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Updated: May 20, 2025

Cell Population Analyses During Skin Carcinogenesis
Published on: August 21, 2013
Recurrent Metastatic Basal Cell Carcinomas of the Face in a Patient with Gorlin-Goltz Syndrome
Petko Petrov1, Dobromira Shopova2, Georgi Goranov3
1Department of Maxillofacial Surgery, Faculty of Dental Medicine, Medical University-Plovdiv, 4000 Plovdiv, Bulgaria.
Abstract:
Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome (NBCCS), is a rare, inherited autosomal dominant disorder primarily caused by mutations in the PTCH1 gene, which regulates the Hedgehog signaling pathway. This genetic defect leads to the uncontrolled proliferation of basal cells, resulting in the formation of multiple basal cell carcinomas (BCCs) and odontogenic keratocysts (OKCs). This study aims to present a complex clinical case of a patient with Gorlin-Goltz syndrome who developed multiple recurrent metastatic basal cell carcinomas on the facial region, detailing the multidisciplinary treatment strategies employed and the challenges encountered during the management of the disease. The patient, diagnosed with a pathogenic PTCH1 gene mutation, underwent a series of treatment interventions over several years. These included multiple surgical excisions aimed at tumor removal, diverse radiotherapy approaches for residual or inoperable lesions, and systemic targeted therapy with Hedgehog pathway inhibitors to control tumor progression. The recurrent and aggressive nature of the basal cell carcinomas resulted in extensive facial tissue loss, posing significant challenges for radical tumor excision and subsequent reconstructive procedures. Multimodal therapeutic strategies, including Mohs micrographic surgery for precise tumor clearance and targeted systemic therapy with vismodegib, were implemented. However, the aggressive progression of lesions required ongoing surgical interventions, highlighting the limitations of current treatment modalities in achieving long-term disease control. This case underscores the critical need for a comprehensive, multidisciplinary approach to managing Gorlin-Goltz syndrome. Successful management requires close collaboration between dermatologists, oncologists, maxillofacial surgeons, and plastic surgeons to balance effective tumor control with optimal functional and aesthetic outcomes. The integration of advanced surgical techniques and targeted molecular therapies shows promise in improving patient outcomes. Nonetheless, early diagnosis, rigorous follow-up, and patient education remain essential components in minimizing disease progression and enhancing the quality of life for affected individuals.
Insights
Gorlin-Goltz syndrome (nevoid basal cell carcinoma syndrome) involves PTCH1 gene mutations, leading to aggressive basal cell carcinomas. This case highlights challenges in managing recurrent facial tumors, emphasizing multidisciplinary care and targeted therapies.
Area of Science:
- Genetics and Molecular Biology
- Dermatology
- Oncology
Background:
- Gorlin-Goltz syndrome (nevoid basal cell carcinoma syndrome) is an autosomal dominant disorder caused by PTCH1 gene mutations affecting Hedgehog signaling.
- This leads to uncontrolled basal cell proliferation, manifesting as basal cell carcinomas (BCCs) and odontogenic keratocysts (OKCs).
Observation:
- A complex case of Gorlin-Goltz syndrome with multiple, recurrent, metastatic facial BCCs is presented.
- The patient experienced extensive facial tissue loss due to aggressive tumor progression, complicating treatment.
Findings:
- Multimodal treatment included surgical excisions, radiotherapy, and Hedgehog pathway inhibitors (vismodegib).
- Despite interventions like Mohs surgery and targeted therapy, aggressive recurrence necessitated ongoing surgical management, indicating treatment limitations.
Implications:
- This case underscores the need for a multidisciplinary approach involving dermatology, oncology, and surgery for Gorlin-Goltz syndrome.
- Integrating advanced surgical techniques and molecular therapies is crucial for improving outcomes, alongside early diagnosis and patient education.
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