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Necrolytic migratory erythema (NME) is a red, blistering rash that spreads across the skin. It particularly affects the skin around the mouth and distal extremities; but may also be found on the lower abdomen, buttocks, perineum , and groin.
Idiopathic craniofacial erythema is a medical condition characterized by uncontrollable and frequently unprovoked facial blushing. Blushing can occur at any time and is frequently triggered by even mundane events, such as talking to friends, paying for goods in a shop, asking for directions or even simply making eye contact with another person.
Erythromelanosis follicularis faciei et colli is characterized by patches of erythema (with or without telangiectasia), follicular papules (follicular plugging), and bilateral and symmetrical hyperpigmentation (reddish-brown pigmentation) that start on the preauricular areas and cheeks and can eventually migrate to the submandibular portions of the neck.
Chronic treatment with topical corticosteroids may lead to telangiectasia. [11] Spider angiomas are a radial array of tiny arterioles that commonly occur in pregnant women and in patients with hepatic cirrhosis and are associated with palmar erythema. In men, they are related to high estrogen levels secondary to liver disease. TEMPI syndrome
Rombo syndrome is inherited in an autosomal dominant manner [1] Rombo syndrome is a very rare genetic disorder characterized mainly by atrophoderma vermiculatum of the face, [ 2 ] : 580 multiple milia , telangiectases , acral erythema , [ 3 ] peripheral vasodilation with cyanosis , [ 4 ] and a propensity to develop basal cell carcinomas .
Majocchi's disease is a chronic condition for which there is no cure. It often follows a recurrent course of alternating improvement and flares. There are treatments available to help improve the symptoms for some individuals, but responses vary. Some of these treatments include the application of topical steroids and ultraviolet therapy.
Telangiectasia macularis eruptiva perstans (TMEP) is persistent, pigmented, asymptomatic eruption of macules usually less than 0.5 cm in diameter with a slightly reddish-brown tinge. [ 1 ] : 616 [ 2 ]
FACES syndrome is a syndrome of unique facial features , a norexia, c achexia, eye and skin anomalies. [ 1 ] It is a rare disease and estimated to occur in less than 1 in 1 million people.