Lichenoid pseudovesicular papular eruption on nose: A papular facial dermatosis probably related to actinic lichen nitidus or micropapular polymorphous light eruption.

BACKGROUND: Facial papules are a feature of several clinical conditions and may present both diagnostic and therapeutic challenges. AIM: To describe a grouped papular eruption on the nose and adjoining cheeks that has not been well characterized previously. MATERIALS AND METHODS: A series of consecutive patients with a papular eruption predominantly involving nose and cheeks were evaluated, treated and followed up prospectively at tertiary care centers. Demographic details, clinical features, histopathology and response to treatment were recorded. RESULTS: There were five men and six women (mean age 29.9 ± 6.9 years) who had disease for a mean duration of 17.3 ± 11.1 months. All patients presented with a predominantly asymptomatic eruption of monomorphic, pseudovesicular, grouped, skin colored to slightly erythematous papules prominently involving the tip of nose, nasal alae, philtrum and the adjoining cheeks. A total of 15 biopsies from 11 patients were analyzed and the predominant finding was a dense, focal lymphoid infiltrate restricted to the upper dermis with basal cell damage and atrophy of the overlying epidermis. The eruption ran a chronic course from several months to years. LIMITATIONS: Direct immunofluorescence could not be performed except in one case. Immunohistochemical stains for CD4 and CD8 could not be done owing to nonavailability. Phototesting was undertaken in one patient only. CONCLUSION: Small grouped papules on the nose and adjoining skin with a lichenoid histopathology appear to represent a distinct clinicopathological entity. It may be related to actinic lichen nitidus/micropapular variant of polymorphous light eruption.

Lesiones queratósicas en las palmas de las manos y alteraciones ungueales / Keratotic Lesions on the Palms and Nail Abnormalities

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Liquen nitidus generalizado. A propósito de un caso / Widespread lichen nitidus. A case report

El liquen nitidus es una dermatosis poco frecuente de origen desconocido caracterizada por pequeñas pápulas hemiesféricas, brillantes y del color de la piel, habitualmente asintomáticas o ligeramente pruriginosas. Tiene predilección por genitales, glúteos, abdomen inferior y superficies flexoras de antebrazos y muñecas. Ocasionalmente tiene una distribución generalizada. Su evolución es benigna con resolución espontánea en meses o años. Presentamos un caso de liquen nitidus generalizado (AU)

Lichen nitidus is a rare dermatosis of unknown etiology; it consists of small, hemispherical, shiny and flesh-coloured papules commonly asymptomatic or sometimes itchy. It has predilection on the genitals, lower abdomen, flexor surfaces of forearms and wrists. There are rare reports of patients having a more generalized distribution of lesions. Lichen nitidus lesions resolve spontaneously in months or years. We present a case of generalized lichen nitidus (AU)

Generalized lichen nitidus in Russell-Silver syndrome.

Generalized lichen nitidus is a rare disease, and there are only a few reports associating it with a genetic disorder. Here we report a case of generalized lichen nitidus in Russell-Silver syndrome.

Generalized Lichen nitidus associated with Down's syndrome: case report.

Lichen nitidus is a disease of unknown etiology, characterized by flesh-colored, shiny papules of 1-2 mm and generally asymptomatic or with mild pruritus. The most common sites of occurrence are genitalia, upper limbs, trunk and abdomen. The generalized form is rare. This is the fourth reported case of lichen nitidus associated with Down Syndrome.

Generalized Lichen nitidus associated with Down's syndrome: case report / Liquen nítido geneneralizado associado à síndrome de Down: relato de caso

Lichen nitidus is a disease of unknown etiology, characterized by flesh-colored, shiny papules of 1-2 mm and generally asymptomatic or with mild pruritus. The most common sites of occurrence are genitalia, upper limbs, trunk and abdomen. The generalized form is rare. This is the fourth reported case of lichen nitidus associated with Down Syndrome.

Líquen nítido é uma doença de etiologia desconhecida, caracterizada por pápulas normocrômicas, brilhantes medindo de 1 a 2 milímetros de diâmetro, geralmente assintomáticas ou com leve prurido. A forma mais comum é a localizada nos genitais, membros superiores, tronco e abdome. A forma generalizada é rara. Este é o quarto relato de caso descrito de líquen nítido associado à Síndrome de Down.

Liquen nitidus: respuesta favorable a fototerapia UVB de banda estrecha. Presentación de dos casos / No disponible

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Generalized lichen nitidus, with perioral and perinasal accentuation, in association with Down syndrome.

Generalized cases of lichen nitidus are rare, but have been infrequently reported in association with Down syndrome. We report the third such case, with unusual perioral and perinasal accentuation.

Multiple endocrine neoplasia type 2b associated with lichen nitidus.

Multiple endocrine neoplasia (MEN) type 2B syndrome is an autosomal dominantly inherited endocrine disorder with rare skin manifestations. We report the case of a 19-year-old Turkish girl who presented with skin-colored flat papules scattered all over the trunk and extremities. Additionally, she had marfanoid habitus, thick lips, and multiple flesh-colored papules over the inner eyelids and oral mucosa. Histopathological examination of one of the trunk lesions was consistent with lichen nitidus. Her past medical history was significant for medullary thyroid carcinoma. Genetic testing showed a point mutation in exon 16 at codon 918 (M918T) in the RET proto-oncogene. Based on all these findings, MEN type 2B was diagnosed. To the best of our knowledge we report the first case of MEN type 2B associated with lichen nitidus.