Department of Oral Surgery, University of Padova, Institute of Clinical Dentistry, Padova, Italy.
J Periodontol. 2012 Apr;83(4):465-76. doi: 10.1902/jop.2011.110261. Epub 2011 Aug 22.
Destructive membranous periodontal disease, or ligneous gingivitis, is a rare condition involving nodular gingival enlargement with ulceration and periodontal tissue destruction. This review gives a brief account of the cases reported in the literature. An effort is also made to define the periodontal disease caused by plasminogen deficiency with a view to its potential inclusion in the classification of periodontal diseases.
A MEDLINE/PubMed and manual search was conducted to find papers describing ≥1 case of ligneous disease involving the oral mucosa.
We identified 23 articles reporting 35 cases. For each patient, we analyzed various characteristics, including age, sex, age of onset, oral symptoms, histologic features, plasminogen levels (functional activity, plasma antigen), genetic features, treatment, and results of treatment during the reported follow-up.
Ligneous gingivitis is a rare periodontal disorder closely associated with ligneous conjunctivitis and plasminogen deficiency. Its diagnosis may be supported by the finding of genetic mutations responsible for the condition. Research is focusing on the future development of an effective therapy capable of arresting the destructive evolution of the disease. Additional studies, investigating features such as probing depth and attachment loss, are needed for the appropriate classification of this periodontal disease.
破坏性膜性牙周病,又称木质龈炎,是一种罕见的疾病,表现为结节性牙龈肿大伴溃疡和牙周组织破坏。本文简要介绍了文献中报道的病例。本文还努力定义了由纤溶酶原缺乏引起的牙周病,以期将其纳入牙周病的分类。
通过 MEDLINE/PubMed 和手动搜索,查找描述≥1 例涉及口腔黏膜的木质疾病的论文。
我们确定了 23 篇报道 35 例病例的文章。对于每个患者,我们分析了各种特征,包括年龄、性别、发病年龄、口腔症状、组织学特征、纤溶酶原水平(功能活性、血浆抗原)、遗传特征、治疗以及报告的随访期间的治疗结果。
木质龈炎是一种罕见的牙周疾病,与木质结膜炎和纤溶酶原缺乏密切相关。其诊断可能通过发现导致该病的遗传突变来支持。研究的重点是开发一种有效的治疗方法,能够阻止疾病的破坏性进展。需要进一步的研究来调查如探诊深度和附着丧失等特征,以便对这种牙周病进行适当的分类。