Collagenous fibroma (desmoplastic fibroblastoma): A clinicopathologic analysis of 63 cases of a distinctive soft tissue lesion with stellate-shaped fibroblasts

被引:97
作者
Miettinen, M [1 ]
Fetsch, JF [1 ]
机构
[1] Armed Forces Inst Pathol, Dept Soft Tissue Pathol, Washington, DC 20306 USA
关键词
fibroma; fibroblastoma; soft tissue; diagnosis; immunohistochemistry;
D O I
10.1016/S0046-8177(98)90275-1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Sixty-three cases of collagenous fibroma (desmoplastic fibroblastoma) from the files of the Armed Forces Institute of Pathology were analyzed. These tumors occurred mostly in men (80%) with a median age of 50 years (range, 16 to 81 years). The lesions had a wide anatomic distribution 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 history of a painless, slowly growing mass, often of relatively long duration. The tumors ranged in size from 1 to 20 cm (median, 3.0 cm). The 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 firm consistency and a homogeneous pearl-gray color. Histologically, the tumors often appeared well marginated on low-power examination, but most (78%) infiltrated fat or, less commonly, skeletal muscle. The lesional cells were relatively bland stellate and spindle-shaped fibroblasts separated by a collagenous or myxocollagenous matrix. Mitotic activity was absent or minimal. Some of the lesional cells had a myofibroblastic immunophenotype, as evidenced by focal reactivity for muscle-specific and cu-smooth muscle actins. In a few cases, rare actin-positive cells were also positive for keratins. Desmin, S100 protein, and CD34 were not expressed. None of the 39 patients with follow-up (median, 11 years) developed a recurrence. Collagenous fibroma is a benign fibroblastic/myofibroblastic proliferation. The large size of some of these tumors coupled with slow growth and persistence favors a neoplastic process over a peculiar reactive proliferation. The differential diagnosis includes a variety of reactive and neoplastic fibroblastic lesions, most importantly fibromatosis and low-grade fibromyxoid sarcoma. Simple, conservative excision is the treatment of choice for collagenous fibroma. Copyright (C) 1998 by W.B. Saunders Company.
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页码:676 / 682
页数:7
相关论文
共 29 条
  • [1] ALLEN PW, 1970, CANCER, V26, P857, DOI 10.1002/1097-0142(197010)26:4<857::AID-CNCR2820260420>3.0.CO
  • [2] 2-S
  • [3] [Anonymous], 1995, SOFT TISSUE TUMORS
  • [4] NUCHAL FIBROMA - A CLINICOPATHOLOGICAL STUDY OF 9 CASES
    BALACHANDRAN, K
    ALLEN, PW
    MACCORMAC, LB
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1995, 19 (03) : 313 - 317
  • [5] CHAUBAL A, 1994, ACTA NEUROPATHOL, V88, P454
  • [6] CHUNG EB, 1979, CANCER, V44, P1945, DOI 10.1002/1097-0142(197911)44:5<1945::AID-CNCR2820440558>3.0.CO
  • [7] 2-T
  • [8] ENZINGER FM, 1967, CANCER-AM CANCER SOC, V20, P1131, DOI 10.1002/1097-0142(196707)20:7<1131::AID-CNCR2820200716>3.0.CO
  • [9] 2-8
  • [10] LOW-GRADE FIBROMYXOID SARCOMA - A REPORT OF 12 CASES
    EVANS, HL
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1993, 17 (06) : 595 - 600