Introduction: Morphea and extragenital lichen sclerosus (LSA) are chronic inflammatory dermatoses with overlapping clinical features, requiring invasive biopsy for confirmation. Dermoscopy, a non-invasive tool, may aid by identifying characteristic cutaneous patterns. Objectives: To study the dermoscopic features of LSA, morphea, and their overlap in histopathologically confirmed cases and describe characteristic dermoscopic patterns. Methods: This retrospective observational study was conducted in 2020-2024 in four tertiary care centres across North India. Histopathologically confirmed cases of morphea, LSA, or overlap were included. Dermoscopic evaluation was performed using hand-held dermoscope, and findings were analysed descriptively. Results: Among 90 lesions in 50 patients, 13 were genital LSA, 52 extragenital LSA, 15 morphea and 10 LSA-morphea overlap. Common dermoscopic findings in LSA included white structureless areas (96.15%; shiny 92.31%), pigment change (84.62%), reddish hue (71.15%), violaceous hue (59.62%), scaling (53.85%), dotted vessels (36.54%). Morphea showed white structureless areas (100%; dull and broad, 80%), brown structureless areas (73.33%), pigmentary change (80%), reduced eccrine openings (80%) relative absence of vessels with occasional occurrence of linear-curved vessels (13.33%). Follicular plugging was comparable in both. Overlap cases had a mix of shiny to dull white structureless areas, pigment change (80%, variable pattern), preserved eccrine openings (60%), follicular plugs (50%), vessels (dotted 50%, linear-curved 30%). Genital LSA lesions showed shiny white structureless areas (92.31%), reddish hue (76.92%), violaceous hue (61.54%). Conclusion: Recurring dermoscopic patterns were observed: shiny white structureless areas with reddish/violaceous hue, polymorphous vessels in extragenital LSA; dull white and brown structureless areas, pigment network, reduced eccrine openings in morphea; hybrid features in overlap lesions. Dermoscopy may therefore complement clinical assessment of these entities; however, prospective studies evaluating its diagnostic accuracy are needed before it can inform decisions regarding biopsy.
No takes yet. Share an insight, caveat, or question.
Chauhan et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: