta, David, Rodeberg
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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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Rhabdomyosarcoma of the breast
Clinical Imaging, 2005The aim of this study was to describe the first imaging studies of a primary embryonal rhabdomyosarcoma of the breast in an adult woman.This 45-year-old woman was seen for investigation of a palpable mass in the left breast. Examinations included mammography, Doppler ultrasound, and MRI. The diagnosis was made after surgical biopsy. Treatment consisted
Fabien, Dausse +3 more
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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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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
E G, ST. JOHN, Z P, WOO
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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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