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Cherry angioma, also called cherry hemangioma [1] or Campbell de Morgan Spot, [2] is a small bright red dome-shaped bump on the skin. [3] It ranges between 0.5 – 6 mm in diameter and usually several are present, typically on the chest and arms, and increasing in number with age.
Also known as cherry angiomas. For premium support please call: 800-290-4726 more ways to reach us
Angiomas are benign tumors derived from cells of the vascular or lymphatic vessel walls (endothelium) or derived from cells of the tissues surrounding these vessels. [ 1 ] [ 2 ] Angiomas are a frequent occurrence as patients age, but they might be an indicator of systemic problems such as liver disease.
The most common form, seen in infants, is an infantile hemangioma, known colloquially as a "strawberry mark", most commonly presenting on the skin at birth or in the first weeks of life. A hemangioma can occur anywhere on the body, but most commonly appears on the face, scalp, chest or back.
An angioma refers to any type of benign vascular tumor. [2] Some vascular tumors can be associated with serious blood-clotting disorders, making correct diagnosis critical. [3] A vascular tumor may be described in terms of being highly vascularized, or poorly vascularized, referring to the degree of blood supply to the tumor.
Nonetheless, there have been sporadic cases of angioma serpiginosum in the face, hands, feet, and mucous membranes, among other places. [ 4 ] [ 5 ] According to typical descriptions, angioma serpiginosum has an erythematous backdrop with a purple to coppery-red punctate look that clusters together in serpiginous or gyrate patterns.
Cherry angioma; Cherry hemangioma; Childhood type of generalized eruption of cutaneous mastocytosis; Chondrodermatitis nodularis chronica helicis; Chondrodermatitis nodularis helicis; Chondroid lipoma; Chondroma of soft parts; Chordoma; Choristoma; Collagenoma; Collagenous fibroma; Congenital cutaneovisceral angiomatosis with thrombocytopenia
Glomeruloid hemangioma is a distinctive vascular tumor first described in 1990 when found to be associated with POEMS syndrome and Castleman disease. [1] [2] Glomeruloid hemangiomas can manifest as wine-red sessile or pedunculated papules, papulonodules, subcutaneous bluish compressible tumors, or small, firm, reddish-violaceous, dome-shaped papules.