منابع مشابه
A case of congenital dacryocystocele.
A 6-day-old infant presented with a deeply bluish cystic mass below the right medial canthus. She had been born healthy. Under the impression of a hemangioma brain computed tomography was conducted. As a result, a diagnosis of congenital dacryocystocele was made. We present this case to show that it is important for a dermatologist to correctly identify congenital dacryocystoceles and appropria...
متن کاملCongenital dacryocystocele with intranasal extension.
PURPOSE Congenital dacryocystocele is a rare anomaly in the newborn child. The swelling of lachrymal sac is observed by birth and it is associated with obstruction of lachrymal system either above or below lachrymal sac. METHODS Diagnosis was made by clinical observation. Some ancillary examinations, such as ultrasonography, tomography, and rhinoscopy, were useful. RESULTS The authors descr...
متن کاملForeign body mimicking malignancy in acquired dacryocystocele
A featured malignant-like granulation tissue can be the only preoperative clinical clue of a concealed foreign body in the nasal cavity. Thus, endoscopic Dacryocystorhinostomy (DCR) should be completed with intraoperative nasal exploration to reveal non-apparent foreign bodies that might be the underlying etiology of chronic dacryocystocele.
متن کاملCongenital dacryocystocele: diagnosis and treatment.
Five children were diagnosed with congenital dacryocystocele; in all cases, the cystic lesion was unilateral; age ranged from 7 to 60 days (mean 29 days). The mean ultrasonography diameter of the cyst, at the time of the diagnosis, was 11.51 mm. Topical and systemic antibiotics and massage were prescribed. One patient had no recurrence of the dacryocystocele but 4 showed no improvement with med...
متن کاملComplex choristoma masquerading as a dacryocystocele.
Comment. Deficiency of MBL has been correlated with a variety of infections in otherwise healthy individuals but may also enhance susceptibility to certain infections in persons receiving chemotherapy or those with secondary immunosuppression for other reasons. Genetic polymorphism explains the range of serum concentrations of MBL found in the general population, with severe serum MBL deficienc...
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ژورنال
عنوان ژورنال: Revista Brasileira de Oftalmologia
سال: 2014
ISSN: 0034-7280
DOI: 10.5935/0034-7280.20140066