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原发性干燥综合征与妊娠:18例报告

Primary Sjögren's syndrome and pregnancy: A report of 18 cases.

作者信息

Demarchi Julia, Papasidero Silvia B, Klajn Diana, Alba Paula, Babini Alejandra M, Durigan Virginia, Gobbi Carla, Raiti Laura

机构信息

Servicio de Reumatología, Hospital General de Agudos Dr. Enrique Tornú, Ciudad Autónoma de Buenos Aires, Argentina.

Servicio de Reumatología, Hospital General de Agudos Dr. Enrique Tornú, Ciudad Autónoma de Buenos Aires, Argentina.

出版信息

Reumatol Clin (Engl Ed). 2019 Mar-Apr;15(2):109-112. doi: 10.1016/j.reuma.2017.07.014. Epub 2017 Aug 26.

Abstract

UNLABELLED

Primary Sjögren's syndrome (pSS) is a condition that predominantly affects women. Reports of pregnancy outcome in these patients are limited and contradictory.

OBJECTIVE

To describe pregnancy characteristics and outcomes and newborn morbidity in women with pSS.

MATERIAL AND METHODS

We included women with pSS who became pregnant after the onset of the symptoms of the disease. Clinical and serological characteristics, risk factors and previous maternal comorbidities are described. For each pregnancy in a woman with pSS, we recorded pregnancy course and outcome and newborn condition.

RESULTS

We assessed 11 patients with 18 pregnancies after the onset of pSS symptoms. All of them presented FAN +; 10 anti-Ro / SSA + and 7 anti-La / SSB +. The mean age in years at the onset of symptoms was 24.9 (SD 6.9) and at the time of pregnancy was 30.3 (SD 5.4). Thirteen pregnancies happened before the diagnosis, reporting only one miscarriage. Two preterm births, 1 case of oligohydramnios, 2 of premature membrane rupture and 2 low birthweight babies were reported after the onset of pSS symptoms. There was 1 newborn with congenital atrioventricular block and another with neonatal cutaneous lupus. All the women with pregnancy complications (n=6) had anti-Ro/SSA antibodies.

CONCLUSIONS

Almost half of the pregnancies assessed in women with pSS were associated with complications not attributable to factors other than the disease.

摘要

未标注

原发性干燥综合征(pSS)主要影响女性。关于这些患者妊娠结局的报道有限且相互矛盾。

目的

描述原发性干燥综合征女性患者的妊娠特征、结局及新生儿发病率。

材料与方法

我们纳入了在疾病症状出现后怀孕的原发性干燥综合征女性患者。描述了其临床和血清学特征、危险因素及既往母体合并症。对于每一位原发性干燥综合征女性患者的每次妊娠,我们记录了妊娠过程、结局及新生儿状况。

结果

我们评估了11例患者,在原发性干燥综合征症状出现后有18次妊娠。所有患者均表现为FAN +;10例抗Ro / SSA +,7例抗La / SSB +。症状出现时的平均年龄为24.9岁(标准差6.9),妊娠时为30.3岁(标准差5.4)。13次妊娠发生在诊断之前,仅报告1例流产。在原发性干燥综合征症状出现后,报告了2例早产、1例羊水过少、2例胎膜早破和2例低体重儿。有1例新生儿患有先天性房室传导阻滞,另1例患有新生儿皮肤狼疮。所有有妊娠并发症的女性(n = 6)均有抗Ro/SSA抗体。

结论

在原发性干燥综合征女性患者中评估的几乎一半妊娠与并非由疾病以外因素导致的并发症相关。

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