WELL-DIFFERENTIATED LIPOSARCOMA - THE MAYO-CLINIC EXPERIENCE WITH 58 CASES

被引:162
作者
LUCAS, DR
NASCIMENTO, AG
SANJAY, BKS
ROCK, MG
机构
[1] MAYO CLIN & MAYO FDN,DEPT PATHOL,DIV ANAT PATHOL,ROCHESTER,MN 55905
[2] MAYO CLIN & MAYO FDN,DEPT ORTHOPED,ROCHESTER,MN 55905
关键词
ATYPICAL LIPOMA; SCLEROSING LIPOSARCOMA; WELL-DIFFERENTIATED LIPOSARCOMA;
D O I
10.1093/ajcp/102.5.677
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The clinicopathologic results from 58 patients with well-differentiated liposarcomas are reported. Thirty-two tumors involved the extremities, 20 the retroperitoneum, 4 the scrotum, 1 the abdominal wall, and 1 the cheek. Most tumors were large (mean, 22.6 cm). There were 31 (53%) lipomalike, 23 (40%) sclerosing, and 4 (7%) primary dedifferentiated tumors. Six tumors underwent dedifferentiation after recurrence. The average follow-up period was 9.3 years. Thirty-seven patients (64%) were alive with no evidence of disease; 7 (12%) were alive with disease; 8 (14%) died of disease; and 6 (10%) died of other causes. Dedifferentiation did not indicate imminent death; 5 of the 10 patients were alive with no evidence of disease. Three dedifferentiated tumors subsequently recurred as pure well-differentiated liposarcomas. Patients with extremity tumors had a significantly better prognosis than those with retroperitoneal or scrotal tumors (P = .006). Extremity tumors treated by wide local excision recurred in only 11% of cases, whereas 60% of those treated by marginal or simple excision recurred.
引用
收藏
页码:677 / 683
页数:7
相关论文
共 18 条
  • [1] ATYPICAL AND MALIGNANT NEOPLASMS SHOWING LIPOMATOUS DIFFERENTIATION - A STUDY OF 111 CASES
    AZUMI, N
    CURTIS, J
    KEMPSON, RL
    HENDRICKSON, MR
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1987, 11 (03) : 161 - 183
  • [2] LIPOSARCOMAS - A HISTOGENETIC APPROACH TO THE CLASSIFICATION OF ADIPOSE-TISSUE NEOPLASMS
    BOLEN, JW
    THORNING, D
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1984, 8 (01) : 3 - 17
  • [3] Brooks JJ, 1990, SURG PATHOL, V3, P169
  • [4] CHANG HR, 1989, CANCER, V64, P1514, DOI 10.1002/1097-0142(19891001)64:7<1514::AID-CNCR2820640726>3.0.CO
  • [5] 2-2
  • [6] DAHLIN DC, 1971, CANCER, V28, P461, DOI 10.1002/1097-0142(197108)28:2<461::AID-CNCR2820280227>3.0.CO
  • [7] 2-U
  • [8] Enzinger FM, 1988, SOFT TISSUE TUMORS, P347
  • [9] EVANS HL, 1979, CANCER, V43, P574, DOI 10.1002/1097-0142(197902)43:2<574::AID-CNCR2820430226>3.0.CO
  • [10] 2-7