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Endovascular papillary angioendothelioma (Dabska tumor) of bone

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Abstract 

Endovascular papillary angioendothelioma, also known as Dabska tumor, is a rare vascular neoplasm that usually involves the skin or subcutaneous tissue of children. There have been no reported cases of this lesion occurring in bone. We report a Dabska tumor in the distal femur of a 45-year-old woman who, clinically and radiologically, was felt to have an osteoid osteoma. Histologic study of the lesion showed a hemangioma with budding fronds of endothelial cells, a feature characteristic of the Dabska tumor. We feel that the lesion arose in a pre-existing hemangioma, a hypothesis suggested in a few other case reports. Endovascular papillary angioendothelioma is a low-grade malignant neoplasm, although only one patient has died due to this lesion. Our patient is asymptomatic without evidence of recurrence 1 year post curettage.

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Received: 13 September 1998; Revision requested: 19 October 1998; Revision received: 10 November 1998; Accepted: 12 November 1998

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McCarthy, E., Lietman, S., Argani, P. et al. Endovascular papillary angioendothelioma (Dabska tumor) of bone. Skeletal Radiol 28, 100–103 (1999). https://doi.org/10.1007/s002560050482

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  • DOI: https://doi.org/10.1007/s002560050482

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