Angiokeratoma circumscriptum (Q92109): Difference between revisions

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Angioceratoma circunscrito é caracterizado por agregados de pápulas hiperqueratóticas, eritematosas a violáceas que podem posteriormente se tornar verrucosas e coalescer para formar placas. As mulheres são comumente afetadas, sendo a proporção homem/mulher de 1:3. Pode ser congênita ou adquirida e, embora muitos casos se apresentem ao nascimento, alguns não se desenvolvem antes da infância ou idade adulta. Localizações comuns são a perna, o pé, a coxa e a nádega. Podem, no entanto, ocorrer em outras localizações, incluindo na língua. Formas sistematizadas são reconhecidas.
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Angiokeratoma circumscriptum is characterised by aggregates of hyperkeratotic, erythematous to violaceous papules that may later become verrucous and coalesce to form plaques. Females are commonly affected, with the male-to-female ratio being 1:3. It may be either congenital or acquired and although many cases present at birth, some do not develop until childhood or adulthood. Common sites are the leg, foot, thigh and buttock. They may, however, occur elsewhere including on the tongue. Systematized forms are recognised.

Revision as of 07:15, 16 August 2026

Angiokeratoma circumscriptum is characterised by aggregates of hyperkeratotic, erythematous to violaceous papules that may later become verrucous and coalesce to form plaques. Females are commonly affected, with the male-to-female ratio being 1:3. It may be either congenital or acquired and although many cases present at birth, some do not develop until childhood or adulthood. Common sites are the leg, foot, thigh and buttock. They may, however, occur elsewhere including on the tongue. Systematized forms are recognised.
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    English
    Angiokeratoma circumscriptum
    Angiokeratoma circumscriptum is characterised by aggregates of hyperkeratotic, erythematous to violaceous papules that may later become verrucous and coalesce to form plaques. Females are commonly affected, with the male-to-female ratio being 1:3. It may be either congenital or acquired and although many cases present at birth, some do not develop until childhood or adulthood. Common sites are the leg, foot, thigh and buttock. They may, however, occur elsewhere including on the tongue. Systematized forms are recognised.

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