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作 者:黄敏[1] 左莹[2] HUANG Min;ZUO Ying(Graduate school of North Sichuan Medical College,Sichuan Nanchong 637000,China;Department of Endocrinology and Metabolism,The Affiliated Hospital of North Sichuan Medical College,Sichuan Nanchong 637000,China)
机构地区:[1]川北医学院研究生院,四川南充637000 [2]川北医学院附属医院内分泌代谢科,四川南充637000
出 处:《诊断学理论与实践》2024年第6期624-627,共4页Journal of Diagnostics Concepts & Practice
摘 要:原发性干燥综合征(primary Sjögren syndrome,PSS)作为一种慢性系统性自身免疫性疾病,早期发病往往较为隐匿,患者多以其他系统疾病的临床表现首次就诊,针对其发病机制现暂无明确研究结论。该病除侵犯机体外分泌腺体外,肾脏也常是其受累器官,部分患者可发展为肾小管酸中毒(renal tubular acidosis,RTA),出现难治性低钾血症及相关临床表现,而目前临床尚缺乏有针对性的规范治疗手段。早期诊断该病可以及时干预患者的病情进展,避免或延缓相关系统受累,使患者的临床治疗达最大获益。现报道1例因反复肢体乏力1年入院,最终被诊断为PSS继发Ⅰ型RTA的病例,根据患者自身情况予硫酸羟氯喹调节免疫治疗及对症处理,最终患者的病情好转。Primary Sjögren syndrome(PSS)as a chronic systemic autoimmune disease,many patients with early hid-den symptoms of presented the clinical manifestations of other systemic diseases for the first time,and its pathogenesis was not clear yet.PSS could invade the exocrine glands of body,and the kidney was also the susceptible organ in PSS.Some pa-tients could develop to renal tubular acidosis,and lead to refractory hypokalemia and related clinical manifestations.As lack of effective treatment,the early diagnosis and intervention of the disease could avoid damage or delay the involvement of related organs and maximize the benefits of clinical treatment.This paper reported a patient,who was admitted to hospi-tal with chief complain of repeated limb weakness for one year,was diagnosed as type I renal tubular acidosis secondary to primary Sjögren syndrome.The patients received symptomatic treatment and hydroxychloroquine sulfate immunotherapy,and the symptoms were resolved eventually.
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