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Published in: Pediatric Radiology 12/2010

01-12-2010 | Original Article

Congenital dacryocystocele: prenatal MRI findings

Authors: Zeynep Yazici, Beth M. Kline-Fath, Bulent Yazici, Eva I. Rubio, Maria A. Calvo-Garcia, Leann E. Linam

Published in: Pediatric Radiology | Issue 12/2010

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Abstract

Background

Congenital dacryocystocele can be diagnosed prenatally by imaging. Prenatal MRI is increasingly utilized for fetal diagnosis.

Objective

To present the radiological and clinical features of seven fetuses with congenital dacryocystocele diagnosed with prenatal MRI.

Materials and methods

The institutional database of 1,028 consecutive prenatal MR examinations performed during a period of 4 years was reviewed retrospectively. The cases of congenital dacryocystocele were identified by reading the report of each MRI study.

Results

The incidence of dacryocystocele diagnosed with prenatal MRI was 0.7% (n = 7/1,028). The dacryocystocele was bilateral in three fetuses. Mean gestational age at the time of diagnosis was 31 weeks. The indication for prenatal MRI was the presence or the suspicion of central nervous system abnormality in six fetuses and diaphragmatic hernia in one. Dacryocystocele was associated with an intranasal cyst in six of ten eyes. Prenatal sonography revealed dacryocystocele in only two of seven fetuses. Of eight eyes with postnatal follow-up, four did not have any lacrimal symptoms.

Conclusion

Prenatal MRI can delineate congenital dacryocystocele more clearly and in a more detailed fashion than ultrasonography. Presence of dacryocystocele was symptomatic in only 50% of our patients, supporting that prenatal diagnosis of dacryocystocele might follow a benign course.
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Metadata
Title
Congenital dacryocystocele: prenatal MRI findings
Authors
Zeynep Yazici
Beth M. Kline-Fath
Bulent Yazici
Eva I. Rubio
Maria A. Calvo-Garcia
Leann E. Linam
Publication date
01-12-2010
Publisher
Springer-Verlag
Published in
Pediatric Radiology / Issue 12/2010
Print ISSN: 0301-0449
Electronic ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-010-1719-2

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