{Reference Type}: Case Reports
{Title}: Diagnosis and management of vulvar Darier disease: A case report.
{Author}: Evruke I;Ugurlucan FG;Erdem BY;Sari SO;
{Journal}: Case Rep Womens Health
{Volume}: 39
{Issue}: 0
{Year}: 2023 Sep
暂无{DOI}: 10.1016/j.crwh.2023.e00545
{Abstract}: Darier disease is an autosomal dominant disorder with hyperkeratotic papules affecting primarily seborrheic areas of the upper chest, back, forehead, scalp, nasolabial folds, ears, and, less frequently, the oral mucosa. A typical eruption consists of keratotic and crusted skin-colored papules and plaques. Pruritus occurs in 80% of patients, and pain is rare. Lesions can be triggered by exposure to ultraviolet light, heat, or stress. Secondary infections of the lesions are a common complication. A definitive diagnosis is obtained by a biopsy showing histological features such as acantholysis, suprabasal clefts, and "corps rond and grains". Here we present a 37-year-old woman admitted to the gynecology department with pruritic lesions she had noticed on her vulva and perineum for three months. A vulvar biopsy led to the diagnosis of Darier disease. She was referred to the dermatology department and treated with oral acitretin since systemic retinoids are offered as the first-line treatment of the disease.