Abstract
We report an unusual presentation of a dacryocystocele in a 3-day-old child, with clinical and novel MRI findings. The literature contains extensive CT documentation, but descriptions of the MRI appearances of dacryocystoceles are lacking. Although CT is the standard initial imaging modality, MRI can be helpful if there are questions as to the content of the lesion or a need for further anatomical characterization.
Similar content being viewed by others
References
Meyer JR, Quint DJ, Holmes JM, Wiatrak BJ (1993) Infected congenital mucocele of the nasolacrimal duct. AJNR 14: 1008–1010
Holzberg N, Ward RF (1993) Bilateral congenital dacryocystoceles. Otolaryngol Head Neck Surg 109: 1074–1077
Sevel D (1981) Developmental and congenital abnormalities of the nasolacrimal apparatus. J Pediatr Ophthalmol Strabis 18: 13–19
Castillo M, Merten DF, Weissler MC (1993) Bilateral nasolacrimal duct mucocele, a rare cause of respiratory distress: CT findings in two newborns. AJNR 14: 1011–1013
Bhaya M, Meehan R, Har-El G (1997) Dacryocystocele in an adult: endoscopic management. Am J Otolaryngol 18: 131–134
Sherer DM, Eisenberg C, Schwartz BM, Hammerman RM, Katz N (1997) Prenatal sonographic diagnosis of dacryocystocele: a case and review of the literature. Am J Perinatol 14: 479–481
Rand PK, Ball WS Jr, Kulwin DR (1989) Congenital nasolacrimal mucoceles: CT evaluation. Radiology 173: 691–694
Mansour AM, Cheng KP, Mumma JV (1991) Congenital dacryocele: a collaborative review. Ophthalmology 98: 1744–1751
Edison BJ, Meyer DR (2000) Nasolacrimal duct obstruction and dacryocystocele associated with a concha bullosa mucocele. Ophthalmology 107: 1393–1396
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Farrer, R.S., Mohammed, T.L. & Hahn, F.J. MRI of childhood dacryocystocele. Neuroradiology 45, 259–261 (2003). https://doi.org/10.1007/s00234-003-0942-z
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00234-003-0942-z