COLLAGENOUS FIBROMA (DESMOPLASTIC FIBROBLASTOMA) - A CLINICOPATHOLOGICAL ANALYSIS OF 63 CASES OF A DISTINCTIVE SOFT-TISSUE LESION WITH STELLATE-SHAPED FIBROBLASTS
M. Miettinen et Jf. Fetsch, COLLAGENOUS FIBROMA (DESMOPLASTIC FIBROBLASTOMA) - A CLINICOPATHOLOGICAL ANALYSIS OF 63 CASES OF A DISTINCTIVE SOFT-TISSUE LESION WITH STELLATE-SHAPED FIBROBLASTS, Human pathology, 29(7), 1998, pp. 676-682
Sixty-three cases of collagenous fibroma (desmoplastic fibroblastoma)
from the files of the Armed Forces Institute of Pathology were analyze
d. These tumors occurred mostly in men (80%) with a median age of 50 y
ears (range, 16 to 81 years). The lesions had a wide anatomic distribu
tion and involved the arm (24%), shoulder girdle (19%), posterior neck
or upper back (14%), feet or ankles (14%), leg (14%), hand (8%), and
abdominal wall and hip (6%). The patients typically presented with a h
istory of a painless, slowly growing mass, often of relatively long du
ration. The tumors ranged in size from 1 to 20 cm (median, 3.0 cm). Th
e lesions were predominantly subcutaneous, but fascial involvement was
common, and 27% of cases involved skeletal muscle. Gross examination
typically showed an elongated, lobulated, or disc-shaped mass with a f
irm consistency and a homogeneous pearl-gray color. Histologically, th
e tumors often appeared well marginated on low-power examination, but
most (78%) infiltrated fat or, less commonly, skeletal muscle. The les
ional cells were relatively bland stellate and spindle-shaped fibrobla
sts separated by a collagenous or myxocollagenous matrix. Mitotic acti
vity was absent or minimal. Some of the lesional cells had a myofibrob
lastic immunophenotype, as evidenced by focal reactivity for muscle-sp
ecific and cu-smooth muscle actins. In a few cases, rare actin-positiv
e cells were also positive for keratins. Desmin, S100 protein, and CD3
4 were not expressed. None of the 39 patients with follow-up (median,
11 years) developed a recurrence. Collagenous fibroma is a benign fibr
oblastic/myofibroblastic proliferation. The large size of some of thes
e tumors coupled with slow growth and persistence favors a neoplastic
process over a peculiar reactive proliferation. The differential diagn
osis includes a variety of reactive and neoplastic fibroblastic lesion
s, most importantly fibromatosis and low-grade fibromyxoid sarcoma. Si
mple, conservative excision is the treatment of choice for collagenous
fibroma. Copyright (C) 1998 by W.B. Saunders Company.