Oyama Takeru, Shioya Akihiro, Ikeda Hiroko, Maeda Daichi, Yamada Sohsuke
Department of Pathology and Laboratory Medicine, School of Medicine, Kanazawa Medical University, Uchinada, JPN.
Department of Diagnostic Pathology, Kanazawa University Hospital, Kanazawa, JPN.
Cureus. 2024 Aug 24;16(8):e67697. doi: 10.7759/cureus.67697. eCollection 2024 Aug.
Myoepitheliomas are rare salivary gland-type tumors. The tumors are divided into four histological subtypes (spindle cell, plasmacytoid, epithelioid, and clear cell) and two variants (reticular and mucinous). A myoepithelioma of the mucinous variant, also referred to as mucinous or secretory myoepithelioma, is a novel variant of myoepithelioma characterized by the presence of extracellular mucin. To date, only six benign mucinous myoepitheliomas have been reported. We herein report an 84-year-old man with a four-month history of swelling in the left bucca. Computed tomography revealed a well-demarcated elliptical mass measuring 30 mm in diameter. Fine-needle aspiration (FNA) smears showed an acellular spherical matrix surrounded by basaloid cells with scant cytoplasm resembling mucous globules, in addition to clusters of spindle cells. The mass was initially diagnosed as a pleomorphic adenoma based on the presence of a mucous globule-like structure and cytological variation. The surgically resected tumor showed two different histological components: one was composed of cells arranged in thin cords with a mucoid stroma showing a "sieve-like" structure and the other component was spindle cells. Alcian blue staining confirmed extracellular mucin in both tumor components. The tumor was suspected of being a mucinous myoepithelioma. We encountered a case of a mucinous myoepithelioma with two unique features, namely its cytological features of mucous globules composed of monotonous basaloid cells in the FNA smear and its histological feature of a "sieve-like" structure. The presence of mucous globules in FNA smears might require the inclusion of the mucinous myoepithelioma in the differential diagnosis.
肌上皮瘤是罕见的涎腺型肿瘤。这些肿瘤分为四种组织学亚型(梭形细胞型、浆细胞样型、上皮样型和透明细胞型)和两种变异型(网状型和黏液型)。黏液型变异型肌上皮瘤,也称为黏液性或分泌性肌上皮瘤,是肌上皮瘤的一种新型变异型,其特征是存在细胞外黏液。迄今为止,仅报道过6例良性黏液性肌上皮瘤。我们在此报告1例84岁男性,其左颊部肿胀4个月。计算机断层扫描显示一个边界清晰的椭圆形肿块,直径30 mm。细针穿刺(FNA)涂片显示,除梭形细胞簇外,还有一个无细胞的球形基质,其周围是基底样细胞,胞质稀少,类似黏液球。基于黏液球样结构和细胞学变异,该肿块最初被诊断为多形性腺瘤。手术切除的肿瘤显示出两种不同的组织学成分:一种由排列成细条索状的细胞组成,伴有呈“筛状”结构的黏液样基质,另一种成分是梭形细胞。阿尔辛蓝染色证实两种肿瘤成分中均存在细胞外黏液。该肿瘤疑似为黏液性肌上皮瘤。我们遇到1例具有两个独特特征的黏液性肌上皮瘤,即FNA涂片中由单一基底样细胞组成的黏液球的细胞学特征及其“筛状”结构的组织学特征。FNA涂片中存在黏液球可能需要在鉴别诊断中考虑黏液性肌上皮瘤。