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胎儿磁共振成像(MRI)上先天性小眼畸形的孤立表现。

Isolated presentation of congenital microphthalmia on fetal MRI.

作者信息

Gittens Allison, Gedrich Mark, Khandelwal Meena, Fischer Richard, Germaine Pauline

机构信息

Department of Diagnostic Radiology, Cooper University Hospital, Camden, NJ 08102, USA.

Rowan University, School of Osteopathic Medicine, 1 Medical Center Drive, Stratford, NJ 08084, USA.

出版信息

Radiol Case Rep. 2019 Jun 29;14(9):1069-1071. doi: 10.1016/j.radcr.2019.05.002. eCollection 2019 Sep.

Abstract

A fetal growth scan was performed on a 34-year-old Caucasian woman, G4P3, with a history of gestational diabetes diagnosed at 32 weeks gestation. The examination revealed an absence of normal left globe with an echogenic mass in its expected location with a rim of surrounding hypoechoic fluid. The right orbit and globe were normal, and no other structural anomalies were identified. Prior to this examination, the patient had a normal anatomic survey and fetal echocardiogram at 20 weeks, however due to fetal positioning there was limited visualization of the orbits on initial scan. Fetal MRI was performed at 36 weeks gestation and confirmed near-complete absence of the left globe with asymmetrically smaller size of the left orbit. Normal right orbit and globe were present, and no additional fetal structural abnormalities were observed. Figure 1 congenital microphthalmia was diagnosed based on the imaging findings, preparing the family and alerting the medical team of appropriate care needed postnatally.

摘要

对一名34岁、孕4产3的白人女性进行了胎儿生长扫描,该女性有妊娠糖尿病病史,在妊娠32周时被诊断出。检查发现左侧眼球正常结构缺失,在其预期位置有一个回声团块,周围有一圈低回声液性暗区。右侧眼眶和眼球正常,未发现其他结构异常。在本次检查之前,患者在孕20周时进行了正常的解剖学超声检查和胎儿超声心动图检查,然而由于胎儿体位原因,初次扫描时眼眶的可视化受限。在妊娠36周时进行了胎儿磁共振成像(MRI),证实左侧眼球几乎完全缺失,左侧眼眶不对称性变小。右侧眼眶和眼球正常,未观察到其他胎儿结构异常。根据影像学检查结果诊断为先天性小眼球,告知了家属并提醒医疗团队产后需要采取的适当护理措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4da/6612667/79df53337bfc/gr1.jpg

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