Reiter’s综合征临床较罕见。1916年Reiter’s首先报告以尿道炎、关节炎、结合膜炎为三大主征的疾病。国内第一例是1956年刘倍基报告,其后相继有个案报告。本综合征病因不明,目前提出变态反应性机制、自体免疫学说和遗传因素有关等。它主要见于男性青年。初起先有尿道炎,排尿时有灼热感或剧痛,尿道口红肿。晨起见脓性尿滴出,在尿道炎后数天出现急性、无菌性化脓性结合膜炎。通常在病后两周后出现多发性关节炎。关节症状在三联征中最为突出,有剧烈疼痛及灼热感,进而肿 Reiter’s syndrome is clinically rare. In 1916, Reiter’s first reported urethritis, arthritis, conjunctivitis as the main symptoms of the disease. The first case in China was Liu Peiji’s report in 1956, followed by a case report. The etiology of the syndrome is unknown, the current proposed allergic mechanisms, autoimmune theory and genetic factors. It is mainly seen in male youth. Beginning urethritis, micturition when there is a burning sensation or pain, urethra swollen. Morning onset of purulent urine dripping, urethritis in a few days after the emergence of acute, aseptic purulent conjunctivitis. Multiple arthritis usually occurs two weeks after illness. Joint symptoms in the triad in the most prominent, severe pain and burning sensation, and then swollen