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掌跖角化症伴圆锥角膜

Palmoplantar Keratoderma with Keratoconus.

作者信息

Gupta Ved Prakash, Chaudhari Isha

机构信息

Department of Ophthalmology, University College of Medical Sciences and GTB Hospital, New Delhi, India.

出版信息

Middle East Afr J Ophthalmol. 2018 Jan-Mar;25(1):49-51. doi: 10.4103/meajo.MEAJO_221_17.

DOI:10.4103/meajo.MEAJO_221_17
PMID:29899652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5974819/
Abstract

Palmoplantar keratodermas (PPKs) are a rare heterogeneous group of disorders characterized by abnormal thickening of the skin of palms and soles. Ocular manifestations reported with palmer planter keratosis include scleral melanosis, macular deposits, and congenital cataract. We report, for the first time, a case of bilateral keratoconus in a patient with PPK.

摘要

掌跖角化病(PPKs)是一组罕见的异质性疾病,其特征是手掌和脚底皮肤异常增厚。与掌跖角化症相关的眼部表现包括巩膜黑变病、黄斑沉积物和先天性白内障。我们首次报告了一例患有掌跖角化病的患者出现双侧圆锥角膜的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c83d/5974819/59137002a8dc/MEAJO-25-49-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c83d/5974819/cf65cb044455/MEAJO-25-49-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c83d/5974819/59137002a8dc/MEAJO-25-49-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c83d/5974819/cf65cb044455/MEAJO-25-49-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c83d/5974819/59137002a8dc/MEAJO-25-49-g002.jpg

相似文献

1
Palmoplantar Keratoderma with Keratoconus.掌跖角化症伴圆锥角膜
Middle East Afr J Ophthalmol. 2018 Jan-Mar;25(1):49-51. doi: 10.4103/meajo.MEAJO_221_17.
2
Hereditary palmoplantar keratodermas. Part I. Non-syndromic palmoplantar keratodermas: classification, clinical and genetic features.遗传性掌跖角化病。第一部分。非综合征性掌跖角化病:分类、临床和遗传特征。
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Pain mechanisms in hereditary palmoplantar keratodermas.遗传性掌跖角化病的疼痛机制
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4
Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease.掌跖角化病(PPK):一种并不罕见的疾病的后天性和遗传性病因。
J Dtsch Dermatol Ges. 2014 Sep;12(9):781-8. doi: 10.1111/ddg.12418.
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The palmoplantar keratodermas: much more than palms and soles.掌跖角化病:远不止于手掌和脚掌。
Mol Med Today. 1999 Mar;5(3):107-13. doi: 10.1016/s1357-4310(98)01428-2.
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Lymphology. 2009 Jun;42(2):85-7.
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Hereditary palmoplantar keratodermas. Part II: syndromic palmoplantar keratodermas - Diagnostic algorithm and principles of therapy.遗传性掌跖角化病。第二部分:综合征性掌跖角化病 - 诊断算法和治疗原则。
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本文引用的文献

1
Human bone marrow harbors cells with neural crest-associated characteristics like human adipose and dermis tissues.人类骨髓中含有具有神经嵴相关特征的细胞,类似于人类脂肪组织和真皮组织。
PLoS One. 2017 Jul 6;12(7):e0177962. doi: 10.1371/journal.pone.0177962. eCollection 2017.
2
Prospect of Human Pluripotent Stem Cell-Derived Neural Crest Stem Cells in Clinical Application.人多能干细胞来源的神经嵴干细胞的临床应用前景
Stem Cells Int. 2016;2016:7695836. doi: 10.1155/2016/7695836. Epub 2016 Dec 20.
3
Palmoplantar keratodermas: clinical and genetic aspects.
掌跖角化病:临床与遗传学方面
J Dtsch Dermatol Ges. 2016 Feb;14(2):123-39; quiz 140. doi: 10.1111/ddg.12930.
4
Mal de Meleda with Congenital Cataract: A Novel Case Report.伴先天性白内障的梅勒达病:一例新病例报告
Indian J Dermatol. 2015 Sep-Oct;60(5):524. doi: 10.4103/0019-5154.159655.
5
Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease.掌跖角化病(PPK):一种并不罕见的疾病的后天性和遗传性病因。
J Dtsch Dermatol Ges. 2014 Sep;12(9):781-8. doi: 10.1111/ddg.12418.
6
Bilateral Keratoconus and Corneal Hydrops Associated with Eye Rubbing in a 7-year-old Girl.一名7岁女孩双眼圆锥角膜及角膜水肿与揉眼有关
J Ophthalmic Vis Res. 2014 Jan;9(1):101-5.
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Coexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family: two case reports.突尼斯一个近亲家庭中梅勒达病与先天性白内障并存:两例报告
J Med Case Rep. 2010 Apr 20;4:108. doi: 10.1186/1752-1947-4-108.
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Acquired palmoplantar keratoderma.获得性掌跖角化病。
Am J Clin Dermatol. 2007;8(1):1-11. doi: 10.2165/00128071-200708010-00001.
9
Ocular and dermatologic findings in two siblings with mal de Meleda.两名患有梅勒达病的兄弟姐妹的眼部和皮肤表现
Retina. 1999;19(3):247-50. doi: 10.1097/00006982-199903000-00013.