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Telmisartan-Induced Lichen Planus Eruption Manifested on Vitiliginous Skin

Cutis. 2017 January;99(1):E16-E19
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Practice Points

  • Lichen planus (LP) is a T-cell–mediated autoimmune disease that affects the skin and often the mucosa, nails, and scalp.
  • The etiology of LP is unknown. It can be induced by a variety of medications and may spread through the isomorphic phenomenon.
  • Immune factors play a role in the development of LP, drug-induced LP, and vitiligo.

To the Editor:

A 39-year-old man with a history of hypertension and vitiligo presented with a rapid-onset, generalized, pruritic rash covering the body of 4 weeks’ duration. He reported that the rash progressively worsened after developing mild sunburn. The patient stated that the rash was extremely pruritic with a burning sensation and was tender to touch. He was treated with betamethasone valerate cream 0.1% by an outside physician and an over-the-counter anti-itch lotion with no notable improvement. His only medication was telmisartan-hydrochlorothiazide (HCTZ) for hypertension. He denied any drug allergies.

Physical examination revealed multiple discrete and coalescent planar erythematous papules and plaques involving only the depigmented vitiliginous skin of the forehead, eyelids, and nape of the neck (Figure 1A), and confluent on the lateral aspect of the bilateral forearms (Figure 1B), dorsal aspect of the right hand, and bilateral dorsi of the feet. Wickham striae were noted on the lips (Figure 1C). A clinical diagnosis of lichen planus (LP) was made. The patient initially was prescribed halobetasol propionate ointment 0.05% twice daily. He reported notable relief of pruritus with reduction of overall symptoms and new lesion formation.

Figure 1. Confluent shiny erythoviolaceous papules and plaques on the photodistributed vitiliginous skin of the posterior aspect of the neck (A). Numerous shiny erythroviolaceous papules coalescing into confluent plaques on photodistributed vitiliginous skin of the bilateral lateral forearms (B). Netlike lacy white lines (Wickham striae) on the lower mucosal lip with mild edema on the upper and lower lips (C).

A 4-mm punch biopsy was performed on the left forearm. Histopathology revealed LP. Microscopic examination of the hematoxylin and eosin–stained specimen revealed a bandlike lymphohistiocytic infiltrate that extended across the papillary dermis, focally obscuring the dermoepidermal junction where there were vacuolar changes and colloid bodies. The epidermis showed sawtooth rete ridges, wedge-shaped foci of hypergranulosis, and compact hyperkeratosis (Figure 2).

Figure 2. Histopathology of a specimen from the left forearm revealed a bandlike lymphohistiocytic infiltrate that extended across the papillary dermis, focally obscuring the dermoepidermal junction. The epidermis showed sawtooth rete ridges, wedge-shaped foci of hypergranulosis, and compact hyperkeratosis (H&E, original magnification ×40).