Can Xanthelasma Return After Surgical Removal? Recurrence and the Next Options

Key Takeaways
- Xanthelasma plaques are clusters of lipid-filled immune cells in the upper eyelid dermis, and no removal method changes the biological tendency that forms them, which is why they can return.
- In the Copenhagen City Heart Study of 12,745 adults, people with xanthelasmata had a 48 percent higher rate of heart attack even after adjusting for cholesterol, so recurrence is a cue for a cardiovascular risk review.
- Lowering blood cholesterol rarely shrinks existing plaques but is the measure most consistently associated with fewer new deposits in the descriptive literature.
- Each repeat surgical excision removes more eyelid skin, so surgeons often shift toward trichloroacetic acid peels or ablative laser for thin regrowth, especially on the lower lid where skin shortage risks ectropion.
- Healing windows for excision, peels, laser and cryotherapy all cluster around one to two weeks for surface recovery, with redness fading over subsequent weeks and scars maturing for up to a year.
- Home remedies and online products marketed to dissolve xanthelasma have no controlled evidence and can cause burns and scarring on eyelid skin that are harder to treat than the original plaque.
Yes. Xanthelasma can come back after surgical removal, and published case series report recurrence often enough that surgeons discuss it before treating. The plaques reflect an underlying tendency to deposit cholesterol in eyelid skin, which removal does not change. If xanthelasma comes back after removal, options include repeat excision, trichloroacetic acid peels, ablative laser or cryotherapy, alongside a lipid review with the treating team.
The stitches came out on day six. For a few weeks the inner corner of her left eyelid looked pink, then pale, then simply like eyelid again. Eleven months later, standing at the bathroom mirror with a magnifying light, she noticed a faint buttery smudge exactly where the old patch had been. Smaller, yes. But there.
If that scene feels familiar, you are asking a question that eyelid surgeons and dermatologists hear constantly: why xanthelasma comes back after removal, and what, realistically, can be done the second time around. The honest answer has two halves. The first is about the skin that was treated. The second is about the bloodstream underneath it, which no scalpel or laser touches.
This explainer walks through both halves, without promises, using what mainstream medical evidence actually shows.
Why xanthelasma comes back after removal: the plain truth
Xanthelasma is a soft, yellowish plaque of cholesterol-laden cells that forms in the thin skin of the eyelids, most often near the inner corner. Removing it takes away the visible deposit. It does not remove the reason the deposit formed.
That reason is a local process. Immune cells called histiocytes, which normally patrol tissue for debris, take up lipid and swell into what pathologists call foam cells. Clusters of foam cells sit in the upper layer of the skin and give the plaque its color. Eyelid skin is among the thinnest on the body and is constantly moving, and the region has a rich network of tiny blood vessels. Those features appear to make it a favored spot for lipid to settle, in people whose blood lipids are high and in a sizeable group whose measured cholesterol is normal, as MedlinePlus notes.
So when a surgeon excises a plaque, three things determine whether it returns. Was every foam-cell cluster removed, including the faint edges that shade into normal-looking skin? Is the person still carrying a lipid pattern that encourages fresh deposits? And has enough time passed to know? Recurrence is often slow, arriving over months to a few years rather than weeks.
There is one more layer worth naming early. Xanthelasma that keeps returning is a signal to look again at the whole person, not just the eyelid. Cleveland Clinic and MedlinePlus both describe the plaques as sometimes the first visible clue to an inherited or acquired lipid disorder. A recurrence is frustrating cosmetically, but it can also be genuinely useful information for your physician.
What actually happens under the eyelid skin
Picture the eyelid in cross-section. On top sits a very thin epidermis, the outer protective layer. Beneath it lies the dermis, the supportive layer holding collagen, tiny vessels and immune cells. Under that is a loose plane of connective tissue, then the orbicularis muscle that closes the eye.
Xanthelasma lives in the upper dermis. Cholesterol, largely carried into tissue by low-density lipoprotein (LDL, the particle often labeled bad cholesterol), leaks from small vessels and is taken up by histiocytes. As those cells fill with lipid droplets they lose their normal shape and function, becoming foam cells. Over time they gather into sheets, and the plaque becomes visible as a velvety yellow patch that may be flat or slightly raised.
