Penetrating keratoplasty, often called PK or full-thickness corneal transplant, is an eye surgery where a surgeon removes a circular piece of the patient’s cloudy or damaged cornea and replaces it with a clear, healthy, donor cornea. The cornea is the clear “window” at the front of the eye. It helps focus light so we can see sharply. When the cornea becomes scarred, swollen, thin, or irregular, light cannot enter the eye cleanly. Vision becomes blurry, distorted, or very poor. PK replaces all layers of the bad cornea with a clear donor cornea, so light can pass smoothly again.
PK is done in a sterile operating room. The surgeon uses a circular blade (called a trephine) to remove the patient’s cornea and a matching blade to punch a precise disc from the donor cornea. Tiny nylon stitches hold the donor cornea in place. The surgery usually takes under two hours. Patients go home the same day in most cases. Eye drops are used for many months to prevent rejection and to control inflammation. Stitches are removed slowly over time when the cornea is stable. Vision often improves gradually over months as the cornea heals and astigmatism settles.
PK is full-thickness. That means it replaces the entire cornea, from the front surface (epithelium) all the way to the back layer (endothelium). Today there are also lamellar transplants that replace only part of the cornea (for example, DALK for the front layers or DMEK/DSAEK for the back layer). Doctors choose PK when damage involves most or all layers, when infection or scarring is deep, when the cornea has perforated, or when other transplants are not suitable. PK has been performed for many decades, and surgical methods, tissue handling, and post-operative care are well established.
Below is a simple, long-form explanation of PK, written in plain English for easy reading. It covers types, 20 causes, 15 symptoms, and 20 diagnostic tests grouped by category. Each item includes a short, clear description.
What PK Tries To Fix (in very simple terms)
The cornea must be clear, smooth, and the right shape to focus light into a sharp image on the retina. If the cornea is scarred, light gets scattered. If the cornea is swollen, it becomes cloudy and hurts. If the cornea is thin or cone-shaped, light bends in the wrong way and vision becomes distorted. If the cornea has a hole or is about to perforate, the inside of the eye is at risk. PK removes the damaged window and puts in a new, clear window. The stitches hold it steady while it heals. Over time, the eye learns to see through the new window.
Types of Penetrating Keratoplasty
1) Optical PK (to improve vision).
This is the most common type. The goal is simple: replace a cloudy or misshapen cornea with a clear one to improve sight. It is chosen when scarring, swelling, or distortion is too severe for glasses, contact lenses, or partial-thickness transplants.
2) Therapeutic PK (to control disease).
This PK removes dangerous tissue to stop a harmful process, such as severe infection that does not respond to medicine. The main goal is to remove infected or inflamed cornea to save the eye. Vision improvement is a secondary goal once the eye is safe.
3) Tectonic PK (to restore eye integrity).
“Tectonic” means structural support. This PK is done when the cornea is very thin, has a hole, or is melting. The transplant gives the eye a strong front wall again, so the contents of the eye stay inside and the eye can heal.
4) Emergency PK (urgent surgery).
This is a fast, life-saving step for the eye. It is done when there is an open globe from trauma or a corneal perforation from disease or infection. The priority is to close the wound and protect the inside of the eye. Later, another PK may be done for optical reasons if needed.
5) High-risk PK (special planning).
Some eyes have a high chance of rejection. Reasons include blood vessels growing into the cornea, many past surgeries, active inflammation, or autoimmune disease. These cases need careful planning, strong medicines, and close follow-up to reduce rejection risk.
6) Pediatric PK (for children).
Children’s eyes heal and change quickly, and they are at higher risk of amblyopia (“lazy eye”). Pediatric PK needs special timing, anesthesia, and vision therapy afterward. Parents are taught how to give drops and protect the eye.
7) Repeat PK (regraft).
Sometimes a previous graft fails or becomes cloudy. A repeat PK replaces the old graft with a new one. The risks are higher than a first graft, so careful selection and counseling are important.
8) Combined PK (“triple procedure”).
When a patient also has a cataract, the surgeon may remove the cataract and place an intraocular lens during the PK. This is called a triple procedure (PK + cataract extraction + lens implant). It reduces the number of surgeries and anesthesia sessions.
9) Large-diameter or small-diameter PK (size tailored to the problem).
A large graft may be chosen to remove more diseased tissue or to capture a large scar. A small graft may be used to avoid nearby blood vessels or to fit a small clear area. The size choice balances disease removal, healing, and rejection risk.
10) Eccentric or decentered PK (off-center).
If the main problem is not in the center of the cornea, the surgeon can place the graft slightly off center to replace the worst area while preserving as much healthy host cornea as possible. This is less common but can be useful in unique cases.
Common Causes That Lead to Needing PK
These are the underlying problems that can damage the cornea so badly that a full-thickness transplant is considered. Each cause is explained in simple terms.
1) Keratoconus (advanced).
The cornea becomes thin and cone-shaped. In early stages, glasses or contact lenses help. In late stages, scarring and extreme irregular shape make vision very poor. PK may be needed when other options fail.
2) Post-LASIK or post-refractive ectasia.
After certain refractive surgeries, the cornea in rare cases can weaken and bulge. If bulging and irregularity are severe, and lenses do not work, PK may restore shape and clarity.
3) Fuchs endothelial corneal dystrophy (advanced).
The back layer (endothelium) fails and the cornea swells and becomes cloudy. Today, many patients get back-layer transplants (DMEK/DSAEK), but some advanced or complex cases still require PK.
4) Lattice corneal dystrophy.
Abnormal protein deposits form lines in the cornea and cause scarring. As scarring worsens, PK may be needed to clear the visual axis.
5) Granular corneal dystrophy.
White crumb-like deposits form in the cornea and can merge into scars. When vision drops a lot, PK may be chosen.
6) Macular corneal dystrophy.
This rare dystrophy causes diffuse clouding. It often involves many layers, so PK can be the best choice to replace the full thickness.
7) Congenital hereditary endothelial dystrophy (CHED).
Babies are born with cloudy corneas from endothelial failure. Some cases need PK in childhood when visual development is at risk.
8) Pseudophakic bullous keratopathy (after cataract surgery).
Endothelial cells are lost and cannot pump fluid out of the cornea. The cornea swells and forms blisters that hurt. When medical therapy fails, transplant is needed.
9) Aphakic bullous keratopathy (no lens).
Similar swelling occurs in eyes without a natural or artificial lens. PK may be considered when pain and clouding are severe.
10) Bacterial corneal ulcer with scarring.
A serious infection can leave a dense scar or a thin, weak spot. If the scar blocks vision or the cornea is unstable, PK can help.
11) Herpes simplex keratitis scarring.
The herpes virus can scar the cornea deeply. Once the infection is quiet, PK may be used to restore clarity, often with antiviral medicine to lower recurrence risk.
12) Fungal keratitis scarring.
Fungal infections can be deep and stubborn. After controlling infection, a scar can remain. PK removes the damaged tissue and improves vision.
13) Acanthamoeba keratitis (often from contact lenses) with scarring.
This organism causes intense pain and deep damage. When the disease is finally controlled, PK may be needed to clear the cornea.
14) Corneal trauma with laceration or perforation.
A cut or penetrating injury can leave an irregular scar or a weakened cornea. PK can rebuild a smooth, clear window.
15) Chemical burn (alkali or acid) with scarring.
Chemicals can quickly destroy the cornea and limbus. Once the eye is quiet, PK may be part of the reconstruction plan, often alongside surface and limbal stem-cell procedures.
16) Thermal burn (heat-related).
Heat injuries can cloud and scar the cornea. PK may be required if the damage is full-thickness.
17) Mooren ulcer (autoimmune).
This is a painful, progressive, peripheral corneal ulcer. When medical therapy fails or when perforation threatens, PK can restore the corneal wall.
18) Rheumatoid arthritis–related peripheral ulcerative keratitis (PUK).
Autoimmune inflammation can thin the cornea to the point of perforation. PK may be necessary to save the eye, along with systemic immune therapy.
19) Keratomalacia from severe vitamin A deficiency.
In advanced deficiency, the cornea softens and melts. Emergency measures and nutrition come first; PK may be needed once the eye is stabilized.
20) Failed previous corneal graft (graft failure).
A prior transplant can become cloudy or rejected. A repeat PK can restore clarity when other treatments cannot.
Symptoms People May Notice Before PK
These are the symptoms that commonly push patients and doctors to consider a transplant. Each is described simply.
1) Blurred vision.
Vision looks foggy or smeared, even with glasses. The cornea is not clear enough to let light focus nicely.
2) Hazy or cloudy view of the world.
Things look as if seen through frosted glass. This is common when the cornea is swollen or scarred.
3) Halos around lights.
Rings or halos appear around headlights and streetlights. This happens when light scatters through an irregular or wet cornea.
4) Glare and light sensitivity (photophobia).
Bright light hurts the eyes or makes it hard to see. A rough or swollen corneal surface can cause this.
5) Eye pain.
Pain can be sharp (in ulcers or perforations) or aching (in swelling or inflammation). Blisters on the cornea can be very painful.
6) Excess tearing (watery eye).
The eye tears to protect itself when the surface is rough, irritated, or infected.
7) Redness.
Inflammation makes the white of the eye look red. Infection and active immune disease can be very red.
8) Foreign-body sensation (gritty feeling).
The surface is not smooth, so it feels like something is in the eye. This is common with erosions and scars.
9) Distorted vision.
Straight lines look wavy. The cornea is irregular, so images bend unevenly.
10) Ghost images or monocular double vision.
You may see two images with one eye because of severe irregular astigmatism from scars or cone shape.
11) Fluctuating vision.
Vision may be better some days and worse on others, especially when swelling changes during the day.
12) Contact lens intolerance.
Lenses that once worked now irritate the eye or fall out because the cornea is too irregular.
13) Recurrent discharge or crusting.
Ongoing infection or surface breakdown can produce mucus or pus, which blurs vision and irritates the eye.
14) Sudden sharp pain with tearing after a minor bump or rub.
This can happen if a thin cornea or a previous wound opens or leaks. It needs urgent care.
15) Poor night vision and low contrast sensitivity.
Dim light makes vision particularly bad because scattered light and glare are worse at night.
Diagnostic Tests
Doctors use tests to confirm the cause, plan the surgery, and predict outcomes. Here are 20 tests, broken into Physical Exam, Manual Tests, Lab/Pathological Tests, Electrodiagnostic Tests, and Imaging Tests. Each test is explained in simple language.
A) Physical Exam
1) External eye inspection.
The doctor looks carefully at the eyelids, lashes, and the white of the eye. They check for redness, swelling, scars, eyelid malpositions, or signs of trauma. Healthy lids and surface are important for a good transplant outcome.
2) Pupillary light reflex testing.
A light is shined in each eye. The doctor watches how the pupils react. Poor reaction can point to nerve or retina problems. If the retina or optic nerve is weak, vision after transplant may still be limited.
3) Confrontation visual fields.
You cover one eye. The doctor moves fingers in your side vision. This screens for big blind spots. It helps rule out severe nerve or brain problems that would limit final vision.
4) Lid eversion and ocular surface check.
The doctor gently flips the eyelid to look for hidden foreign bodies, papillae, or scarring. A healthy inner lid and smooth tear film help the new cornea stay clear and comfortable.
B) Manual Tests
5) Visual acuity with and without pinhole.
You read letters on a chart. A pinhole can improve focus by blocking scattered light. If pinhole helps a lot, the retina and nerve likely work well, which is a good sign for post-PK vision.
6) Refraction and retinoscopy.
The doctor measures the exact power of lenses that sharpen your view. Retinoscopy uses a moving light and lenses to see how your eye focuses. This shows how irregular the cornea has become and sets a baseline for after surgery.
7) Slit-lamp biomicroscopy.
