Abstract
Laugier–Hunziker syndrome (LHS) is a rare, benign pigmentary disorder characterized by unique pigmentation over mucosa, nails, and acral sites, arising spontaneously during adulthood. It has no malignant potential or systemic involvement. It has a female preponderance (2:1 ratio). The pigmentary lesions in LHS respond poorly to therapy, and has high recurrence. Since LHS is a diagnosis based on exclusion, we discuss the differential diagnosis of mucocutaneous hyperpigmentation. We present a case of a 66-year-old man with LHS.
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