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Lacrimal punctum
Lacrimal punctum
Lacrimal punctum
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Lacrimal punctum
The tarsal glands, etc., seen from the inner surface of the eyelids. (Puncta lacrimalia visible at center left.)
The lacrimal apparatus. Right side. Note outdated terminology: The "Lacrimal ducts" in Gray's are now called "Lacrimal canals".
Details
Identifiers
Latinpuncta lacrimalia
TA98A15.2.07.065
TA26854
FMA59365
Anatomical terminology

The lacrimal punctum (pl.: puncta) or lacrimal point is a minute opening on the summits of the lacrimal papillae, seen on the margins of the eyelids at the lateral extremity of the lacrimal lake. There are two lacrimal puncta in the medial (inside) portion of each eyelid. Normally, the puncta dip into the lacrimal lake.

Together, they function to collect tears produced by the lacrimal glands. The fluid is conveyed through the lacrimal canaliculi to the lacrimal sac, and thence via the nasolacrimal duct to the inferior nasal meatus of the nasal passage.

Additional images

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  • A close up of a lacrimal punctum.
    A close up of a lacrimal punctum.
  • Lower lacrimal punctum through slit lamp biomicroscope
    Lower lacrimal punctum through slit lamp biomicroscope

See also

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References

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Revisions and contributorsEdit on WikipediaRead on Wikipedia

Lacrimal punctum

View on Grokipedia
from Grokipedia
The lacrimal punctum (plural: lacrimal puncta) is a small opening located at the medial margin of each upper and lower , approximately 6 mm from the medial , serving as the initial entry point for into the lacrimal drainage system. Each punctum measures about 0.2 to 0.3 mm in diameter and is positioned to collect from the ocular surface during , which activates the surrounding to facilitate drainage. There are four puncta in total—two per eye (one superior and one inferior)—and they connect directly to short vertical canaliculi that transition into horizontal canaliculi, ultimately merging into the before flow through the into the .

Anatomy

Location and gross structure

The lacrimal puncta are situated on the medial aspect of the upper and lower s, approximately 6.0 mm and 6.5 mm lateral to the medial , respectively. These openings mark the entry points to the lacrimal drainage system and are positioned such that the inferior punctum lies about 0.5 mm lateral to the superior one, ensuring alignment during closure. In gross appearance, each punctum presents as a small, rounded or oval opening measuring 0.2 to 0.3 mm in diameter, located at the summit of a slightly elevated papilla at the of the eyelid margin. The papillae are subtle elevations, with the overall structure appearing as minute, reddish-brown dots posterior to the anterior lid margin and integrated seamlessly with the surrounding tarsal plate. The puncta are oriented to face each other when the eyelids are closed, facilitating the collection of tears from the lacrimal lake in the medial canthus. Each punctum opens directly into a short vertical canaliculus, approximately 2 mm in length, which then dilates into a fusiform ampulla before curving horizontally to continue as the canalicular system. This positioning places the puncta anterior to the deeper canaliculi and posterior to the free edge of the eyelid margin, serving as the initial conduit in the tear drainage pathway.

Histology

The lacrimal punctum is lined by a non-keratinized that forms a protective barrier at its opening. This epithelial layer transitions gradually from the adjacent conjunctival epithelium, which consists of non-keratinized stratified squamous cells with goblet cells, to a more skin-like stratified squamous structure at the external punctal margin, facilitating seamless integration with the eyelid skin. Beneath the epithelium lies a subepithelial layer of rich in elastic fibers, which provides structural support to the punctal papilla and maintains the patency of the opening. This is reinforced by underlying fibers from the , particularly the pars lacrimalis (Riolan muscle), contributing to the punctum's resilience and aiding in its eversion during blinking. Glandular elements are not intrinsic to the punctum itself, which lacks secretory capabilities; however, accessory lacrimal glands, such as the glands of Krause, are present in nearby conjunctival fornices and contribute to basal tear production without direct involvement in the punctal structure. The region receives a rich vascular supply from the superior and inferior palpebral arteries, branches of the , forming a network that nourishes the epithelial and connective tissues. Sensory innervation is provided by branches of the ophthalmic division of the (cranial nerve V), enabling reflex tearing in response to ocular irritation.

Embryology

Developmental formation

The development of the lacrimal punctum begins as part of the excretory lacrimal system's embryogenesis, originating from the surface in the lacrimal groove between the nasal and maxillary processes around the 5th to 6th week of ( 16–18). At this stage, epithelial thickening forms the lacrimal lamina, which invaginates into the underlying to establish the precursor structure for the drainage apparatus. By the 6th to 8th week (Carnegie stages 19–23), the lacrimal lamina separates from the overlying to form a solid cellular cord, known as the lacrimal cord, whose lateral end bifurcates to create the primordia of the superior and inferior canaliculi; these ectodermal cords elongate toward the future margins, influenced by surrounding facial for proper positioning. Canalization of these solid cords into patent lumina initiates around the 10th week, with central epithelial cell degeneration forming a continuous channel connecting to the by the 4th month of (approximately 16 weeks). The canaliculi continue to elongate between 16 and 20 weeks, establishing the structural framework for tear drainage. The lacrimal puncta, as the distal openings of the canaliculi, achieve patency by the 7th month of (around 28 weeks), coinciding with separation and final maturation of the drainage system. Full functional patency of the puncta is typically present at birth, though minor refinements may occur shortly postpartum due to ongoing mesenchymal interactions. This developmental process is regulated by genetic factors, including transcription factors such as FOXC1 and PITX2, which play roles in the differentiation of the periocular and ectodermal components of the anterior segment, with disruptions linked to congenital drainage anomalies.

