Focal infantile haemangioma (Q39326): Difference between revisions

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Hemangioma infantil é uma neoplasia vascular benigna comum que se desenvolve em cerca de 4% dos bebês. Aparece semanas após o nascimento como uma área esbranquiçada, eritematosa ou telangiectásica que então se prolifera rapidamente por vários meses antes de entrar em um processo prolongado de involução que dura até 12 anos, deixando uma cicatriz residual variavelmente proeminente. Um tumor focal solitário é observado em cerca de 85% dos casos. Mais da metade dos casos estão localizados em cabeça e pescoço. As complicações incluem sangramento, infecção, ulceração e, em tumores próximos ao olho, ambliopia.
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Infantile haemangioma is a common benign vascular neoplasm which develops in about 4% of infants. It appears within weeks of birth as a blanched, blushed, or telangiectatic area that then rapidly proliferates for several months before entering a prolonged process of involution lasting up to 12 years, leaving a residual variably prominent scar. A solitary focal tumour is seen in about 85% of cases. Over half of cases are located on the head and neck. Complications include bleeding, infection, ulceration and, in tumours situated close to the eye, amblyopia.

Revision as of 04:42, 13 August 2026

Infantile haemangioma is a common benign vascular neoplasm which develops in about 4% of infants. It appears within weeks of birth as a blanched, blushed, or telangiectatic area that then rapidly proliferates for several months before entering a prolonged process of involution lasting up to 12 years, leaving a residual variably prominent scar. A solitary focal tumour is seen in about 85% of cases. Over half of cases are located on the head and neck. Complications include bleeding, infection, ulceration and, in tumours situated close to the eye, amblyopia.
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    Focal infantile haemangioma
    Infantile haemangioma is a common benign vascular neoplasm which develops in about 4% of infants. It appears within weeks of birth as a blanched, blushed, or telangiectatic area that then rapidly proliferates for several months before entering a prolonged process of involution lasting up to 12 years, leaving a residual variably prominent scar. A solitary focal tumour is seen in about 85% of cases. Over half of cases are located on the head and neck. Complications include bleeding, infection, ulceration and, in tumours situated close to the eye, amblyopia.

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