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Recurrent intravascular papillary endothelial hyperplasia developing from a pyogenic granuloma
H S Inalöz1, G Patel, A G Knight
1Department of Dermatology, University of Wales College of Medicine, Cardiff, South Wales, UK. serhatinaloz@hotmail.com
Abstract:
Intravascular papillary endothelial hyperplasia (IPEH) is a rare benign vascular tumour. Many histological features are similar to those of low-grade angiosarcoma, a common, but more serious condition. Clinical and histological differentiation is important to avoid overtreatment of this benign condition. We report on a 34-year-old woman who developed recurrent IPEH at the site of a previously excised pyogenic granuloma.
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