Why does this matter for recurrence? Because foam cells do not respect a neat boundary. Under a microscope, the plaque often extends a little beyond the edge you can see with the naked eye, and it may sit deeper in the dermis than its flat appearance suggests. Every removal technique has to trade completeness against the risk of taking too much from an area where the skin is thin, where scarring can pull the lid margin, and where the eye itself is millimeters away.
The same anatomy explains the second route to recurrence. Even if a surgeon clears every foam cell, the vessels, the histiocytes and the circulating lipid remain. If the biological conditions that fed the first plaque persist, the tissue can simply start the process again. Removal resets the clock; it does not stop it.
Is xanthelasma linked to cholesterol and heart risk?
Partly, and the details matter. Many people with xanthelasma have raised total or LDL cholesterol, low HDL, or a genetic lipid disorder such as familial hypercholesterolemia, an inherited condition that keeps LDL very high from childhood. But a substantial share have entirely normal lipid panels, so a normal blood test does not rule out the plaques and the plaques do not prove a lipid problem.
The most cited evidence on wider risk comes from the Copenhagen City Heart Study, published in the BMJ. Researchers followed 12,745 adults for up to 33 years. At the start, 4.4 percent had xanthelasmata. After adjusting for the usual risk factors, including cholesterol levels themselves, people with xanthelasmata had a hazard ratio of 1.48 for heart attack, 1.39 for ischemic heart disease, 1.69 for severe atherosclerosis and 1.14 for death from any cause. A hazard ratio is a comparison of event rates over time; 1.48 means roughly a 48 percent higher rate relative to people without the plaques. The association held even in those with normal blood lipids.
Two cautions. First, an association is not a diagnosis; most people with xanthelasma in that cohort did not have a heart attack. Second, the same study found no such link for arcus corneae, the pale ring around the iris, so the eyelid finding appears to carry specific information.
The practical reading, echoed by Cleveland Clinic, is that xanthelasma deserves a lipid panel and a conversation about cardiovascular risk, especially when it appears before middle age or returns after removal. That conversation belongs with your primary care physician or a lipid specialist, not the aesthetic clinic alone.
What xanthelasma removal procedures actually do
Every method aims to destroy or lift out the foam-cell layer while sparing as much normal eyelid as possible. They differ in how they get there.
Surgical excision removes the plaque with a scalpel under local anesthetic, usually along a natural crease so the fine scar hides in a fold. Small plaques may be closed directly with sutures. Larger ones can require a small skin graft or a rearrangement of nearby skin, which is why operative planning for extensive plaques is a separate conversation.
Trichloroacetic acid (TCA) is a chemical peeling agent. Applied precisely to the plaque, it causes controlled protein coagulation in the upper skin layers; the treated tissue frosts white, then sheds over the following days as new skin forms underneath. Several sessions may be needed for thicker plaques.
Ablative lasers, chiefly carbon dioxide and erbium types, vaporize thin layers of tissue with heat, allowing the operator to work down to the plaque base while watching the color change. Some centers use lasers that target blood vessels or pigment instead.
Cryotherapy freezes the tissue with liquid nitrogen so that lipid-filled cells rupture and are cleared; electrodesiccation uses a fine electrical current to dry and destroy tissue point by point.
None of these alters cholesterol metabolism. Each carries a chance of pigment change (lighter or darker skin), fine scarring, and, rarely, an outward turn of the lower lid margin called ectropion when too much skin is removed. Which technique suits a given plaque depends on its size, depth, position and the person’s skin type, and that judgment sits with the treating surgeon or dermatologist.
What is the xanthelasma recurrence rate, honestly?
There is no guideline-endorsed number, and anyone quoting a single figure with confidence is simplifying. Here is what the evidence actually looks like.
Both MedlinePlus and Cleveland Clinic state plainly that xanthelasma can come back after treatment. Beyond that, the recurrence data come from case series: reports from individual departments describing their own patients, often a few dozen at a time, followed for varying lengths. These series differ in technique, in how they define recurrence (a visible spot? any yellow tint on close inspection?), and in how long patients were watched. Short follow-up flatters every method, because recurrence tends to be slow.
Across that literature a consistent pattern emerges even though exact percentages do not. Recurrence is common enough that it should be part of the pre-treatment conversation. It is more likely when plaques are large or involve all four eyelids, when the person has a lipid disorder that is untreated or difficult to control, and after a second or third removal at the same site, where scar tissue complicates complete clearance. Recurrence appears less frequent when the lipid picture has been addressed, though no controlled trial has tested that directly.
