Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Introduction: Congenital dacryocystoceles are a rare condition caused by nasolacrimal duct obstruction. Symptoms include epiphora, nasal obstruction, and swelling in the medial canthus. Treatment usually entails probing Hasner's valve open and, if necessary, intubating the nasolacrimal duct. We present a minimally invasive, endoscopic procedure with marsupialisation of the endonasal portion of the cele. The operation avoids additional manipulation of the lacrimal duct to prevent iatrogenic injury.

Methods: This retrospective analysis included a total of nineteen infants or young children (21 eyes) aged 3 days to 39 months. Two of the patients were suffering from acute respiratory distress, seven from recurrent infections with persistent epiphora, and twelve from acute dacryocystitis with orbital phlegmon.

Results: The endonasal portion of the dacryocele was detected in all cases and resected endonasally using an endoscope. Recurrences required revision surgery involving dacryocystorhinostomy after primary surgery in two patients aged of 22 and 39 months. All other seventeen patients were free of recurrence.

Summary: Our results show endoscopic endonasal marsupialisation without additional intubation or probing of the lacrimal ducts to be a successful treatment strategy for congenital dacryocystoceles. This avoids iatrogenic scarring, false passages, or postoperative bacteraemia. The surgical technique presented here shows a lower success rate in older children with a history of inflammation.

Download full-text PDF

Source
http://dx.doi.org/10.1055/a-2409-0958DOI Listing

Publication Analysis

Top Keywords

congenital dacryocystoceles
12
minimally invasive
8
nasolacrimal duct
8
endonasal portion
8
long-term outcomes
4
outcomes minimally
4
invasive surgical
4
surgical approach
4
approach paediatric
4
patients
4

Similar Publications

Bilateral congenital dacryocystocele is a rare, congenital anomaly of the lacrimal drainage system in a newborn. Herein, we report a case of infected congenital bilateral dacryocystocele in a newborn. The case was determined to be a bilateral dacryocystocele after an endoscopic examination and confirmed by a magnetic resonance imaging (MRI) scan.

View Article and Find Full Text PDF

Endoscopic endonasal dacryocystectomy.

Am J Ophthalmol Case Rep

March 2025

Govindram Seksaria Institute of Dacryology, L.V. Prasad Eye Institute, Hyderabad, India.

Purpose: To report an exceptionally rare instance of Endoscopic endonasal dacryocystectomy.

Observations: Dacryocystectomy (DCT), a procedure of surgical extirpation of the lacrimal sac is normally approached by an external route. However, an endoscopic endonasal approach DCT is rare and usually reserved in cases where intellectual disabilities of a patient become a restrictive factor in maintenance of a healthy external wound.

View Article and Find Full Text PDF
Article Synopsis
  • Congenital dacryocystoceles are uncommon birth defects linked to blocked tear ducts, presenting symptoms like excessive tearing and swelling around the eye.
  • A new minimally invasive endoscopic procedure was tested on 19 infants and young children, focusing on resecting the affected tissue without further manipulating the lacrimal duct, aiming to reduce complications.
  • The treatment was effective, with a recurrence in only two older patients, while the rest showed no issues post-surgery, suggesting this method is beneficial but may be less successful in older children with previous infections.
View Article and Find Full Text PDF

Meningocele, a rare subtype of cephalocele, can manifest in various positions and exhibit diverse characteristics. On the other hand, dacryocystocele, also a rare anatomical disorder, typically presents as a cyst located between the nose and the eye. Generally, distinguishing between these 2 lesions is not difficult.

View Article and Find Full Text PDF

Objective: To determine the incidence and present our experience with prenatal diagnosis and postnatal outcome of dacryocystocele.

Material And Methods: All cases of congenital dacryocystocele diagnosed in our center between 2020 and 2022 were identified in our database to establish the incidence of these defects. The medical records were then reviewed for gestational age, gender, size, and side of dacryocystocele and postnatal outcome.

View Article and Find Full Text PDF