Carapina Mirela, Jurić Mario, Bubalo Pero, Leventić Miro
Clinical Institute of Pathology, Cytology and Forensic Medicine, University Hospital Mostar, Mostar, Bosnia and Herzegovina.
Coll Antropol. 2010 Mar;34 Suppl 1:283-6.
Rare malignant tumor of the salivary gland, a myoepithelial carcinoma, arose de novo in the right parotid gland. The initial tumor was composed predominantly of myoepithelial cells. Subsequently the tumor recurred three times, with infiltration of the bones of the cranial base. Histological examination showed sarcomatoid neoplasm composed of malignant spindle cells with high mitotic rate and perineural invasion. There was no involvement of cervical lymph nodes. Immunohistochemistry demonstrated myoepithelial differentiation: tumor cells were positively stained with vimentin, alpha smooth muscle actin and S-100 protein antibodies, and focal positively was noticed with cytokeratin (AE1/AE3) antibody. Large number of tumor cells nuclei was reactive with the monoclonal anti-p63 antibody, clone 4A4. Myoepithelial carcinomas exhibit a wide spectrum of morphological heterogeneity and for that reason could be confused with many tumors. Cytoarchitectural patterns and immunohistochemical profile are crucial for identification. These tumors are malignant neoplasms with diverse clinical outcomes, sometimes very aggressive.
涎腺罕见恶性肿瘤——肌上皮癌,原发于右侧腮腺。初始肿瘤主要由肌上皮细胞构成。随后肿瘤复发三次,侵犯颅底骨质。组织学检查显示为肉瘤样肿瘤,由有高有丝分裂率的恶性梭形细胞组成,并伴有神经周围侵犯。颈部淋巴结未受累。免疫组化显示肌上皮分化:肿瘤细胞波形蛋白、α平滑肌肌动蛋白和S-100蛋白抗体呈阳性染色,细胞角蛋白(AE1/AE3)抗体呈局灶阳性。大量肿瘤细胞核与单克隆抗p63抗体(克隆号4A4)反应阳性。肌上皮癌表现出广泛的形态学异质性,因此可能与许多肿瘤混淆。细胞结构模式和免疫组化特征对于鉴别至关重要。这些肿瘤是具有不同临床结局的恶性肿瘤,有时极具侵袭性。