Background
Epiphora is defined as the overflow of tears. The clinical spectrum of epiphora ranges from the occasionally bothersome trickle to the chronically irritating overflow. Epiphora is caused by a disruption in the balance between tear production and tear drainage. The lacrimal drainage system is a continuous and complex membranous channel whose function is dependent on the interaction of anatomy and physiology.
When faced with a patient who complains of tearing, the first step is to determine whether the epiphora is caused by an increase in lacrimation or a decrease in tear drainage. Trichiasis, superficial foreign bodies, eyelid malpositions, diseases of the eyelid margins, tear deficiency or instability, and cranial nerve V irritation may cause an abnormal increase in tear production. In the absence of these conditions, an abnormality in tear drainage is the most likely cause.
Abnormalities of tear drainage may be subdivided further into functional and anatomical. Functional failure is related to poor lacrimal pump function, which may be due to a displaced punctum, eyelid laxity, weak orbicularis, or cranial nerve VII palsy. Anatomical obstruction may occur at any point along the lacrimal drainage pathway and may be congenital or acquired. Congenital obstructions tend to produce symptoms during the neonatal period and are the subject of another article, Nasolacrimal Duct, Congenital Anomalies.
Classification of nasolacrimal drainage obstruction
The 2 types of acquired nasolacrimal drainage obstructions (NLDO) are primary and secondary. In 1986, Linberg and McCormick coined the term primary acquired nasolacrimal duct obstruction (PANDO) to describe an entity of nasolacrimal duct obstruction caused by inflammation or fibrosis without any precipitating cause.[1] Bartley proposed an etiologic classification system for secondary acquired lacrimal drainage obstruction (SALDO) based on published cases.[2, 3, 4]
Pathophysiology
PANDO is more common in middle-aged and elderly females. Using CT scans, Groessl and colleagues demonstrated that women have significantly smaller dimensions in the lower nasolacrimal fossa and middle nasolacrimal duct.[5] They noted that changes in the anteroposterior dimensions of the bony nasolacrimal canal coincide with osteoporotic changes throughout the body. These quantitative measurements may help explain the higher incidence of PANDO in women. Others have suggested menstrual and hormonal fluctuations and a heightened immune status as factors that may contribute to the disease process. These may explain the prevalence in middle-aged and elderly females. Hormonal changes that bring about a generalized de-epithelialization in the body may cause the same within the lacrimal sac and duct. An already narrow lacrimal fossa in women predispose them to obstruction by the sloughed off debris.
The general categories of causes of SALDO include infectious, inflammatory, neoplastic, traumatic, and mechanical. Bacteria, viruses, fungi, and parasites have been implicated as causes of infectious lacrimal drainage obstruction. Bacteria, such as Actinomyces, Propionibacterium, Fusobacterium, Bacteroides, Mycobacterium, and Chlamydia species, have been associated with lacrimal drainage obstruction. Other bacteria include Nocardia, Enterobacter, Aeromonas, Treponema pallidum, and Staphylococcus aureus.
Viral causes of obstruction most commonly are seen with herpetic infection (eg, herpes simplex, herpes zoster, chickenpox, epidemic keratoconjunctivitis). The obstruction is due to the damage of the substantia propria of the canalicular elastic tissue and/or the adherence of the inflammatory membranes to the raw epithelial surface of the canaliculus.
Fungi may obstruct lacrimal passages by forming a stone (dacryolith) or cast. Species associated with obstruction are Aspergillus, Candida, Pityrosporum, and Trichophyton. Parasitic obstruction is rare but is reported in patients infected with Ascaris lumbricoides, which enters the lacrimal system through the valve of Hasner.
Inflammation may be endogenous or exogenous in origin. Wegener granulomatosis and sarcoidosis are 2 examples of conditions that lead to obstruction due to progressive inflammation within the nasal and lacrimal sac mucosa. Other endogenously arising inflammations associated with lacrimal obstruction are cicatricial pemphigoid, sinus histiocytosis, Kawasaki disease, and scleroderma.
Exogenous causes of cicatricial lacrimal drainage obstruction are eye drops, radiation, systemic chemotherapy, and bone marrow transplantation. Ophthalmic medications are the most common cause of iatrogenic punctal and canalicular scarring. Radiotherapy of the medial canthal area may cause a sufficiently severe inflammatory reaction to lead to punctal stenosis, although published reports vary on the amount of radiation causing the inflammation. Systemic chemotherapy with 5-fluorouracil (5-FU) has been known to occlude the puncta and canaliculi, although the incidence has declined since oncologic regimens today use much lower doses for shorter durations.
