Gengler Carole, Coindre Jean-Michel, Leroux Agnés, Trassard Martine, Ranchère-Vince Dominique, Valo Isabelle, Michels Jean-Jacques, Guillou Louis
Department of Pathology, University Institute of Pathology, Lausanne, Switzerland.
Cancer. 2007 Apr 15;109(8):1584-98. doi: 10.1002/cncr.22586.
Cutaneous vascular proliferations that occur in the field of prior radiotherapy include angiosarcoma and small, cutaneous lesions with a pseudosarcomatous pattern that previously were reported as atypical vascular lesions or benign lymphangiomatous papules.
The objective of this study was to investigate the clinicopathologic features and outcomes of 56 radiation-induced vascular proliferations that occurred in 36 patients who received previous treatment for breast carcinoma. Data from all patients were retrieved from the files of the French Sarcoma Group. Immunostaining with D2.40 antibody was performed in 24 lesions.
All patients (median age, 52 years) had received external radiotherapy. Small papules developed within the field of prior radiotherapy (median latency interval, 66 months). Microscopically, the lesions were relatively well circumscribed, and they were located mostly in the superficial/middermis. They were composed of dilated or irregular-jagged vascular channels that were lined by a single layer of bland endothelial cells, and they demonstrated either a predominately lymphangioendothelioma-like or lymphangioma/lymphangioma circumscriptum-like growth pattern. Micropapillary tufts were common findings. Ten lesions showed additional cytologic and/or architectural atypia. Twenty of 24 lesions showed D2.40 positivity. Follow-up information was available for 31 patients (median follow-up, 48 months): Five women developed new cutaneous lesions, and 1 woman had spontaneous regression of her lesions. None of the patients developed cutaneous angiosarcoma. Five patients were lost to follow-up.
Although vascular proliferations in irradiated skin may mimic angiosarcoma morphologically, the large majority of these lesions showed a benign clinical outcome. Despite relatively limited follow-up, the current results indicate the benign nature of these vascular proliferations.
先前放疗区域出现的皮肤血管增殖性病变包括血管肉瘤以及一些小的、具有假肉瘤样形态的皮肤病变,这些病变以前被报道为非典型血管病变或良性淋巴管瘤样丘疹。
本研究的目的是调查56例放射诱导的血管增殖性病变的临床病理特征及转归,这些病变发生在36例曾接受过乳腺癌治疗的患者中。所有患者的数据均从法国肉瘤研究组的档案中获取。对24个病变进行了D2.40抗体免疫染色。
所有患者(中位年龄52岁)均接受过外照射放疗。在先前放疗区域内出现小丘疹(中位潜伏期为66个月)。显微镜下,病变边界相对清晰,主要位于表皮浅层/中层。病变由扩张或不规则锯齿状的血管腔隙构成,内衬单层温和的内皮细胞,表现为主要为淋巴管内皮瘤样或淋巴管瘤/局限性淋巴管瘤样生长模式。微乳头簇是常见表现。10个病变显示有额外的细胞学和/或结构异型性。24个病变中有20个显示D2.40阳性。31例患者有随访信息(中位随访时间48个月):5名女性出现了新的皮肤病变,1名女性病变自发消退。所有患者均未发生皮肤血管肉瘤。5例患者失访。
尽管照射皮肤中的血管增殖性病变在形态上可能类似血管肉瘤,但这些病变绝大多数临床转归为良性。尽管随访相对有限,但目前结果表明这些血管增殖性病变具有良性本质。