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首页> 外文期刊>Clinical Cancer Investigation Journal >Sclerosing mucoepidermoid carcinoma of the submandibular gland: Report of two rare cases
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Sclerosing mucoepidermoid carcinoma of the submandibular gland: Report of two rare cases

机译:下颌下腺硬化性粘液表皮样癌:两例罕见病例报告

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Although mucoepidermoid carcinoma is the most common primary malignancy of the salivary glands, the sclerosing morphologic variant of this tumor is extremely rare, with only 15 reported cases. As its name suggests, sclerosing mucoepidermoid carcinoma is characterized by an intense central sclerosis that occupies the entirety of an otherwise typical tumor, frequently with an inflammatory infiltrate of plasma cells, eosinophils, and/or lymphocytes at its peripheral regions. The sclerosis associated with these tumors may obscure their typical morphologic features and result in diagnostic difficulties. Two cases of mucoepidermoid carcinoma of the submandibular gland associated with extensive central sclerosis and peripheral lymphoid response are reported. This unusual but distinctive variant of mucoepidermoid carcinoma can be difficult to recognize and may be confused with chronic sialoadenitis or even metastasis to an intra-parotid lymph node.
机译:尽管粘液表皮样癌是涎腺最常见的原发性恶性肿瘤,但这种肿瘤的硬化形态学变异极为罕见,仅报道了15例。顾名思义,硬化性粘液表皮样样癌的特征是强烈的中央硬化,其占据了整个原本典型的肿瘤,并在其周围区域经常发生浆细胞,嗜酸性粒细胞和/或淋巴细胞的炎性浸润。与这些肿瘤有关的硬化症可能掩盖其典型的形态学特征并导致诊断困难。据报道有两例颌下腺黏液表皮样癌,伴有广泛的中央硬化和外周淋巴样反应。粘液表皮样癌的这种异常但独特的变体可能难以辨认,并且可能与慢性唾液腺炎甚至腮腺内淋巴结转移相混淆。

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