模仿唾液腺良性囊性病变的低级别粘液表皮样癌:诊断难题。

IF 0.9 Q4 ONCOLOGY
Rare Tumors Pub Date : 2024-03-23 eCollection Date: 2024-01-01 DOI:10.1177/20363613241242397
Wangpan Shi, Timothy Law, Kevin Thomas Brumund, Jennifer Chang, Charmi Patel, Grace Lin, Jingjing Hu
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引用次数: 0

摘要

黏液表皮样癌(MEC)是一种常见的腮腺恶性肿瘤。腮腺黏液表皮样癌的诊断通常仅依据其形态特征,其特征是含有黏液细胞、中间细胞和表皮样细胞。然而,当囊性变性呈弥漫性时,要将 MEC 与其他良性囊性肿瘤区分开来就很困难了。本病例报告的是一名 58 岁的白种男子,他出现了腮腺肿块。肿块的 H&E 切片显示,多发性囊肿内衬为平淡无奇的上皮,仅有罕见的乳头状结构。乳头状增生包含粘液细胞和表皮细胞,p63 免疫组化检查结果突出显示了这一点。FISH结果显示MAML2(11q21)重排阳性,确诊该病。患者接受了腮腺切除术,术后6个月无病。MEC伴囊性变性是一种常见的诊断误区,它可以模拟唾液腺中的许多良性病变。我们介绍了一例罕见的伴有广泛囊变的MEC病例、其分子和病理结果,并回顾了MEC的诊断特征、其良性假象以及区分这些实体的有用工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-grade mucoepidermoid carcinoma mimicking benign cystic lesions in the salivary gland: A diagnostic dilemma.

Mucoepidermoid carcinoma (MEC) is a common malignancy arising in the parotid gland. The diagnosis of MEC is typically based on its morphological features alone, characteristically containing mucocytes, intermediate cells and epidermoid cells. However, when cystic degeneration is diffuse, it is challenging to distinguish MEC from other benign cystic tumors. This is a case report of a 58-year-old Caucasian man who presented with a parotid mass. H&E sections of the mass reveal multiloculated cysts lined by bland-looking epithelium with only rare papillary architectures. The papillary proliferation contains mucocytes, and epidermoid cells highlighted by the p63 immunohistochemistry study. The diagnosis was confirmed by FISH result of positive MAML2 (11q21) rearrangement. Patient underwent parotidectomy and is disease-free 6 months post-surgery. MEC with cystic degeneration is a common diagnostic pitfall which can mimic many benign lesions in the salivary gland. We present a rare case with MEC with extensive cystic change, its molecular and pathologic findings and review the diagnostic features of MEC, its benign mimickers and useful tools for distinguishing these entities.

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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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