The use of I(131) for thyroid carcinoma is associated with a 3.4% incidence of documented NLDO and an overall 4.6% incidence of documented or suspected obstruction.
Canalicular and nasolacrimal duct obstruction is a common adverse effect of weekly docetaxel therapy used for metastatic breast cancer and non-small cell lung cancer.
Neoplasms may cause lacrimal obstruction by primary growth, secondary spread, or metastatic spread. Primary neoplasms may arise in the puncta, canaliculi, lacrimal sac, or nasolacrimal duct. Secondary spread from nearby tissues is more common than primary tumors. They are most commonly eyelid cancers (eg, basal cell carcinoma, squamous cell carcinoma), although spread from the maxillary antrum and the nasopharynx also have been reported. Studies have documented oncocytoma and cylindroma from direct extension. Metastatic spread, an extremely rare phenomenon, has been reported with primary sites from the breast and prostate.
Trauma may be iatrogenic in the case of scarring of the lacrimal passage after overly aggressive lacrimal probing. Iatrogenic causes of NLDO also may follow orbital decompression surgery, paranasal, nasal, and craniofacial procedures. Noniatrogenic traumatic causes are either blunt or sharp and most commonly involve the canaliculus, lacrimal sac, and nasolacrimal duct.
Posttraumatic dacryostenosis was found to have a frequent association with delayed treatment of facial fracture repair or bone loss in the lacrimal district.
Mechanical lacrimal drainage obstructions may be due to intraluminal foreign bodies, such as dacryoliths or casts. These may be caused by infection (eg, Actinomyces, Candida) as well as long-term administration of topical medications. Mechanical obstruction also may be caused by external compression from rhinoliths, nasal foreign bodies, or mucoceles.
Dentigerous cyst in the maxillary sinus has been reported to have caused nasolacrimal duct obstruction.
Epidemiology
Frequency
United States
This condition is relatively common, but the exact frequency is not known.
International
The incidence rate worldwide is unknown.
Mortality/Morbidity
Epiphora can be a nuisance; if untreated, nasolacrimal duct obstruction can cause significant problems.
Race
No predilection to race has been established.
Sex
- PANDO is more prevalent in women. Theories regarding this predilection in women are discussed in Pathophysiology.
- No gender predilection of SALDO exists.
Age
- PANDO most commonly is diagnosed in middle-aged women. Previous studies have noted a high incidence of PANDO in individuals aged 50-70 years.
Linberg JV, McCormick SA. Primary acquired nasolacrimal duct obstruction. A clinicopathologic report and biopsy technique. Ophthalmology. Aug 1986;93(8):1055-63. [Medline].
Bartley GB. Acquired lacrimal drainage obstruction: an etiologic classification system, case reports, and a review of the literature. Part 1. Ophthal Plast Reconstr Surg. 1992;8(4):237-42. [Medline].
Bartley GB. Acquired lacrimal drainage obstruction: an etiologic classification system, case reports, and a review of the literature. Part 2. Ophthal Plast Reconstr Surg. 1992;8(4):243-9. [Medline].
Bartley GB. Acquired lacrimal drainage obstruction: an etiologic classification system, case reports, and a review of the literature. Part 3. Ophthal Plast Reconstr Surg. 1993;9(1):11-26. [Medline].
Groessl SA, Sires BS, Lemke BN. An anatomical basis for primary acquired nasolacrimal duct obstruction. Arch Ophthalmol. Jan 1997;115(1):71-4. [Medline].
Kashkonli MB, Rezaee R, Nilforonshan N, et al. Topical antiglaucoma medications and lacrimal drainage system obstruction. Ophthal Plast Reconstr Surg. May-Jun 2008;24(3):175-6.
Seider N, Miller B, Beiran I. Topical glaucoma therapy as a risk factor for nasolacrimal duct obstruction. Am J Ophthalmol. Jan 2008;145(1):120-123. [Medline].
Berry-Brincat A, Tomlins P, Hall A, Quinlan M, Cheung D. Primary extrasac orbital lymphoma presenting as nasolacrimal obstruction. Orbit. 2008;27(3):175-7. [Medline].
Golub JS, Parikh SL, Budnick SD, Bernardino CR, DelGaudio JM. Inverted papilloma of the nasolacrimal system invading the orbit. Ophthal Plast Reconstr Surg. Mar-Apr 2007;23(2):151-3. [Medline].
