Lü W, Sun G
Department of Medicine, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
Zhonghua Nei Ke Za Zhi. 2001 Nov;40(11):747-9.
Primary biliary cirrhosis (PBC) is a chronic non-suppurative destructive cholangitis of unknown etiology. It has been reported that patients with PBC suffer from xerostomia and keratoconjunctivitis at high prevalence and PBC has been shown to be associated with Sjögren's syndrome. This study investigated the relationship between PBC and Sjögren's syndrome.
20 cases diagnosed as PBC consented to the evaluation for Sjögren's syndrome which included clinical and serological features, Schirmer's test, measurement of parotid flow rate and labial minor salivary gland biopsy.
The main manifestations of PBC are jaundice, pruritus, hepatosplenomegaly. M2 subtype of antimitochondrial antibody is of great specificity for PBC. Many PBC patients are suffering from xerostomia and keratoconjunctivitis sicca but do not have typical serological and pathological presentations of primary Sjögren's syndrome. Corticosteroids and immunosuppressive agents have disappointing effects in the treatment. Ursodeoxycholic acid is effective to certain extent.
It was indicated that Sjögren's syndrome associated with PBC appears to be a secondary form differing from primary Sjögren's syndrome.
原发性胆汁性肝硬化(PBC)是一种病因不明的慢性非化脓性破坏性胆管炎。据报道,PBC患者口干和角结膜炎的患病率很高,并且已证明PBC与干燥综合征有关。本研究调查了PBC与干燥综合征之间的关系。
20例诊断为PBC的患者同意接受干燥综合征评估,评估内容包括临床和血清学特征、Schirmer试验、腮腺流速测量和唇小唾液腺活检。
PBC的主要表现为黄疸、瘙痒、肝脾肿大。抗线粒体抗体M2亚型对PBC具有高度特异性。许多PBC患者患有口干和干眼症,但没有原发性干燥综合征的典型血清学和病理学表现。皮质类固醇和免疫抑制剂治疗效果不佳。熊去氧胆酸在一定程度上有效。
表明与PBC相关的干燥综合征似乎是一种不同于原发性干燥综合征的继发形式。