Lichen sclerosus (LS) is a benign, chronic, inflammatory dermatosis that mainly affects the
genitalia and is characterized by pearly-white papules.[1-3] Its etiology is still
unknown; however, genetic factors and autoimmunity have been implicated.[1-3] It
may occur in all age groups and is more prevalent in females than males, with a ratio of
10: 1.[1,4] LS shows bimodal distribution with a peak incidence in prepubertal
girls and postmenopausal women.[3] It
preferably affects the genital area and extra-genital lesions are rare, especially in
children.[1] This report describes
the case of a female child with an exuberant clinical presentation of LS with genital and
disseminated extra-genital lesions.A 11-year-old, white, female patient had a 3-year history of hypochromic pruritic lesions
in the genital area and disseminated hypochromic lesions on the face, trunk, and limbs.
Dermatological examination revealed numerous pearly-white papules, some with atrophy,
distributed in the frontal region, trunk and limbs, predominating on the dorsal surface of
the hands and feet (Figure 1A-C). In some areas, they formed plaques and linear lesions, showing the
Koebner phenomenon (Figure 1D). In the genital area,
we observed papules and a hypochromic plaque on the labia majora, and erosion and
hypochromia on the labia minora and perineum (Figure
2).
FIGURE 1
A - Multiple pearly-white papules on the forehead. B -
Multiple lesions on the back. C - Pearly-white papules and plaques with
a parchment-like aspect in the acromial region. D - Linear lesions
showing the Koebner phenomenon on the lower back
FIGURE 2
Papules and hypochromic plaque on the left labia majora, and erosion and hypochromia
on the labia minora and perineum
A - Multiple pearly-white papules on the forehead. B -
Multiple lesions on the back. C - Pearly-white papules and plaques with
a parchment-like aspect in the acromial region. D - Linear lesions
showing the Koebner phenomenon on the lower backPapules and hypochromic plaque on the left labia majora, and erosion and hypochromia
on the labia minora and perineumBiopsies of the lesions on the trunk, back of the hand and genital area were obtained.
Histopathological examination of the genital lesion showed hyperkeratosis, basal layer
rectification, in the epidermis, and a band-like mononuclear infiltrate as well as an area
of edema and sclerosis, in the dermis, which are features compatible with LS (Figure 3). According to these findings we concluded that
it was a case of disseminated LS. Treatment was started with clobetasol propionate 0.05%
ointment, applied to the genital area and most affected regions. The itching in genital
lesions improved with treatment. In the other regions, the improvement was not pronounced.
The proposed treatment was phototherapy with narrowband UVB, but the patient did not follow
the treatment plan.
FIGURE 3
Histopathological examination of the genital area revealed hyperkeratosis and basal
layer rectification in the epidermis, and a band-like mononuclear infiltrate as well
as an area of edema and sclerosis in the dermis. (HE, 40x)
Histopathological examination of the genital area revealed hyperkeratosis and basal
layer rectification in the epidermis, and a band-like mononuclear infiltrate as well
as an area of edema and sclerosis in the dermis. (HE, 40x)Approximately 5-15% of LS cases occur in children.[1] In children, LS almost always affects the genital area. Only 6% of
patients have extra-genital manifestations of LS.[1] The patient in the case reported here belongs to this small group of
pediatric patients with extra-genital lesions that may mimic other dermatoses, which makes
diagnosis more difficult. The main differential diagnosis of the genital lesions are
vitiligo, lichen simplex chronicus and sexual abuse, whereas the main differential
diagnosis of the extra-genital lesions are localized scleroderma, lichen planus, lichen
nitidus, vitiligo and psoriasis. About LS's relationship with localized scleroderma, a
recent study with 472 patients has indicated that the frequency of LS in patients with
localized scleroderma is higher than in the general population, which raises the hypothesis
of a common autoimmune pathophysiological mechanism.[5]In our case, the complaint of itching and the clinical examination of the genital area were
fundamental to the clinical diagnosis.This case report of a child with an exuberant clinical presentation of genital LS with
disseminated extra-genital lesions aims to illustrate a rare clinical presentation of LS,
in order to support the clinical diagnosis of LS and draw attention to the importance of
examining the genital area of these patients.
Authors: Alexander Kreuter; Jana Wischnewski; Sarah Terras; Peter Altmeyer; Markus Stücker; Thilo Gambichler Journal: J Am Acad Dermatol Date: 2012-04-24 Impact factor: 11.527