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. Primary breast angiosarcoma is a very rare tumor and accounts   for 0.04% of all breast malignant tumors and most commonly occur in young   women. Kasabach-Merritt syndrome (KMS) is described as consumption   coagulopathy with thrombocytopenia, and without adequate therapy almost   certainly leads to a very fast lethal outcome. Case report. We present a   rare case of 60-year-old postmenopausal woman with metastatic primary   angiosarcoma of the breast associated with a picture like Kasabach-Merritt's   syndrome (thrombocytopenia and anemia without the coagulation factor   disorder with massive bleeding in the tumor). Conclusion. Primary breast   angiosarcoma in postmenopausal women is a very rare tumor, and may be   associated with anemia and thrombocytopenia without other laboratory   parameters for Kasabach-Merritt's syndrome. Anemia and thrombocytopenia are   refractory to standard treatment protocols, and also significantly reduces   the quality of life of these patients. The literature contains only a few   cases of Passociated with thrombocytopenia or with KMS and there are no   clear defined protocols for the treatment of these patients, which requires   the presentation of as many cases as possible.

Primary breast angiosarcoma in postmenopausal women with a picture like Kasabach-Merritt syndrome: A case report