CASE REPORT | https://doi.org/10.5005/jp-journals-10009-1665 |
Bilateral Congenital Dacryocystoceles: HDlive Silhouette Image
1,6Department of Obstetrics and Gynecology, Miyake Clinic, Ofuku, Minami-ku, Okayama, Japan; Department of Perinatology and Gynecology, Kagawa University Graduate School of Medicine, Ikenobe, Miki, Kagawa, Japan
2–5Department of Obstetrics and Gynecology, Miyake Clinic, Ofuku, Minami-ku, Okayama, Japan
Corresponding Author: Toshiyuki Hata, Department of Obstetrics and Gynecology, Miyake Clinic, Ofuku, Minami-ku, Okayama, Japan; Department of Perinatology and Gynecology, Kagawa University Graduate School of Medicine, Ikenobe, Miki, Kagawa, Japan, Phone: +81-(0)87-891-2174, e-mail: toshi28@med.kagawa-u.ac.jp
How to cite this article Hata T, Bouno S, Koyanagi A, et al. Bilateral Congenital Dacryocystoceles: HDlive Silhouette Image. Donald School J Ultrasound Obstet Gynecol 2020;14(4):349–350.
Source of support: Nil
Conflict of interest: None
ABSTRACT
HDlive Silhouette can demonstrate inner echo-free structures of the fetal body. In our case, this technique clearly showed fetal bilateral dacryocystoceles just below the medial canthal area under the orbits at 28 weeks and 3 days of gestation. We could clearly identify spatial relationships between the mouth, nose, orbits, and dacryocystoceles. These dacryocystoceles became obscure with advancing gestation. HDlive Silhouette may be a useful diagnostic technique for evaluating inner echo-free structures in fetal orbital regions.
Keywords: Antenatal diagnosis, Bilateral congenital dacryocystoceles, HDlive Silhouette, HDlive Studio.
INTRODUCTION
The overall incidence of fetal dacryocystocele is 0.016–0.43%.1,2 The rare combination of an imperforate membrane of Hasner and malfunction of Rosenmuller’s valve is the main cause.3 Most cases of congenital dacryocystocele resolve spontaneously before birth or just after delivery.2,4 Two-dimensional (2D) sonographic characteristics of fetal dacryocystocele are uni- or bilateral hypoechoic, periorbital, and round masses.4 Three-dimensional (3D) surface-rendering imaging showed swelling below the medial canthal area.4–10 There has been only one report on HDlive Silhouette diagnosis of unilateral congenital dacryocystocele.11 However, the whole face view was not shown in that study. In the current study, we present HDlive Silhouette diagnosis of bilateral congenital dacryocystoceles in a fetus at 28 weeks and 3 days of gestation.
CASE DESCRIPTION
A 37-year-old pregnant Japanese woman, gravida 1, para 0, received routine third-trimester ultrasound screening at 28 weeks and 3 days of gestation. Two-dimensional sonography showed bilateral round cysts in the lower and medial areas of the orbits (Fig. 1). HDlive Studio revealed a small dimple in the lower and medial area of the right orbit and swelling below the left medial canthal area (Fig. 2). HDlive Silhouette (Voluson E10 BT20, GE Healthcare Japan, Tokyo, Japan) clearly showed fetal bilateral dacryocystoceles just below the medial canthal area under the orbits (Fig. 3). Fetal biometry was normal, and there was no other abnormality. These dacryocystoceles became obscure with advancing gestation.
At 40 weeks and 4 days of gestation, an emergency cesarean section was performed due to delivery arrest, resulting in a viable, single male newborn weighing 3,520 g, with a height of 52 cm. The Apgar scores were 9 (1 minute) and 10 (5 minutes), and the umbilical artery blood pH was 7.28. The pediatric examination showed no newborn facial abnormalities (Fig. 4). The mother and neonate both followed a favorable course after the delivery.
