Oral Lichen Planus: A Narrative Review Navigating Etiologies, Clinical Manifestations, Diagnostics, and Therapeutic Approaches

Author:

Nukaly Houriah Yasir1ORCID,Halawani Ibrahim R.2ORCID,Alghamdi Saja Mohammed S.3,Alruwaili Araa Ghanem4,Binhezaim Alhanouf5,Algahamdi Rana Ali A.3ORCID,Alzahrani Rayan Abdullah J.3,Alharamlah Faisal Saad S.6ORCID,Aldumkh Shahad Hamad S.7,Alasqah Hamad Majid A.8,Alamri Awadh910,Jfri Abdulhadi911

Affiliation:

1. Medicine Program, Batterjee Medical College, Jeddah 21442, Saudi Arabia

2. Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia

3. College of Medicine, Albaha University, Albaha 65799, Saudi Arabia

4. College of Medicine, Jouf University, Sakaka 72388, Saudi Arabia

5. Saudi Board in Pediatric Dentistry [SB-PD], Department of Pedodontics, Prince Sultan Military Medical City, Riyadh 12233, Saudi Arabia

6. College of Dentistry, Imam Abdulrahman Bin Faisal University, Dammam 34212, Saudi Arabia

7. College of Medicine, King Saud University, Riyadh 11421, Saudi Arabia

8. College of Dentistry, King Saud University, Riyadh 11421, Saudi Arabia

9. College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Jeddah 11481, Saudi Arabia

10. King Abdulaziz Medical City, Jeddah 22384, Saudi Arabia

11. King Abdullah International Medical Research Center, Jeddah 21423, Saudi Arabia

Abstract

Background/Objectives: Oral Lichen Planus (OLP) is a common immune-mediated inflammatory disorder affecting the oral mucosa, impacting 0.5% to 2% of the global population, primarily middle-aged women. Immunological dysregulation is a key factor in OLP’s pathogenesis, involving CD4+ T helper and CD8+ T cytotoxic cells. The World Health Organization (WHO) classifies OLP as a potentially malignant disorder, with a risk of oral squamous cell carcinoma (OSCC) developing in up to 2% of lesions. This narrative review aims to provide a comprehensive overview of the etiopathogenesis, clinical manifestations, diagnostic criteria, and therapeutic strategies for OLP, informing clinical practice and guiding future research. Methods: A review of the literature from the PubMed and Google Scholar databases was conducted up to December 2023, focusing on studies addressing the etiopathogenesis, diagnosis, clinical manifestations, and treatment of OLP. Results: OLP’s pathogenesis is driven by immune dysregulation, with CD4+ and CD8+ cells playing crucial roles. Clinically, OLP presents as reticular, erosive, bullous, and plaque-like lesions. Diagnosis relies on clinical examination, histopathology, and direct immunofluorescence. Recent advancements in diagnostic markers and imaging techniques have improved detection and monitoring. Treatment primarily involves corticosteroids, but novel therapies such as curcumin, retinoids, and laser therapy are increasingly used for their effectiveness and reduced side effects. These treatments show promise in symptom reduction and recurrence prevention, although long-term data are needed. Conclusions: Regular screenings and biopsies are essential due to OLP’s likelihood of malignant transformation. This study urges further investigation into long-term results, improved diagnostic techniques, and evidence-based treatment regimens.

Publisher

MDPI AG

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