Lichen nitidus
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Lichen nitidus is a chronic inflammatory disease of unknown etiology[1], characterized by 1-2mm, discrete and uniform, shiny, flat-topped, pale flesh-colored or reddish-brown papules[1][1] that may be hypopigmented in blacks, and, occasionally, minimal scaling is present or can be induced by rubbing the surface[1], a disease process that usually affects children and young adults[1], and is painless and nonpruritic, though protracted pruritus may be occur.[1][1]
Presentation
Linear arrangements of these papules is common (referred to as a Koebner Phenomenon), especially on the forearms[1][1], but may occasionally be grouped, though not confluent, on flexural areas.[1] Generally, the initial lesions are localized, and remain so, to the chest, abdomen, glans penis, and flexor aspects of the upper extremities[1]; however, less commonly, the disease process can (1) be strictly isolated to the palms and soles[1], presenting with many hyperkeratotic, yellow papules that may coalesce into plaques that fissure[1][1] or “...sometimes a non-specific keratoderma resembling chronic eczema,”[1] or (2) become more widespread, with papules widely distributed on the body—the extensor surfaces of the elbows, wrists, and hands, folds of the neck, submammary region in females, groin, thighs, ankles, and feet[1][1]—and fusing into erythematous, minimally scaled plaques, with reddness that develops tints of violet, brown, and yellow[1][1].
Pathology
The histology of lichen nitidus is significant for a "...localized granulomatous lymphohistiocytic infiltrate in an expanded dermal papilla with thinning of overlying epidermis and downward extension of the rete ridges at the lateral margin of the infiltrate, producing a typical 'claw clutching a ball' picture...."[1]
Treatment
Generally, lichen nitidus is asymptomatic and self-limited; therefore, no treatment is required. However, if persistent pruritus is present, or the appearance “...interferes with daily activities or outlook...”[1] topical glucocorticoids may be tried. If the disease processes is symptomatic, generalized and extensive, oral glucocorticoids may be indicated.[1] Other reported treatments include PUVA, UVA/UVB phototherapy[1], astemizole[1], acitretin, and etretinate.[1]
Footnotes
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
