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涎腺透明细胞硬化性癌

Hyalinizing clear cell carcinoma of salivary gland.

作者信息

Milchgrub S, Gnepp D R, Vuitch F, Delgado R, Albores-Saavedra J

机构信息

Department of Pathology, University of Texas Southwestern Medical Center, Dallas 75235-9072.

出版信息

Am J Surg Pathol. 1994 Jan;18(1):74-82. doi: 10.1097/00000478-199401000-00007.

Abstract

We describe 11 patients with a distinctive salivary gland neoplasm. Most of the patients were adult women who presented with a painless mass. Nine tumors arose in minor salivary glands of the oral cavity (82%). Microscopically, they were characterized by the formation of trabeculae, cords, islands, and/or nests of monomorphic clear cells that were glycogen rich and mucin negative and were surrounded by hyalinized bands with foci of myxohyaline stroma. Cells with eosinophilic and granular cytoplasm were also noted. Both cell types showed minimal nuclear pleomorphism and a very low mitotic index. The neoplasms all had infiltrative borders. Immunohistochemically, the tumor cells expressed cytokeratins and epithelial membrane antigen, but not S-100 protein and smooth muscle actin. Ultrastructurally, the tumor cells contained abundant glycogen, desmosomes, peripheral tonofilaments, and prominent interdigitating microvilli without actin myofilaments or dense bodies. These immunohistochemical and ultrastructural findings provide evidence of epithelial differentiation without myoepithelial differentiation. For these tumors, we propose the name, hyalinizing clear cell carcinoma (HCCC). These are low-grade malignant neoplasms. Two patients had ipsilateral cervical lymph node metastases at presentation, but with surgical excision and either preoperative or post-operative radiotherapy in three cases, eight of 10 patients with clinical follow-up are alive and well without evidence of recurrence. The mean clinical follow-up is 3.6 years, with a range of 6 months to 11 years. One patient died as a result of surgery, another died of unrelated causes, and one patient was lost to follow-up.

摘要

我们描述了11例患有一种独特唾液腺肿瘤的患者。大多数患者为成年女性,表现为无痛性肿块。9个肿瘤发生于口腔小唾液腺(82%)。显微镜下,其特征为形成梁状、索状、岛状和/或巢状的单形性透明细胞,这些细胞富含糖原且黏液阴性,周围有玻璃样变带及黏液透明基质灶。还可见到具有嗜酸性和颗粒状细胞质的细胞。两种细胞类型均显示核异型性极小且有丝分裂指数极低。这些肿瘤均具有浸润性边界。免疫组化显示,肿瘤细胞表达细胞角蛋白和上皮膜抗原,但不表达S-100蛋白和平滑肌肌动蛋白。超微结构上,肿瘤细胞含有丰富的糖原、桥粒、周边张力丝和突出的指状微绒毛,无肌动蛋白微丝或致密小体。这些免疫组化和超微结构结果提供了上皮分化而非肌上皮分化的证据。对于这些肿瘤,我们提议命名为透明细胞癌(HCCC)。这些是低级别恶性肿瘤。2例患者初诊时出现同侧颈部淋巴结转移,但经手术切除,3例患者接受了术前或术后放疗,10例接受临床随访的患者中有8例存活且情况良好,无复发迹象。平均临床随访时间为3.6年,范围为6个月至11年。1例患者死于手术,另1例死于无关原因,1例患者失访。

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