Sjögren综合征的喉、牙学表现

B. Kamiński, K. Błochowiak
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引用次数: 1

摘要

Sjögren 's综合征(SS)影响许多不同的领域,许多专家可能参与SS的诊断和治疗。耳鼻喉科和牙科表现,神经功能障碍和听力损失可能是SS的初始症状。本章描述了SS最常见的耳鼻喉科和口腔表现,其病理机制和可能的病因。干燥伴SS有许多临床意义。SS的口干率从最初诊断时的41%到诊断后10年的84%不等。根据目前的EULAR/ACR标准,非刺激唾液流速为0.1 ml/min,对5项的加权和给予1分。唾液腺导管和腺泡周围单核细胞聚集的存在导致这些腺体的功能和结构改变,并损害其分泌功能。最常见的口腔体征和症状是龋齿、蛀牙、真菌感染、创伤性口腔病变、吞咽困难、发音困难和唾液腺炎症。SS患者唾液的特点是乳铁蛋白、钾和胱抑素C浓度升高,淀粉酶、碳酸酐酶、粘蛋白、组蛋白、IgA、他汀蛋白、富含脯氨酸的蛋白质浓度降低,唾液缓冲特性丧失。这些生理防御机制的缺乏增加了机会性感染的风险,主要是由白色念珠菌引起的真菌感染。念珠菌病伴有角唇炎、单纯性唇炎和剥脱性唇炎。SS患者的唾液腺以慢性炎症为特征,横纹管周围存在淋巴细胞浸润。这些管周病灶可能导致有组织异位淋巴样结构的发展,类似于次级淋巴样器官,具有分离的T细胞和b细胞区,以及高内皮小静脉。鼻黏膜萎缩、咽喉干燥、吞咽困难、声音嘶哑、耳鸣、胃食管反流和慢性咳嗽。与一般人群相比,SS患者有更高的感音神经性听力障碍患病率。特发性听力损失可能是SS的初始表现。此外,作者介绍并讨论了SS的主要神经系统症状。约20%的SS患者报告了神经系统表现。SS患者可能出现神经系统表现,如周围神经病变和其他形式的神经病,包括感觉共济失调、无感觉共济失调的疼痛性感觉神经病、多发性单神经病变、多发性颅神经病变、自主神经病变,根状神经病变口内和口外感觉异常,感觉减退,三叉神经
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Laryngological and Dental Manifestations of Sjögren’s Syndrome
Sjögren’s syndrome (SS) affects numerous different areas, and many special-ists may be involved in the diagnosis and treatment of SS. Otolaryngological and dental manifestations, neurological impairment, and hearing loss may be the initial symptoms of SS. This chapter describes the most common otolaryngological and oral manifestations of SS, its pathomechanism and possible etiology. Dryness accompanying SS is associated with many clinical implications. The rate of dry mouth in SS ranged from 41% at initial diagnosis to 84% 10 years after diagnosis. An unstimulated salivary flow rate of 0.1 ml/min in sialometry gives a score of 1 to the weighted sum of 5 items according to the current EULAR/ACR criteria. The presence of mononuclear cell aggregates around the ducts and acini of salivary glands results in functional and structural alterations at the level of these glands and impairs their secretory function. The most common oral signs and symptoms are dental caries, tooth decay, fungal infections, traumatic oral lesions, dysphagia, dysgeusia, and inflammation of the salivary glands. Saliva in SS is characterized by the increased concentration of lactoferrin, potassium and cystatin C and the decreased concentration of amylase, carbonic anhydrase, mucins, histatines, IgA, statherins, proline-rich proteins, and the loss of salivary buffer properties. The lack of these physiological defense mechanisms increases the risk of opportunistic infections, mainly fungal infections by Candida albicans . Candidiasis accompanies angular cheilitis, simple cheilitis, and exfoliative cheilitis. The salivary glands of SS patients are characterized by chronic inflammation with the presence of lymphocytic infiltrates located around the striated ducts. These periductal foci may lead to the development of organized ectopic lymphoid structures resembling secondary lymphoid organs with segregated T- and B-cell areas, and high endothelial venules. 2 or atrophy of the nasal mucosa, dryness of the throat, dysphagia, hoarseness, otalgia and tinnitus, gastro-esophageal reflux, and chronic cough. Patients with SS tend to have a higher prevalence of sensorineural hearing impairment compared with the general population. Idiopathic hearing loss may represent the initial manifestation of SS. Furthermore, authors present and discuss the main neurological symptoms of SS. Neurological manifestations are reported in about 20% of patients with SS. In patients with SS, neurological manifestations may occur, such as peripheral neuropathy and other forms of neuropathies, including sensory ataxia, painful sensory neuropathy without sensory ataxia, multiple mononeuropathy, multiple cranial neuropathy, autonomic neuropathy, radiculoneuropathy intra- and extraoral paresthesias, hypaesthesia, trigeminal
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