Losito Nunzia Simona, Botti Gerardo, Ionna Franco, Pasquinelli Gianandrea, Minenna Pasquale, Bisceglia Michele
Department of Pathology, National Cancer Institute, Fondazione G. Pascale, Naples, Italy.
Pathol Res Pract. 2008;204(5):335-44. doi: 10.1016/j.prp.2007.11.006. Epub 2008 Jan 18.
Myoepithelial carcinoma (MC) is an uncommon neoplasm of the salivary glands, and cases of the clear-cell (CC) variant are extremely rare. Two cases of MC of the CC variant arising in the left submandibular gland are described herein. Both cases, which involved elderly women, almost exclusively consisted of large glycogen-rich CCs. Both cases were immunopositive for several epithelial and myoepithelial markers, and electron microscopy (EM) demonstrated hybrid epithelial and myoid differentiation in both. Case 1 arose in a pre-existing pleomorphic adenoma ("ex mixed tumor MC"), while Case 2 was a "de novo MC". CC-MC is an aggressive tumor with frequent recurrence, lymph node, and systemic metastases. A total of 14 cases of this type of neoplasm have been reported so far in the salivary glands, two arising from the submandibular gland. To date, only four cases have been studied using EM. The cases of CC-MC presented here are the third and fourth ones, respectively, originating from the submandibular glands, and the first two cases arising from this location, in which EM investigation succeeded in demonstrating myoepithelial differentiation. CC-MC needs to be distinguished from diverse primary and secondary CC neoplasms.
肌上皮癌(MC)是涎腺的一种罕见肿瘤,透明细胞(CC)变异型病例极为罕见。本文描述了2例发生于左下颌下腺的CC变异型MC。这2例均为老年女性,几乎完全由富含糖原的大透明细胞组成。2例对多种上皮和肌上皮标志物均呈免疫阳性,电子显微镜(EM)显示二者均有上皮和肌样混合分化。病例1发生于先前存在的多形性腺瘤(“混合瘤型MC”),而病例2为“原发性MC”。CC-MC是一种侵袭性肿瘤,常复发,易发生淋巴结转移和全身转移。迄今为止,涎腺中总共报道了14例这种类型的肿瘤,其中2例起源于下颌下腺。到目前为止,仅有4例使用EM进行了研究。本文报道的CC-MC病例分别是起源于下颌下腺的第3例和第4例,也是该部位前2例成功通过EM研究证实有肌上皮分化的病例。CC-MC需要与多种原发性和继发性CC肿瘤相鉴别。