European Interbalkan Medical Center, Pylaia, Greece.
3rd Surgical Department, University General Hospital of Thessaloniki "AHEPA", School of Medicine, Faulty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Am J Case Rep. 2023 Apr 24;24:e939117. doi: 10.12659/AJCR.939117.
BACKGROUND Gorlin syndrome, also known as basal cell nevus syndrome (BCNS), nevoid basal cell carcinoma syndrome (NBCCS), and Jaw cyst-Basal cell nevus-Bifid rib syndrome, is a rare multisystemic syndrome that can affect a remarkable number of tissues and organs in the human body. Patients with this syndrome are in jeopardy of developing basal cell skin cancer during puberty or early adulthood. CASE REPORT Herein, we report a case of a 58-year-old woman who had multiple pigmented skin lesions and a palpable tumor of the left scapula. The patient underwent surgical excision of the above-mentioned lesions. The histopathological examination revealed that 10 of them were basal cell skin carcinomas (BCCs); therefore, the patient was proven to have the syndrome. She had a history of similar skin lesions, which were removed before the age of 20. CONCLUSIONS This case highlights that rare phenomena, such as the presence of multiple BCCs, require additional investigations and a multidisciplinary approach since a rare and potentially life-threating condition might be the underlying cause. Early diagnosis of Gorlin syndrome is of paramount importance to facilitate the appropriate therapeutic approach, as directed by a multidisciplinary team. Patients with multiple skin lesions need to have regular assessments by their general practitioner or dermatologist, with dermoscopy serving as an important preventive measure. Furthermore, because pathogenesis of the syndrome is characterized by development of basal cell carcinomas, consecutive follow-up is of a great significance.
背景 基底细胞痣综合征(Gorlin 综合征),又称基底细胞痣病(BCNS)、基底细胞癌痣综合征(NBCCS)和颌骨囊肿-基底细胞痣-分叉肋综合征,是一种罕见的多系统综合征,可累及人体许多组织和器官。患有这种综合征的患者在青春期或成年早期有发生基底细胞皮肤癌的风险。
病例报告 在此,我们报告了一例 58 岁女性,她有多个色素性皮肤病变和左肩胛骨可触及的肿瘤。患者接受了上述病变的手术切除。组织病理学检查显示其中 10 个为基底细胞皮肤癌(BCC);因此,该患者被证实患有该综合征。她有类似皮肤病变的病史,这些病变在 20 岁之前已被切除。
结论 本例强调了罕见现象,如多发性 BCC 的存在,需要进行额外的调查和多学科方法,因为潜在的罕见且危及生命的疾病可能是潜在的原因。早期诊断 Gorlin 综合征至关重要,以便由多学科团队指导进行适当的治疗方法。多发性皮肤病变的患者需要由全科医生或皮肤科医生定期评估,皮肤镜检查是一种重要的预防措施。此外,由于该综合征的发病机制是基底细胞癌的发展,因此连续随访具有重要意义。
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