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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.
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http://dx.doi.org/10.1055/a-2409-0958 | DOI Listing |
Indian J Otolaryngol Head Neck Surg
March 2025
Department of Otorhinolaryngology, Hospital Raja Perempuan Zainab II, Kelantan, Malaysia.
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 PDFAm 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.
Klin Monbl Augenheilkd
March 2025
Klinik für Hals-Nasen-Ohrenheilkunde, Universitätsklinikum Essen, Deutschland.
Glob Pediatr Health
September 2024
Thien Hanh Hospital, Buon Ma Thuot, Vietnam.
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 PDFTaiwan J Obstet Gynecol
September 2024
Nimotech, Brno, Czech Republic.
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.