Udhay P, Noronha OV, Mohan RE. Helical computed tomographic dacryocystography and its role in the diagnosis and management of lacrimal drainage system blocks and medial canthal masses. Indian J Ophthalmol. Jan-Feb 2008;56(1):31-7. [Medline].
Gökçek A, Argin MA, Altintas AK. Comparison of failed and successful dacryocystorhinostomy by using computed tomographic dacryocystography findings. Eur J Ophthalmol. Sep-Oct 2005;15(5):523-9. [Medline].
Karagülle T, Erden A, Erden I, Zilelioglu G. Nasolacrimal system: evaluation with gadolinium-enhanced MR dacryocystography with a three-dimensional fast spoiled gradient-recalled technique. Eur Radiol. Sep 2002;12(9):2343-8. [Medline].
Anderson NG, Wojno TH, Grossniklaus HE. Clinicopathologic findings from lacrimal sac biopsy specimens obtained during dacryocystorhinostomy. Ophthal Plast Reconstr Surg. May 2003;19(3):173-6. [Medline].
Moscato EE, Dolmetsch AM, Silkiss RZ, Seiff SR. Silicone intubation for the treatment of epiphora in adults with presumed functional nasolacrimal duct obstruction. Ophthal Plast Reconstr Surg. Jan 2012;28(1):35-9. [Medline].
Goldberg RA, Samimi DB, Tsirbas A, Douglas RS. The hydrogel lacrimal stent for dacryocystorhinostomy: preliminary experience. Ophthal Plast Reconstr Surg. Mar-Apr 2008;24(2):85-9. [Medline].
Erkan AN, Yilmazer C, Altan-Yaycioglu R. Otologic T-tube in endonasal dacryocystorhinostomy: a new approach. Acta Otolaryngol. Dec 2007;127(12):1316-20. [Medline].
Oghan F, Ozcura F. A novel stenting technique in endoscopic dacryocystorhinostomy. Eur Arch Otorhinolaryngol. Aug 2008;265(8):911-5. [Medline].
Kim KR, Song HY, Shin JH, Kim JH, Choi EK, Lee YJ. Efficacy of mitomycin C irrigation after removal of an occluded nasolacrimal stent. J Vasc Interv Radiol. Apr 2007;18(4):519-25. [Medline].
Kim KR, Song HY, Shin JH, et al. Eficacy of Mitomycin-C irrigation after balloon dacryoplasty. J Vasc Interv Radiol. Jun 2007;18(6):757-62.
Nemet AY, Wilcsek G, Francis IC. Endoscopic dacryocystorhinostomy with adjunctive mitomycin C for canalicular obstruction. Orbit. Jun 2007;26(2):97-100. [Medline].
Tabatabaie SZ, Heirati A, Rajabi MT, Kasaee A. Silicone intubation with intraoperative mitomycin C for nasolacrimal duct obstruction in adults: a prospective, randomized, double-masked study. Ophthal Plast Reconstr Surg. Nov-Dec 2007;23(6):455-8. [Medline].
Yildirim C, Yaylali V, Esme A, Ozden S. Long-term results of adjunctive use of mitomycin C in external dacryocystorhinostomy. Int Ophthalmol. Feb 2007;27(1):31-5. [Medline].
Ashenhurst ME, Hill VE, Keyhani K. Restrictive strabismus following Jones tube insertion: a case series of 8 patients. Can J Ophthalmol. Aug 2007;42(4):613-6. [Medline].
Bajaj MS, Mahindrakar A, Pushker N. Dentigerous cyst in the maxillary sinus: a rare cause of nasolacrimal obstruction. Orbit. Dec 2003;22(4):289-92. [Medline].
Becelli R, Renzi G, Mannino G, Cerulli G, Iannetti G. Posttraumatic obstruction of lacrimal pathways: a retrospective analysis of 58 consecutive naso-orbitoethmoid fractures. J Craniofac Surg. Jan 2004;15(1):29-33. [Medline].
Burns JA, Morgenstern KE, Cahill KV, Foster JA, Jhiang SM, Kloos RT. Nasolacrimal obstruction secondary to I(131) therapy. Ophthal Plast Reconstr Surg. Mar 2004;20(2):126-9. [Medline].
Camara JG, Bengzon AU, Henson RD. The safety and efficacy of mitomycin C in endonasal endoscopic laser-assisted dacryocystorhinostomy. Ophthal Plast Reconstr Surg. Mar 2000;16(2):114-8. [Medline].
Camara JG, Santiago MD. Success rate of endoscopic laser-assisted dacryocystorhinostomy. Ophthalmology. Mar 1999;106(3):441-2. [Medline].
