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Signs and symptoms [ edit ] 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 ...
Cutis marmorata telangiectatica congenita (CMTC) is a rare congenital vascular disorder that usually manifests in affecting the blood vessels of the skin. The condition was first recognized and described in 1922 by Cato van Lohuizen, [2] a Dutch pediatrician whose name was later adopted in the other common name used to describe the condition – Van Lohuizen syndrome.
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 ]
Maffucci syndrome (multiple enchondromas and hemangiomas) Hereditary hemorrhagic telangiectasia (Osler–Weber–Rendu syndrome) Ataxia–telangiectasia; Sturge–Weber syndrome, a nevus formation in the skin supplied by the trigeminal nerve and associated with facial port-wine stains, glaucoma, meningeal angiomas and intellectual disabilities
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.
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 .
PMO symptoms often resolve after a few days or weeks, though in some cases they can linger for years. Sharrah said he still sees demonic faces. There are fewer than 100 published case reports of PMO.
EDP does not usually have symptoms beside the macules and patches of discolored skin; however, some itching in these areas may occur. Because EDP is an uncommon disease of the skin, it is important to consider other skin diseases that may resemble erythema dyschromicum perstans, such as infectious diseases (i.e. leprosy or pinta ), reaction to ...