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帕皮永-勒费夫尔综合征:一例病例报告。

Papillon-Lefevre syndrome: A case report.

作者信息

Pavankumar Kalwa

机构信息

Department of Periodontics, Navodaya Dental College and Hospital, Navodaya Nagar, Raichur 584103, Karnataka, India.

出版信息

Saudi Dent J. 2010 Apr;22(2):95-8. doi: 10.1016/j.sdentj.2010.02.009. Epub 2010 Feb 6.

Abstract

Papillon-Lefevre syndrome (PLS) is a rare autosomal recessive disorder of keratinization, characterized by palmoplantar hyperkeratosis, periodontal involvement and precocious loss of dentition. The purpose of this report was to describe the case of an 18-year-old girl who presented to the out patient department of Navodaya Dental College and Hospital, Raichur, Karnataka, India, with the chief complaint of multiple loss of teeth. Her gingiva appeared erythematous, edematous and bled readily on probing, and the teeth were mobile. Hyperkeratosis of palms and soles were found. These findings are consistent with Papillon-Lefèvre syndrome. The clinical presentation, differential diagnosis, complications and management of this syndrome are discussed.

摘要

掌跖角化-牙周破坏综合征(PLS)是一种罕见的常染色体隐性角化障碍性疾病,其特征为掌跖角化过度、牙周受累和牙齿过早缺失。本报告的目的是描述一名18岁女孩的病例,该女孩前往印度卡纳塔克邦赖丘尔市纳沃代亚牙科学院和医院门诊部就诊,主诉为多颗牙齿缺失。她的牙龈呈红斑状、水肿,探诊时容易出血,牙齿松动。发现有掌跖角化过度。这些发现与掌跖角化-牙周破坏综合征相符。本文讨论了该综合征的临床表现、鉴别诊断、并发症及治疗。

相似文献

1
Papillon-Lefevre syndrome: A case report.帕皮永-勒费夫尔综合征:一例病例报告。
Saudi Dent J. 2010 Apr;22(2):95-8. doi: 10.1016/j.sdentj.2010.02.009. Epub 2010 Feb 6.
3
Papillon- Lefèvre Syndrome: Report of a case and its management.掌跖角化-牙周破坏综合征:1例报告及其治疗
J Clin Exp Dent. 2012 Feb 1;4(1):e77-81. doi: 10.4317/jced.50594. eCollection 2012 Feb.

本文引用的文献

2
Papillon-Lefevre syndrome in two brothers.
Indian J Dermatol Venereol Leprol. 2002 May-Jun;68(3):155-6.
5
Papillon-Lefèvre syndrome.
Indian Pediatr. 2003 Dec;40(12):1197-200.
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Dermatologic and oral findings in a cohort of 47 patients with Papillon-Lefèvre syndrome.
J Am Acad Dermatol. 2003 Mar;48(3):345-51. doi: 10.1067/mjd.2003.197.
9
Papillon-Lefevre syndrome: a case report of four affected siblings.
J Am Acad Dermatol. 2002 Feb;46(2 Suppl Case Reports):S8-10. doi: 10.1067/mjd.2002.104968.

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