Poikiloderma vasculare atrophicans (Q44164): Difference between revisions
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Poiquilodermia vascular atrófica é um padrão de reação cutânea caracterizado por hiper e hipomelanose mosqueada, telangiectasias e atrofia dérmica e epidérmica progressivas. Pode se manifestar como um componente da micose fungoide estabelecida, mas pode preceder o desenvolvimento desta última em muitos anos e, em alguns casos, pode persistir indefinidamente sem progressão para linfoma franco. Deve ser distinguida de outras causas de poiquilodermia, como aquela observada na dermatomiosite. | |||
| description / en | description / en | ||
Poikiloderma vasculare atrophicans is a cutaneous reaction pattern characterised by mottled hyper- and hypomelanosis, telangiectasia and progressive dermal and epidermal atrophy. It may manifest as a component of established mycosis fungoides but may precede the development of the latter by many years and, in some cases, may persist indefinitely without progression to frank lymphoma. It should be distinguished from other causes of poikiloderma such as may be seen with dermatomyositis. | |||
Revision as of 11:31, 13 August 2026
Poikiloderma vasculare atrophicans is a cutaneous reaction pattern characterised by mottled hyper- and hypomelanosis, telangiectasia and progressive dermal and epidermal atrophy. It may manifest as a component of established mycosis fungoides but may precede the development of the latter by many years and, in some cases, may persist indefinitely without progression to frank lymphoma. It should be distinguished from other causes of poikiloderma such as may be seen with dermatomyositis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | EK91.1 |
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| English | Poikiloderma vasculare atrophicans |
Poikiloderma vasculare atrophicans is a cutaneous reaction pattern characterised by mottled hyper- and hypomelanosis, telangiectasia and progressive dermal and epidermal atrophy. It may manifest as a component of established mycosis fungoides but may precede the development of the latter by many years and, in some cases, may persist indefinitely without progression to frank lymphoma. It should be distinguished from other causes of poikiloderma such as may be seen with dermatomyositis. |
