A Rare Case of Dacryocystocele Diagnosed by Antenatal Ultrasonography at 26 Weeks of Gestation

被引:0
|
作者
Ganesan, Parvathy [1 ,3 ]
Balakrishnan, Bijoy K. [2 ]
Parasuram, Meenu Batra [2 ]
机构
[1] Pran Fertil & Well Women Ctr, Dept Fetomaternal Med, Thiruvananthapuram, Kerala, India
[2] CIMAR Cochin Hosp, Dept Fetomaternal Med, Kochi, Kerala, India
[3] Pran Fertil & Well Women Ctr, Dept Fetomaternal Med, Thiruvananthapuram 695011, Kerala, India
关键词
dacryocyctocele; prenatal diagnosis; Inner canthus; inferomedial; complete resolution; CONGENITAL DACRYOCYSTOCELE; SONOGRAPHIC DIAGNOSIS;
D O I
10.1055/s-0043-57003
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Dacryocystocele is a rare variant of obstruction of the nasolacrimal duct that results in a fluid-filled, closed sac. It often resolves by the spontaneous perforation of the distal membrane during the early neonatal period, resulting in drainage of the accumulated fluid. If persisting, this benign condition can be usually treated postnatally. If the cysts occur bilaterally, there can be an obstruction to the nasal passage due to their possible intranasal extension and might require surgical intervention postnatally to prevent or treat respiratory distress. Also, it may be a part of a few syndromes, which makes the early prenatal diagnosis very important. In this case report, we present a case of unilateral dacryocystocele reported as early as 26 weeks, 3 days of gestation detected by ultrasound that spontaneously resolved by 33 weeks. This is one of the earliest reported three-dimensional/four-dimensional ultrasound diagnosis of dacryocystocele.
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收藏
页码:82 / 84
页数:3
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