Lymphocytic Infiltrate of Jessner is a rare chronic skin condition characterized by the presence of lymphocytes infiltrating the skin. It primarily affects middle-aged adults, with a slight female predominance. The exact prevalence of this condition is unknown, as it is often underdiagnosed or misdiagnosed. However, it is considered a relatively uncommon disorder. Lymphocytic Infiltrate of Jessner typically presents as multiple red or pink papules or plaques on the face, neck, or upper trunk. The condition is usually benign and self-limiting, with treatment options including topical corticosteroids or immunomodulatory agents.
Lymphocytic infiltrate of Jessner, also known as Jessner lymphocytic infiltrate or Jessner-Kanof syndrome, is a rare chronic skin condition characterized by the presence of infiltrating lymphocytes in the skin. It primarily affects middle-aged adults, with a slight female predominance.
The exact prevalence of lymphocytic infiltrate of Jessner is not well-established due to its rarity and underdiagnosis. However, it is considered to be a relatively uncommon condition. It has been reported in various populations worldwide, but no specific geographic or ethnic predisposition has been identified.
The clinical presentation of lymphocytic infiltrate of Jessner typically involves the development of multiple, small, red to violaceous papules or plaques on the face, neck, or upper trunk. These lesions are usually asymptomatic or mildly pruritic. The diagnosis is confirmed through skin biopsy, which reveals a dense infiltrate of lymphocytes in the dermis.
Treatment options for lymphocytic infiltrate of Jessner include topical or intralesional corticosteroids, systemic corticosteroids, or immunomodulatory agents. However, the condition is often chronic and recurrent, and complete resolution may not always be achieved.