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Pigmented actinic lichen planus: a case report.

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Actinic lichen planus (ALP), a rare sun-sensitive skin condition, can affect older individuals, as shown in this case report. Early diagnosis via biopsy and treatment combining topical therapies with photoprotection are key for managing pigmented ALP.

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Area of Science:

  • Dermatology
  • Photosensitive dermatoses
  • Cutaneous oncology

Background:

  • Actinic lichen planus (ALP) is a rare, photosensitive variant of lichen planus (LP).
  • It typically affects younger, dark-skinned individuals in tropical/subtropical regions, with limited European case reports.
  • Common presentations include annular, pigmented (melasma-like), dyschromic, and classic lichenoid forms.

Observation:

  • A case of a 68-year-old Caucasian male with a 9-year history of a solitary, mildly pruritic, hyperpigmented nasal patch is presented.
  • The patient's presentation is atypical given the typical demographic and geographic distribution of ALP.

Findings:

  • Histopathological examination revealed classic lichen planus features, including epidermal atrophy, pigmentary incontinence, and solar elastosis.
  • These findings led to the diagnosis of pigmented actinic lichen planus.
  • Treatment with topical pimecrolimus, tretinoin, and strict photoprotection resulted in significant improvement with residual hyperpigmentation.

Implications:

  • This case expands the known demographic profile of actinic lichen planus to include older Caucasian individuals.
  • Highlights the importance of histopathological correlation for accurate diagnosis, differentiating ALP from other facial hyperpigmented lesions.
  • Emphasizes the need for a combined therapeutic approach addressing both pigmentary and inflammatory aspects, alongside rigorous photoprotection, for effective management and recurrence prevention.