Pigment International

THE CLINICAL PICTURE
Year
: 2019  |  Volume : 6  |  Issue : 2  |  Page : 115--116

Koebnerization and lichen planus pigmentosus: Is it a reality?


Seema Manjunath, Divya Kamat, Muthu Sendhil Kumaran 
 Department of Dermatology, Venereology and Leprology, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Correspondence Address:
Additional Professor Muthu Sendhil Kumaran
Department of Dermatology, Venereology and Leprology, PGIMER, Chandigarh, India 160012
India




How to cite this article:
Manjunath S, Kamat D, Kumaran MS. Koebnerization and lichen planus pigmentosus: Is it a reality?.Pigment Int 2019;6:115-116


How to cite this URL:
Manjunath S, Kamat D, Kumaran MS. Koebnerization and lichen planus pigmentosus: Is it a reality?. Pigment Int [serial online] 2019 [cited 2022 May 21 ];6:115-116
Available from: https://www.pigmentinternational.com/text.asp?2019/6/2/115/273464


Full Text



Two middle-aged females presented with 6-months history of asymptomatic bluish grey macules over the back and chest conforming to the impression of their undergarment ([Figure 1]a, 1b). They denied any history of preceding erythema or scaling or significant sun exposure, any drug intake, contact with chemicals, perfumes, or plants. On examination, multiple greyish black-colored macules coalescing to form patches surface changes were present on chest and back, localized to the area beneath the undergarments. Few similar greyish blue macules were also seen over both arms. On dermatooscopy, multiple brown-black dots were seen sparing the eccrine glands. In addition, brown to bluish-grey dots, globules, and blotches in diffuse brownish background were noted ([Figure 2]). Histopathology of skin biopsy in both patients revealed orthokeratosis with basal cell vacuolization, pigment incontinence, and upper dermal perivascular lymphocytic infiltrate suggestive of lichen planus pigmentosus ([Figure 3]). Both patients were treated with topical mometasone 0.1% cream and tacrolimus 0.1% ointment for 6 months without any improvement.{Figure 1}{Figure 2}{Figure 3}

Lichen planuspigmentosus (LPP) is considered a variant of lichen planus (LP) with controversial nosological status.[1] It is thought to be a type IV hypersensitivity reaction to unknown antigen with lichenoid inflammation, leading to melanin incontinence and superficial dermal pigmentation without any clinical evidence of inflammation. The face, neck, trunk, arms, and legs are the most common areas of presentation, whereas involvement of the scalp, nails, or oral mucosa is relatively rare. Pigmentation is usually symmetrical, and most frequently seen pattern is diffuse followed by reticular, blotchy, and perifollicular; rare patterns include linear/blaschkoid LPP and zosteriform LPP. Presentation as seen in our patients—undergarment-like distribution pattern is unique and rare. The underlying cause of this varied presentation could be koebnerization due to friction or due to tight clothing.[2] This peculiar distribution leads to speculation about role of the phenomenon of koebnerisation which is commonly reported in LP.

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Conflicts of interest

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References

1Kumaran MS, Dabas G, Parsad D, Vinay K. Lichen planus pigmentosus − An appraisal. International Journal of Dermatology 2018;57:748-50. doi:10.1111/ijd.13982.
2Kim BS, Park KD, Chi SG et al. Two cases of lichen planus pigmentosus-inversus arising from long-standing lichen planus-inversus. Annals of Dermatology 2008;20:254. doi:10.5021/ad.2008.20.4.254.