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首页> 外文期刊>Cutis >Epidermolytic hyperkeratosis and congenital platelike osteoma cutis in a child.
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Epidermolytic hyperkeratosis and congenital platelike osteoma cutis in a child.

机译:小儿表皮溶解性角化过度和先天性板状骨瘤。

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摘要

Epidermolytic hyperkeratosis is a rare congenital ichthyosis. Platelike osteoma cutis also is a rare diagnosis and is associated with abnormal ossification of cutaneous or subcutaneous tissue. A 17-month-old Hispanic girl presented with a plate of subcutaneous bone since birth as well as considerable scaling and hyperkeratosis centered around the joints. Histologic examination confirmed the diagnosis of both epidermolytic hyperkeratosis and osteoma cutis. Although there have been some cases of epidermolytic hyperkeratosis with other dermatologic conditions, we report a rare case of epidermolytic hyperkeratosis and platelike osteoma cutis.
机译:表皮溶解性角化病是一种罕见的先天性鱼鳞病。板状骨质瘤也很少见,与皮肤或皮下组织的骨化异常有关。自出生以来,一个17个月大的西班牙裔女孩就出现了一块皮下骨板,并且以关节为中心出现了明显的鳞屑和角化过度。组织学检查证实了表皮溶解性角化过度和角质瘤的诊断。尽管有些表皮溶解性角化过度并伴有其他皮肤病学情况,但我们报告了罕见的表皮溶解性角化过度和板状骨瘤。

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