先天性肿甲1型口腔表现:Jadassohn lewandowsky综合征

Natasha Byahatti
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引用次数: 0

摘要

先天性厚甲症(PC),是一种罕见的遗传性疾病,常染色体显性,角化疾病。这种疾病的特征是皮肤表现,主要是皮肤和粘膜角化过度以及指甲肥大。在这种情况下,几乎50%的患者会发生口腔白细胞角化病。本文报告一例15岁女孩,表现为指甲营养不良,指甲和脚趾甲增厚,甲下角化过度,掌足底角化病,颊粘膜角化过度斑块。组织学检查显示棘层增生,角化不全,上皮细胞呈球状,这些特征与白细胞角化症一致,诊断为先天性肿甲1型。这是一种罕见的情况,因此有报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral manifestation of pachyonychia congenita type 1: Jadassohn lewandowsky syndrome
Pachyonychia congenital (PC), is a rare genetic disorder, autosomal dominant, disorder of keratinization. This condition is characterized by cutaneous manifestation mainly hyperkeratosis of skin and mucosae and hypertrophy of nails. In this condition, almost 50% of the patients will have oral leukokeratosis. The case report here is of a 15 years old girl, presented with dystrophic, thickened fingernails and toenails with subungual hyperkeratosis, palmoplantar keratoderma, hyperkeratotic plaques in buccal mucosae. Histological examination shows acanthosis, parakeratosis and ballooning of epithelial cells, these features were consistent leukokeratosis, and has been diagnosed as Pachyonychia Congenita type 1. This is a rare condition hence, has been reported.
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