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Dacryocystitis is the inflammation of the nasolacrimal sac related to impairment in the lacrimal drainage system and superimposed infection.
Dacryocystitis has a bimodal distribution: neonates due to congenital abnormalities and when acquired, usually affect individuals older than 40 years of age 3.
Dacryocystitis is typically characterized by epiphora, erythema, and edema in the region of the medial epicanthus and lacrimal puncta as the result of an infection of the nasolacrimal sac. There is often mucopurulent discharge from the puncta and associated conjunctivitis.
Obstruction or stricture of the nasolacrimal drainage is an underlying factor.
Most cases in infants represent congenital abnormalities, such as incomplete canalization or atresia of the nasolacrimal duct, dacryocystocele and facial clefts. Whereas in adults it is usually the result of an acquired abnormality, including:
The microbiology of dacryocystitis mimics normal conjunctival flora in most instances.
In chronic dacryocystitis, there may be superinfection with fungal species.
Diagnosis is usually made clinically; however, imaging may help to exclude complications. Imaging is indicated to exclude orbital cellulitis or orbital abscess; both of which are uncommon as the orbital septum acts as a barrier preventing post septal spread 3.
CT findings include well-circumscribed round lesions with peripheral enhancement around the inner canthus, with adjacent soft tissue thickening and fat stranding,
Treatment and prognosis
Treatment is usually with antibiotics in the acute phase. In some cases, intervention (including external dacryocystorhinostomy) may be necessary.
Chronic dacryocystitis typically requires surgery or an interventional procedure.
Differentials on imaging include: