Unilateral acrosyringeal lichen planus of palm

Lichen planus (LP) is a pruritic, benign, papulosquamous, inflammatory dermatosis of unknown etiology that affects either or all of the skin, mucus membrane, hair and nail. It presents with varied morphology on the palms and soles. Here we present a case of unusual acrosyringeal variant of LP on palm. The diagnosis was confirmed histologically

Acitretin: A good treatment option for hypertrophic lichen planus

Lichen planus (LP) is a chronic inflammatory dermatosis of unknown etiology characterized by pruritic violaceous papules. Here, we share our experience of a long standing case of disseminated hypertrophic LP treated with oral acitretin. A 48-year-old married male, presented with multiple highly itchy dark raised lesions over bilateral legs since 15 years. There was no history of any preceding trauma, any recent drug intake before eruption, dental metal fillings, hepatitis, or any other infection. Patient was treated with oral antihistamines and topical moisturizers and topical steroid and salicylic acid combination ointments in the past with only temporary relief. Clinical examination revealed multiple hyperpigmented keratotic papulonodular lesions over bilateral legs and few on feet. Mucous membranes were normal. He was started on acitretin 25 mg twice daily along with oral hydroxyzine 25 mg and topical moisturizer and clobetasol and 6% salicylic acid ointment. After 2 weeks, patient noted up to 30–40% improvement in lesions and some became flat. Furthermore, itching was reduced. His lipid and liver profile showed no abnormality. Acitretin 25 mg bid and antihistamines were continued along with moisturizer for another 2 weeks. Since patient tolerated acitretin well without any major side effects,except for mucosal dryness and slight hair loss, it was continued for another 1 month. At the end of 2 months, there was almost 90% improvement in most of the lesions. Acitretin was stopped after 4 months. There was no recurrence reported up to 6 months posttreatment. Our case of HLP showed a good response to acitretin and it can be considered one of the treatment options for such severe, highly itchy cases of LP affecting quality of life

Progressive cribriform and zosteriform hyperpigmentation

Here we report a case of a healthy 30-year-old male who presented to us with progressively increasing reticulate pigmented lesions following lines of Blaschko on the right side of abdomen and back. Skin biopsy revealed increased basal layer pigmentation without nevus cells. A diagnosis of progressive cribriform and zosteriform hyperpigmentation (PCZH) was made on clinicopathological correlation. We also discuss clinicopathological differentials of this peculiar pigmentary disorder

Bullous scabies in an adult: A case report with review of literature

Scabies is an infestation caused by Sarcoptes scabiei, characterized by polymorphous lesions that may include burrows, papules, nodules, excoriation, and crusts. Vesicular and bullous lesions are rather rare. Bullous scabies is regarded as a distinct subtype of scabies, closely resembling bullous pemphigoid. Here, we report a case of bullous scabies in an adult male and review the literature

Pseudolymphomatous folliculitis: A distinctive cutaneous lymphoid hyperplasia

Pseudolymphomatous folliculitis (PLF) was first described in 1986 as a distinct variant of pseudolymphoma, characterized by a dense lymphoid infiltrate and accompanied by hyperplastic hair follicles. Here in we report a case of PLF presenting as an erythematous plaque with pustules and satellite lesions on forehead in an otherwise healthy adult male patient

Unilateral multiple facial angiofibromas: A case report with brief review of literature

Tuberous sclerosis (TSC) is an autosomal dominant hereditary condition with many varied forms of clinical presentation. The most frequent cutaneous findings in TSC include multiple angiofibromas, hypopigmented macules, periungual fibromas, and shagreen patch. Rarely, unilateral multiple facial angiofibromas have been reported. We report a case of unilateral multiple facial angiofibromas without any other manifestations of TSC. Although rare, unilateral multiple facial angiofibromas may be a mosaic form of TSC