Chen Mingxia, Zhang Wei, Qu Jianli, Li Lei, Sun Qing
Department of Pathology, Qian-Fo-Shan Hospital Affiliated Shandong University 16766 Jingshi Road, Jinan 250014, China ; Department of Pathology, Yatai Yaitaishan Hospital 91 Jiefang Road, Yatai 264001, China.
Department of Pathology, Yatai Yaitaishan Hospital 91 Jiefang Road, Yatai 264001, China.
Int J Clin Exp Pathol. 2014 Dec 1;7(12):9099-103. eCollection 2014.
Bone epithelioid angiosarcoma (EA) is rare and characterized by large, mildly to moderately pleomorphic epithelioid cells, with abundant eosinophilic cytoplasm, vesicular nuclei, and prominent nucleoli. The tumors may arise in various locations in bone and the patients may present with unifocal or multifocal osseous disease. We present a unifocal lesion case of EA of the ilium in a 62-year-old woman. A needle biopsy of the ilium was performed and first diagnosed poorly differentiated adenocarcinoma based on CKpan and CK18 immunopositivity. The tumor was treated initially with curettage followed by chemotherapy. The final diagnosis on the surgical specimen was epithelioid angiosarcoma.
骨上皮样血管肉瘤(EA)较为罕见,其特征为具有大量、轻度至中度多形性的上皮样细胞,胞质丰富嗜酸性,核呈泡状,核仁明显。肿瘤可发生于骨骼的各个部位,患者可能表现为单灶性或多灶性骨病变。我们报告一例62岁女性髂骨EA单灶性病变病例。对髂骨进行了针吸活检,最初基于广谱细胞角蛋白(CKpan)和细胞角蛋白18(CK18)免疫阳性诊断为低分化腺癌。该肿瘤最初接受了刮除术,随后进行化疗。手术标本的最终诊断为上皮样血管肉瘤。