Recognising angiosarcoma presenting as an enlarging ecchymotic plaque
Cutaneous angiosarcoma (cAS) is a rare malignant neoplasm of vascular endothelial origin with an unfavourable prognosis. Its diagnosis often faces delays due to its manifestation as an inconspicuous 'bruise-like' lesion in an otherwise asymptomatic individual, leading to a generally low index of suspicion for angiosarcoma. Here, we present a case of a man who presented to his general practitioner with an ecchymotic plaque on his forehead, initially thought to be benign. Over the subsequent 6 weeks, the lesion progressively enlarged and became ulcerated, prompting the patient to represent to his general practitioner. He was urgently referred to a dermatologist and a subsequent biopsy confirmed the diagnosis of cAS. Our presentation of this case serves as a reminder for physicians to maintain a high index of suspicion and low threshold for biopsy for patients with atraumatic ecchymotic lesions.
Authors
- Michelle Wu (ORCID: https://orcid.org/0000-0003-2013-1860)
- Theone Papps
- Bruno Blaya-Alvarez
Institutions
- Royal Prince Alfred Hospital (AU)
- Royal North Shore Hospital (AU)
- St Vincent's Hospital Sydney (AU)
Publication Details
- Journal
- BMJ Case Reports
- Published
- 2024-09-01
- DOI
- https://doi.org/10.1136/bcr-2023-258751
- Primary Topic
- Vascular Tumors and Angiosarcomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00