Results 211 to 220 of about 39,428 (277)
Editorial: Advances in spinal cord injury prevention during endovascular and open aortic repairs. [PDF]
Front SurgRahouma M, Baudo M, El-Sayed Ahmed M.
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Hepatic Angiosarcoma Associated with Chronic Schistosomiasis in a Patient with Decompensated Cirrhosis: A Rare Case Report. [PDF]
Case Rep GastroenterolSwaid T +3 more
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Primary pulmonary angiosarcoma: A case study with genetic insights and potential therapeutic targets. [PDF]
Oncol LettZhu Y, Guo C.
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Angiosarcoma of the Breast: Overview of Current Data and Multimodal Imaging Findings
Journal of Imaging, 2023 Angiosarcoma of the breast is a rare breast cancer, which can arise de novo (primary breast angiosarcoma, PBA) or as a secondary malignancy (secondary breast angiosarcoma, SBA) as a result of a biological insult.
Marco Conti +2 more
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Clinical activity of checkpoint inhibitors in angiosarcoma: A retrospective cohort study
Cancer, 2022Systemic treatments for angiosarcoma remains an area of unmet clinical need. The authors conducted this retrospective study to assess the clinical activity of checkpoint inhibitors in patients with angiosarcoma.
V. Ravi +21 more
semanticscholar +1 more source
The Lancet Oncology, 2010
Angiosarcomas are rare soft-tissue sarcomas of endothelial cell origin that have a poor prognosis. They can arise anywhere in the body, most commonly presenting as cutaneous disease in elderly white men, involving the head and neck and particularly the scalp.
Robin J, Young +4 more
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Angiosarcomas are rare soft-tissue sarcomas of endothelial cell origin that have a poor prognosis. They can arise anywhere in the body, most commonly presenting as cutaneous disease in elderly white men, involving the head and neck and particularly the scalp.
Robin J, Young +4 more
openaire +2 more sources
Cancer, 1980
A case of angiosarcoma of the breast with a fatal outcome is reported, and the world literature on this rare type of breast tumor is reviewed. Familiarity with the clinical and pathologic features of this entity is essential in avoiding underdiagnosis and delay of definitive treatment. The three-year survival rate of reported cases was 38%.
K T, Chen, D D, Kirkegaard, J J, Bocian
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A case of angiosarcoma of the breast with a fatal outcome is reported, and the world literature on this rare type of breast tumor is reviewed. Familiarity with the clinical and pathologic features of this entity is essential in avoiding underdiagnosis and delay of definitive treatment. The three-year survival rate of reported cases was 38%.
K T, Chen, D D, Kirkegaard, J J, Bocian
openaire +2 more sources
International Journal of Dermatology, 1999
An 82-year-old woman was seen at our Dermatology Department for a plaque on the right parietal scalp that had recently increased in size, and bled. The lesion had been present for 3 months. The patient had a previous diagnosis of chronic bronchitis, noninsulin-dependent diabetes mellitus, and hypertension, but no previous history of cancer.
María Del Mar +3 more
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An 82-year-old woman was seen at our Dermatology Department for a plaque on the right parietal scalp that had recently increased in size, and bled. The lesion had been present for 3 months. The patient had a previous diagnosis of chronic bronchitis, noninsulin-dependent diabetes mellitus, and hypertension, but no previous history of cancer.
María Del Mar +3 more
openaire +2 more sources
Urology, 1998
Sarcoma of the penis is rare. We report an angiosarcoma that was essentially an incidental finding, despite the presence of metastatic lesions, in a 46-year-old man who presented with hematemesis and melena. The diagnosis of the primary lesion was confirmed by histology, and the presence of secondary lesions by fine needle aspiration cytology.
R J, Webber +3 more
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Sarcoma of the penis is rare. We report an angiosarcoma that was essentially an incidental finding, despite the presence of metastatic lesions, in a 46-year-old man who presented with hematemesis and melena. The diagnosis of the primary lesion was confirmed by histology, and the presence of secondary lesions by fine needle aspiration cytology.
R J, Webber +3 more
openaire +2 more sources