DISCUSSION
HDlive Silhouette can demonstrate inner echo-free structures of the fetal body.12–15 In our previous report,11 HDlive Silhouette showed spatial relationships among the dacryocystocele, lens, eyeball, and optic nerve. However, a clear image of the whole fetal face could not be observed. In the current investigation, a good quality image of the whole fetal face could be obtained, and the true shape and exact location of bilateral dacryocystoceles were noted. Moreover, assessment of spatial relationships between the mouth, nose, orbits, and dacryocystoceles, and delineation of their contours enabled the location of the lesions to be assessed. HDlive Silhouette may be a useful diagnostic technique for evaluating inner echo-free structures in fetal orbital regions.
REFERENCES
1. Li S, Luo G, Tian X, et al. Prenatal diagnosis and perinatal outcome of congenital dacryocystocele: ba large case series. Prenata Diagn 2015;35(2):103–107. DOI: 10.1002/pd.4494.
2. Kim YH, Lee YJ, Song MJ, et al. Dacryocystocele on prenatal ultrasonography: diagnosis and postnatal outcomes. Ultrasonography 2015;34(1):51–57. DOI: 10.14366/usg.14037.
3. Suma V, Marini A, Bellitti F, et al. Prenatal sonographic diagnosis of dacryocystocele. Ultrasound Obstet Gynecol 1999;14(1):74. DOI: 10.1046/j.1469-0705.1999.14010074.x.
4. Bonilla-Musoles F, Jimenez LC, Castillo JC. Congenital dacryocystocele: a rare and benign nasolacrimal duct syst condition. Donald School J Ultrasound Obstet Gynecol 2012;6(3):233–236. DOI: 10.5005/jp-journals-10009-1247.
5. Petrikovsky BM, Kaplan GP. Fetal dacryocystcele: comparing 2D and 3D imaging. Pediatr Radiol 2003;33(8):582–583. DOI: 10.1007/s00247-002-0843-z.
6. Sepulveda W, Wojakowski AB, Elias D, et al. Congenital dacryocystocele. Prenatal 2- and 3-dimensional sonographic findings. J Ultrasound Med 2005;24(2):225–230. DOI: 10.7863/jum.2005.24.2.225.
7. Lembet A, Bodur H, Selam B, et al. Prenatal two- and three-dimensional sonographic diagnosis of dacryocystocele. Prenat Diagn 2008;28(6):554–555. DOI: 10.1002/pd.2015.
8. Brown K, Adhate A, Apuzzio J. Prenatal diagnosis of bilateral dacryocystocele using 3-D/4-D ultrasound technology: a case report. J Reprod Med 2011;56:178–80.
9. Bingol B, Basgul A, Guducu N, et al. Prenatal early diagnosis of dacryocystocele, a case report and review of literature. J Turk Ger Gynecol Assoc 2011;12(4):259–262. DOI: 10.5152/jtgga.2011.60.
10. Kanshaiym S, El-Din MHN, Abdelazim IA, et al. Congenital dilatation of the nasolacrimal sac (dacryocystocele): case report. J Family Med Prim Care 2019;8(3):1284–1286. DOI: 10.4103/jfmpc.jfmpc_17_19.
11. Hata T, Koyanagi A, Yamanishi T, et al. HDlive silhouette for diagnosis of congenital dacryocystocele. Donald School J Ultrasound Obstet Gynecol 2020;14(2):83–84. DOI: 10.5005/jp-journals-10009-1631.
12. AboEllail MAM, Hanaoka U, Numoto A, et al. HDlive image of giant fetal hemangioma. J Ultrasound Med 2015;34(12):2313–2318. DOI: 10.7863/ultra.15.01070.
13. AboEllail MAM, Kanenishi K, Marumo G, et al. Fetal HDlive sulhouette mode in clinical practice. Donald School J Ultrasound Obstet Gynecol 2015;9(4):413–419. DOI: 10.5005/jp-journals-10009-1428.
14. AboEllail MAM, Tanaka H, Mori N, et al. HDlive silhouette mode in antenatal diagnosis of jejunal atresia. Ultrasound Obstet Gynecol 2016;48(1):131–132. DOI: 10.1002/uog.15737.
15. Hata T, AboEllail MAM, Sajapala S, et al. HDlive silhouette mode with spatiotemporal correlation for assessment of the fetal heart. J Ultrasound Med 2016;35(7):1489–1495. DOI: 10.7863/ultra.15.08061.
________________________
© The Author(s). 2020 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.