Lichen nitidus
From Wikipedia, the free encyclopedia
| Lichen nitidus Classification and external resources |
|
| ICD-10 | L44.1 |
|---|---|
| ICD-9 | 697.1 |
| DiseasesDB | 34283 |
| eMedicine | derm/232 |
| MeSH | D017513 |
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[2][3] that may be hypopigmented in blacks, and, occasionally, minimal scaling is present or can be induced by rubbing the surface[3], a disease process that usually affects children and young adults[4], and is painless and nonpruritic, though protracted pruritus may be occur.[3][5]
Contents |
[edit] Presentation
Linear arrangements of these papules is common (referred to as a Koebner Phenomenon), especially on the forearms[2][5], but may occasionally be grouped, though not confluent, on flexural areas.[2] Generally, the initial lesions are localized, and remain so, to the chest, abdomen, glans penis, and flexor aspects of the upper extremities[6]; however, less commonly, the disease process can (1) be strictly isolated to the palms and soles[7], presenting with many hyperkeratotic, yellow papules that may coalesce into plaques that fissure[7][3] or “...sometimes a non-specific keratoderma resembling chronic eczema,”[7] 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][2]—and fusing into erythematous, minimally scaled plaques, with reddness that develops tints of violet, brown, and yellow[4][3].
[edit] 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]
[edit] 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...”[2] topical glucocorticoids may be tried. If the disease process is symptomatic, generalized and extensive, oral glucocorticoids may be indicated.[2] Other reported treatments include PUVA, UVA/UVB phototherapy[6], astemizole[1], acitretin, and etretinate.[2]
[edit] References
- ^ a b c d Al-Mutairi, N., et al. "Generalized lichen nitidus." Pediatr Dermatol. 2005;22(2):158-60. PMID 15804308.
- ^ a b c d e f g Odom, Richard, et al. Andrews' Diseases of the Skin: Clinical Dermatology. W.B. Saunders Company. Pages 277-280. ISBN 0721658326.
- ^ a b c d e Freedberg, Irwin, et al. Fitzpatrick's Dermatology in General Medicine. McGraw-Hill Professional Publishing. Pages 577-581. ISBN 0079129382.
- ^ a b Soroush, V., et al. "Generalized lichen nitidus: case report and literature review." Cutis. 1999;64(2):135-6. PMID 10467510.
- ^ a b Maeda, M. "A case of generalized lichen nitidus with Koebner's phenomenon." J Dermatol. 1994;21(4):273-7.
- ^ a b Do, M.O., et al. "Generalized lichen nitidus successfully treated with narrow-band UVB phototherapy: two cases report." J Korean Med Sci. 2007;22(1):163-6. PMID 17297274.
- ^ a b c Thibaudeau, A., et al. "Palmoplantar lichen nitidus: a rare cause of palmoplantar hyperkeratosis." Ann Dermatol Venereol. 2004;131(8-9):822-4. PMID 15505553.
