Key result
Primary malignant fibrous histiocytoma of bone resulted in pulmonary metastases in 81.8% of patients within 21 months, with an average survival of 12 months in untreated patients.
Observational (n=11)
Primary malignant fibrous histiocytoma of bone is an aggressive tumor with a high rate of early pulmonary and lymph node metastases and poor survival without secondary treatment.
Early pulmonary metastases and short untreated survival mark malignant fibrous histiocytoma of bone; hypothesis-generating for adjuvant responses in this rare tumor.
A review of over 400 primary bone tumors yielded 11 lesions with features allowing classification as malignant fibrous histiocytoma on a purely histological basis. Correlation with roentgenograms and clinical data indicated that these tumors occurred as osteolytic lesions associated with a high incidence of pathologic fractures in the metaphyses of skeletally mature long bones. Nine patients developed pulmonary metastases and 3 developed lymph node metastases within 21 months following diagnosis. The average survival was 12 months in 6 of the 9 patients who had no secondary treatment of their metastases. Treatment of 3 patients with metastatic lesions with chemotherapy or radiotherapy has been clinically encouraging. Some evidence was obtained that either or both the histiocytic and fibroblastic component may metastasize. There is a need for biopsy of metastatic lesions and autopsy followup to more accurately assess the mode of spread and histologic type of the metastases.
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Spanier et al. (1975) conducted an observational in Primary malignant fibrous histiocytoma of bone (n=11). Primary malignant fibrous histiocytoma of bone was evaluated on Pulmonary metastases. Primary malignant fibrous histiocytoma of bone resulted in pulmonary metastases in 81.8% of patients within 21 months, with an average survival of 12 months in untreated patients.
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