Sclerosing Central Mucoepidermoid Carcinoma: Rare Case Series and Review

A. Haleem, R. R. Al-Ani
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Abstract

Introduction: The most frequent malignant tumour of the salivary glands is mucoepidermoid carcinoma which accounts for 30% of all malignancies of the salivary glands. There are numerous histologic variations with various levels of differentiation. Sclerosing MEC (SMEC) is a rare subtype of MEC that has the potential to be misdiagnosed as a low-grade non-SMEC malignancy or a benign reactive condition. There have been no cases of the extremely rare sclerosing variant of central or intraosseous MEC reported as of yet. Case reports: We present two cases of Sclerosing Central MEC, in which histologic analysis revealed relatively well-circumscribed, nonencapsulated tumours made up of dispersed epithelial islands of low-grade MEC and extensive central sclerosis. Similar sclerotic stroma was present in the tumor in the second case, but the epithelial component was of intermediate grade. Both cases showed abundant intracytoplasmic mucin and positive Mayer mucicarmine and PAS stains. Conclusions: Sclerosing central mucoepidermoid carcinoma was identified as the cause. Both cases underwent a complete resection of the tumor and have since been free of the disease.
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硬化性中央黏液表皮样癌:罕见病例系列及回顾
涎腺最常见的恶性肿瘤是粘液表皮样癌,占所有涎腺恶性肿瘤的30%。有许多不同程度分化的组织学变异。硬化性MEC (SMEC)是一种罕见的MEC亚型,有可能被误诊为低级别非SMEC恶性肿瘤或良性反应性疾病。到目前为止,还没有极为罕见的中央或骨内MEC硬化变体的病例报道。病例报告:我们报告了两例硬化性中央MEC,其中组织学分析显示相对明确的,非包膜肿瘤由分散的低级别MEC上皮岛和广泛的中央硬化组成。第二例肿瘤中也有类似的硬化间质,但上皮成分为中等级别。两例均显示胞浆内黏液蛋白丰富,Mayer黏液胺和PAS染色阳性。结论:硬化性中心性黏液表皮样癌为病因。这两个病例都接受了肿瘤的完全切除,并从此摆脱了疾病。
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审稿时长
12 weeks
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