Results 21 to 30 of about 384 (163)
Process of spontaneous resolution in the conservative management of congenital dacryocystocele
Masashi Mimura,1,2 Mari Ueki,1 Hidehiro Oku,1 Bunpei Sato,2 Tsunehiko Ikeda11Department of Ophthalmology, Osaka Medical College, Takatsuki, 2Department of Ophthalmology, Osaka Kaisei Hospital, Osaka, JapanPurpose: To assess efficacy of the conservative ...
Mimura M, Ueki M, Oku H, Sato B, Ikeda T
doaj +1 more source
Prenatal diagnosis and outcome of congenital dacryocystoceles
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
Veronika Frisova +2 more
doaj +2 more sources
Special congenital dacryocystocele. [PDF]
Congenital Dacryocystocele is a rare disease of the eye and nose, which originates from congenital obstruction of lacrimal duct system, but accounts for a low proportion in congenital obstruction of lacrimal duct system. We present a case of congenital dacryocystocele to analyze the clinical features and to explore the clinical treatment effect of ...
Han LP, Wang FX, Zhang CY.
europepmc +3 more sources
Sinonasal Myxoma With Intraorbital Expansion: A Rare Case. [PDF]
OTO Open, Volume 5, Issue 3, July‐September 2021.
Kondamuri NS +3 more
europepmc +2 more sources
Selected Abstracts of the 12th International Workshop on Neonatology • 10 P PEDIATRICS: NOTES FOR THE FUTURE • Cagliari (Italy) • October 19th-22nd, 2016 ABS 1. ABNORMAL FETAL GROWTH ALTERS THE METABOLIC PROFILE OF EARLY HUMAN MILK • A. Kontogeorgou,
--- Various Authors
doaj +2 more sources
A full-term baby girl showed a bluish mass at birth in the right medial canthal area. She later demonstrated dacryocystitis and cellulitis. Although probing was performed, it was unsuccessful, and the dacryocystitis and cellulitis worsened. Computed tomography showed a dilated lacrimal sac, an enlarged nasolacrimal canal and a nasal cyst.
Hirohiko, Kakizaki +4 more
openaire +3 more sources
Lacrimo-auriculo-dento-digital syndrome: A case report and literature review. [PDF]
We report a healthy 18-year-old male Saudi with bilateral agenesis of the lacrimal puncta and canaliculi associated with large dacryocystocele on the right side without tearing or inflammation, detected in conjunction with other characteristic features ...
Alhamadi R +4 more
europepmc +2 more sources
Congenital Dacryocystocele: A Major Review
Purpose: To provide a systematic review of the literature on congenital dacryocystoceles (CDCs) and summarize their presentations, investigations, management, and outcomes. Methods: The authors performed a PubMed search of all articles published in English on CDCs.
Swati, Singh, Mohammad Javed, Ali
openaire +3 more sources
Routine 36-week scan: diagnosis of fetal abnormalities. [PDF]
ABSTRACT Objectives To investigate further the incidence and types of fetal abnormality identified at a routine 36‐week ultrasound examination, which had not been diagnosed in previous scans at 20 weeks and 12 weeks' gestation, and to report the fetal abnormalities that are diagnosed only postnatally.
Syngelaki A +5 more
europepmc +2 more sources
Purpose The aim of this study was to detect the prevalence of adult encysted dacryocystocele among patients with lacrimal passage obstruction and to evaluate its management by canaliculo-dacryocystorhinostomy (canaliculo-DCR).
Mohamed Farag K Ibrahiem +2 more
doaj +1 more source

