A case of myoepithelioma in the upper lip

Q3 Dentistry
Shuji Yoshida , Akira Watanabe , Yoshihiko Akashi , Kenichi Matsuzaka , Masayuki Takano
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引用次数: 0

Abstract

A myoepithelioma is a type of salivary gland tumor composed entirely of myoepithelial cells. Previously, this was considered a subtype of pleomorphic adenoma. Here, we report an extremely rare case of myoepithelioma of the upper lip. A 33-year-old female patient presented with a painless mass on her upper lip. Magnetic resonance imaging revealed a 23 mm × 18 mm well-defined tumor. We clinically suspected a benign minor salivary gland tumor and the patient underwent complete resection of the tumor under general anesthesia. Since the tumor was diagnosed as a myoepithelioma by rapid pathological examination, it was resected with a safety margin of approximately 5 mm. Pathologically, this tumor showed mild to moderate cell atypia, and focal invasion into the capsule. Immunohistochemical findings showed that the tumor was positive for the S-100 protein and vimentin. The Ki-67 labeling index was less than 1%, and there were no malignant findings. The postoperative clinical course has been good for approximately 5 years, and satisfactory results were obtained both functionally and esthetically. Herein, we also discussed the clinical and immunohistochemical features of myoepitheliomas.

上唇肌上皮瘤1例
肌上皮瘤是一种完全由肌上皮细胞组成的唾液腺肿瘤。以前,这被认为是多形性腺瘤的一种亚型。在这里,我们报告了一个极其罕见的上唇肌上皮瘤病例。一位33岁的女性患者上唇出现无痛肿块。磁共振成像显示一个23毫米×18毫米的清晰肿瘤。我们临床上怀疑是良性小涎腺肿瘤,患者在全身麻醉下接受了肿瘤的完全切除。由于该肿瘤通过快速病理检查被诊断为肌上皮瘤,因此以约5毫米的安全裕度切除。病理学上,该肿瘤显示轻度至中度细胞异型性,并局灶性侵犯包膜。免疫组化结果显示肿瘤S-100蛋白和波形蛋白阳性。Ki-67标记指数小于1%,无恶性发现。术后临床过程良好约5年,在功能和美观方面都取得了令人满意的结果。在此,我们还讨论了肌上皮瘤的临床和免疫组织化学特征。
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来源期刊
Oral and Maxillofacial Surgery Cases
Oral and Maxillofacial Surgery Cases Medicine-Otorhinolaryngology
CiteScore
0.60
自引率
0.00%
发文量
43
审稿时长
69 days
期刊介绍: Oral and Maxillofacial Surgery Cases is a surgical journal dedicated to publishing case reports and case series only which must be original, educational, rare conditions or findings, or clinically interesting to an international audience of surgeons and clinicians. Case series can be prospective or retrospective and examine the outcomes of management or mechanisms in more than one patient. Case reports may include new or modified methodology and treatment, uncommon findings, and mechanisms. All case reports and case series will be peer reviewed for acceptance for publication in the Journal.
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