Anatomical variations

The lacrimal punctum exhibits several anatomical variations, ranging from congenital absences to duplications and positional deviations, which can influence tear drainage efficiency. Punctal agenesis, or complete absence of the opening, is a rare congenital anomaly, most commonly affecting the lower punctum, and occurs due to failed embryonic canalization. While exact is not well-established, it is frequently associated with systemic conditions rather than isolated occurrences, with bilateral involvement in approximately 59% of reported cases. Supernumerary puncta, characterized by extra openings along the margin, are also uncommon congenital variants, with an estimated incidence of about 1 in 60,000 eyes, predominantly affecting the lower lid in a slit-like form. Positional anomalies include membranous puncta, where a thin epithelial membrane covers the opening at birth, often resolving spontaneously within the first few months without intervention, though manual probing may be required in persistent cases. Ectropic puncta, or punctal ectropion, involve eversion of the punctum away from the globe due to lower eyelid laxity, which can misalign the opening and impair initial tear entry. These positional shifts are typically acquired with age but can have congenital underpinnings in cases of eyelid maldevelopment. Variations in size and shape encompass imperforate puncta, a severe form of congenital where the opening fails to perforate, and stenotic puncta, which narrow progressively and are classified into types such as membranous, slit, horseshoe, or pinpoint based on morphology. The lower punctum is generally larger than the upper (average 0.64 mm versus smaller in comparative studies), with racial differences noted; for instance, punctal tends to be slightly smaller in Asian populations (e.g., 0.61 mm in ) compared to Caucasians (e.g., 0.65 mm). These shape variations are more prevalent in older adults, with affecting up to 63% in those over 65 years. Certain systemic syndromes are linked to punctal variations, particularly those impacting ectodermal development. In (trisomy 21), nasolacrimal anomalies including punctal or occur in up to 22% of cases, often involving multiple drainage system defects. syndromes similarly feature high rates of lacrimal drainage obstruction, with punctal reported in about 33% and overall obstruction in 40% of affected individuals, underscoring the role of genetic factors in patency disruptions.

Function

Tear drainage mechanism

Tears originating from the lacrimal glands and accessory glands spread across the ocular surface as a thin film before pooling in the lacrimal lake at the medial canthus. From there, they enter the lacrimal puncta primarily through and , which draw the fluid into the small openings without requiring active muscular effort during interblink periods. The lower punctum plays the dominant role in this initial entry, accounting for approximately 80% of total tear drainage due to its more dependent position relative to tear flow dynamics. Once inside the puncta, tears flow into the canalicular system, beginning with the vertical segment of the canaliculus, which measures about 2 mm in length and collects fluid into a dilated . This vertical portion transitions into the horizontal canaliculus, spanning 8–10 mm, which conveys the medially toward the . In approximately 90% of individuals, the upper and lower horizontal canaliculi converge to form a short common canaliculus (3–5 mm long) before entering the sac, optimizing the pathway for efficient drainage. The primary propulsion of tears through the canaliculi occurs via the mechanism, which acts as a pump driven by the . During closure, contraction of the preseptal and pretarsal portions of this muscle compresses the elastic canalicular walls, increasing intraluminal pressure and forcing toward the ; upon lid opening, creates negative pressure, aiding further inflow. This dynamic process ensures effective movement even against gravity, with each blink contributing to the overall tear propulsion. The lacrimal drainage system is calibrated to manage basal tear production, which occurs at a rate of 1–2 μL/min per eye, maintaining ocular surface through continuous, low-volume outflow that prevents accumulation and overflow under normal conditions.

