Congenital dacryocystocele is a relatively rare type of nasolacrimal duct obstruction that may induce respiratory distress during the early neonatal period. We encountered a case of bilateral congenital dacryocystoceles with intranasal cysts in a premature infant delivered at 34 weeks of gestation. The patient developed symptoms of respiratory failure immediately after birth, but no ophthalmologic symptoms. Treatment with nasal continuous positive airway pressure via a nasal mask, instead of a nasal prong, effectively relieved the symptoms. Early diagnosis and appropriate treatment are critical for infants with nasal obstruction.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1111/ped.12516 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
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.
Long-term Outcomes of a Minimally Invasive Surgical Approach in Paediatric Patients with Congenital Dacryocystoceles.
Klin Monbl Augenheilkd
December 2024
Klinik für Hals-Nasen-Ohrenheilkunde, Universitätsklinikum Essen, Deutschland.
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.
Unusual Case of Fetal Meningocele Mimicking Dacryocystocele.
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 PDFPrenatal diagnosis and outcome of congenital dacryocystoceles.
Taiwan 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.
Bilateral Dacryocystoceles in Congenital Arhinia.
Ophthalmic Plast Reconstr Surg
November 2024
Ophthalmic Plastic Surgery Service, Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, U.S.A.
Congenital arhinia is a rare anomaly characterized by a syndrome called Bosma arhinia microphthalmia syndrome. A 22-year-old woman with a history of congenital arhinia presented with bilateral discharge and enlarged bilateral lacrimal sacs, with imaging consistent with bilateral dacryocystoceles and complete absence of nasal structures. This is the first case in the literature that describes surgical management of bilateral dacryocystoceles in a patient with Bosma arhinia microphthalmia syndrome.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!