BACKGROUND. Primary malignant fibrous histiocytoma (MFH) of the lung i
s a rare clinical entity. Only 23 reports of 49 cases have been report
ed in the literature. Surgery was the primary mode of therapy, with hi
gh rates of local and distant recurrence reported. The role of radiati
on therapy and chemotherapy has never been clearly defined. METHODS. T
he records of the Mayo Clinic in Scottsdale and Rochester from 1970 to
1990 were reviewed for cases of primary pulmonary MFH. A review of th
e literature was also undertaken. RESULTS. Four cases from the Mayo re
cords and 49 cases from a review of the literature were identified. Ei
ght patients were alive at 5 years from diagnosis; all had been treate
d with surgery as the primary modality. No definite relationship betwe
en histologic subtype of MFH and survival could be identified and no d
efinite role of radiation therapy or chemotherapy could be defined. CO
NCLUSIONS. MFH of the lung should be treated by surgical resection if
technically feasible. The role of adjuvant therapy remains undefined.
(C) 1996 American Cancer Society.