02745nas a2200253 4500000000100000008004100001260002300042653002400065653001600089100001300105700001300118700001200131700001300143700001200156700001200168700001400180700001100194700001300205245007800218856011100296300000800407520205100415022002502466 2024 d bScientific Scholar10aInfectious Diseases10aDermatology1 aAnkad BS1 aSharma A1 aVinay K1 aRathod S1 aMehta H1 aBhat YJ1 aAshwini P1 aJha AK1 aNarang T00aDermatoscopic evaluation of leprosy: A multi-centre cross-sectional study uhttps://ijdvl.com/dermatoscopic-evaluation-of-leprosy-a-multi-centre-cross-sectional-study/#tab_default_03 a1-83 a

Background: Leprosy is known to be a great mimicker. Its dermatoscopic evaluation may be of value in establishing diagnosis.

Objective: To study the dermatoscopic findings encountered across the leprosy spectrum.

Methods: This was a multi-centre cross-sectional study of leprosy patients, where after a thorough cutaneous and neurological evaluation, representative skin lesions from the study patients were photographed in standard settings, and the most representative skin lesions were chosen for dermatoscopic evaluation. Data was entered in a structured proforma and a descriptive analysis of dermatoscopic patterns was carried out.

Results: A total of 53 cases of ages between 14 and 80 years, ranging from tuberculoid to the lepromatous spectrum of disease, with active skin lesions in the form of patches and plaques were included. The spectrum of leprosy as per Ridley-Jopling classification at diagnosis was indeterminate in 1 (1.9%), tuberculoid in 1 (1.9%), borderline tuberculoid in 25 (21.5%), borderline lepromatous in 9 (17%), lepromatous in 14 (26.4%) and histoid in 3 (5.7%). Dermatoscopic features included distorted pigment network in 48 (90.6%), focal white areas in 40 (75.5%), reduced eccrine and follicular openings in 43 (81.1%), widened skin lines in 28 (52.8%), circle hairs in 15 (28.3%) and white shiny streaks in 17 (32.1%).

Conclusion: Dermatoscopy is a practical, non-invasive device to assess skin lesions of leprosy and provide cues to its diagnosis, spectral classification and differentiating it from other granulomatous disorders. However, dermatoscopy alone cannot reliably differentiate between the various types of leprosy and future large-scale studies are required.

Limitations of the study: The numbers for each subtype were variable and few in some spectrum of leprosy patients. A dermatoscopic-histologic correlation was not done.

 a0973-3922, 0378-6323