Camara JG, Santiago MD, Rodriguez RE, Medalle RA, Young DA, Atebara NH. The Micro-Reflux Test: a new test to evaluate nasolacrimal duct obstruction. Ophthalmology. Dec 1999;106(12):2319-21. [Medline].
Couch SM, White WL. Endoscopically assisted balloon dacryoplasty treatment of incomplete nasolacrimal duct obstruction. Ophthalmology. Mar 2004;111(3):585-9. [Medline].
de Bree R, Scheeren RA, Kummer A, Tiwari RM. Nasolacrimal duct obstruction caused by an oncocytoma. Rhinology. Sep 2002;40(3):165-7. [Medline].
Dolman PJ. Comparison of external dacryocystorhinostomy with nonlaser endonasal dacryocystorhinostomy. Ophthalmology. Jan 2003;110(1):78-84. [Medline].
Esmaeli B, Hidaji L, Adinin RB, et al. Blockage of the lacrimal drainage apparatus as a side effect of docetaxel therapy. Cancer. Aug 1 2003;98(3):504-7. [Medline].
Katowitz JA, Low JE. Lacrimal surgery. In: Duane's Ophthalmology. Vol 5. [book on CD-ROM]; 1998:Chapter 79.
Kloos RT, Duvuuri V, Jhiang SM, Cahill KV, Foster JA, Burns JA. Nasolacrimal drainage system obstruction from radioactive iodine therapy for thyroid carcinoma. J Clin Endocrinol Metab. Dec 2002;87(12):5817-20. [Medline].
Lueder GT. Balloon catheter dilation for treatment of older children with nasolacrimal duct obstruction. Arch Ophthalmol. Dec 2002;120(12):1685-8. [Medline].
Lueder GT. Endoscopic treatment of intranasal abnormalities associated with nasolacrimal duct obstruction. J AAPOS. Apr 2004;8(2):128-32. [Medline].
Mauffray RO, Hassan AS, Elner VM. Double silicone intubation as treatment for persistent congenital nasolacrimal duct obstruction. Ophthal Plast Reconstr Surg. Jan 2004;20(1):44-9. [Medline].
Mirza S, Al-Barmani A, Douglas SA, Bearn MA, Robson AK. A retrospective comparison of endonasal KTP laser dacryocystorhinostomy versus external dacryocystorhinostomy. Clin Otolaryngol Allied Sci. Oct 2002;27(5):347-51. [Medline].
Nguyen LK, Linberg JV. Evaluation of the lacrimal system. In: Surgery of the eyelid, orbit, and lacrimal system. American Academy of Ophthalmology. 1995;3:254-69.
Oztürk S, Konuk O, Ilgit ET, Unal M, Erdem O. Outcome of patients with nasolacrimal polyurethane stent implantation: do they keep tearing?. Ophthal Plast Reconstr Surg. Mar 2004;20(2):130-5. [Medline].
Paul L, Pinto I, Vicente JM. Treatment of complete obstruction of the nasolacrimal system by temporary placement of nasolacrimal polyurethane stents: preliminary results. Clin Radiol. Nov 2003;58(11):876-82. [Medline].
Shepler TR, Sherman SI, Faustina MM, Busaidy NL, Ahmadi MA, Esmaeli B. Nasolacrimal duct obstruction associated with radioactive iodine therapy for thyroid carcinoma. Ophthal Plast Reconstr Surg. Nov 2003;19(6):479-81. [Medline].
Tao S, Meyer DR, Simon JW, Zobal-Ratner J. Success of balloon catheter dilatation as a primary or secondary procedure for congenital nasolacrimal duct obstruction. Ophthalmology. Nov 2002;109(11):2108-11. [Medline].
Tsirbas A, Davis G, Wormald PJ. Mechanical endonasal dacryocystorhinostomy versus external dacryocystorhinostomy. Ophthal Plast Reconstr Surg. Jan 2004;20(1):50-6. [Medline].
Tsirbas A, Wormald PJ. Endonasal dacryocystorhinostomy with mucosal flaps. Am J Ophthalmol. Jan 2003;135(1):76-83. [Medline].
Wobig JL, Dailey RA. Surgery of the Lacrimal System. In: Surgery of the eyelid, orbit, and lacrimal system. American Academy of Ophthalmology. 1995;3:270-87.
Woog JJ, Kennedy RH, Custer PL, Kaltreider SA, Meyer DR, Camara JG. Endonasal dacryocystorhinostomy: a report by the American Academy of Ophthalmology. Ophthalmology. Dec 2001;108(12):2369-77. [Medline].

