1995
DOI: 10.1001/archotol.1995.01890120079016
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Respiratory Distress in the Neonate: Sequela of a Congenital Dacryocystocele

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Cited by 46 publications
(24 citation statements)
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“…The canal may expand and take the form of a sac as fluid accumulates [3]. The swelling of lacrimal sac is observed at birth; but newborns diagnosed in the prenatal ultrasonographic screening have also been reported [3,5,9,[16][17][18][19][20]. Prolapse or expansion of the mucocele into nose may lead to respiratory distress and diffulty in feeding, as newborns are preferential nose breathers [16].…”
Section: Discussionmentioning
confidence: 99%
“…The canal may expand and take the form of a sac as fluid accumulates [3]. The swelling of lacrimal sac is observed at birth; but newborns diagnosed in the prenatal ultrasonographic screening have also been reported [3,5,9,[16][17][18][19][20]. Prolapse or expansion of the mucocele into nose may lead to respiratory distress and diffulty in feeding, as newborns are preferential nose breathers [16].…”
Section: Discussionmentioning
confidence: 99%
“…Cases of either proximal or distal obstruction may present with epiphora, which is generally self-resolving. Obstruction both proximally and distally results in the formation of a dacryocystocoele, the majority of which present as a unilateral fluctuant mass at the medial canthus, often with blue discoloration and associated epiphora [12,13]. Some authors believe that the valve of Rosenmuller may not have to be completely obstructed, but may behave as a unidirectional valve, preventing the escape of secretions collected against an imperforate valve of Hasner inferiorly [5,11].…”
Section: Discussionmentioning
confidence: 99%
“…Symptomatic congenital obstruction of the nasolacrimal system is a common problem affecting 5-6% of newborns [12]. Eighty-five to 95% of those with uncomplicated nasolacrimal obstruction will experience spontaneous resolution within 1 year.…”
Section: Nasolacrimal Duct Cyst (Dacryocystocele)mentioning
confidence: 99%