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Tearing: A Merck Manual of Patient Symptoms podcast
Excess tearing may cause a sensation of watery eyes or result in tears falling down the cheek (epiphora).
Pathophysiology
Tears are produced in the lacrimal gland and drain through the upper and lower puncta into the canaliculi and then into the lacrimal sac and nasolacrimal duct (see Fig. 2: Symptoms of Ophthalmologic Disorders: Anatomy of the lacrimal system. ). Obstruction of tear drainage can lead to stasis and infection. Recurrent infection of the lacrimal sac (dacryocystitis) can sometimes spread, potentially leading to orbital cellulitis.
Etiology
Overall, the most common causes of tearing are
Tearing can be caused by increased tear production or decreased nasolacrimal drainage.
Increased tear production:
The most common causes are
Any disorder causing conjunctival or corneal irritation can increase tear production (see Table 12: Symptoms of Ophthalmologic Disorders: Some Causes of Tearing ). However, most patients with corneal disorders that cause excess tearing (eg, corneal abrasion, corneal ulcer, corneal foreign body, keratitis) or with primary angle-closure glaucoma or anterior uveitis present with eye symptoms other than tearing (eg, eye pain, redness). Most people who have been crying do not present for evaluation of tearing.
Decreased nasolacrimal drainage:
The most common causes are
Nasolacrimal drainage system obstruction may be caused by strictures, tumors, or foreign bodies (eg, stones, often associated with subclinical infection by Actinomyces). Obstruction can also be a congenital malformation. Many disorders and drugs can cause stricture or obstruction of nasolacrimal drainage.
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Table 12
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| Some Causes of Tearing |
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Cause
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Suggestive Findings
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Disorders causing excess tear production
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Dry eyes with reflex tearing
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Worse on cold or windy days or with exposure to cigarette smoke or dry heat
Intermittent foreign body sensation
In patients with a disorder known to cause dry eyes (eg, blepharitis)
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Ocular surface irritation (eg, allergic conjunctivitis, corneal abrasion or erosion or ulcer, foreign body, hordeolum, infectious conjunctivitis, irritant chemicals, keratitis, trichiasis, irritation with punctate lesions due to paresis of blink muscles as in facial nerve palsy)
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Grittiness
Redness
In patients with corneal lesions, pain, constant foreign body sensation, and photophobia
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Allergic conjunctivitis
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Itching
Possibly follicles on tarsal conjunctiva
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Nasal irritation and inflammation (eg, allergic rhinitis, URI)
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Rhinorrhea, sneezing, nasal congestion
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Disorders causing nasolacrimal drainage obstruction
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Congenital nasolacrimal duct obstruction
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Symptoms that begin shortly after age 2 wk
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Idiopathic age-related nasolacrimal duct stenosis
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Usually normal examination except for evidence of obstruction
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Dacryocystitis
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Nasal pain
Often swelling, redness, and warmth over the lacrimal sac and, with palpation, tenderness and expression of pus
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Tumors
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Hard mass in the nasolacrimal duct system, particularly in the elderly
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Other causes of nasolacrimal drainage stricture or obstruction (see text)
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Often risk factors
Often no characteristic examination findings other than obstruction
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Disorders causing decreased drainage without obstruction
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Misalignment between tear film and puncta (eg, ectropion, entropion)
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Usually visible on examination
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Other causes of nasolacrimal drainage stricture or obstruction include
Evaluation
History:
History of present illness addresses the duration, onset, and severity of symptoms, including whether tears drip down the cheek (true epiphora). The effects of weather, environmental humidity, and cigarette smoke are ascertained.
Review of symptoms should seek symptoms of possible causes, including itching, rhinorrhea, or sneezing, particularly when occurring perennially or after exposure to specific potential allergens (allergic reaction); eye irritation or pain (blepharitis, corneal abrasion, irritant chemicals); and pain near the medial canthus (dacryocystitis). Other symptoms are of lower yield but should be sought; they include positional headache, purulent rhinorrhea, nocturnal cough, and fever (sinusitis, granulomatosis with polyangiitis); rash (Stevens-Johnson syndrome); cough, dyspnea, and chest pain (sarcoidosis); and epistaxis, hemoptysis, polyarthralgias, and myalgias (granulomatosis with polyangiitis).
