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Angiosarcoma associated with Kasabach-Merritt syndrome presenting with typical signs and symptoms of pulmonary tuberculosis: a case report.
J Med Case Rep
December 2024
Shifa International Hospital/Shifa Tameer e Millat University, Islamabad, Pakistan.
Background: Angiosarcoma is a rapidly proliferating vascular tumor that originates in endothelial cells of vessels. Rarely, it can be associated with consumptive coagulopathy due to disseminated intravascular coagulation eventually leading to thrombocytopenia and microangiopathic hemolytic anemia. This specific manifestation is termed Kasabach-Merritt syndrome.
View Article and Find Full Text PDFChest Pain and ST-Segment Elevation: Angiosarcoma Discovered With Coronary Angiography.
JACC Case Rep
December 2024
Rush University Medical Center, Chicago, Illinois, USA.
Primary cardiac angiosarcomas are rare malignant tumors that can cause chest pain and heart failure symptoms. They can be diagnosed using multimodality imaging, primarily echocardiogram, with formal diagnosis requiring biopsy. A 56-year-old man with history of hypertension and dyslipidemia presented with acute crushing chest pain and shortness of breath.
View Article and Find Full Text PDFCount Me In: patient-partnered research to address disparities for rare cancer patients.
Ther Adv Rare Dis
December 2024
Count Me In, Cambridge, MA, USA.
Background: Approximately 25% of cancer patients are diagnosed with rare cancers and face unique challenges. Decentralized patient-partnered research efforts, like Count Me In provide an avenue for patients to participate in research that overcomes key barriers to address disparities in rare cancer research to accelerate discovery.
Objectives: Projects in metastatic breast cancer (The Metastatic Breast Cancer Project; MBCproject) and angiosarcoma (The Angiosarcoma Project; ASCproject) highlight disparities that exist for all cancer patients and underscore those that are compounded for rare cancer patients.
Epithelioid angiosarcoma at a non-functioning arteriovenous fistula site in a renal transplant patient.
Skeletal Radiol
December 2024
Manchester University NHS Foundation Trust, Manchester, UK.
We present a case of biopsy-proven epithelioid angiosarcoma in an arteriovenous fistula (AVF). Angiosarcomas developing in non-functioning AVF in renal transplant recipients are rare clinical entities with poor prognosis. A 59-year-old male adequately immunosuppressed kidney transplant patient presented with pain and swelling at the site of a previously asymptomatic fistula.
View Article and Find Full Text PDFHemorrhagic muscular metastasis of primary splenic hemangiosarcoma in a dog.
Can Vet J
December 2024
Department of Clinical Sciences (Padilla, Enders, Traverson) and Department of Molecular Biomedical Sciences (Nelson) and Department of Population Health and Pathobiology (Watanabe, Womble), College of Veterinary Medicine, North Carolina State University, 1060 William Moore Drive, Raleigh, North Carolina 27606, USA.
This report describes the presentation and management of an incidental primary splenic hemangiosarcoma with hemorrhagic muscle metastasis following an incisional biopsy of a temporalis mass in a dog. In the absence of clinical signs related to the primary splenic lesion, skeletal muscle metastasis of hemangiosarcoma could be misdiagnosed as isolated primary tumor, resulting in failure to provide an accurate prognosis and effective treatment of the primary tumor itself. A thorough diagnostic imaging workup in patients presenting with blood-filled subcutaneous or muscular masses is fundamental to rule out a primary visceral hemangiosarcoma.
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