Results 301 to 310 of about 556,852 (338)
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Pediatric Clinics of North America, 2015
Malignant bone tumors (osteosarcoma, Ewing sarcoma) and soft-tissue sarcomas (rhabdomyosarcoma, nonrhabdomyosarcoma) account for approximately 14% of childhood malignancies. Successful treatment of patients with sarcoma depends on a multidisciplinary approach to therapy, including oncology, surgery, radiation oncology, radiology, pathology, and ...
Josephine H, HaDuong +3 more
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Malignant bone tumors (osteosarcoma, Ewing sarcoma) and soft-tissue sarcomas (rhabdomyosarcoma, nonrhabdomyosarcoma) account for approximately 14% of childhood malignancies. Successful treatment of patients with sarcoma depends on a multidisciplinary approach to therapy, including oncology, surgery, radiation oncology, radiology, pathology, and ...
Josephine H, HaDuong +3 more
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Mayo Clinic Proceedings, 2007
Sarcomas comprise a heterogeneous group of mesenchymal neoplasms. They can be grouped into 2 general categories, soft tissue sarcoma and primary bone sarcoma, which have different staging and treatment approaches. This review includes a discussion of both soft tissue sarcomas (malignant fibrous histiocytoma, liposarcoma, leiomyosarcoma, synovial ...
Keith M, Skubitz, David R, D'Adamo
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Sarcomas comprise a heterogeneous group of mesenchymal neoplasms. They can be grouped into 2 general categories, soft tissue sarcoma and primary bone sarcoma, which have different staging and treatment approaches. This review includes a discussion of both soft tissue sarcomas (malignant fibrous histiocytoma, liposarcoma, leiomyosarcoma, synovial ...
Keith M, Skubitz, David R, D'Adamo
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2011
Sarcomas are a diverse group of malignancies originating in the connective tissue. The approach of a patient with a mass suspect for sarcoma starts with performing a biopsy to obtain tissue for evaluation by pathology. The main role of the current imaging modalities, in general, is to recognize patients with typically benign disease, in whom further ...
Ceyssens, Sarah, Stroobants, Sigrid
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Sarcomas are a diverse group of malignancies originating in the connective tissue. The approach of a patient with a mass suspect for sarcoma starts with performing a biopsy to obtain tissue for evaluation by pathology. The main role of the current imaging modalities, in general, is to recognize patients with typically benign disease, in whom further ...
Ceyssens, Sarah, Stroobants, Sigrid
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Journal of the American Academy of Orthopaedic Surgeons, 2013
Sarcomas are a rare, heterogeneous group of malignant tumors of the bone or soft tissue. Although historically intended for the pharmaceutical treatment of microbes, today chemotherapy is used in orthopaedic oncology and is arguably the primary reason for improved survivorship.
Brian E, Walczak, Ronald B, Irwin
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Sarcomas are a rare, heterogeneous group of malignant tumors of the bone or soft tissue. Although historically intended for the pharmaceutical treatment of microbes, today chemotherapy is used in orthopaedic oncology and is arguably the primary reason for improved survivorship.
Brian E, Walczak, Ronald B, Irwin
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Cancer, 1966
Sixty three patients with Kaposi's sarcoma (1935–1963) have been reviewed. Of this group 18 patients died of a secondary primary. The second primaries included 5 cases of Hodgkin's disease, 3 of lymphosarcoma, 3 of carcinoma of the colon and one each of multiple myeloma, malignant melanoma, carcinoma of the prostate, carcinoma of the tongue, carcinoma ...
P H, O'Brien, R D, Brasfield
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Sixty three patients with Kaposi's sarcoma (1935–1963) have been reviewed. Of this group 18 patients died of a secondary primary. The second primaries included 5 cases of Hodgkin's disease, 3 of lymphosarcoma, 3 of carcinoma of the colon and one each of multiple myeloma, malignant melanoma, carcinoma of the prostate, carcinoma of the tongue, carcinoma ...
P H, O'Brien, R D, Brasfield
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Blood, 2009
We present two cases where GS was sole presentations, months before the diagnosis of AML.
J B, Ghosh, Mahua, Roy, Anirban, Halder
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We present two cases where GS was sole presentations, months before the diagnosis of AML.
J B, Ghosh, Mahua, Roy, Anirban, Halder
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New England Journal of Medicine, 2000
In 1872, Moritz Kaposi, a Hungarian dermatologist, described five men with aggressive “idiopathic multiple pigmented sarcomas of the skin.”1 One patient died of gastrointestinal bleeding 15 months after the initial appearance of the skin lesions, and an autopsy showed visceral lesions in the lungs and the gastrointestinal tract.
K, Antman, Y, Chang
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In 1872, Moritz Kaposi, a Hungarian dermatologist, described five men with aggressive “idiopathic multiple pigmented sarcomas of the skin.”1 One patient died of gastrointestinal bleeding 15 months after the initial appearance of the skin lesions, and an autopsy showed visceral lesions in the lungs and the gastrointestinal tract.
K, Antman, Y, Chang
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Hematology/Oncology Clinics of North America, 2019
Cutaneous sarcomas are rare malignancies that may present with a variety of clinical manifestations. This article focuses on 4 of the most common cutaneous sarcomas (Kaposi sarcoma, cutaneous angiosarcoma, dermatofibrosarcoma protuberans, and cutaneous leiomyosarcoma) and reviews clinical, diagnostic, and therapeutic aspects of these rare skin ...
Mehul D, Bhatt, Vinod E, Nambudiri
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Cutaneous sarcomas are rare malignancies that may present with a variety of clinical manifestations. This article focuses on 4 of the most common cutaneous sarcomas (Kaposi sarcoma, cutaneous angiosarcoma, dermatofibrosarcoma protuberans, and cutaneous leiomyosarcoma) and reviews clinical, diagnostic, and therapeutic aspects of these rare skin ...
Mehul D, Bhatt, Vinod E, Nambudiri
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