Physiological regulation

The physiological of the lacrimal punctum involves integrated neural, , and hormonal mechanisms that modulate tear drainage efficiency and punctal patency. Neural control primarily stems from the , with parasympathetic fibers originating from the (cranial nerve VII) providing secretomotor innervation to the , thereby increasing tear production and subsequent flow through the punctum during lacrimation. Sympathetic modulation, via postganglionic fibers from the , influences vasoregulation in the lacrimal drainage apparatus, adjusting vascular tone to support epithelial health and fluid dynamics around the punctum. Additionally, somatic motor innervation from cranial nerve VII to the , particularly its pars lacrimalis, facilitates mechanical compression and release at the punctum to propel tears into the canaliculi. Reflex pathways enhance punctal function through sensory-motor loops, where afferent signals from the trigeminal nerve (cranial nerve V), via its ophthalmic and maxillary divisions, detect ocular surface irritation and trigger protective responses. These signals synapse in the brainstem, eliciting punctal closure and opening via orbicularis oculi contraction, which optimizes tear entry and prevents overflow. The blink reflex, a key component, amplifies pump efficiency by repeatedly compressing the canaliculi against the punctum during eyelid closure, generating negative pressure to draw tears inward at rates aligned with basal secretion. This reflex integrates with lacrimal gland activation to maintain homeostasis. Adaptive responses allow the punctum to handle varying tear loads, such as during irritation-induced reflex tearing, which can elevate production to approximately 100 μL/min, far exceeding the basal rate of 1-2 μL/min and necessitating enhanced drainage throughput. Diurnal variations in tear meniscus volume, which is higher upon awakening and decreases throughout the day, further influence punctal throughput by altering the hydrostatic gradient and evaporation rates across the day. Hormonal influences indirectly regulate punctal patency through effects on nearby epithelial and secretory tissues. Androgens, acting via receptors in the lacrimal acinar cells and conjunctival , promote responses and maintain structural integrity, supporting unobstructed punctal function. Estrogens similarly modulate epithelial and production in the ocular surface, influencing tear composition and flow dynamics that affect punctal clearance. These sex steroid effects ensure adaptive patency under physiological fluctuations, such as during hormonal cycles.

Clinical significance

Associated disorders

Punctal stenosis refers to the narrowing or occlusion of the lacrimal punctum opening, often resulting from aging, chronic inflammation such as , or certain medications including systemic chemotherapy agents like . This condition commonly manifests as epiphora, or excessive tearing, and accounts for 8% to 54% of epiphora cases depending on the patient population studied. Congenital imperforate punctum arises from a failure in the canalization of the lacrimal drainage system during embryonic development, preventing the formation of the punctal opening. This rare anomaly can lead to neonatal through tear stasis and secondary infection in the , with congenital —a related condition—affecting approximately 6% to 20% of newborns, though imperforate punctum specifically occurs in a smaller subset. Punctal eversion, often associated with lower eyelid , occurs due to laxity or malposition of the margin, which displaces the punctum away from the tear meniscus and impairs effective tear drainage. This misalignment results in symptoms including epiphora from inadequate drainage as well as dry eye manifestations such as ocular irritation and exposure keratopathy. Inflammatory conditions affecting the lacrimal punctum include chronic , which induces persistent and scarring of the and adjacent structures, potentially leading to punctal occlusion. Similarly, herpes zoster ophthalmicus can involve the punctal epithelium, causing chronic scarring that results in and obstructive epiphora. Systemic autoimmune diseases, such as Sjögren's syndrome, are linked to secondary punctal through chronic lymphocytic infiltration and of the ocular surface, exacerbating lacrimal dysfunction and tear drainage issues.

Diagnosis and procedures

Diagnosis of lacrimal punctum issues typically begins with slit-lamp biomicroscopy to evaluate punctal patency and identify or occlusion. The fluorescein dye disappearance test involves instilling 2% fluorescein into the conjunctival fornix and observing clearance time, with normal drainage occurring within 5 minutes; delayed clearance indicates potential obstruction. Lacrimal irrigation and probing assess anatomical patency by cannulating the punctum with a lacrimal attached to a saline-filled ; free passage into the confirms openness, while reflux through the opposite punctum suggests blockage. For more complex cases, imaging modalities such as dacryocystography provide detailed visualization of the lacrimal drainage system by injecting contrast into the canaliculus to detect strictures or diverticula. Computed tomography (CT) or dacryocystography is employed when or trauma is suspected, offering non-invasive assessment of bony structures and soft tissues around the punctum and . The Jones dye test differentiates pre-sac from post-sac obstructions: in the primary (Jones I) test, fluorescein is placed in the eye and nasal recovery after 5 minutes indicates canalicular patency; the secondary (Jones II) test irrigates the inferior canaliculus, with dye in the nasal effluent confirming to duct flow. Therapeutic interventions for punctal stenosis include punctal dilation, sometimes followed by insertion of temporary perforated punctal plugs to maintain patency. Punctoplasty enlarges a stenotic punctum through incisions: the one-snip procedure involves a single vertical cut in the posterior canalicular wall, while the two-snip technique adds a horizontal incision connecting vertical cuts in the medial and lateral walls for greater opening. Adjunctive application of during punctoplasty can help prevent restenosis. For conditions involving refractory dry eye, such as in association with or Sjögren's syndrome, surgical options include thermal or radiofrequency to permanently close the punctum, applying heat to the punctal opening under to induce and prevent tear drainage. For chronic blockages, lacrimal involves placing tubes (e.g., Crawford or Ritleng) through the canaliculi into the to maintain patency, often after probing or , with tubes left in place for 3-6 months. Punctoplasty achieves anatomical success rates around 91% and functional success rates of 64-93%, though long-term restenosis can occur in up to 20% of cases. Complications of these procedures include , over-drainage leading to epiphora, canalicular trauma, or formation, with risks minimized through precise technique and postoperative care.

References

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