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Case Report
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Prenatal diagnosis of unilateral dacryocystocele: A rare case report

Year 2019, Volume: 41 Issue: 1, 234 - 236, 28.03.2019

Cihan İnan

https://doi.org/10.7197/223.vi.487385

Abstract

Dacryocystocele is a rare benign
cystic formation seen in the lacrimal sac as a result of obstruction of the
nasolacrimal duct. This lesion may coexist with additional anomalies. Most
cases resolve spontaneously in the late intrauterine or early neonatal periods. They
are usually unilateral and more common in female fetuses. In
the literature, a very limited numbers of prenatal dacryocystocele cases have
been reported. We
presented a case of unilateral dacryocystocele accompanied by polyhydramnios in
a male fetus which was diagnosed with obstetric ultrasonography at 29 weeks of
gestation.

Keywords

Dacryocystocele fetus prenatal diagnosis

References

  • Referans 1. Lorena SHT, Gonçalves ED, Silva JAF. Congenital dacryocystocele: case report and treatment. Rev Bras Oftalmol 2014; 73: 243-5.
  • Referans 2. Kim YH, Lee YJ, Song MJ, Han BH, Lee YH, Lee KS. Dacryocystocele on prenatal ultrasonography: diagnosis and postnatal outcomes. Ultrasonography 2015; 34: 51-7.
  • Referans 3. Veleva N, Chernodrinska V, Mladenov O. Bilateral congenital dacryocystocele-A case report. Biomedical Research 2018; 29: 2134-5.
  • Referans 4. Bachelard-Serra M, Chau C, Farinetti A, Roman S, Triglia JM, Nicollas R. Prenatal diagnosis of congenital dacryocystocele. Int J Pediatr Otorhinolaryngol 2013; 77: 847-9.
  • Referans 5. Li SL, Luo GY, Tian XX, et al. Prenatal diagnosis and perinatal outcome of congenital dacryocystocele: a large case series. Prenat Diagn 2015; 35: 103-7.
  • Referans 6. Bonilla-Musoles F, Jimenez LC, Castillo JC. Congenital dacryocystocele: a rare and benign nasolacrimal duct cyst condition. Donald School J Ultrasound Obstet Gynecol 2012; 6: 233-6.
  • Referans 7. Sakin O, Kars K, Karşıdağ AYK, Demir C, Büyükbayrak EE. Prenatal diagnosis of dacryocystocele. CausaPedia 2015; 4: 1117-21.
  • Referans 8. Adam SH, Meulles L, Jain V. Antenatal diagnosis of dacryocystocele. J Obstet Gynaecol Can 2013; 35: 591.
  • Referans 9. Bingöl B, Başgül A, Güdücü N, Işci H, Dünder I. Prenatal early diagnosis of dacryocystocele, a case report and review of literature. J Turk Ger Gynecol Assoc 2011; 12: 259-62.
  • Referans 10. Vázquez-Osorio I, Hernández-Martín A. Usefulness of Ultrasonography in the Diagnosis of Neonatal Dacryocystocele. Pediatr Dermatol 2017; 34: 209-10.

Unilateral dakriyosistoselin prenatal tanısı: Nadir bir olgu sunumu

Year 2019, Volume: 41 Issue: 1, 234 - 236, 28.03.2019

Cihan İnan

https://doi.org/10.7197/223.vi.487385

Abstract

Dakrosistosel nazolakrimal kanalın obstrüksiyonu sonucu lakrimal
kesede görülen oldukça nadir benign bir kistik oluşumdur. Bu lezyon ek
anomalilerle birlikte bulunabilirler. Birçok vaka, geç intrauterin veya erken
neonatal periyotta genellikle spontan rezolüsyona uğrar. Genellikle unilateral
olurlar ve kız fetuslarda daha sık görülürler. Literatürde oldukça sınırlı
sayıda prenatal dakrosistosel vakası sunulmuştur. Biz de gebeliğin 29.
haftasında erkek fetusta obstretrik obstetrik ultrasonografi ile tanısı
konulan, polihidramniosun eşlik ettiği, tek taraflı dakrosistosel vakasını
sunduk. 

Keywords

Dakrosistosel fetus prenatal tanı

References

  • Referans 1. Lorena SHT, Gonçalves ED, Silva JAF. Congenital dacryocystocele: case report and treatment. Rev Bras Oftalmol 2014; 73: 243-5.
  • Referans 2. Kim YH, Lee YJ, Song MJ, Han BH, Lee YH, Lee KS. Dacryocystocele on prenatal ultrasonography: diagnosis and postnatal outcomes. Ultrasonography 2015; 34: 51-7.
  • Referans 3. Veleva N, Chernodrinska V, Mladenov O. Bilateral congenital dacryocystocele-A case report. Biomedical Research 2018; 29: 2134-5.
  • Referans 4. Bachelard-Serra M, Chau C, Farinetti A, Roman S, Triglia JM, Nicollas R. Prenatal diagnosis of congenital dacryocystocele. Int J Pediatr Otorhinolaryngol 2013; 77: 847-9.
  • Referans 5. Li SL, Luo GY, Tian XX, et al. Prenatal diagnosis and perinatal outcome of congenital dacryocystocele: a large case series. Prenat Diagn 2015; 35: 103-7.
  • Referans 6. Bonilla-Musoles F, Jimenez LC, Castillo JC. Congenital dacryocystocele: a rare and benign nasolacrimal duct cyst condition. Donald School J Ultrasound Obstet Gynecol 2012; 6: 233-6.
  • Referans 7. Sakin O, Kars K, Karşıdağ AYK, Demir C, Büyükbayrak EE. Prenatal diagnosis of dacryocystocele. CausaPedia 2015; 4: 1117-21.
  • Referans 8. Adam SH, Meulles L, Jain V. Antenatal diagnosis of dacryocystocele. J Obstet Gynaecol Can 2013; 35: 591.
  • Referans 9. Bingöl B, Başgül A, Güdücü N, Işci H, Dünder I. Prenatal early diagnosis of dacryocystocele, a case report and review of literature. J Turk Ger Gynecol Assoc 2011; 12: 259-62.
  • Referans 10. Vázquez-Osorio I, Hernández-Martín A. Usefulness of Ultrasonography in the Diagnosis of Neonatal Dacryocystocele. Pediatr Dermatol 2017; 34: 209-10.
There are 10 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Case Reports
Authors

Cihan İnan 0000-0002-4872-1689

Publication Date March 28, 2019
Acceptance Date March 20, 2019
Published in Issue Year 2019 Volume: 41 Issue: 1

Cite

AMA İnan C. Prenatal diagnosis of unilateral dacryocystocele: A rare case report. CMJ. March 2019;41(1):234-236. doi:10.7197/223.vi.487385