| Palmoplantar
lichen nitidus: a rare cause of palmoplantar hyperkeratosis.
Ann Dermatol
Venereol. 2004 Aug-Sep;131(8-9):822-4.
BACKGROUND: Lichen
nitidus is a rare condition, which may be a cause of palmoplantar
hyperkeratosis. We report two cases. CASE REPORTS: A 53 year-old woman
presented with a dry and fissured palmoplantar hyperkeratosis. Histological
examination of a biopsy showed the typical features of lichen nitidus.
Significant improvement was obtained with acitretin. A few months later,
multiple lichen nitidus papules appeared on the limbs and the abdomen. A 67
year-old woman was referred to us for a fissured, disabling palmoplantar
hyperkeratosis refractory to topical steroids. Histological examination led
to the diagnosis of lichen nitidus. Local PUVA therapy resulted in the
cleaning of her lesions. Later, typical papules of lichen nitidus appeared
on her elbows. DISCUSSION: Nineteen cases of palmoplantar localization of
lichen nitidus have been described. The features are usually tiny yellow
papules but sometimes a non-specific keratoderma resembling chronic eczema.
Palmoplantar involvement of lichen nitidus may be isolated or associated
with cutaneous lesions on unusual sites. Oral retinoids and local PUVA are
effective treatments.
Purpuric generalized
lichen nitidus: an unusual eruption simulating pigmented purpuric
dermatosis.Dermatology.
2004;208(2):167-70.
BACKGROUND:
Generalized haemorrhagic lichen nitidus is rare. To our knowledge, this form
of presentation has only been reported once. OBJECTIVE: To describe a new
case of generalized haemorrhagic lichen nitidus simulating a pigmented
purpuric dermatosis. METHODS AND RESULTS: We document a 24-year-old man who
presented with an 8-month history of a progressive non-pruritic, red-brown
papular eruption on the dorsa of the feet, ankles and distal third of the
legs. A diagnosis of Schamberg's progressive pigmentary dermatosis was made,
and no treatment was prescribed. Two months later, the lesions had extended
to the abdomen, groins, forearms, elbows and wrists. Biopsy of the skin of
the right foot revealed lesions typical of lichen nitidus with subepidermal
extravasation of red cells and capillary wall hyalinization. Macrophages and
T lymphocytes were abundant in the infiltrate. CONCLUSION: Purpuric
generalized lichen nitidus should be included in the differential diagnosis
of pigmented purpuric dermatoses. |