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DOI: 10.1055/s-0043-122396
Successful Treatment of a Child With Generalized Lichen Ruber Planus
Kindlicher Lichen ruber planus als therapeutische HerausforderungPublication History
Publication Date:
12 March 2018 (online)
Introduction
Lichen planus is an autoimmune inflammatory mucocutaneous disease. The etiology of LP is poorly understood, but is believed to be the result of an autoimmune disorder including misled CD8+-T-Cells targeting basal keratinocytes (Lehman, J.S., M.M. Tollefson, and L.E. Gibson, Int J Dermatol, 2009. 48(7): p. 682–694). Multiple other associated factors, such as cytokines, hepatitis C and drugs are discussed.
It occurs in 0.5–1% (Weston, G. and M. Payette, International Journal of Women's Dermatology, 2015. 1(3): p. 140–149.) of the population and is rarely seen in children (1-4% of total cases)( Pandhi, D., A. Singal, and S.N. Bhattacharya, Pediatr Dermatol, 2014. 31(1): p. 59–67.), although a higher proportional percentage has been reported in certain studies (Kumar, V., et al., J Dermatol, 1993. 20(3): p. 175–177;). Although a racial predilection has not been shown for LP, 5 of 9 existing large LP-childhood-studies have been carried out in India (Payette, M.J., et al., Clin Dermatol, 2015. 33(6): p. 631–643.). Furthermore an U.S.-study showed a higher incidence of LP in African-American patients (Walton, K.E., et al., Pediatr Dermatol, 2010. 27(1): p. 34–38). No gender prevalence has been shown in the majority of the large childhood-studies. ([Table 1])
Author, Year |
Study type/number of cases/age |
Used therapy or treatment recommendations |
---|---|---|
D. Pandhi et al., 2014 |
Record of cases/316 patients/2–14 years |
|
A. Kanwar et al., 2010 |
Record of cases/100 patients/2–18 years |
|
D. Cohen et al., 2009 |
Case report/1 patient/6 years |
|
P. Basak, 2002 |
Case report/1 patient/9 years |
|
R. Sharma et al., 1999 |
Record of cases/50 patients/0–14 years |
|
There is a great variety to clinical presentations of LP. Our 11-year old patient suffered from classical cutaneous lesions with darker pigmented, nearly violaceous flat-topped papules, partly coalescing, covering the whole integument and responded very well to the treatment.