Introduction: Epithelioid hemagioendothelioma (HHE) is a rare mesenchymal tumor of vascular origin and epithelial appearance, which develops like angiosarcoma to mimic endothelial cells. According to the literature, its prognosis is variable and remains unpredictable.
Case report: We report a 72-year-old man who presented with an inflammatory pain in the left lower limb. Several osteolytic lesions involving the knee, the upper third of the tibia, the medial malleolus and the left calcaneus were identified. The diagnosis HHE was obtained by histological examination of a bone sample. The patient died after 5 months, despite taxol chemotherapy.
Conclusion: No therapeutic behavior is standardized in this uncommon type of cancer.
Keywords: Epithelioid hemagioendothelioma; Hémangioendothéliome épithélioïde; Multiple myeloma; Myélome; Primary bone tumor; Tumeur osseuse primitive; Tumeur vasculaire; Vascular tumor.
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