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

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2025-01-25 DOI:10.1186/s13256-025-05036-1
Noura Abdul Rahman, Fatima Breim, Joud Zakour, Zainab Srouji, Silva Ishkhanian
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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.

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瘤状基底细胞癌综合征(Gorlin综合征)1例。
背景:基底细胞痣综合征,也称为Gorlin或Gorlin- goltz综合征,是一种由补丁基因突变引起的遗传性疾病。该综合征表现为广泛的临床表现,包括基底细胞癌、颌骨囊肿和骨骼异常。诊断是基于特定的标准,治疗通常包括手术切除基底细胞癌。病例介绍:一名36岁中东男性,其面部、头皮和躯干出现多发性色素溃疡性病变,符合基底细胞癌。先前的颌骨囊肿切除史和特征性的体格检查结果导致了Gorlin-Goltz综合征的诊断。治疗包括手术切除高危病变和5-氟尿嘧啶局部注射浅表病变。患者对治疗表现出积极的反应,大多数病变完全愈合,其他病变正在改善。观察到最小的副作用,突出了这种新方法在治疗与Gorlin-Goltz综合征相关的基底细胞癌方面的潜在疗效。结论:Gorlin综合征是一种罕见的遗传性疾病,临床表现多样,以基底细胞癌为突出特征。诊断是基于特定的主要和次要标准,多学科的方法是有效管理的关键。Gorlin综合征的基底细胞癌更常发生在阳光照射的区域,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,基于病变特征。本病例报告描述了一种使用5-氟尿嘧啶注射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。观察到的副作用很小,证明了这种治疗方式的潜在疗效。
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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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