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.

PubMed

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.