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Targetoid hemosiderotic hemangioma manifests as a single, tiny, reddish-violaceous to brown targetoid lesion that can grow centrifugally in the acute phase is encircled by a hemorrhagic halo. [3] The halo may vanish in later phases, leaving just a central papule. [4] [5] There have been reports of certain cases without targetoid development. [6]
Microvenular hemangioma is an acquired benign vascular tumor that presents as an asymptomatic, slowly growing, 0.5- to 2.0 cm reddish lesion on the forearms or other sites of young to middle-aged adults. [2] The cause of microvenular hemangioma is unknown, however it has been associated with immunosuppression.
Approximately 5% of adults have liver hemangiomas in the United States, but most are asymptomatic. [30] Liver hemangiomas usually occur between the ages of 30 and 50 and more commonly in women. [4] Cases of infantile liver cavernomas are extremely rare. Cavernous hemangioma of the eye is more prevalent in women than men and between the ages of ...
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. [3] [4] If scratched, they may bleed. [5]
An infantile hemangioma, also called a strawberry angioma, on a child's arm. Angiomas usually appear at or near the surface of the skin anywhere on the body, and may be considered bothersome depending on their location.
A hemangioma or haemangioma is a usually benign vascular tumor derived from blood vessel cell types. 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.
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.
Kasabach–Merritt syndrome (KMS), also known as hemangioma with thrombocytopenia, [1] is a rare disease, usually of infants, in which a vascular tumor leads to decreased platelet counts and sometimes other bleeding problems, [2] which can be life-threatening. [3] It is also known as hemangioma thrombocytopenia syndrome.