Past medical history asks about known disorders that can cause tearing, including granulomatosis with polyangiitis, sarcoidosis, and cancer treated with chemotherapy drugs; disorders that cause dry eyes (eg, RA, sarcoidosis, Sjögren syndrome); and drugs, such as echothiophate, epinephrine, and pilocarpine. Previous ocular and nasal history, including infections, injuries, surgical procedures, and radiation exposure, is ascertained.
Physical examination:
Examination focuses on the eye and surrounding structures.
The face is inspected; asymmetry suggests congenital or acquired obstruction of nasolacrimal duct drainage. When available, a slit lamp should be used to examine the eyes. The conjunctivae and corneas are inspected for lesions, including punctate spots, and redness. The cornea is stained with fluorescein and examined. The lids are everted to detect hidden foreign bodies. The eyelids, including the lacrimal puncta, are closely inspected for foreign bodies, blepharitis, hordeola, ectropion, entropion, and trichiasis. The lacrimal sac (near the medial canthus) is palpated for warmth, tenderness, and swelling. Any swellings are palpated for consistency and to see whether pus is expressed.
The nose is examined for congestion, purulence, and bleeding.
Red flags:
The following findings are of particular concern:
Interpretation of findings:
Findings that suggest obstruction of nasolacrimal drainage include
A cause is often evident from the clinical evaluation (see Symptoms of Ophthalmologic Disorders: Some Causes of Tearing ).
Testing:
Testing is often unnecessary because the cause is usually evident from the examination.
Schirmer test with a large amount of wetting (eg, > 25 mm) suggests an evaporative dry eye as the etiology of tearing. Schirmer test with very little wetting (< 5.5 mm) suggests an aqueous tear-deficient dry eye. Usually, Schirmer test is done by an ophthalmologist to ensure it is done and interpreted correctly.
Probing and saline irrigation of the lacrimal drainage system can help detect anatomic obstruction of drainage, as well as stenosis due to complete obstruction of the nasolacrimal drainage system. Irrigation is done with and without fluorescein dye. Reflux through the opposite punctum or canaliculus signals fixed obstruction; reflux and nasal drainage signify stenosis. This test is considered adjunctive and is done by ophthalmologists.
Imaging tests and procedures (dacryocystography, CT, nasal endoscopy) are sometimes useful to delineate abnormal anatomy when surgery is being considered or occasionally to detect an abscess.
Treatment
Underlying disorders (eg, allergies, foreign bodies, conjunctivitis) are treated.
The use of artificial tears lessens tearing when dry eyes or corneal epithelial defects are the cause.
Congenital nasolacrimal duct obstruction often resolves spontaneously. In patients < 1 yr, manual compression of the lacrimal sac 4 or 5 times/day may relieve the distal obstruction. After 1 yr, the nasolacrimal duct may need probing with the patient under general anesthesia. If obstruction is recurrent, a temporary drainage tube may be inserted.
In acquired nasolacrimal duct obstruction, irrigation of the nasolacrimal duct may be therapeutic when underlying disorders do not respond to treatment. As a last resort, a passage between the lacrimal sac and the nasal cavity can be created surgically (dacryocystorhinostomy).
In cases of punctal or canalicular stenosis, dilation is usually curative. If canalicular stenosis is severe and bothersome, a surgical procedure that places a glass tube leading from the caruncle into the nasal cavity can be considered.
Geriatrics Essentials
Idiopathic age-related nasolacrimal duct stenosis is the most common cause of unexplained epiphora in elderly patients; however, tumors should also be considered.
Key Points
Last full review/revision November 2012 by Kathryn Colby, MD, PhD
Content last modified December 2012
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