Shi Wangpan, Law Timothy, Brumund Kevin Thomas, Chang Jennifer, Patel Charmi, Lin Grace, Hu Jingjing
Department of Pathology, University of California, San Diego, CA, USA.
Department of Pathology, California Northstate University, College of Medicine, La Jolla, CA, USA.
Rare Tumors. 2024 Mar 23;16:20363613241242397. doi: 10.1177/20363613241242397. eCollection 2024.
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.
黏液表皮样癌(MEC)是腮腺常见的恶性肿瘤。MEC的诊断通常仅基于其形态学特征,其特征性地包含黏液细胞、中间细胞和表皮样细胞。然而,当囊性变弥漫时,将MEC与其他良性囊性肿瘤区分开来具有挑战性。这是一例58岁白种男性腮腺肿块的病例报告。肿块的苏木精-伊红(H&E)切片显示多房性囊肿,内衬外观平淡的上皮,仅有罕见的乳头结构。乳头增生包含黏液细胞,p63免疫组化研究突出显示了表皮样细胞。MAML2(11q21)重排阳性的荧光原位杂交(FISH)结果证实了诊断。患者接受了腮腺切除术,术后6个月无疾病。伴有囊性变的MEC是一个常见的诊断陷阱,可模仿唾液腺中的许多良性病变。我们报告了一例罕见的伴有广泛囊性改变的MEC病例,其分子和病理结果,并回顾了MEC的诊断特征、其良性模仿者以及区分这些实体的有用工具。