Suppr超能文献

痣样基底细胞癌综合征(戈林综合征):一例报告

Nevoid basal cell carcinoma syndrome (Gorlin syndrome): a case report.

作者信息

Abdul Rahman Noura, Breim Fatima, Zakour Joud, Srouji Zainab, Ishkhanian Silva

机构信息

Department of Dermatology and Venereology, Faculty of Medicine, University of Aleppo, Aleppo, Syria.

Faculty of Medicine, University of Aleppo, Aleppo, Syria.

出版信息

J Med Case Rep. 2025 Jan 25;19(1):36. doi: 10.1186/s13256-025-05036-1.

Abstract

BACKGROUND

Basal cell nevus syndrome, also known as Gorlin or Gorlin-Goltz syndrome, is a hereditary condition caused by mutation in the PATCHED gene. The syndrome presents with a wide range of clinical manifestations, including basal cell carcinomas, jaw cysts, and skeletal anomalies. Diagnosis is based on specific criteria, and treatment typically includes surgical removal of basal cell carcinomas.

CASE PRESENTATION

A 36-year-old Middle Eastern man presented with multiple pigmented ulcerated lesions on his face, scalp, and trunk, consistent with basal cell carcinomas. A history of a previous jaw cyst excision and characteristic physical examination findings led to the diagnosis of Gorlin-Goltz syndrome. Treatment included surgical excision of high-risk lesions and intralesional 5-fluorouracil injections for superficial lesions. The patient showed positive responses to the treatment, with most lesions healing completely and others showing ongoing improvement. Minimal side effects were observed, highlighting the potential efficacy of this novel approach in managing basal cell carcinomas associated with Gorlin-Goltz syndrome.

CONCLUSION

Gorlin syndrome is a rare genetic disorder characterized by various clinical manifestations, with basal cell carcinomas being a prominent feature. Diagnosis is based on specific major and minor criteria, and a multidisciplinary approach is crucial for effective management. Basal cell carcinomas in Gorlin syndrome tend to occur more commonly in sun-exposed areas, necessitating sun protection. Treatment options include surgical excision, cryotherapy, photodynamic therapy, and topical chemotherapeutics, based on lesions characteristics. This case report describes a novel approach to treating multiple basal cell carcinomas associated with basal cell nevus syndrome using intralesional 5-fluorouracil injections. The observed side effects were minimal, demonstrating the potential efficacy of this treatment modality.

摘要

背景

基底细胞痣综合征,也称为戈林或戈林 - 戈尔茨综合征,是一种由PTCH基因的突变引起的遗传性疾病。该综合征表现出广泛的临床表现,包括基底细胞癌、颌骨囊肿和骨骼异常。诊断基于特定标准,治疗通常包括手术切除基底细胞癌。

病例报告

一名36岁的中东男子面部、头皮和躯干出现多个色素沉着的溃疡性病变,符合基底细胞癌的表现。既往有颌骨囊肿切除病史以及特征性的体格检查结果导致诊断为戈林 - 戈尔茨综合征。治疗包括手术切除高危病变以及对浅表病变进行皮损内注射5 - 氟尿嘧啶。患者对治疗有积极反应,大多数病变完全愈合,其他病变也在持续改善。观察到的副作用最小,突出了这种新方法在治疗与戈林 - 戈尔茨综合征相关的基底细胞癌方面的潜在疗效。

结论

戈林综合征是一种罕见的遗传性疾病,具有多种临床表现,基底细胞癌是其突出特征。诊断基于特定的主要和次要标准,多学科方法对于有效管理至关重要。戈林综合征中的基底细胞癌往往更常见于暴露于阳光的部位,因此需要防晒。治疗选择包括手术切除、冷冻疗法、光动力疗法和局部化疗,具体取决于病变特征。本病例报告描述了一种使用皮损内注射5 - 氟尿嘧啶治疗与基底细胞痣综合征相关的多发性基底细胞癌的新方法。观察到的副作用最小,证明了这种治疗方式的潜在疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a1a/11762882/85849ca3295b/13256_2025_5036_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验