Objective. A bone infarct may occasionally dedifferentiate to osteogen
ic sarcoma, fibrosarcoma or malignant fibrous histiocytoma. However, t
he association of an angiosarcoma with a bone infarct is extremely rar
e. Such an association is presented in three patients. Their clinical
course is compared with that of patients with bone infarcts associated
with other sarcomas. Design and patients. The three patients were men
with a mean age of 43 years. Cases 1 and 3 presented with a pathologi
cal fracture at the site of the angiosarcoma. Plain radiography was do
ne in the three patients, computed tomography (CT) was performed in ca
ses 1 and 3 and magnetic resonance imaging (MRI) in case 3. The femur
was the site of the three tumors: midshaft in cases 1 and 3 and distal
shaft in case 2. On the basis of the radiographic findings, and clini
cal examination, an open biopsy was performed for the three men, which
confirmed the diagnosis of a high-grade angiosarcoma associated with
a bone infarct. Results. Case 1 was treated with high-above knee amput
ation and is still alive after 18 months from the time of operation. S
egmental resection of the distal femur with adjuvant chemotherapy and
local irradiation was the treatment for case 2, who is still alive wit
h no tumor recurrence on metastatic disease 3 years from the operation
. Intramedullary redding was done for case 3 who died 6 months later.
Conclusion. The association of an angiosarcoma with a bone infarct has
been established in only five cases. Although the number of such asso
ciations is small, it seems that such an association may be prognostic
ally more or less the same as in those cases in which a bone infarct i
s associated with either osteosarcoma, fibrosarcoma or malignant fibro
us histiocytoma, where the survival rate is unfavorable. A cause-and-e
ffect relationship may exist between a bone infarct and subsequent dev
elopment of a bone sarcoma.