Results 291 to 300 of about 99,358 (330)
Pulmonary Artery Rhabdomyosarcoma: Diagnostic Challenges and Evolving Management. [PDF]
JACC Case RepMorrison AM, Fong PP, Aday AW, Matta M.
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Alveolar Rhabdomyosarcoma With Bone Marrow Metastases and Disseminated Intravascular Coagulation Mimicking Acute Lymphoblastic Leukemia: A Case Report. [PDF]
CureusChu S, Zhang H, Niu Q, Zhang L, Li L.
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The Indian Journal of Pediatrics, 1977
Six cases of rhabdomyosarcoma have been reported. Three of them were in the bladder, one in the tongue, one in the gluteal region and one in the leg muscles. The leg tumour was successfully treated by combined triple regimen of surgery, deep-X-ray therapy and D-Actinomycin.
T. Viswanatha Rao, C. V. Satyanaryana
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Six cases of rhabdomyosarcoma have been reported. Three of them were in the bladder, one in the tongue, one in the gluteal region and one in the leg muscles. The leg tumour was successfully treated by combined triple regimen of surgery, deep-X-ray therapy and D-Actinomycin.
T. Viswanatha Rao, C. V. Satyanaryana
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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.
Jayant Radhakrishnan, Andrea L. Stuart
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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.
Jayant Radhakrishnan, Andrea L. Stuart
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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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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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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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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.
ANIK, YONCA +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.
ANIK, YONCA +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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