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妊娠晚期钩端螺旋体病的不典型表现。

Unusual presentation of leptospirosis in the late stage of pregnancy.

作者信息

Gaspari R, Annetta M G, Cavaliere F, Pallavicini F, Grillo R, Conti G, Antonelli M, Tafani C, Proietti R

机构信息

Department of Anaestesiology and Intensive Care, Catholic University, Rome, Italy.

出版信息

Minerva Anestesiol. 2007 Jul-Aug;73(7-8):429-32.

Abstract

Here we report a case of leptospirosis without fever during the late stage of pregnancy in which the initial clinical presentation was more suggestive of a pregnancy-related liver dysfunction rather than an infectious disease. A 32-year-old primipara at 37 week of gestation was hospitalised with a 10-day history of nausea, vomiting, and abdominal pain without fever. Initial routine blood tests showed hyperbilirubinemia, a moderate increase in transaminase levels, severe coagulopathy and an increased creatinine level. On clinical suspicion of pregnancy-related liver dysfunction such as HELLP syndrome (hemolysis, elevated liver enzyme levels, low platelet count) or acute fatty liver of pregnancy (AFLP), emergency caesarean section was performed and a healthy baby was delivered. Postoperatively, the patient was stable, but 5 days later she developed clouding of consciousness, severe jaundice and respiratory failure. At this time, an infectious disease was considered and leptospirosis was confirmed by serological tests. In conjunction with intensive care management, antibiotic therapy was given; the patient was discharged in good condition and her baby did not develop signs of active leptospirosis. While leptospirosis is rare in pregnancy, this is the first report of acute infection without fever mimicking the clinical pattern of HELLP syndrome or AFLP

摘要

在此,我们报告一例妊娠晚期无发热的钩端螺旋体病病例,其最初的临床表现更提示为妊娠相关肝功能障碍而非传染病。一名37孕周的32岁初产妇因恶心、呕吐和腹痛10天入院,无发热。初始常规血液检查显示高胆红素血症、转氨酶水平中度升高、严重凝血功能障碍及肌酐水平升高。临床怀疑为妊娠相关肝功能障碍,如HELLP综合征(溶血、肝酶水平升高、血小板计数降低)或妊娠急性脂肪肝(AFLP),遂行急诊剖宫产,娩出一健康婴儿。术后患者情况稳定,但5天后出现意识模糊、严重黄疸及呼吸衰竭。此时考虑为传染病,经血清学检查确诊为钩端螺旋体病。结合重症监护管理,给予抗生素治疗;患者康复出院,其婴儿未出现钩端螺旋体病活动迹象。虽然妊娠期间钩端螺旋体病罕见,但这是首例无发热的急性感染病例,其临床表现类似HELLP综合征或AFLP。

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