Dermoscopy of Graham–Little–Piccardi–Lassueur Syndrome
January 2025
in “
Indian Journal of Dermatopathology and Diagnostic Dermatology
”
Studysummary In this case report, a rare instance of Graham–Little–Piccardi–Lassueur syndrome coexisting with linear lichen planus was identified in a 35-year-old male, highlighting the condition's rarity in males, with dermoscopy aiding diagnosis through distinctive scalp and trunk lesion features.
Our plain-language summary. Not medical advice or a treatment recommendation. Consult a qualified healthcare professional before changing treatment. Full disclaimer
Graham–Little–Piccardi–Lassueur syndrome (GLPLS) is a rare variant of lichen planopilaris, characterized by a triad of symptoms including patchy cicatricial alopecia of the scalp, non-cicatricial alopecia of the axilla and groin, and follicular spinous papules on the body. This case study describes a 35-year-old male with GLPLS and coexisting linear lichen planus, a combination not previously reported. Dermoscopy revealed features consistent with lichen planopilaris, aiding in early diagnosis. Treatment aimed to halt disease progression using topical medications, but the patient was lost to follow-up. The study highlights the rarity of GLPLS in males and the importance of dermoscopy in diagnosis.
