Hovorková E, Ryska A
Fingerlandův ústav patologie FN, Hradec Králové.
Cesk Patol. 1999 Jul;35(3):85-9.
A case of malignant myoepithelioma of the parotid gland in a 34-year-old female is presented. In the fine-needle aspiration material, there was predominance of poorly cohesive polygonal cells with marked nuclear pleomorphism; no mitotic figures were observed. Focally, fragments of myxoid metachromatic intercellular material were also present. Histologically, the tumor was encepsulated, showing focal invasion of the capsule and tumor thrombi in the capsular vessels. The tumor was predominantly solid and myxoid, composed of cells with epithelioid features, marked anisonucleosis and a low mitotic activity. Immunohistochemically, the cells revealed positive staining for S-100 protein, vimentin, cytokeratins, glial acidic fibrillary protein and carcinoembryonic antigen; only several cell groups expressed smooth muscle actin and desmin; muscle specific actin was uniformly negative. In differential diagnosis, it was important to distinguish malignant myoepitelioma mainly from pleomorphic adenoma (mixed tumor), benign myoepithelioma, carcinoma ex pleomorphic adenoma and malignant melanoma. The criteria of malignancy in myoepithelial tumors are discussed.
本文报告一例34岁女性腮腺恶性肌上皮瘤。在细针穿刺材料中,主要为黏附性差的多边形细胞,核异型性明显;未见有丝分裂象。局部还可见黏液样异染性细胞间物质碎片。组织学上,肿瘤有包膜,可见包膜局灶性侵犯及包膜血管内瘤栓形成。肿瘤主要为实性和黏液样,由具有上皮样特征、明显核大小不一和低有丝分裂活性的细胞组成。免疫组化显示,细胞S-100蛋白、波形蛋白、细胞角蛋白、胶质酸性纤维蛋白和癌胚抗原染色阳性;仅少数细胞群表达平滑肌肌动蛋白和结蛋白;肌肉特异性肌动蛋白均为阴性。在鉴别诊断中,主要将恶性肌上皮瘤与多形性腺瘤(混合瘤)、良性肌上皮瘤、多形性腺瘤恶变及恶性黑色素瘤相鉴别。文中讨论了肌上皮肿瘤的恶性标准。