Myoepithelial carcinoma of the skin: a case report.

IF 0.5 Q4 SURGERY Journal of Surgical Case Reports Pub Date : 2025-03-19 eCollection Date: 2025-03-01 DOI:10.1093/jscr/rjaf151
Sarra Ben Rejeb, Yasmine Chaabane, Amani Hachicha, Senda Turki
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Abstract

Cutaneous myoepithelial carcinoma (MEC) is extremely rare and its diagnosis is challenging due to its broad morphological spectrum. We reported the case of a 50-year-old woman with a 7 mm cutaneous nodule on the left nasal wing, initially misdiagnosed as a fibrous papule. The lesion recurred 6 months after excision. Histopathological analysis revealed a dermal neoplasm with epithelioid cells exhibiting moderate atypia and mitotic activity. Immunohistochemical analysis confirmed a myoepithelial phenotype with positive staining for CK7 and S-100, while excluding adnexal, vascular, muscular, histiocytic, plasmacytic, and melanocytic origins. A diagnosis of primary cutaneous MEC was established. The patient underwent complete surgical excision with clear margins, and no recurrence or metastasis was observed after 6 years of follow-up. This case highlights the diagnostic challenges associated with primary cutaneous MEC and underscores the importance of complete surgical excision. Increased awareness and further case reporting are necessary to refine diagnostic and therapeutic approaches for this rare malignancy.

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皮肤肌上皮癌1例报告。
皮肤肌上皮癌(MEC)是非常罕见的,其诊断是具有挑战性的,由于其广泛的形态学谱。我们报告了一例50岁的女性,在左鼻翼有一个7毫米的皮肤结节,最初被误诊为纤维丘疹。病变在切除后6个月复发。组织病理学分析显示真皮肿瘤上皮样细胞表现出中度异型性和有丝分裂活性。免疫组织化学分析证实了肌上皮表型,CK7和S-100染色阳性,而排除了附件、血管、肌肉、组织细胞、浆细胞和黑素细胞起源。建立了原发性皮肤MEC的诊断。患者行手术切除,边缘清晰,随访6年未见复发转移。该病例强调了原发性皮肤MEC的诊断挑战,并强调了完全手术切除的重要性。提高认识和进一步的病例报告是必要的,以完善诊断和治疗方法,为这种罕见的恶性肿瘤。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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