A special microscope with a thin beam of light lets the doctor see the cornea in fine detail. They can find scars, blood vessels, thinning, edema (swelling), and signs of infection. It is the key tool for corneal evaluation.
8) Fluorescein staining (including Seidel leak check when needed).
A yellow dye highlights damaged areas on the cornea under blue light. It shows scratches, ulcers, and dry spots. When the doctor looks for a leak (Seidel test), a stream of diluted dye reveals fluid escaping from a wound.
9) Tonometry (eye pressure measurement).
A small device gently touches or puffs the eye to measure pressure. High pressure can damage the optic nerve. Pressure also matters before and after PK, because glaucoma can limit vision and affect graft health.
C) Lab & Pathological Tests
10) Corneal scraping with Gram stain/KOH prep.
If infection is suspected, a tiny sample from the ulcer is examined right away under the microscope with special stains. This can quickly suggest bacteria or fungi, so the right treatment starts fast.
11) Culture and sensitivity testing.
The same sample is placed on plates to grow germs. The lab tests which antibiotics or antifungals kill them best. This guides precise treatment and can prevent graft infection or failure.
12) Viral PCR (e.g., for herpes simplex or varicella-zoster).
Sometimes a virus is the cause. PCR detects viral genetic material from tears or tissue. Knowing the virus helps plan long-term antiviral therapy around the time of PK.
13) Histopathology of the excised corneal “button.”
After PK, the removed cornea can be examined under a microscope. The pathologist confirms the exact disease, checks for organisms, and documents depth and severity. This helps guide post-op care and prognosis.
D) Electrodiagnostic Tests
14) Electroretinography (ERG).
Small contact lens electrodes measure how the retina responds to flashes of light. If the retina is very weak, even a clear cornea may not give sharp vision. ERG is helpful when the cornea is too opaque to see the retina directly.
15) Visual evoked potential (VEP).
Sensors on the scalp measure the brain’s response to visual stimuli. A poor signal suggests optic nerve or brain pathway problems. This test helps set realistic expectations for vision after PK.
16) Electrooculogram (EOG).
This test measures electrical changes as the eye moves. It checks certain retinal pigment functions. While used less often, it can add information in complex cases where the media are too cloudy to examine.
E) Imaging Tests
17) Corneal topography or tomography (Placido or Scheimpflug).
A camera maps the curvature and shape of the cornea. It shows steep or flat areas and irregular astigmatism. Tomography also measures the back surface and overall thickness map. This is crucial for planning and later for tracking astigmatism after stitches.
18) Anterior segment optical coherence tomography (AS-OCT).
AS-OCT uses light waves to create cross-section images of the cornea and the front of the eye. It shows layers, scars, fluid pockets, and very thin areas. It helps measure healing and detect interface problems after surgery.
19) Specular microscopy (endothelial cell analysis).
A camera images the back cells of the cornea (endothelium). It counts cells and looks at their shape. Low counts in donor tissue predict faster clouding. Checking the host eye’s other endothelium and the donor specs guide safety and prognosis.
20) B-scan ultrasound or ultrasound biomicroscopy (when the cornea is too opaque).
If the cornea is so cloudy that the doctor cannot see inside, ultrasound checks the lens, vitreous, and retina for detachments or masses. This ensures there is no hidden problem that would limit vision after the transplant.
Disclaimer: Each person’s journey is unique, treatment plan, life style, food habit, hormonal condition, immune system, chronic disease condition, geological location, weather and previous medical history is also unique. So always seek the best advice from a qualified medical professional or health care provider before trying any treatments to ensure to find out the best plan for you. This guide is for general information and educational purposes only. Regular check-ups and awareness can help to manage and prevent complications associated with these diseases conditions. If you or someone are suffering from this disease condition bookmark this website or share with someone who might find it useful! Boost your knowledge and stay ahead in your health journey. We always try to ensure that the content is regularly updated to reflect the latest medical research and treatment options. Thank you for giving your valuable time to read the article.
The article is written by Team RxHarun and reviewed by the Rx Editorial Board Members
Last Updated: August 20, 2025.
