Primary mucoepidermoid carcinoma of scalp: a case report.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2025-02-25 DOI:10.1186/s13256-025-05035-2
Jay Lodhia, Mujaheed Suleman, Vanessa Poppe, Felister Uisso, Zuwena Alhinai, Angela Pallangyo, Goodluck Ndibalema, Happiness Rabiel
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Abstract

Background: Mucoepidermoid carcinoma of the skin is an exceedingly rare neoplasm, with only a limited number of cases documented in the literature. Typically, mucoepidermoid carcinoma arises in the salivary glands, where it accounts for 30% of all malignant salivary gland tumors and generally presents as a low-grade malignancy with a low probability of metastasis.

Case presentation: We report a case of a 49-year-old female patient of African origin who presented to our tertiary center with a longstanding scalp lesion that had been present for approximately 10 years. Initially, the lesion was roughly the size of a tennis ball and remained stable until about 3 months prior to presentation, when it was excised at a peripheral primary health center. Unfortunately, no histological analysis or follow-up was conducted after the excision, and the lesion recurred, progressively increasing in size. The patient reported no cardinal B-symptoms or central nervous system symptoms at any point. Histopathological analysis of the recurrent mass confirmed a diagnosis of mucoepidermoid carcinoma, and a complete surgical excision was subsequently performed. Following surgery, the patient was referred to the national oncology center for radiotherapy as part of her comprehensive oncological management. She is currently 8 months post-excision, receiving radiotherapy, and exhibits no clinical signs of recurrence.

Conclusion: Mucoepidermoid carcinoma originating in cutaneous sites is particularly unusual and may stem from the embryonic development of ectopic salivary glands within the skin. In this case report, we describe a unique presentation of primary mucoepidermoid carcinoma on the scalp, which demonstrated aggressive characteristics with suspected metastasis to the vertebral body. This case highlights the importance of considering mucoepidermoid carcinoma in the differential diagnosis of scalp masses and underscores the need for further investigation into its pathogenesis and metastatic potential.

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头皮原发性黏液表皮样癌1例。
背景:皮肤粘液表皮样癌是一种极为罕见的肿瘤,文献记载的病例数量有限。粘液表皮样癌通常发生于唾液腺,占所有恶性唾液腺肿瘤的30%,通常表现为低级别恶性肿瘤,转移概率低。病例介绍:我们报告了一个49岁的非洲裔女性患者,她以大约10年的长期头皮病变来到我们的三级中心。最初,病变约为网球大小,并保持稳定,直到发病前约3个月,在周边初级卫生中心切除。不幸的是,切除后没有进行组织学分析或随访,病变复发,体积逐渐增大。患者在任何时候均未报告基本b症状或中枢神经系统症状。复发肿块的组织病理学分析证实了粘液表皮样癌的诊断,并随后进行了完全的手术切除。手术后,患者被转到国家肿瘤中心进行放射治疗,作为其综合肿瘤治疗的一部分。她目前在手术后8个月,正在接受放疗,无临床复发迹象。结论:起源于皮肤部位的黏液表皮样癌特别罕见,可能源于皮肤内异位唾液腺的胚胎发育。在这个病例报告中,我们描述了一个独特的原发性头皮粘液表皮样癌的表现,其表现出侵袭性特征,怀疑转移到椎体。本病例强调了在头皮肿块鉴别诊断中考虑黏液表皮样癌的重要性,并强调了进一步研究其发病机制和转移潜力的必要性。
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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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