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原发性皮肤上皮样血管肉瘤:13 例罕见肿瘤的临床病理研究,这些肿瘤发生于常规血管肉瘤之外,且好发于四肢。

Primary cutaneous epithelioid angiosarcoma: a clinicopathologic study of 13 cases of a rare neoplasm occurring outside the setting of conventional angiosarcomas and with predilection for the limbs.

机构信息

Department of Dermatopathology, St John's Institute of Dermatology, St Thomas' Hospital, London, UK.

出版信息

Am J Surg Pathol. 2011 Jan;35(1):60-9. doi: 10.1097/PAS.0b013e3181fee872.

Abstract

Epithelioid angiosarcomas are rare aggressive neoplasms that occur most frequently in deep soft tissues. Primary cutaneous lesions are rare, and there are discrepant findings in the literature regarding their behavior. In this study, we report a series of 13 cases of primary cutaneous epithelioid angiosarcoma and analyze their clinicopathologic features. The tumors arising in the conventional settings for cutaneous angiosarcoma (ie, in the head and neck region of elderly patients, and those occurring postradiation or associated with lymphedema) were excluded. Primary cutaneous epithelioid angiosarcoma occurred in adults (mean age, 66 y) with an equal sex distribution, and presented as solitary (n=10) or multiple (n=3) nodules ranging in size from 8 to 80 mm, with a predilection for the limbs (n=10). Histopathologically, the tumors comprised infiltrative sheets of atypical epithelioid cells within the dermis with or without the involvement of the subcutis. Vascular channel formation and intracytoplasmic lumina were seen, at least focally, in most cases. Mitoses were readily identified and necrosis was seen in 40% of the cases. The tumors were immunoreactive for vascular markers, with CD31 and FLI-1 offering the highest sensitivity. Pancytokeratin was positive in two thirds of the cases, and epithelial membrane antigen was positive in one-quarter of the cases. There was rare focal expression of Melan-A (n=2) and smooth muscle actin (n=3). Follow-up information was available for 11 patients. Six patients died of metastatic disease after a median follow-up of 12 months (range, 3 to 36 mo), and 1 patient died of unrelated causes. These findings suggest that primary cutaneous epithelioid angiosarcoma occurring outside the conventional settings of angiosarcoma is a highly aggressive malignant tumor with mortality rates in excess of 55% after 3 years.

摘要

上皮样血管肉瘤是一种罕见的侵袭性肿瘤,最常发生于深部软组织。原发性皮肤病变罕见,文献中关于其行为的报道存在差异。在本研究中,我们报告了 13 例原发性皮肤上皮样血管肉瘤病例,并分析了其临床病理特征。我们排除了发生在皮肤血管肉瘤常规部位(即老年患者的头颈部,以及放疗后或与淋巴水肿相关的部位)的肿瘤。原发性皮肤上皮样血管肉瘤发生于成年人(平均年龄 66 岁),男女比例相等,表现为单发(n=10)或多发(n=3)结节,大小 8 至 80mm 不等,好发于四肢(n=10)。组织病理学上,肿瘤由真皮内浸润性的不典型上皮样细胞组成,可伴有或不伴有皮下组织受累。大多数病例至少局灶性可见血管腔形成和胞质内管腔。很容易识别有丝分裂象,40%的病例可见坏死。肿瘤对血管标志物呈免疫反应性,CD31 和 FLI-1 的敏感性最高。大多数病例的细胞角蛋白广谱(pancytokeratin)阳性(n=2/3),上皮膜抗原(epithelial membrane antigen)阳性(n=1/4)。Melan-A(n=2)和平滑肌肌动蛋白(smooth muscle actin)(n=3)的表达呈罕见的局灶性。11 例患者的随访信息可用。中位随访 12 个月(范围 3 至 36 个月)后,6 例患者死于转移性疾病,1 例患者死于无关原因。这些发现表明,发生在血管肉瘤常规部位以外的原发性皮肤上皮样血管肉瘤是一种高度侵袭性恶性肿瘤,3 年后死亡率超过 55%。

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