What about the frequently searched question of success rate? Success can mean complete clearance in one session, an acceptable cosmetic result, or no recurrence at a given time point, and the case series rarely use the same yardstick. No systematic review sets a benchmark that applies to an individual. Ask your surgeon what their experience has been with plaques like yours, and ask how they define a good result. That is a more useful question than a percentage.
Who is usually offered removal, and who is asked to wait
Xanthelasma is harmless to the eye and to vision. Removal is therefore a choice, made for appearance or, occasionally, because a very large plaque feels heavy or interferes with the lid margin. That framing shapes who is usually treated straight away and who is asked to pause.
Removal is commonly considered when the plaques are stable in size, the person understands they can return, the lipid workup has been done or is under way, and there is no active skin infection or inflammation around the eyes. Small, flat, well-defined plaques near the inner corner of the upper lid are the most straightforward case for most techniques.
A clinician may suggest waiting in several situations. When plaques are still enlarging quickly, treating a moving target often means treating again soon. When a lipid disorder has just been identified and treatment is starting, many physicians prefer to see the metabolic picture settle first. When the plaques are extensive, involve the lower lids or sit close to the lash line, planning may need to include an oculoplastic surgeon, a specialist in surgery around the eye, because skin shortage there risks ectropion. People with a history of raised or keloid scars, active eczema or rosacea on the lids, recent isotretinoin use, or conditions that impair healing are also usually assessed more carefully.
Younger adults with xanthelasma face a specific version of this. Plaques appearing in the twenties raise the chance of an inherited lipid disorder, and both Mayo Clinic and MedlinePlus advise lipid testing in that setting. Sorting that out first does not prevent later removal; it simply puts the more consequential question ahead of the cosmetic one.
Xanthelasma removal options side by side
No single method wins on every measure. The table below summarizes how the main approaches compare on the questions patients tend to ask. It is a general guide drawn from the descriptive literature, not a ranking, and your clinician’s judgment about your specific plaques takes precedence.
| Method | How it removes the plaque | Typical healing window | Main trade-offs | Suits |
|---|---|---|---|---|
| Surgical excision | Cuts out the plaque; closes with sutures, sometimes a graft | Sutures out around one week; redness fades over weeks | Fine scar; skin shortage risk on lower lid; allows tissue examination | Discrete plaques along a natural crease |
| Trichloroacetic acid peel | Chemically coagulates the plaque, which sheds | Crust separates within about one to two weeks | May need repeat sessions; pigment change, especially in darker skin | Thin, superficial plaques |
| Ablative laser | Vaporizes tissue layer by layer | Raw surface re-epithelializes over roughly one to two weeks | Equipment-dependent; pigment change; heat injury if too deep | Flat or moderately raised plaques |
| Cryotherapy | Freezes and ruptures lipid-filled cells | Blister and crust resolve over one to two weeks | Less precise depth control; swelling; pigment loss | Small plaques where other options are unsuitable |
| Electrodesiccation | Destroys tissue with fine electrical current | Small crusts heal over about one to two weeks | Operator-dependent depth; scarring if aggressive | Very small, scattered spots |
Two observations from this comparison. Excision is the only option that produces a specimen a pathologist can examine, which occasionally matters when the diagnosis is uncertain. And the healing windows overlap heavily, so the choice usually turns on plaque depth, skin type and the surgeon’s experience rather than on downtime.
What the days and weeks after removal usually look like
Recovery timelines vary with technique and with the individual, but the broad shape is consistent enough to describe, and Cleveland Clinic outlines a similar course.
In the first two or three days, expect swelling, some bruising if a scalpel was used, and tenderness. After a peel or laser, the treated skin looks raw or crusted and may weep slightly. Cold compresses and keeping the head elevated at night are the usual comfort measures; your team will give specific wound-care instructions, and those instructions override anything general.
Toward the end of the first week, sutures from an excision typically come out. Crusts from chemical or laser treatment begin to separate on their own; picking them off early risks scarring and pigment change. New skin underneath is pink and shiny.
Over weeks two to six, redness fades gradually. Pinkness at a laser or peel site can persist for several weeks, longer in fair skin, and temporary darkening can appear in olive or brown skin. Strict sun protection during this period is one of the few interventions with clear benefit for the final appearance.
