INTRODUCTION
Prurigo nodularis is an intensely pruritic disease in which dome-shaped papulonodules result from chronic scratching and picking of the skin.1 Lesions typically occur on the extensor surfaces, back, chest, face and other areas that are easily accessible.1 Treatment is often challenging and unsatisfying. The pathogenesis of PN remains unclear but its association with atopic dermatitis (AD) intuitively allows for overlap in the treatment options to consider. In this case report, we present a patient with recalcitrant PN who failed many therapies for PN. The patient’s primary complaint was severe pruritis. Initiation of dupilumab significantly decreased pruritis and the size and number of new lesions also improved
CASE SYNOPSIS
We present a 43-year-old type III Hispanic female who presented with intensely pruritic papules and nodules that were firm and tan-to-brown-violaceous in color (Figure 1 A-B). Several lesions had hyperkeratotic scale. Pathology demonstrated psoriasiform epidermal hyperplasia with hypergranulosis, overlying compact hyperkeratosis and sparse papillary dermal perivascular lymphocytic infiltrate (Figure 2 A-B). Initially, only a handful of lesions were present, but new lesions continuously appeared and lesions never resolved. Over a 3-year period, treatment attempts with topical clobetasol, flurandrenolide tape, intralesional triamcinolone, cryotherapy, narrowband ultraviolet B therapy, and ultimately methotrexate (max dose 15 mg/week) failed to provide any improvement in the quality of the lesions or severe pruritis.
The patient was lost to follow-up for nearly 6 months, after which she returned with innumerable lesions. At that time,
The patient was lost to follow-up for nearly 6 months, after which she returned with innumerable lesions. At that time,
