Keratoderma Spotted Disseminated Symmetrical

Keratoderma spotted disseminated symmetrical (k. maculosa disseminata symmetrica) is a rare genetically determined skin disease characterized by the appearance of multiple spots and plaques covered with horny layers.

Synonyms for this disease: beignet symmetrical erythematous keratoderma, Buschke-Fischer-Brock syndrome.

Main clinical manifestations:

1. Symmetrical spots and plaques on the skin, covered with horny layers
2. Damage predominantly to the extensor surfaces of the limbs, buttocks, and lower back
3. Itching and peeling of affected areas
4. Gradual spread of rashes

Diagnosis is based on the clinical picture and histological examination. Treatment is mainly symptomatic. The prognosis depends on the prevalence of the process.

Keratoderma macular disseminated symmetric (KPDDS) is a rare skin disorder characterized by the appearance of symmetrical patches of skin that may be covered with crusts or scales. This disease can cause discomfort and pain in patients, as well as lead to cosmetic problems.

Symptoms of KPDDS can appear as spots of various sizes and shapes that are usually reddish in color. These spots may have scales or crusts on the surface, which can cause the skin to peel.

The causes of KPDDS are still unclear, but it is known that the disease may be associated with genetic factors, infectious diseases, immune system disorders, and other factors.

Treatment for KPDDS may include the use of topical and systemic medications such as corticosteroids, antihistamines, vitamins, and others. Treatments such as phototherapy or surgery may also be required.

It is important to note that KPDDS is a rare disease and can be difficult to diagnose. Therefore, it is necessary to consult a dermatologist for an accurate diagnosis and prescription of appropriate treatment.