Perez-Davidi M
Dept. of Prosthodontics, The Hebrew University Hadassah, Faculty of Dental Medicine, Jerusalem, Israel.
Refuat Hapeh Vehashinayim (1993). 2011 Oct;28(4):12-8, 37.
With a prevalence of 1% in western populations, Celiac disease (CD) is one of the most common inflammatory disorders of the small intestine. CD is often assumed to have its onset in childhood, but it has recently been suggested that adults can also develop CD. Clinical manifestations vary according to age group: infants and young children present with diarrhea, abdominal distention, and failure to thrive, whereas adults that develop CD not only present with diarrhea, but also with silent manifestations such as anemia, osteoporosis, or neurological symptoms. In the small intestine of celiac disease patients, dietary wheat gluten and similar proteins in barley and rye trigger an inflammatory response. While strict adherence to a gluten-free diet induces full recovery in most patients, a small percentage of patients fail to recover. In a subset of these refractory celiac disease patients, an (aberrant) oligoclonal intraepithelial lymphocyte population develops into overt lymphoma. Celiac disease is strongly associated with HLA-DQ2 and/or HLA-DQ8, as both genotypes predispose for disease development. mmunohistochemistry of the small intestine of patients shows villous atrophy, crypt hyperplasia, and elevated levels of intraepithelial lymphocytes (IELs). The only therapy until now is a gluten-free diet, which will normalize the clinical and histological manifestations and allows the patients to live an otherwise normal life. part of the symptoms are oral manifestations as dental enamel defects, aphthous ulcers and Atrophic Glossitis. The prevalence of caries in CD patiens is law as compared to the healthy population and in some cases the normal eruption sequence of the teeth was damaged. Part of the undiagnosed CD patients are among our patients and the enamel defects they present are misdiagnosed as tetracycline pigmentation or white spot lesions it is the practitioners responsibility to add CD as a possible cause to the findings and refer the patient to further examination. The case report in this paper presents a 47 years old female patient who was a patient in my practice for 25 years. When she became 40 she was diagnosed as CD and treated accordingly over the years enamel defects were treated conservatively. As the lesions became more frequent and unpredictable the patient demanded a full mouth solution that would restore both the functional and esthetical problems she had with her dentition. A full Porcelane Fused to Metal (PFZ) crowns were fabricated and the patient got a solution to both here demands. The crowns used were 3M Lava zirconia crowns and the case is presented as step by step sequence.
在西方人群中,乳糜泻(CD)的患病率为1%,是小肠最常见的炎症性疾病之一。人们通常认为CD在儿童期发病,但最近有人提出成年人也会患上CD。临床表现因年龄组而异:婴幼儿表现为腹泻、腹胀和发育不良,而成年CD患者不仅有腹泻症状,还会有无症状表现,如贫血、骨质疏松或神经症状。在乳糜泻患者的小肠中,膳食中的小麦麸质以及大麦和黑麦中的类似蛋白质会引发炎症反应。虽然严格遵循无麸质饮食能使大多数患者完全康复,但仍有一小部分患者无法康复。在这些难治性乳糜泻患者的一个亚组中,(异常的)寡克隆上皮内淋巴细胞群会发展为明显的淋巴瘤。乳糜泻与HLA - DQ2和/或HLA - DQ8密切相关,因为这两种基因型都易引发疾病。对患者小肠进行免疫组织化学检查显示有绒毛萎缩、隐窝增生以及上皮内淋巴细胞(IELs)水平升高。到目前为止,唯一的治疗方法是无麸质饮食,这将使临床和组织学表现恢复正常,并使患者能够过上正常生活。部分症状表现为口腔问题,如牙釉质缺陷、阿弗他溃疡和萎缩性舌炎。与健康人群相比,CD患者的龋齿患病率较低,在某些情况下,牙齿的正常萌出顺序也会受到影响。我们的患者中有一部分是未被诊断出的CD患者,他们出现的牙釉质缺陷被误诊为四环素色素沉着或白斑病变,医生有责任将CD作为这些症状的可能病因,并将患者转诊进行进一步检查。本文的病例报告介绍了一位47岁的女性患者,她在我的诊所就诊了25年。40岁时她被诊断为CD,并接受了相应治疗,多年来牙釉质缺陷一直采用保守治疗。随着病变越来越频繁且难以预测,患者要求进行全口修复,以解决她在牙列方面的功能和美观问题。制作了全瓷熔附金属(PFZ)冠,患者的两个需求都得到了解决。使用的冠是3M Lava氧化锆冠,并按步骤顺序展示了该病例。