Palmoplantar keratoderma with scleroatrophy of the extremities (Q84896): Difference between revisions

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Transtorno autossômico dominante raro caracterizado por atrofia e fibrose da pele dos membros, hipoplasia ungueal e ceratodermia palmoplantar. Carcinoma espinocelular agressivo da pele afetada ocorre em cerca de 1 em cada 6 indivíduos afetados, principalmente na terceira a quarta década, com formação precoce de metástases. Há também um risco aumentado de câncer de intestino.
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A rare autosomal dominant disorder characterised by atrophy and fibrosis of the skin of the limbs, nail hypoplasia and palmoplantar keratoderma. Aggressive squamous cell carcinoma of affected skin occurs in about 1 in 6 affected individuals, mostly in the third to fourth decade, with early metastasis formation. There is also an increased risk of bowel cancer.

Revision as of 10:15, 15 August 2026

A rare autosomal dominant disorder characterised by atrophy and fibrosis of the skin of the limbs, nail hypoplasia and palmoplantar keratoderma. Aggressive squamous cell carcinoma of affected skin occurs in about 1 in 6 affected individuals, mostly in the third to fourth decade, with early metastasis formation. There is also an increased risk of bowel cancer.
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ID_1466864301
    English
    Palmoplantar keratoderma with scleroatrophy of the extremities
    A rare autosomal dominant disorder characterised by atrophy and fibrosis of the skin of the limbs, nail hypoplasia and palmoplantar keratoderma. Aggressive squamous cell carcinoma of affected skin occurs in about 1 in 6 affected individuals, mostly in the third to fourth decade, with early metastasis formation. There is also an increased risk of bowel cancer.

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