Dacryocystocele is an uncommon condition presenting at birth as a bluish swelling approximately 1 cm in diameter located below and nasal to the medial canthus. It represents a cystic swelling of the lacrimal sac due to obstruction of the lacrimal drainage system both above and below the sac. The ave
Antenatal sonographic diagnosis of a dacryocystocele
β Scribed by Dr. Geraldine Walsh; Paul A. Dubbins
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 394 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0091-2751
No coin nor oath required. For personal study only.
β¦ Synopsis
Antenatal sonography accurately identifies structural abnormalities of the fetal face including cyclopia, hemangiomata, and facial
We describe the sonographic and clinical features of a dacryocystocele from the time of its initial imaging at 36 weeks, menstrual age (MA), through to its complete resolution in early infancy.
CASE REPORT
A 17-year-old gravida 3, para 0 woman presented at 36 weeks, MA, having moved to this area. Routine ultrasonography earlier in the pregnancy at another center had been normal. A repeat examination was performed in our department to resolve a scan-clinical fetal age discrepancy. This revealed a hypoechoic mass measuring 9 mm in diameter medial to the right orbit (Figure 1). The globes were symmetrical and appeared normal, and no intracranial abnormality was identified.
At 41 weeks, a female infant weighing 3.23 kg was born by spontaneous vaginal delivery. Physical examination revealed a blue-gray cystic swelling at the medial canthus of the right eye. Ultrasonography at 48 hours showed bilateral cystic areas, 11 mm in diameter on the right and 5 mm in diameter on the left, in the region of the lacrimal apparatus abutting onto the ethmoid air cells (Figure 2). Cranial ultrasound was normal and facial x-rays showed soft-tissue swelling over both orbits, that on the right side more marked (Figure 3). There was no associated bony abnormality. Clinically the right-sided swelling resolved at 1 week. The lesions were much less ap--
π SIMILAR VOLUMES
## Abstract We report a case of a large fetal oropharyngeal teratoma in a 19βweek fetus evaluated with 3βdimensional (3D) sonography. The 3D sonographic surface and maximum mode rendering of the tumor allowed detailed visualization of the mass lesion and thus enabled active patient participation in
Eighteen cases of congenital clubfoot were diagnosed sonographically be-From Diagnostic Ultrasound Associates, Boston, Massachusetts, and