Consultoria em Patologia, Botucatu, SP, Brazil.
Am J Surg Pathol. 2010 Sep;34(9):1334-43. doi: 10.1097/PAS.0b013e3181ee4eaf.
We report 18 cases of cutaneous angiosarcoma with predominant or exclusive epithelioid morphology. Both sexes were similarly affected. Patients' ages ranged from 2 to 97 years, median 77.5 years; 2 were pediatric patients. In elderly patients scalp or facial lesions and cutaneous lesions arising within irradiated breast skin predominated. Limb lesions were seen in younger patients. Microscopically, the tumors were composed of packed polygonal cells with focal evidence of endothelial differentiation. Diverging phenotypes included syncytial growth of large cells with clear nuclei and prominent nucleoli, micronodules of tumor cells scattered in dermis, predominance of discohesive plasmacytoid polygonal cells with abundant bright eosinophilic cytoplasm, sheets of clear cells with coarse granular cytoplasm, trabecular and cord arrangement of tumor cells splaying the dermal collagen, or a pseudoglandular appearance owing to clear cell tubular arrangement with open lumina. These cases posed further diagnostic challenges simulating lymphoma, melanoma, lymphoepithelioma-like carcinoma, adnexal carcinoma, and neuroendocrine carcinoma. Immunohistochemical studies showed positivity for CD31 and CD34; no immunoreactivity was documented for other tested antigens including cytokeratins, S100 protein, melanocytic antigens, leukocyte common antigen, and desmin. Therapeutic modalities included combined local excision, chemotherapy, and radiotherapy, depending on patient clinical status. Of the 9 patients available for follow-up, 5 were alive and apparently well, 2 had recurrent disease, and 2 had died of tumor. Our data show that epithelioid cutaneous angiosarcoma may have a broad morphological spectrum, raising interpretive challenges on microscopy. In addition, its clinical presentation seems to differ in nonelderly patients, with lesions likely related to lymphedema or vascular malformations.
我们报告了 18 例以上皮样形态为主或仅为上皮样形态的皮肤血管肉瘤。男女发病率相似。患者年龄 2-97 岁,中位年龄 77.5 岁;2 例为儿童。老年患者以头皮或面部病变和放疗后乳房皮肤出现的皮肤病变为主,年轻患者以肢体病变为主。镜下,肿瘤由排列紧密的多边形细胞组成,局灶性具有内皮分化的证据。不同的表型包括大细胞的合胞体生长,细胞核透明,核仁明显,肿瘤细胞微结节散在真皮中,以分离的浆细胞样多边形细胞为主,胞质丰富、嗜酸性明亮,透明细胞呈片状,胞质粗糙颗粒状,肿瘤细胞呈小梁状和索状排列,将真皮胶原撑开,或由于透明细胞管状排列形成的假腺样外观,管腔开放。这些病例进一步增加了诊断挑战,模拟淋巴瘤、黑色素瘤、淋巴上皮样癌、附属器癌和神经内分泌癌。免疫组织化学研究显示 CD31 和 CD34 阳性;其他检测的抗原包括细胞角蛋白、S100 蛋白、黑色素细胞抗原、白细胞共同抗原和结蛋白均无免疫反应性。治疗方式包括根据患者临床状况,选择联合局部切除、化疗和放疗。在 9 例可随访的患者中,5 例存活且情况良好,2 例复发,2 例死于肿瘤。我们的数据表明,上皮样皮肤血管肉瘤可能具有广泛的形态学谱,在显微镜下具有解释上的挑战。此外,其临床表现在非老年患者中似乎有所不同,病变可能与淋巴水肿或血管畸形有关。