Luo Shuai, Tian Xiaoxue, Xu Ting, Wang Jinjing
Department of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Front Oncol. 2024 Oct 16;14:1436178. doi: 10.3389/fonc.2024.1436178. eCollection 2024.
Myoepithelial carcinoma (MECA) is a malignant tumor primarily affecting the salivary gland, most frequently in the parotid gland. It can manifest as primary or secondary to pleomorphic adenoma or benign myoepithelioma. MECA exhibits aggressive behaviors. In particular, primary MECA is more aggressive, frequently recurring or metastasizing distantly. Its morphological and immunohistochemical characteristics overlap with various tumors, posing challenges in its recognization as a distinct entity. Consequently, MECA may be frequently misdiagnosed, mainly when occurred in the mammary gland. This chance for misdiagnosis poses significant challenges in clinical diagnosis and treatment.
A 77-year-old woman with a history of pleomorphic adenoma presented with a palpable lump in the right breast for 3 months. Subsequent core needle biopsy (CNB) and modified radical mastectomy were performed, with samples subjected to histopathological examination. Based on the patient's history, histomorphologic features, immunohistochemistry (IHC) results and results of FISH, the pathological diagnosis confirmed MECA in the mammary gland. Postoperative chemotherapy was administered, and the patient exhibited a favorable prognosis during a 40-month follow-up period.
Primary MECA in the mammary gland is exceedingly rare, metastasis from the salivary gland MECA to the mammary gland is even rarer and has not been previously reported. This study presents the first documented case of MECA originating from the parotid gland metastasizing to the mammary gland (also known as breast). Highlighting this case aims to raise awareness among clinical pathologists to prevent underdiagnosis and misdiagnosis of this tumor entity.
肌上皮癌(MECA)是一种主要影响唾液腺的恶性肿瘤,最常见于腮腺。它可表现为原发性,或继发于多形性腺瘤或良性肌上皮瘤。MECA具有侵袭性。特别是原发性MECA更具侵袭性,常复发或远处转移。其形态学和免疫组化特征与多种肿瘤重叠,将其识别为一个独特的实体具有挑战性。因此,MECA可能经常被误诊,主要是在发生于乳腺时。这种误诊的可能性给临床诊断和治疗带来了重大挑战。
一名77岁有过多形性腺瘤病史的女性,右乳出现可触及肿块3个月。随后进行了粗针穿刺活检(CNB)和改良根治性乳房切除术,并对样本进行了组织病理学检查。根据患者病史、组织形态学特征、免疫组化(IHC)结果和荧光原位杂交(FISH)结果,病理诊断确诊为乳腺MECA。术后给予化疗,患者在40个月的随访期内预后良好。
乳腺原发性MECA极其罕见,唾液腺MECA转移至乳腺更为罕见,此前未见报道。本研究首次记录了起源于腮腺并转移至乳腺(也称为乳房)的MECA病例。强调该病例旨在提高临床病理学家的认识,以防止对该肿瘤实体的漏诊和误诊。