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Clinicodermoscopic features of lichen scrofulosorum – A rare form of cutaneous tuberculosis
*Corresponding author: Siddhartha Dash, Department of Dermatology, and Venereology, S.C.B. Medical College and Hospital, Cuttack, Odisha, India. siddharth101990@gmail.com
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Accepted: ,
How to cite this article: Dash S, Bhoi A, Mohanty S. Clinicodermoscopic features of lichen scrofulosorum – A rare form of cutaneous tuberculosis. CosmoDerma. 2024;4:36. doi: 10.25259/CSDM_11_2024
A 35-year-old male presented with multiple asymptomatic, skin-colored to erythematous, grouped, and discrete follicular papules of size ranging from 3 to 5 mm, mostly over the trunk for 15 days [Figure 1a]. There was no history of cough, fever, night sweats, weight loss or any other systemic complaints. He denied any past or family history of tuberculosis. Bacillus Calmette-Guerin scar was present on his left arm. Systemic examination was unremarkable.
Dermoscopy under polarized light (DermLite, DL4, ×10 magnification) revealed pale round monomorphic grouped perifollicular large dots with a central black follicular plug with perilesional erythema [Figure 1b]. Differential diagnoses of lichen scrofulosorum, papular mucinosis, papular sarcoidosis, and histoid leprosy were kept. Mantoux test showed 3 mm induration after 48 h. The biochemical, hematological, and radiological investigations were within normal limits. Histopathology revealed superficial non-caseating tuberculoid granuloma around hair follicles and sweat ducts [Figure 1c]. Based on clinical and histopathological findings, a final diagnosis of lichen scrofulosorum was kept, and the patient was started on antitubercular treatment (ATT) with complete resolution after six months [Figure 1d]. Our case presented with typical morphology, dermoscopic, and histopathologic picture. Although the Mantoux test was negative, there was a complete response to ATT.
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