Stewart-Treves syndrome
Year: 2012
Type: article
Abstract: Stewart-Treves syndrome is a rare cutaneous angiosarcoma with a poor prognosis. Physicians must be aware of this lethal syndrome, especially in patients who have been treated for breast cancer with radiation and lymph-node dissection (such as the case reported here). Patients who develop unexplained enlarging plaques of coalescing purple papules should have immediate biopsy for early diagnosis of Stewart-Treves syndrome. MRI, along with PET/CT, can help evaluate the extent of disease and help with treatment strategies.
Source: Radiology Case Reports
DOI: 10.2484/rcr.v7i4.693
Authors: Roy Gottlieb, Rukhsana Serang, David Chi, Harry Menco
Institution: Western University of Health Sciences
Language: English
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $600
OpenAlex ID: W2264913478
