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Solar purpura (also known as "Actinic purpura," and "Senile purpura") is a skin condition characterized by large, sharply outlined, 1- to 5-cm, dark purplish-red ecchymoses appearing on the dorsa of the forearms and less often the hands. [1] The condition is most common in elderly people of European descent.
Typically, senile pruritus is diagnosed following an exclusion process starting with a complete physical exam. If a person is exhibiting signs and symptoms of senile pruritus, a laboratory exam may not be recommended by a doctor at the initial doctor's visit unless there are other indicators of an underlying disease.
Eliminating harsh skin regimens or products will be necessary to minimize potential for further purpura or trauma, skin sensitivity, and potential infection. Steroid-induced skin atrophy [ 14 ] [ 15 ] is often permanent, though if caught soon enough and the topical corticosteroid discontinued in time, the degree of damage may be arrested or ...
Purpura (/ ˈ p ɜːr p jʊər ə / [1]) is a condition of red or purple discolored spots on the skin that do not blanch on applying pressure. The spots are caused by bleeding underneath the skin secondary to platelet disorders, vascular disorders, coagulation disorders, or other causes. [ 2 ]
Ducas and Kapetanakis pigmented purpura; Lichen aureus; Although vascular damage may be present, it is insufficient for these conditions to be considered forms of vasculitis. [2] A few very small non-blinded studies of treatment with narrow-band ultraviolet light have been reported as promising. [3]
Actinic keratosis (AK), sometimes called solar keratosis or senile keratosis, [1] [2] is a pre-cancerous [3] area of thick, scaly, or crusty skin. [4] [5] Actinic keratosis is a disorder of epidermal keratinocytes that is induced by ultraviolet (UV) light exposure ().
Current treatments can relieve some of the symptoms, and new disease-modifying treatments are not widely available. Now, researchers have developed a nasal spray that, in a mouse model, slows down ...
Treatment is geared towards decreasing the amount of the involved protein. [2] This may sometimes be achieved by determining and treating the underlying cause. [2] AL amyloidosis occurs in about 3–13 per million people per year and AA amyloidosis in about two per million people per year. [2]
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