SOLITARY FIBROUS TUMOR OF SOFT-TISSUE - A REPORT OF 15 CASES, INCLUDING 5 MALIGNANT EXAMPLES WITH LIGHT-MICROSCOPIC, IMMUNOHISTOCHEMICAL, AND ULTRASTRUCTURAL DATA
Gp. Nielsen et al., SOLITARY FIBROUS TUMOR OF SOFT-TISSUE - A REPORT OF 15 CASES, INCLUDING 5 MALIGNANT EXAMPLES WITH LIGHT-MICROSCOPIC, IMMUNOHISTOCHEMICAL, AND ULTRASTRUCTURAL DATA, Modern pathology, 10(10), 1997, pp. 1028-1037
We describe 15 soft tissue solitary fibrous tumors (SFTs) occurring in
patients 24 to 78 years old (average, 50.6 yr). Ten tumors were benig
n and arose in the head and neck area (three tumors), thigh (two), vul
va (two), upper arm (one), lower leg (one), and retroperitoneum (one).
Five tumors were histologically malignant and arose in the thigh (two
), abdominal wall (one), buttock (one), and retroperitoneum (one). All
of the tumors were grossly well circumscribed. The benign tumors meas
ured from 2 to 10 cm (average, 4.8 cm) and the malignant ones from 3 t
o 5.5 cm (average, 4.3 cm) in greatest diameter. Microscopically, the
benign tumors showed areas of hypercellularity with variable amounts o
f collagenous and myxoid stroma; one had amianthoid fibers. The malign
ant tumors were composed of cytologically atypical cells enmeshed in a
collagenous or myxoid extracellular matrix. Ultrastructural study of
three benign and three malignant tumors showed fibroblastic differenti
ation; one benign tumor showed myofibroblastic differentiation. Immuno
histochemically, all of the tumors examined were immunoreactive for vi
mentin, and seven of nine were positive for CD34, including all of the
malignant ones. There was focal staining for muscle actin in two beni
gn tumors and for Leu-7 in one benign tumor; there was no staining for
cytokeratin, desmin, S-100 protein, epithelial membrane antigen, or s
mooth muscle actin in any of the examined tissues. Follow-up was avail
able for eight patients for 6 to 21 months (average, 12 mo). No tumor
recurred locally or metastasized. The SFTs reported herein support the
experiences of others who recently described these tumors in the soma
tic soft tissues, In addition, our series highlights the occurrence of
malignant SFTs in the soft tissues, SFTs should be separated from oth
er spindle cell sarcomas, with which they can be confused.