Results 1 to 10 of about 20,071 (176)

Intraoral angiosarcoma with unusual clinical presentation: A case report

open access: yesHeliyon, 2023
Introduction: Angiosarcoma is a rare and highly aggressive soft tissue malignancy originating from vascular and lymphatic endothelial cells. Epithelioid angiosarcoma is the rarest subtype of angiosarcoma, characterized by the proliferation of large ...
Mohammed Matooq AlAli   +3 more
doaj   +2 more sources

Cutaneous angiosarcoma–A report of 20 Taiwanese patients

open access: yesDermatologica Sinica, 2018
Angiosarcoma is a rare soft tissue sarcoma of poor prognosis. A retrospective single-center study was conducted to characterize cutaneous angiosarcoma. Twenty patients were enrolled. The mean age was 76 years and male to female ratio 3:1.
Yi-Hsin Chan   +4 more
doaj   +2 more sources

Epithelioid angiosarcoma in pleural fluid: Cytological features and literature review

open access: yesHuman Pathology: Case Reports, 2018
Epithelioid angiosarcoma is a rare vascular neoplasm with an aggressive clinical course and poor prognosis. The cytological diagnosis of epithelioid angiosarcoma is challenging.
Jane H. Zhou   +2 more
doaj   +2 more sources

Patient-partnered multiomics reveals the molecular architecture of angiosarcoma [PDF]

open access: yesNature Communications
Angiosarcoma is a poorly understood sarcoma due to its high heterogeneity and rarity. Here we show a comprehensive clinical and molecular analysis of a large cohort of 254 angiosarcoma patients through the patient-partnered Angiosarcoma Project.
Hoyin Chu   +32 more
doaj   +2 more sources

Post-Radiation Angiosarcoma (PRA) of the Small Bowel: Report of a Case and Review of the Literature

open access: yesSurgeries, 2023
Angiosarcoma is a rare and aggressive neoplasia of endothelial cells which represents only 2% of all soft-tissue tumors and frequently occurs in the skin and subcutaneous tissues.
Marco La Gatta   +6 more
doaj   +1 more source

Nectin cell adhesion molecule 4 regulates angiogenesis through Src signaling and serves as a novel therapeutic target in angiosarcoma

open access: yesScientific Reports, 2022
Angiosarcoma is a rare, life-threatening soft tissue sarcoma with malignant endothelial cells that is mainly found in the skin. Multidisciplinary approaches are used to treat patients with unresectable metastasized lesions; considering the cellular ...
Yuka Tanaka   +4 more
doaj   +1 more source

Clinicopathological analysis and prognostic treatment study of angiosarcoma of the breast: a SEER population-based analysis

open access: yesWorld Journal of Surgical Oncology, 2023
Introduction Breast angiosarcoma is a rare malignancy of endovascular origin, accounting for less than 1% of all mammary cancers. Our aim was to explore clinicopathological features and the factors associated with prognosis.
Lizhi Teng   +5 more
doaj   +1 more source

Enrichment of Immune-Related Genes in Aggressive Primary Breast Angiosarcoma: A Case Report

open access: yesCase Reports in Oncology, 2023
Primary breast angiosarcoma is an extremely rare disease with a poor prognosis. Primary angiosarcoma is distinct from secondary angiosarcoma, which usually occurs in patients who have been previously treated for breast cancer.
Ryoichi Matsunuma   +9 more
doaj   +1 more source

Angiosarcoma in HIV-negative patients is not associated with HHV-8 [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2016
: BACKGROUND: Angiosarcoma is an aggressive, malignant neoplasm of vascular or lymphatic origin. Herpes virus 8 (HHV-8) is a member of the herpes family with a tropism for endothelial cells and it has been proven to induce vascular neoplasms, such as ...
João Avancini   +8 more
doaj   +2 more sources

Primary multicentric angiosarcoma of bone: true entity or metastases from an unknown primary? Value of comparative genomic hybridization on paraffin embedded tissues

open access: yesRare Tumors, 2013
Multicentric primary angiosarcoma of bone has been described as a distinct entity from bone metastases from angiosarcoma. Bone angiosarcoma accounts for less than 1% of sarcomas.
Juliette Thariat   +8 more
doaj   +1 more source

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