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青少年牙周炎

Juvenile periodontitis.

作者信息

Genco R J, Christersson L A, Zambon J J

出版信息

Int Dent J. 1986 Sep;36(3):168-76.

PMID:3533789
Abstract

Juvenile periodontitis occurs in children and young adults and can be classified into: periodontitis which occurs in otherwise healthy individuals, and periodontitis which occurs in juveniles with systemic disease. The periodontitis which occurs in otherwise healthy individuals consists of two major forms: juvenile periodontitis, also called periodontosis or localized juvenile periodontitis (LJP), and generalized juvenile periodontitis which includes early onset adult periodontitis, recurrent necrotizing ulcerative periodontitis and the true generalized form of juvenile periodontitis. Periodontitis in systemically diseased individuals can be divided into three subgroups: juvenile periodontitis associated with primary neutrophil disorders, juvenile periodontal disease in which neutrophils are secondarily abnormal, and juvenile periodontitis associated with other diseases. Juvenile periodontitis is perhaps the best understood form of periodontal disease. A major infecting organism, Actinobacillus actinomycetemcomitans, is strongly associated with the disease, and may be an exogenous pathogen since it is not found in healthy individuals or in healthy sites in LJP patients. It is virulent with marked leukaggressive properties and it induces a marked antibody response in infected patients. Eradication of Actinobacillus actinomycetemcomitans requires attention to the fact that it invades the tissue and hence systemic antimicrobials or surgical excision of the tissues is necessary for eradication. Marked suppression of the organism from subgingival sites is associated with healing. Host responses in LJP have also been well described and most immune functions studied appear to be normal. The notable exception is neutrophil chemotaxis which is depressed. Associated with depressed neutrophil chemotaxis is a reduction of neutrophil receptors for several chemotactic factors including C5a, the fifth component of complement.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

青少年牙周炎发生于儿童和年轻人,可分为:发生于健康个体的牙周炎,以及发生于患有全身性疾病青少年的牙周炎。发生于健康个体的牙周炎主要有两种形式:青少年牙周炎,也称为牙周变性或局限性青少年牙周炎(LJP),以及广泛性青少年牙周炎,其中包括早发性成人牙周炎、复发性坏死性溃疡性牙周炎和真正的广泛性青少年牙周炎。全身性疾病个体的牙周炎可分为三个亚组:与原发性中性粒细胞疾病相关的青少年牙周炎、中性粒细胞继发性异常的青少年牙周疾病,以及与其他疾病相关的青少年牙周炎。青少年牙周炎可能是人们了解最多的牙周疾病形式。一种主要的感染病原体——伴放线放线杆菌与该疾病密切相关,并且可能是一种外源性病原体,因为在健康个体或LJP患者的健康部位未发现该菌。它具有毒性,具有显著的白细胞侵袭特性,并且在感染患者中会引发明显的抗体反应。根除伴放线放线杆菌需要注意其会侵入组织,因此根除需要全身使用抗菌药物或手术切除组织。从龈下部位显著抑制该菌与愈合相关。LJP中的宿主反应也有详细描述,大多数研究的免疫功能似乎正常。明显的例外是中性粒细胞趋化性降低。与中性粒细胞趋化性降低相关的是,包括补体第五成分C5a在内的几种趋化因子的中性粒细胞受体减少。(摘要截选至250词)

相似文献

1
Juvenile periodontitis.青少年牙周炎
Int Dent J. 1986 Sep;36(3):168-76.
2
Periodontal disease: an overview for physicians.牙周病:给医生的概述
Mt Sinai J Med. 1998 Oct-Nov;65(5-6):362-9.
3
Actinobacillus actinomycetemcomitans and localized juvenile periodontitis. Clinical, microbiologic and histologic studies.伴放线放线杆菌与局限性青少年牙周炎。临床、微生物学及组织学研究。
Swed Dent J Suppl. 1993;90:1-46.
4
1985 Kreshover lecture. Molecular factors influencing neutrophil defects in periodontal disease.1985年克雷肖弗讲座。影响牙周病中性粒细胞缺陷的分子因素。
J Dent Res. 1986 Dec;65(12):1379-91. doi: 10.1177/00220345860650120201.
5
Early-onset periodontitis.早发性牙周炎
Curr Opin Periodontol. 1996;3:45-58.
6
Neutrophil function in patients with localized juvenile periodontitis and with rapidly progressive periodontitis.局限性青少年牙周炎和快速进展性牙周炎患者的中性粒细胞功能
J Biol Buccale. 1988 Sep;16(3):151-6.
7
Periodontal diseases affecting children and young adults.影响儿童和年轻人的牙周疾病。
J Can Dent Assoc. 1996 Aug;62(8):650-2, 655-6.
8
Decreased lactoferrin content in granulocytes from subjects with Actinobacillus actinomycetemcomitans associated periodontal diseases.
J Parodontol. 1990 May;9(2):195-9.
9
Clinical, laboratory, and immunological studies of a family with a high prevalence of generalized prepubertal and juvenile periodontitis.
J Periodontol. 1992 May;63(5):457-68. doi: 10.1902/jop.1992.63.5.457.
10
Neutrophil chemotaxis and serum factor modulation in Brazilian periodontitis patients.巴西牙周炎患者的中性粒细胞趋化性及血清因子调节
Arch Med Res. 1997 Winter;28(4):531-5.

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J Clin Imaging Sci. 2014 May 27;4(Suppl 2):2. doi: 10.4103/2156-7514.133258. eCollection 2014.
2
LL-37 opsonizes and inhibits biofilm formation of Aggregatibacter actinomycetemcomitans at subbactericidal concentrations.LL-37 在亚抑菌浓度下调理并抑制伴放线放线杆菌生物膜的形成。
Infect Immun. 2013 Oct;81(10):3577-85. doi: 10.1128/IAI.01288-12. Epub 2013 Jul 8.
3
A clinically hidden but severely destructive entity.一种临床隐匿但具有严重破坏性的病症。
BMJ Case Rep. 2013 Jun 27;2013:bcr2013009601. doi: 10.1136/bcr-2013-009601.