Congenital dilatation of the nasolacrimal sac (Dacryocystocele): Case report
| Autor: | Tatyana Starchenko, Sakiyeva Kanshaiym, Mohamed E S Hamed, Mohamed Hassan Naser El-Din, Ibrahim A. Abdelazim |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
Fetus
medicine.medical_specialty business.industry lcsh:R lcsh:Medicine Case Report 030209 endocrinology & metabolism medicine.disease Third trimester Dacryocystocele Congenital 03 medical and health sciences Cystic lesion 0302 clinical medicine medicine.anatomical_structure In utero nasolacrimal Medicine Congenital dilatation 030212 general & internal medicine Radiology dilatation business dacryocystocele Orbit (anatomy) |
| Zdroj: | Journal of Family Medicine and Primary Care, Vol 8, Iss 3, Pp 1284-1286 (2019) Journal of Family Medicine and Primary Care |
| ISSN: | 2249-4863 |
| DOI: | 10.4103/jfmpc.jfmpc_17_19 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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