Cornec Divi, Saraux Alain, Jousse-Joulin Sandrine, Pers Jacques-Olivier, Boisramé-Gastrin Sylvie, Renaudineau Yves, Gauvin Yves, Roguedas-Contios Anne-Marie, Genestet Steeve, Chastaing Myriam, Cochener Béatrice, Devauchelle-Pensec Valérie
Department of Rheumatology, Brest Teaching Hospital, Brest, France.
EA2216, INSERM ESPRI, ERI29, Université de Brest, Brest, France.
Clin Rev Allergy Immunol. 2015 Dec;49(3):278-87. doi: 10.1007/s12016-014-8431-1.
Primary Sjögren's syndrome (pSS) is a frequent autoimmune systemic disease, clinically characterized by eyes and mouth dryness in all patients, salivary gland swelling or extraglandular systemic manifestations in half of the patients, and development of lymphoma in 5 to 10 % of the patients. However, patients presenting with sicca symptoms or salivary gland swelling may have a variety of conditions that may require very different investigations, treatments, or follow-up. Eye and/or mouth dryness is a frequent complaint in clinical setting, and its frequency increases with age. When evaluating a patient with suspected pSS, the first step is to rule out its differential diagnoses, before looking for positive arguments for the disease. Knowledge of normal and abnormal lachrymal and salivary gland physiology allows the clinician to prescribe the most adapted procedures for evaluating their function and structure. New tests have been developed in recent years for evaluating these patients, notably new ocular surface staining scores or salivary gland ultrasonography. We describe the different diagnoses performed in our monocentric cohort of 240 patients with suspected pSS. The most frequent diagnoses are pSS, other systemic autoimmune diseases, idiopathic sicca syndrome and drug-induced sicca syndrome. However, other diseases are important to rule out due to their specific management, such as sarcoidosis, granulomatosis with polyangeitis, IgG4-related disease, chronic hepatitis C virus or human immunodeficiency virus infections, graft-versus-host disease, and head and neck radiation therapy. At the light of these data, we propose a core of minimal investigations to be performed when evaluating a patient with suspected pSS.
原发性干燥综合征(pSS)是一种常见的自身免疫性全身性疾病,临床上所有患者均以眼干和口干为特征,半数患者伴有唾液腺肿大或腺外系统性表现,5%至10%的患者会发展为淋巴瘤。然而,出现干燥症状或唾液腺肿大的患者可能患有多种疾病,可能需要非常不同的检查、治疗或随访。眼干和/或口干在临床环境中是常见的主诉,且其发生率随年龄增长而增加。在评估疑似pSS的患者时,第一步是排除其鉴别诊断,然后再寻找支持该疾病的阳性依据。了解正常和异常的泪腺及唾液腺生理学知识,有助于临床医生选择最适合的程序来评估它们的功能和结构。近年来已开发出用于评估这些患者的新测试,特别是新的眼表染色评分或唾液腺超声检查。我们描述了在我们单中心队列中对240例疑似pSS患者进行的不同诊断。最常见的诊断是pSS、其他系统性自身免疫性疾病、特发性干燥综合征和药物性干燥综合征。然而,由于其特殊的治疗方法,其他疾病也很重要,需要排除,如结节病、肉芽肿性多血管炎、IgG4相关疾病、慢性丙型肝炎病毒或人类免疫缺陷病毒感染、移植物抗宿主病以及头颈部放射治疗。根据这些数据,我们提出了在评估疑似pSS患者时应进行的一组最小化检查的核心内容。