Annular Lichen Planus with Central Clearing

Keywords

Lichen planus, Annular lichen planus, Dermatosis.

Patient History

An 82 year-old white woman with a history of basal cell carcinoma presented for routine follow up and was noted to have a 2.5 cm hyper-pigmented annular plaque on her left lower abdomen. She reported that the plaque had been present and stable for over one year. Examination also revealed small hyperpigmented macules in her right axilla. The remainder of her skin exam, including her buccal mucosa and nails, was unremarkable. Her past dermatologic history was significant for scalp psoriasis, which responded to topical steroids and had remained in remission for several years. Three biopsies were obtained, two from the larger annular plaque and one from an axillary lesion. All demonstrated histologic findings consistent with lichen planus. A review of her medications failed to identify mediations associated with lichenoid drug eruptions.

Discussion

Lichen planus is an inflammatory dermatosis involving the skin and mucous membranes characterized by an autoimmune reaction mediated by CD8+ T cells [1].Several variants of lichen planus are recognized and all may exhibit differing features during acute or chronic phases (Table 1). Although annular lichen planus (ALP) is a long-recognized clinical variant of lichen planus, it is rare. Tinea, granuloma annulare, porokeratosis, mycobacterial infection, figurate erythema, borrelia infection, as well as other annular eruptions all need to be considered in the histologic differential diagnosis. Furthermore, ALP may present with striking central atrophy, which is typically classified as annular atrophic lichen planus [2]. A retrospective review of 20 patients identified the distribution and presentation of annular lichen planus and found that the morphology typically included violaceous plaques with an annular configuration and a narrow rim of activity and residual hyperpigmentation [3]. ALP commonly involves the male genitalia and intertriginous areas such as the axilla and groin folds [4]. In addition, characteristic oral mucosal, vulval, scalp or nail lesions that are associated with other variants of lichen planus are typically absent in ALP. Similarly, pruritus, a symptom that occurs often in typical lichen planus, is very slight or altogether absent in ALP, with recurrence and aggravation related to long exposure to sunlight [5].

---

---

References in table:[6-11]

Our patient’s presentation and clinical course are typical and illustrative. She presented with an annular lesion with indurated borders and a tendency toward central clearing (Figure 1). Biopsy captured the inflammatory component of both sides of the annular rim as well as the quiescent midline area. Microscopic examination revealed a patchy lichenoidlymphohistiocytic inflammatory infiltrate with melanophages in the papillary dermis. Discrete areas demonstrated lichenoid inflammation (Figure 2a). Higher power revealed typical hypergranulosis with dyskeratotic keratinocytes and a band-like lymphocytic infiltrate (Figure 2b). Eosinophils and plasma cells were not conspicuous within the inflammatory infiltrate. The histologic findings confirmed the clinical diagnosis of ALP. Mainstays of therapy include topical corticosteroids. In our patient, the lesions were asymptomatic and not cosmetically apparent, and so the patient elected to forgo treatment.

---

---

---

---

---

---

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.