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唾液腺的嗜酸细胞瘤:临床病理和免疫组化研究。

Oncocytoma of the salivary glands: a clinicopathologic and immunohistochemical study.

机构信息

Department of Oral Pathology, Peking University School and Hospital of Stomatology, Beijing, PR China.

出版信息

Oral Oncol. 2009 Dec;45(12):e232-8. doi: 10.1016/j.oraloncology.2009.08.004. Epub 2009 Sep 30.

Abstract

We present a clinicopathologic and immunohistochemical study of 21 Chinese patients with oncocytoma of salivary gland origin, a rare benign tumour composed exclusively of large epithelial cells with eosinophilic granular cytoplasm (oncocytes). The median age was 60.1 years with a male predominance (67%). All the tumours occurred in the parotid except one in the palate. A painless mass was the most common feature, although intermittent pain was complained of in four cases. All the patients were treated by superficial parotidectomy, with no recurrence or metastasis. Histologically, most tumours displayed an encapsulated nodular growth pattern, but one case presented with an aggressive growing tendency. Typical oncocytes were observed in all cases, with one clear cell variant found. The oncocytes were arranged in solid sheets, trabecular or duct-like structures. Rarely, small foci of hemorrhage or lymphoid stroma were observed, but germinal centres were always absent. Phosphotungstic acid hematoxylin staining illustrated dark-blue cytoplasmic granules, demonstrated as mitochondria by electron microscopy. All the tumours showed immunoreactivity for CK5/6, CK8/18, CK10/13, CK19 and EMA, but were negative for SMA or S-100. MIB-1 antibody, used to identify the dividing cells by staining of the nucleus, was found to stain the cytoplasm of the oncocytes. In summary, clinical diagnosis for an oncocytoma is challenging for its similar features to other benign tumours. Histopathological diagnosis is reliable with histochemical and electron microscopic conformation of the oncocytes, but differential diagnosis is still challenging. MIB-1 immunostaining might be considered as a diagnostic aid.

摘要

我们报告了 21 例源自唾液腺的嗜酸细胞瘤的临床病理和免疫组化研究,这是一种罕见的良性肿瘤,仅由具有嗜酸性颗粒细胞质(嗜酸性细胞)的大上皮细胞组成。中位年龄为 60.1 岁,男性居多(67%)。除 1 例发生在腭部外,所有肿瘤均发生在腮腺。最常见的特征是无痛性肿块,尽管有 4 例患者诉间歇性疼痛。所有患者均行腮腺浅叶切除术治疗,无复发或转移。组织学上,大多数肿瘤表现为包膜性结节生长模式,但有 1 例表现出侵袭性生长趋势。所有病例均观察到典型的嗜酸细胞瘤,其中发现 1 例透明细胞变异型。嗜酸细胞瘤排列成实性片状、小梁状或管状结构。罕见情况下,观察到小灶性出血或淋巴间质,但始终无生发中心。磷钨酸苏木精染色显示深蓝色细胞质颗粒,电镜下表现为线粒体。所有肿瘤均对 CK5/6、CK8/18、CK10/13、CK19 和 EMA 具有免疫反应性,但对 SMA 或 S-100 呈阴性。MIB-1 抗体用于通过细胞核染色识别分裂细胞,发现其可染色嗜酸细胞瘤的细胞质。总之,由于其与其他良性肿瘤相似的特征,临床诊断嗜酸细胞瘤具有挑战性。组织病理学诊断可靠,通过组织化学和电镜证实嗜酸细胞瘤的存在,但鉴别诊断仍具有挑战性。MIB-1 免疫组化可能被视为一种诊断辅助手段。

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