By around three months, most scars have softened and flattened to a fine pale line, though full maturation continues for up to a year. This is also the earliest window to judge the cosmetic result. A faint yellow tint appearing at the margin in the first weeks may be residual plaque that was intentionally left to protect the lid rather than true recurrence; your surgeon can usually tell the difference.
On exercise, a question people search frequently: most teams ask patients to avoid heavy lifting, bending and sweaty workouts for several days to a week after excision, because raised blood pressure and moisture can disturb the wound. Confirm the timing with your own team.
Will xanthelasma go away if I lower my cholesterol?
Usually not on its own, and this is one of the most persistent hopes worth addressing directly.
Xanthelasma plaques are deposits of lipid already sitting inside cells in the dermis. Lowering the concentration of cholesterol circulating in the blood reduces the supply of new lipid to that tissue, and there are scattered case reports of plaques shrinking or fading after aggressive lipid lowering, particularly in people with very high starting levels. But MedlinePlus and Cleveland Clinic describe the plaques as persistent and note that they generally do not disappear without treatment. The foam cells tend to stay put.
The distinction to hold onto is between shrinking existing plaques, which lipid lowering does unreliably, and slowing the formation of new ones, which is biologically plausible and the reason most clinicians want the lipid picture addressed before or alongside removal.
Where medication enters the conversation, it enters through your prescribing physician, not the aesthetic pathway. The most widely used class is statins, which reduce the liver’s cholesterol production and increase clearance of LDL from the blood; effects on lipid levels are measurable within weeks, according to NHS guidance. Other classes work by blocking cholesterol absorption in the gut or by prolonging the life of LDL receptors on liver cells. Whether any of these is appropriate depends on your overall cardiovascular risk, not on your eyelids, and the decision to start, adjust or stop belongs to the prescribing clinician.
Lifestyle changes that the American Heart Association recommends for lipid management, including replacing saturated fat with unsaturated fat, adding fiber, regular physical activity and not smoking, support the same goal. They are worth doing for the heart regardless of what happens to the plaques.
How to prevent xanthelasma recurrence: what the evidence supports
Nobody can promise that xanthelasma will not return. What follows is the set of measures with a reasonable evidence basis or a strong mechanistic rationale, ranked by how much they seem to matter.
First, identify and address any lipid disorder. This is the single step most consistently associated with lower recurrence in the descriptive literature, and it is the only one that also addresses the cardiovascular association found in the Copenhagen study. A standard fasting or non-fasting lipid panel is the starting point; if levels are very high or there is a family history of early heart disease, your physician may consider testing for familial hypercholesterolemia, as Mayo Clinic describes.
Second, check for conditions that raise lipids indirectly. An underactive thyroid, poorly controlled diabetes, certain kidney and liver conditions and some medicines can all push cholesterol up. Treating the underlying cause changes the lipid environment that feeds the plaques.
Third, get complete clearance the first time, within the limits of safety. Ask your surgeon how they assess the plaque margin and depth, and understand that leaving a thin rim to protect the lid is sometimes the right call even though it raises the chance of regrowth.
Fourth, protect the healing skin. Sun exposure does not cause xanthelasma, but it worsens pigment changes and makes any residual or recurrent plaque more visible against blotchy skin.
Finally, keep realistic surveillance. A once-yearly look with a good mirror and light is enough. Catching a recurrence when it is a few millimeters wide makes every subsequent option simpler than waiting until it matches the original.
When xanthelasma comes back after removal: the next options
A recurrence is not a failure of the first treatment so much as a reminder of the biology. The path forward usually runs through three questions in order.
Is it actually recurrence? A pale yellow rim visible weeks after surgery may be residual plaque that was deliberately left, and a small bump along a scar may be a suture reaction or a tiny cyst rather than new xanthelasma. A clinician can usually tell by inspection; occasionally a small biopsy settles it.
Has anything changed medically? Recurrence is the natural moment to repeat the lipid panel, review thyroid and glucose results, and revisit cardiovascular risk with your primary physician. If a lipid disorder was never fully addressed, that becomes the priority alongside any cosmetic plan.
Which technique now? Options broadly mirror the first round, with some shifts. Repeat excision is often feasible for a small recurrence, but each operation removes more skin, and on the lower lid that raises ectropion risk; surgeons may prefer a peel or laser for a thin regrowth on scarred skin. TCA or laser can be repeated in sessions, which suits plaques that return as a scatter of small spots. Cryotherapy remains an option for very small lesions. Where a plaque returns extensively after several removals, an oculoplastic assessment may include skin grafting or lid-tightening procedures, and some people at that point decide that watchful acceptance is the better choice.
