Double Lacrimal Puncta: Clinical Presentation and Potential Mechanisms of Epiphora

被引:23
作者
Satchi, Khami [1 ]
McNab, Alan A. [1 ]
机构
[1] Royal Victorian Eye & Ear Hosp, Orbital Plast & Lacrimal Clin, Melbourne, Australia
关键词
CONGENITAL REDUPLICATION; DOWNS-SYNDROME; CANALICULUS; MANAGEMENT; ANOMALIES; FISTULA;
D O I
10.1016/j.ophtha.2009.06.054
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: Congenital supernumerary lacrimal puncta and canaliculi are rarely reported. Our purpose is to present the largest series of patients with supernumerary puncta and to describe the clinical presentation and associated lacrimal anomalies. Design: Observational retrospective case series. Participants: All patients diagnosed with supernumerary puncta by a single surgeon between 1988 and 2008. Methods: Retrospective case note review. Main Outcome Measures: Patient demographics, clinical presentation, lacrimal and systemic examination findings, management, and surgical outcomes. Results: Twenty-three patients (12 female, 11 male) with a median presenting age of 54 years (range, 1-88 years) had unilateral double lower lid puncta. In 5 patients the presence of a double punctum was an incidental examination finding. Eighteen patients had unilateral tearing on the same side as the double punctum. In 6 children presenting with tearing, associated congenital lacrimal anomalies included nasolacrimal duct obstruction, a lacrimal fistula, a lacrimal sac diverticulum, and absence of the upper canaliculus. Associated systemic findings in 3 children included Down syndrome (1 patient) and preauricular sinuses (2 patients). Of 12 adult patients presenting with ipsilateral tearing, 5 had complete nasolacrimal duct obstruction and 6 had either partial nasolacrimal duct obstruction or functional epiphora. Dacryocystorhinostomy was performed in 12 patients and resulted in improvement or resolution of symptoms in 11 patients (92%). Conclusions: Double lower lacrimal puncta may be associated with epiphora. In younger patients, tearing may be due to associated congenital anomalies of the nasolacrimal system. A proportion of patients presenting with onset of tearing in adulthood have patent lacrimal systems and otherwise normal adnexal examination results, suggesting that the presence of double puncta may be associated with compromised canalicular function. Reflux of tears through the accessory canaliculus is a potential mechanism and would be consistent with a recently proposed 2-compartment model of lacrimal canalicular drainage.
引用
收藏
页码:180 / U218
页数:6
相关论文
共 24 条
[1]  
BACSKULIN J, 1964, Klin Monbl Augenheilkd, V144, P418
[2]   Congenital reduplication of the lacrimal punctum and canaliculus in a patient with dry eye [J].
Bair, PJ ;
Tsai, YY ;
Lin, JM .
OPHTHALMIC SURGERY LASERS & IMAGING, 2004, 35 (02) :156-158
[3]   MANAGEMENT OF CONGENITAL LACRIMAL SAC FISTULA [J].
BIRCHANSKY, LD ;
NERAD, JA ;
KERSTEN, RC ;
KULWIN, DR .
ARCHIVES OF OPHTHALMOLOGY, 1990, 108 (03) :388-390
[4]  
BOTHMAN L, 1932, AM J OPHTHALMOL, V15, P214
[5]  
CARVILL M, 1909, ARCH OPHTHALMOL-CHIC, V38, P585
[6]  
CHANCE B, 1922, AM J OPHTHALMOL, V5, P297
[7]   DOUBLE PUNCTUM AND CANALICULUS [J].
CHIGNELL, AH .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1968, 65 (05) :736-&
[8]   Nasolacrimal outflow drainage anomalies in Down's syndrome [J].
Coats, DK ;
McCreery, KMB ;
Plager, DA ;
Bohra, L ;
Kim, DS ;
Paysse, EA .
OPHTHALMOLOGY, 2003, 110 (07) :1437-1441
[9]  
Duke-Elder S, 1964, SYSTEM OPHTHALMOLO 2, V3, P928
[10]  
FLOM L, 1955, ARCH OPHTHALMOL-CHIC, V54, P760