Keratoderma, Palmoplantar

角质病,掌足底
  • 文章类型: Journal Article
    掌plant角化病(PPK)是角化性疾病的统称,其主要临床症状是手掌和脚底的角化过度。为了建立日本皮肤病学会批准的第一个日本指南,以管理PPK,PPKs管理委员会是作为罕见难治性疾病研究小组的一部分成立的.这些指南旨在为日本的PPK管理提供最新信息。根据证据,他们总结了临床表现,病理生理学,诊断标准,疾病严重程度确定标准,治疗,和治疗建议。由于PPKs的稀有性,只有很少的临床研究有高度的证据。因此,这些准则的几个部分是根据委员会的意见制定的。为了进一步优化指南,根据新证据定期修订是必要的。
    Palmoplantar keratoderma (PPK) is a collective term for keratinizing disorders in which the main clinical symptom is hyperkeratosis on the palms and soles. To establish the first Japanese guidelines approved by the Japanese Dermatological Association for the management of PPKs, the Committee for the Management of PPKs was founded as part of the Study Group for Rare Intractable Diseases. These guidelines aim to provide current information for the management of PPKs in Japan. Based on evidence, they summarize the clinical manifestations, pathophysiologies, diagnostic criteria, disease severity determination criteria, treatment, and treatment recommendations. Because of the rarity of PPKs, there are only few clinical studies with a high degree of evidence. Therefore, several parts of these guidelines were established based on the opinions of the committee. To further optimize the guidelines, periodic revision in line with new evidence is necessary.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

公众号