BACKGROUND. Most pathologists generally accept malignant fibrous histi
ocytoma (MFH) as the most common soft tissue sarcoma in adults. This s
tudy examines the authors' aspiration cytopathology experience with th
is tumor, describes its cytomorphology, and determines the reliability
of such a diagnosis by fine-needle aspiration biopsy (FNAB). METHODS.
The authors' files were reviewed for cases diagnosed as MFH by FNAB,
and for surgical pathology cases of MFH previously aspirated but not d
iagnosed as such by cytology. RESULTS. Fifty-two cases of MFH (by FNAB
or histology) were recovered from the combined files; 42 aspirates ha
d tissue confirmation. Patient age ranged from 15-88 years (mean, 63 y
ears); the male:female ratio was 1.2. Thirty aspirates were from prima
ry tumors, and 12 were from recurrences or metastases. From the 29 asp
irates diagnosed as MFH, 24 (83%) were determined to be MFH on subsequ
ent surgical excision. Four of the remaining cases were other sarcoma
subtypes, and there was one organizing thrombus (false-positive). The
remaining 13 aspirates were identified as unqualified sarcoma (11 case
s) or a different sarcoma subtype (2 cases). Eleven of these were hist
ologically diagnosed as MFH, and 2 as other sarcomas. No single cytolo
gic feature or combination of features distinguished MFH. Patterns ran
ged from single cells to large storiform fragments. Spindled, plasmacy
toid, and pleomorphic cell shapes were found; pleomorphic cells were o
ften multinucleated. AU cases of MFH had malignant nuclear morphology.
Diagnostic pitfalls included low cellularity, obscuring blood and inf
lammation, and inadequate clinical and/or radiologic information. CONC
LUSIONS. The diagnostic role of FNAB in soft tissue lesions remains co
ntroversial. FNAB is important in the initial triage of patients with
soft tissue tumors, and is particularly accurate for confirming recurr
ent or metastatic disease. Although making an initial diagnosis of sar
coma by FNAB is reliable, specific subtyping of them as MFH is more pr
oblematic. (C) 1997 American Cancer Society.