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CASE REPORT
Year : 2019  |  Volume : 8  |  Issue : 3  |  Page : 1284-1286

Congenital dilatation of the nasolacrimal sac (Dacryocystocele): Case report


1 Department of Obstetrics and Gynecology №1, Marat Ospanov, West Kazakhstan State Medical University, Aktobe, Kazakhstan
2 Ain Shams University, Cairo, Egypt
3 Ain Shams University, Cairo, Egypt; Ahmadi Hospital, Kuwait Oil Company, Ahmadi, Kuwait

Correspondence Address:
Prof. Ibrahim A Abdelazim
Department of Obstetrics and Gynecology, Ain Shams University, Cairo, Egypt and Ahmadi Kuwait Oil (KOC) Company Hospital, Ahmadi

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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jfmpc.jfmpc_17_19

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Congenital dacryocystoceles are usually diagnosed in the third trimester by parental ultrasound as a cystic lesion adjacent to the medial and inferior aspects of the fetal orbit. A considerable number of dacryocystocele are bilateral and resolve spontaneously in utero and/or immediately after delivery. Persistent dacryocystoceles need ophthalmological consultation to avoid the possible potential complications. This case report represents a case of congenital dacryocystocele diagnosed by antenatal 2D and 3D ultrasounds, which disappeared spontaneously 2 days after birth. To highlight that, the diagnosis of congenital dacryocystoceles is important to avoid additional postnatal diagnostic techniques and to manage the potential postnatal complications.


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