Whatever is chosen, the same honesty applies: the next removal can also be followed by recurrence. Deciding how many rounds are worthwhile is a personal calculation about appearance, inconvenience and risk, made with your treating team.
What people often get wrong about xanthelasma coming back
Myth: if it returned, the surgeon did a poor job. Incomplete removal is one cause, but recurrence also happens after meticulous excision with clear margins, because the process that made the plaque is still running. Reasonable surgeons discuss this before the first procedure.
Myth: a normal cholesterol test means it is purely cosmetic. Many people with the plaques do have normal lipids, yet the Copenhagen data showed the cardiovascular association persisted after adjusting for cholesterol. Normal lipids are reassuring, not a reason to skip the risk conversation.
Myth: there is a permanent removal method. Every technique clears existing tissue; none changes the tendency to form new deposits. Claims of permanence are marketing, not evidence.
Myth: home remedies such as garlic, castor oil or apple cider vinegar dissolve the plaques. No controlled evidence supports any of these, and applying acids or irritants to eyelid skin can cause burns, scarring and pigment change that are harder to treat than the original plaque. Products sold online as xanthelasma removers fall into the same category.
Myth: it will eventually go away by itself. Spontaneous resolution is rare enough that both MedlinePlus and Cleveland Clinic describe the plaques as persistent without treatment.
Myth: it only affects older people. It is more common in middle age, but it appears in young adults, and in that group it more often points to an inherited lipid disorder worth finding.
Myth: xanthelasma is a growth that could turn cancerous. It is a deposit, not a tumor, and has no malignant potential. Its significance lies in what it may say about the arteries, not the skin.
Questions to ask your care team before a second removal
A recurrence conversation goes better when you arrive with specific questions. These are the ones that tend to change decisions.
- Is what I am seeing a true recurrence, residual plaque that was left for safety, or something else along the scar?
- Have my lipids, thyroid and glucose been checked since the first removal, and do the results change what you would recommend?
- Given my age, family history and these results, should I be assessed for familial hypercholesterolemia or referred to a lipid specialist?
- Which technique do you suggest this time, and why is it preferable to what was done before?
- How much eyelid skin remains to work with, and how does that affect the risk of the lid margin pulling outward?
- What has your experience been with recurrence after this technique in plaques like mine, and how do you define a good outcome?
- How will pigment changes be managed, given my skin type?
- What does aftercare involve, and when can I return to work, exercise, contact lenses and eye makeup?
- If it returns a third time, what would the options be, and is there a point at which you would advise stopping?
- Would a biopsy or a photograph for the record be useful for future comparison?
Write the answers down. Recurrence decisions unfold over months and years, and a clear record of what was done, what was found and what was advised is genuinely useful the next time you sit in the chair. If the answers you receive lean heavily on guarantees or on urgency, that is a reason to seek a second opinion from a dermatologist or oculoplastic surgeon.
When to call your doctor
Xanthelasma itself is not an emergency, and a slow return of yellow color months after treatment can wait for a routine appointment. Certain signs, however, should prompt a prompt call to your treating team or, where noted, urgent care.
Contact your surgeon or dermatologist the same day if the treated area becomes increasingly red, hot, swollen or painful after the first two or three days, if it produces yellow or green discharge, or if you develop a fever; these suggest wound infection. Call if a wound edge separates, if bleeding does not stop with ten minutes of gentle pressure, or if the eyelid begins to pull away from the eye so that the pink inner lining shows or the eye waters constantly, which can indicate developing ectropion.
Seek urgent care for any change in vision, new sensitivity to light, severe eye pain, a feeling that something is scratching the eye surface, or a spreading rash or blistering after a chemical or laser treatment. Sudden pigment loss or a raised, thickening scar in the weeks after treatment is not urgent but warrants an earlier review, because early intervention gives more options.
Separately from the eyelid, take the recurrence itself as a prompt to see your primary care physician for a lipid panel and cardiovascular risk review if that has not happened within the past year. And if you ever experience chest pressure, breathlessness on exertion, or sudden weakness or speech difficulty, treat those as the emergencies they are and call emergency services; the eyelid finding is a risk marker, not a cause, but the arteries it hints at are the ones that matter.
