Not Found

Find information on medical topics, symptoms, drugs, procedures, news and more, written for the health care professional.

* This is the Professional Version. *


By James Garrity, MD

Click here for
Patient Education

Dacryostenosis is obstruction or stenosis of the nasolacrimal duct, causing excess tearing.

Nasolacrimal obstruction may be congenital or acquired. One cause of congenital obstruction is inadequate development of any part of the nasolacrimal ducts. Typically, a membrane at the distal end of the nasolacrimal duct persists. There is tearing and purulent discharge; the condition may manifest as chronic conjunctivitis, usually beginning after the age of 2 wk (most often at age 3 to 12 wk).

There are many causes of acquired nasolacrimal duct obstruction. The cause is most often age-related stenosis of the nasolacrimal duct. Other causes include past nasal or facial bone fractures and sinus surgery, which disrupt the nasolacrimal duct; inflammatory diseases (eg, sarcoidosis, granulomatosis with polyangiitis [formerly Wegener granulomatosis]); tumor [eg, maxillary and ethmoid sinus tumors]; and dacryocystitis.

Causes of punctal or canalicular stenosis include chronic conjunctivitis (especially herpes simplex), certain types of chemotherapy, adverse reactions to eye drops (especially topical echothiophate iodide), and radiation.

Causes of Acquired Nasolacrimal Duct Obstruction

Dacryolith (a concretion)

Granulomatosis with polyangiitis (formerly Wegener granulomatosis)

Idiopathic (usually age-related)


Trauma (including surgical, especially previous sinus surgery)



  • Clinical evaluation

Diagnosis is usually based on clinical criteria. Sometimes ophthalmologists probe and irrigate the lacrimal drainage system with saline, with or without fluorescein dye. Reflux indicates stenosis.


  • Manual or surgical decompression

  • Treatment of underlying disorder

Congenital nasolacrimal duct obstruction often resolves spontaneously by about age 6 to 9 mo; before 1 yr, manual compression of the lacrimal sac 4 or 5 times/day may relieve the obstruction. After age 1 yr, the nasolacrimal duct may need probing, usually under general anesthesia; if obstruction is recurrent, a temporary silastic tube may be inserted.

In acquired nasolacrimal duct obstruction, the underlying disorder is treated when possible. If treatment is not possible or is ineffective, 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 (conjunctivo-dacryocystorhinostomy or C-DCR) that places a tube made of low thermal-expansion borosilicate glass (Jones tube) leading from the caruncle into the nasal cavity can be considered.

Key Points

  • Dacryostenosis is either congenital or acquired.

  • Symptoms include excessive tearing.

  • Reflux of saline or fluorescein dye when flushing the lacrimal drainage system confirms the diagnosis.

  • In congenital dacryostenosis, symptoms usually resolve by 9 mo; manual decompression of the lacrimal sac may help.

  • In acquired dacryostenosis, treat the underlying disorder.

  • For both congenital and acquired dacryostenosis, surgery may be needed if symptoms persist.

Resources In This Article

* This is the Professional Version. *