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Laugier-Hunziker syndrome: A case report
1Department of Oral Medicine, Nanjing Stomatological Hospital, Medical School of Nanjing University, 210008 Nanjing, China.
Journal of Stomatology, Oral and Maxillofacial Surgery
|December 17, 2017
Summary
Laugier-Hunziker syndrome (LHS) is a rare benign pigmentary condition. This report details a case study, reviewing clinical, dermoscopic, and histopathologic features for accurate diagnosis.
Area of Science:
- Dermatology
- Genetics
- Pathology
Background:
- Laugier-Hunziker syndrome (LHS) is a rare, benign, acquired disorder characterized by hyperpigmentation.
- It primarily affects the lips, oral mucosa, and acral areas, often accompanied by longitudinal melanonychia.
Observation:
- A case report of a 45-year-old female diagnosed with Laugier-Hunziker syndrome is presented.
- The patient exhibited characteristic clinical manifestations of the condition.
Findings:
- Detailed review of clinical, dermoscopic, and histopathologic findings in LHS.
- Discussion of key features aiding in the diagnosis of Laugier-Hunziker syndrome.
Implications:
- Highlights the importance of recognizing LHS and its distinct features.
- Emphasizes the need for thorough differential diagnosis to exclude other pigmentary disorders.
- Provides a comprehensive overview for clinicians managing patients with suspected LHS.