Every decision described in this article, from whether to treat again to which method to use, rests with you and your treating team.
Frequently asked questions
Can xanthelasma grow back after removal?
Yes. MedlinePlus and Cleveland Clinic both state that xanthelasma can return after treatment by any method. Removal clears the visible deposit but does not alter the underlying tendency of eyelid tissue to accumulate cholesterol-filled cells. Regrowth is often gradual, appearing over months to years, and is more likely when plaques were large, when a lipid disorder remains unaddressed, or after repeated removal at the same site.
How do I permanently remove xanthelasma?
There is no method proven to remove xanthelasma permanently. Excision, chemical peels, laser, cryotherapy and electrodesiccation all clear existing plaque tissue, and each can be followed by recurrence. The closest approach to durability is combining thorough removal with identification and management of any lipid or metabolic disorder, which addresses the conditions that feed new deposits. Any claim of a permanent fix should be treated with skepticism.
What is the xanthelasma recurrence rate after surgery?
No guideline or systematic review sets a single recurrence rate. Published figures come from small case series that differ in technique, follow-up length and how recurrence is defined, so quoted percentages vary widely and short follow-up flatters every method. The consistent finding is that recurrence is common enough to discuss before treatment, and more likely with extensive plaques, untreated lipid disorders and repeat procedures on scarred skin.
What is the success rate of xanthelasma removal?
Success has no standard definition in this field. It may mean complete clearance in one session, an acceptable cosmetic result, or no recurrence at a set time, and studies rarely measure the same thing. Mainstream sources describe all main techniques as capable of clearing plaques, with trade-offs in scarring and pigment change. Ask your surgeon how they define a good result for plaques like yours rather than seeking a percentage.
Will xanthelasma go away if I lower my cholesterol?
Usually not by itself. Existing plaques are lipid already stored inside dermal cells, and both MedlinePlus and Cleveland Clinic describe them as persistent without treatment. Isolated reports describe fading after intensive lipid lowering in people with very high levels, but this is unreliable. Lowering cholesterol is more plausibly useful for slowing new deposits and, more importantly, for cardiovascular health. Decisions about lipid treatment rest with your prescribing physician.
Does a xanthelasma removal scar fade completely?
Most scars from eyelid excision become fine, pale lines hidden in a natural crease, but they do not vanish entirely. Redness typically fades over weeks and the scar continues to soften for up to a year. Peels and lasers leave less linear scarring but can cause lighter or darker patches, particularly in olive or brown skin. Sun protection during healing is one of the few measures clearly shown to improve the final appearance.
I am in my twenties with xanthelasma. Does that mean something serious?
Not necessarily, but it is a reason to be checked. Xanthelasma appearing in young adults is more often linked to an inherited lipid disorder such as familial hypercholesterolemia, which Mayo Clinic notes can keep LDL very high from childhood. A lipid panel, a family history review and, if indicated, further testing let your physician assess cardiovascular risk early, when management makes the most difference.
Can I exercise after xanthelasma removal surgery?
Light walking is usually fine within a day or two. Most teams ask patients to avoid heavy lifting, bending, swimming and sweaty workouts for several days to about a week after excision, because raised blood pressure can cause bleeding and moisture can disturb the wound. After peels or laser, similar caution applies until the surface has healed. Confirm timing with your own surgeon, whose instructions take precedence.
Are xanthelasma home remedies or online removal creams safe?
No controlled evidence supports garlic, castor oil, vinegar or products marketed online for dissolving xanthelasma. Eyelid skin is extremely thin and sits millimeters from the eye, so acids and irritants applied there can cause chemical burns, permanent pigment change and scarring that are more difficult to treat than the original plaque. If appearance troubles you, a dermatologist or oculoplastic surgeon can review safer options.
Which specialist should I see if xanthelasma comes back after removal?
Two appointments are usually worthwhile. A dermatologist or oculoplastic surgeon, a specialist in surgery around the eye, can confirm true recurrence and discuss repeat removal options suited to the remaining eyelid skin. Your primary care physician should repeat a lipid panel and review cardiovascular risk, and may refer you to a lipid specialist if levels are very high or a family history of early heart disease exists.
References
This article is for general information only and is not a substitute for professional medical advice. Please consult a qualified doctor about your individual situation.
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