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Schamberg's disease, (also known as "progressive pigmentary dermatosis of Schamberg", [1] "purpura pigmentosa progressiva" (PPP), [1] and "Schamberg's purpura" [1]) is a chronic discoloration of the skin found in people of all ages, usually only affecting the feet, legs or thighs or a combination. It may occur as a single event or subsequent ...
Erythrasma is a superficial skin infection that causes brown, scaly skin patches. It is caused by Corynebacterium minutissimum bacteria, a normal part of skin flora (the microorganisms that are normally present on the skin). There are two types of erythrasma: generalized and interdigital. Interdigital is the most common bacterial infection of ...
Here, the entire bottom of the feet becomes rough and scaly.” Treatment: Athlete’s foot can be treated with over-the-counter antifungal creams. If twice daily use after 2 to 4 weeks is not ...
[19] [20] Clinically, the diagnosis of any particular skin condition is made by gathering pertinent information regarding the presenting skin lesion(s), including the location (such as arms, head, legs), symptoms (pruritus, pain), duration (acute or chronic), arrangement (solitary, generalized, annular, linear), morphology (macules, papules ...
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Capillaritis can take many forms but is made up of tiny red or brown dots that may be spread out or in a group forming a red or brown patch on the skin. One variation, Majocchi purpura, forms concentric rings. [2] Capillaritis is a mild condition not requiring treatment.
Keratosis pilaris (KP; also follicular keratosis, lichen pilaris, or colloquially chicken skin. [1]) is a common, autosomal-dominant, genetic condition of the skin's hair follicles characterized by the appearance of possibly itchy, small, gooseflesh-like bumps, with varying degrees of reddening or inflammation. [2]
Ichthyosis (also named fish scale disease) [1] is a family of genetic skin disorders characterized by dry, thickened, scaly skin. [2] The more than 20 types of ichthyosis range in severity of symptoms, outward appearance, underlying genetic cause and mode of inheritance (e.g., dominant, recessive, autosomal or X-linked). [3]
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