angiokeratomas

angiokeratomas, angiokeratomata

References in periodicals archive ?
1978), hemangiossarcomas (LIAPIS & GENOVESE, 2004), angiokeratomas (GEORGE & SUMMERS, 1990), lymphomas {Hong, 2011, Mucosa-associated lymphoid tissue lymphoma of the third eyelid conjunctiva in a dog}(HONG et al.
Clinical manifestations of disease are hypohidrosis, acroparesthesias, heat intolerance, angiokeratomas, corneal opacities, cardiac arrhythmias, left ventricular hypertrophy, proteinuria, renal insufficiency and cerebrovascular accidents.
Angiokeratomas are characterized by asymptomatic hyperkeratotic vascular skin lesions characterized histologically by papillary dermal vascular ectasia and epidermal hyperkeratosis.
Angiokeratomas have been reported to develop over arteriovenous malformations and in the area of lymphangioma circumscriptum following repeated local trauma.
1) Angiokeratomas are composed of a series of subepidermal dilated capillaries that have a characteristic hyperkeratotic surface and bleed easily.
The insidious onset of this disease in childhood or the early teen years can begin with temperature-sensitive aching in the hands and feet and/or very small angiokeratomas on the extremities or groin.
Angiokeratomas in Fabry's disease and Fordyce's disease.
Symptoms of the disease typically begin in childhood and include pain in the hands and feet, angiokeratomas, and changes in the cornea.
Widespread angiokeratomas also occur in patients with several additional enzyme deficiencies, which include a-fucosidase (fucosidosis), neuraminidase (sialodosis), aspartylglycosaminase (aspartylglucosaminuria), AY-mannosidase (AY- mannosidosis), a-N-acetylgalactosaminidase (Kansaki disease), and AY-galactosidase (adult- onset GM1 gangliosidosis).
En esta, explica la evolucion y distincion de los angiokeratomas nombrados en la epoca: "akroasphycticum y corporis naeviforme" y resume lo que los autores previos describian con los hallazgos de sus investigaciones, no solo mencionando una descripcion clinica, sino tambien etiologica (8) (Figura 7).
While mortality is associated primarily with cardiac, renal, and cerebrovascular manifestations of the disease, dermatologic findings--including widespread angiokeratomas and telangiectases--also are prominent in many patients.
This X-linked lysosomal storage disease leads to an accumulation of glycophospholipids in cells throughout the body The insidious onset of this disease in childhood or the early teens can begin with temperature-sensitive aching in the hands and feet and/or very small angiokeratomas on the extremities or groin.