Amano Yusuke, Sakaguchi-Tamba Mio, Sasaki Yumiko, Oshiro Hisashi, Fukushima Noriyoshi, Fujita Takashi, Masuda Shinobu, Niki Toshiro
Department of Pathology.
Department of Breast Surgery, Jichi Medical University, Shimotsuke, Tochigi.
Medicine (Baltimore). 2020 Oct 16;99(42):e22665. doi: 10.1097/MD.0000000000022665.
Breast adenomyoepithelioma (AME) is a rare tumor composed of myoepithelial cells and ductal or luminal cells. Most cases of AME are benign, but rare cases in which either or both cell types exhibited malignant features have been reported. Due to its rarity, no diagnostic criteria for malignancy have been established for AME.
A 64-year-old woman presented with a mass in her right breast. Fine-needle aspiration cytology and biopsy examinations revealed lesions composed of spindle-shaped cells and round epithelial cells. AME was suspected, and partial mastectomy was performed.
The tumor specimen showed AME, which mainly consisted of spindle-shaped myoepithelial cells with slight atypia, admixed with tubular luminal cells and small areas of atypical intraductal proliferative lesions. No apparent features of malignancy, such as necrosis or invasion, were seen in the myoepithelial cells or the luminal or intraductal component. However, the atypical intraductal component exhibited focal nuclear atypia, a cribriform pattern, and moderate to strong membranous human epidermal growth factor receptor 2 (HER2) immunoreactivity. HER2 amplification was detected in focal regions of the atypical intraductal component by fluorescence in situ hybridization (FISH), which resulted in a diagnosis of AME with ductal carcinoma in situ.
The patient did not receive further therapy and was free from tumor recurrence at 23 months after the operation.
HER2 FISH might be useful for evaluating suspected AME tumors for malignancy when an atypical ductal lesion that lacks definitive features of malignancy is encountered.
乳腺腺肌上皮瘤(AME)是一种由肌上皮细胞和导管或管腔细胞组成的罕见肿瘤。大多数AME病例为良性,但也有报道称罕见病例中一种或两种细胞类型表现出恶性特征。由于其罕见性,尚未建立AME的恶性诊断标准。
一名64岁女性因右乳肿块就诊。细针穿刺细胞学检查和活检显示病变由梭形细胞和圆形上皮细胞组成。怀疑为AME,遂行部分乳房切除术。
肿瘤标本显示为AME,主要由轻度异型性的梭形肌上皮细胞组成,混有管状管腔细胞和小面积的非典型导管内增生性病变。在肌上皮细胞、管腔或导管内成分中未见明显的恶性特征,如坏死或浸润。然而,非典型导管内成分表现出局灶性核异型性、筛状结构以及中度至强的膜性人表皮生长因子受体2(HER2)免疫反应性。通过荧光原位杂交(FISH)在非典型导管内成分的局灶区域检测到HER2扩增,从而诊断为伴有导管原位癌的AME。
患者未接受进一步治疗,术后23个月无肿瘤复发。
当遇到缺乏明确恶性特征的非典型导管病变时,HER2 FISH可能有助于评估疑似AME肿瘤的恶性程度。