Goldblum J R, Reith J D, Weiss S W
Department of Anatomic Pathology of the Cleveland Clinic Foundation, Ohio 44195, USA.
Am J Surg Pathol. 2000 Aug;24(8):1125-30. doi: 10.1097/00000478-200008000-00010.
There is a prevailing view that sarcomas arising in dermatofibrosarcoma protuberans (DFSP) have a higher risk of metastasis than ordinary DFSP, but these data are based on cases with variable and often suboptimal treatment. There has not been a large study of sarcomas arising in DFSP in which all cases were treated by wide local excision, thereby arguably altering outcome. Clinicopathologic features of 18 cases of sarcomas arising in DFSP treated by wide local excision and having follow up of at least 5 years were analyzed. An estimate of the proportion of sarcoma and DFSP was made. The number of mitotic figures and degree of CD34 immunoreactivity were assessed in each case. The cohort included 13 females and 5 males (age, 23-87 yrs; median, 47 yrs). The tumors involved the trunk (7), scalp (4), extremities (4), and inguinal region (3), and ranged from 1.5 to 7 cm (median, 4 cm). Sarcoma occurred de novo in 15 cases and in a recurrence in three. Sarcomas resembled fibrosarcoma (17) or malignant fibrous histiocytoma (1) and occupied between 20% and 80% of the tumor (median, 60%). Mitotic activity ranged from 2 to 16 per 10 high-power field (HPF; median 7 per 10 HPF) in the sarcomatous component and 0 to 3 per 10 HPF (median, 1 per 10 HPF) in the DFSP component. All tumors expressed CD34 in the DFSP component but only nine (50%) in the sarcomatous component. All patients were treated by wide local excision with negative margins; three additionally received radiation. Four patients (22%) developed recurrences, but none developed metastasis during the follow-up period of 62 months to 17 years (median, 81.5 mos). In contrast to earlier studies, we demonstrate that patients with sarcomas arising in DFSP do not have an increased risk of distant metastasis within a 5-year follow-up period, provided they are treated by wide local excision with negative margins. This probably reflects the fact that wide local excision results in eradication of local tumor, thereby eliminating the source for subsequent dissemination. However, we cannot completely exclude the possibility that tumors in which clear margins are achieved represent a less aggressive subset, as has been suggested for high-grade extremity sarcomas. Previous studies showing increased metastasis for sarcomas arising in DFSP should be re-evaluated to determine if, with treatment stratification, metastatic rate varies.
有一种普遍的观点认为,隆突性皮肤纤维肉瘤(DFSP)中发生的肉瘤比普通DFSP具有更高的转移风险,但这些数据是基于治疗方式多样且往往不够理想的病例。目前尚未有对DFSP中发生的肉瘤进行的大型研究,其中所有病例均采用广泛局部切除治疗,从而可能改变了结果。分析了18例经广泛局部切除治疗且随访至少5年的DFSP中发生的肉瘤的临床病理特征。估计了肉瘤和DFSP的比例。评估了每个病例的有丝分裂象数量和CD34免疫反应程度。该队列包括13名女性和5名男性(年龄23 - 87岁;中位数47岁)。肿瘤累及躯干(7例)、头皮(4例)、四肢(4例)和腹股沟区(3例),大小范围为1.5至7厘米(中位数4厘米)。肉瘤新发于15例,3例发生于复发时。肉瘤类似纤维肉瘤(17例)或恶性纤维组织细胞瘤(1例),占肿瘤的20%至80%(中位数60%)。肉瘤成分的有丝分裂活性为每10个高倍视野(HPF)2至16个(中位数每10个HPF 7个),DFSP成分的有丝分裂活性为每10个HPF 0至3个(中位数每10个HPF 1个)。所有肿瘤在DFSP成分中均表达CD34,但在肉瘤成分中仅9例(50%)表达。所有患者均接受了切缘阴性的广泛局部切除;3例额外接受了放疗。4例患者(22%)出现复发,但在62个月至17年(中位数81.5个月)的随访期间均未发生转移。与早期研究不同,我们证明,DFSP中发生肉瘤的患者,若接受切缘阴性的广泛局部切除治疗,在5年随访期内远处转移风险并未增加。这可能反映了广泛局部切除可根除局部肿瘤,从而消除后续播散来源这一事实。然而,我们不能完全排除切缘阴性的肿瘤代表侵袭性较低的亚组的可能性,正如对高级别肢体肉瘤所提示的那样。应重新评估先前显示DFSP中发生的肉瘤转移增加的研究,以确定随着治疗分层,转移率是否会有所不同。