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Erythema annulare centrifugum (EAC), is a descriptive term for a class of skin lesion [2] presenting redness in a ring form (anulare) that spreads from a center (centrifugum). It was first described by Darier in 1916.
Annular erythema of infancy (AEI) consists of self-limited eruptions of erythematous, annular to polycyclic patches and plaques. It is an idiopathic figurate erythema. [1] Over several days, a single lesion disappears without leaving behind any scale or hyperpigmentation. Mostly affecting the trunk, face, and extremities, this rash has no symptoms.
The most common lesions are erythema nodosum, plaques, maculopapular eruptions, subcutaneous nodules, and lupus pernio. Treatment is not required, since the lesions usually resolve spontaneously in two to four weeks. Although it may be disfiguring, cutaneous sarcoidosis rarely causes major problems. [1]
This rash was known as erythema chronicum migrans, the skin rash found in early-stage Lyme disease. [18] In the 1920s, French physicians Garin and Bujadoux described a patient with meningoencephalitis, painful sensory radiculitis, and erythema migrans following a tick bite, and they postulated the symptoms were due to a spirochetal infection
Erythema annulare centrifugum (deep gyrate erythema, erythema perstans, palpable migrating erythema, superficial gyrate erythema) Erythema gyratum repens (Gammel's disease) Erythema migrans (erythema chronicum migrans) Erythema multiforme; Erythema multiforme minor (herpes simplex-associated erythema multiforme) Erythema palmare; Generalized ...
Papules and plaques of tumid lupus erythematosus can create an annular pattern in certain patients, resembling annular subacute cutaneous lupus erythematosus (SCLE), with less edema at the center. A Blaschkoid distribution, [ 9 ] [ 10 ] scalp involvement resembling alopecia areata , [ 11 ] and periorbital edema are less frequent signs of tumid ...
Erythema multiforme minor–erythema multiforme von Hebra: 0 Folliculosebaceous cystic hamartoma: 0 Ehrlichiosis: File:Blue morpho butterfly.jpg: 1 Focal epidermolytic palmoplantar keratoderma: 0 Davis Colley disease: 0 Conditions of the skin appendages: 0 Congenital self-healing reticulohistiocytosis: 0 Cutaneous sinus of dental origin: 0
Sweet syndrome (SS), or acute febrile neutrophilic dermatosis, [1] [2] is a skin disease characterized by the sudden onset of fever, an elevated white blood cell count, and tender, red, well-demarcated papules and plaques that show dense infiltrates by neutrophil granulocytes on histologic examination.