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Papillon-Lefèvre综合征伴沟纹舌1例 被引量:2

A case of Papillon-Lefèvre syndrome with fissured tongue
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摘要 报告1例Papillon-Lefèvre综合征伴沟纹舌。患者男,23岁。自幼牙龈化脓,近4年来掌跖部弥漫性角化,并伴有沟纹舌。临床诊断为Papillon-Lefèvre综合征。给予阿维A治疗后皮损得到控制。 A case of Papillon-efevre syndrome is reported,The patient was a 23-year-old male,who developed gingivitis within the first month of life and presented with plantar keratoderma 4 years age.He also had fissured tongue when he was 3 years old.The lesions got improved by administration of acitretin.
出处 《临床皮肤科杂志》 CAS CSCD 北大核心 2006年第2期94-95,共2页 Journal of Clinical Dermatology
关键词 Papillon-Lefevre综合征 沟纹舌 Papillon-Lefevre syndrome fissured tongue
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参考文献5

  • 1Angel TA. Hsu S. Kornbleuth Sl. et al. Pupillon-Lefevre svndrome:a case report of four affected siblings[J]. J Am Acad Dermatol,2002,46(2 Suppl):S8-10.
  • 2Hathway R. Papillon-Lefevre syndrome[J].Br Dent J. 1982,153(10):370-371.
  • 3杨勤萍,方丽.掌跖角化牙周病综合征2例[J].临床皮肤科杂志,1998,27(5):331-331. 被引量:1
  • 4Ullbro C. Crossner CG. Nederfors T. et al. Dermaoligic and oral findings in a cohort of 47 patients with Papillon-Lefevre syndrome[J]. J Am Acad Dermatol ,2003,48(3):345-351.
  • 5Gorlin RJ, Sednno H ,Anderson VE. The syndrome of palmarplantar hyperkeratosis and premature periodontal destruction of the tecth. A clinical genetic analysis of the Papillon-Lefevre syndrome[J].J Pediatr,1946,65:895-908.

同被引文献37

  • 1张雄,章锦才,李兰超.掌跖角化-牙周破坏综合征牙周治疗一例[J].中华口腔医学杂志,2006,41(2):72-73. 被引量:3
  • 2Papillon MM, Lefevre P. Two cases of symmetrically familial pal- mar and plantar hyperkeratosis ( Meleda disease) within brother and sister combined with severe dental alterations in both cases [ J ]. Bull Soc Fr Dermatol SyphiligP, 1924,31 (2) : 82 - 87.
  • 3Dhanrajani PJ. Papillon-LeFevre syndrome : clinical presentation and a brief review [ J ]. Oral Surg Oral Med Oral Pathol Oral Radiol Endod,2009,108 ( 1 ) : 1 - 7.
  • 4Toomes C, James J, Wood A J, et al. Loss-of-function mutation cathepsin C gene result in periodontal disease and palmoplanter keratosis [ J ]. Nat Genet, 1999,23:421 - 424.
  • 5Hart PS, Zhang Y, Firatli E, et al. Identification of eathepsin C mutations in ethnically diverse Papillon- Lefevre syndrome patients [ J ]. Med Genet,2000,37:927 - 932.
  • 6Hart TC, Bowden DW, Ghaffar KA, et al. Sublocalization of the Papillon-Lefevre syndrome locus on llq14-q21 [J]. Am J Med Genet, 1998, 79 : 134 - 139.
  • 7Guay D, Beaulieu C, Percival MD. Therapeutic utility and me- dicinal chemistry of cathepsin C inhibitors [ J ]. Curt Top Med Chem,2010,10:708 - 716.
  • 8Hart TC, Hart PS. Genetic studies of craniofacial anomalies: clinical implications and applications [ J ]. Orthod Craniofac Res, 2009,12:212 - 220.
  • 9于世凤,汪说之,何志秀,等.口腔组织病理学[M].5版.北京:人民卫生出皈社.2006:179-182.
  • 10Meade JL , de Wynter EA, Brett P, et al. A family with Papil- lon-LeFevre syndrome reveals a requirement for cathepsin C in granzyme B activation and NK cell cytolytic activity [ J ]. Blood, 2006, 107(9) : 3665 -3668.

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