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The conjunctiva is the transparent membrane covering the white of the eye and the inner surface of the lids. Most growths that arise there are benign, but malignant types such as melanoma and squamous cell carcinoma also occur. The distinction is made by examination and, where needed, pathological study, and treatment rests on surgical removal.
Examination of a mass on the conjunctiva

What Are Conjunctival Tumors?

The conjunctiva is the thin transparent membrane covering the white of the eye, the sclera, and the inner surface of the eyelids. Growths that arise in this membrane are called conjunctival tumors. Because they sit in a directly visible area, they are often noticed early; most of my patients come because they have seen a lump or a change in colour in the mirror.

The majority of these growths are benign. Even so, malignant tumors such as melanoma and squamous cell carcinoma do arise in the conjunctiva, and in their early stages they can resemble benign lesions. My basic approach follows from that: a lesion on the ocular surface should be shown to be benign, by examination or where necessary by pathology, rather than dismissed on appearance.

Benign Conjunctival Tumors

Conjunctival naevus: a mole on the white of the eye. It usually appears in childhood or adolescence, is brown in tone and may contain small cystic spaces. Most remain unchanged for life. Slight darkening during adolescence and pregnancy is expected, but growth, increased vascularity or spread into a new area calls for follow-up.

Pinguecula: a yellowish elevation near the corneal edge, usually on the nasal side, linked to sun, wind and dust exposure. It is a degenerative change rather than a tumor and is generally monitored.

Pterygium: a triangular sheet of tissue advancing from the conjunctiva onto the cornea, covered in detail on the pterygium page.

Papilloma: cauliflower-like vascular growths associated with human papillomavirus. More common in children and young adults and often multifocal.

Dermoid and dermolipoma: congenital yellowish-white masses, typically at the lower outer corneal edge or on the outer part of the white of the eye.

Inclusion cyst: a thin-walled sac containing clear fluid, usually following trauma or previous surgery.

Pyogenic granuloma: red tissue that grows quickly and bleeds easily after injury, a stye or surgery. Despite the name it is not an infection.

Malignant Conjunctival Tumors

Conjunctival melanoma arises from pigment cells. It may develop within an existing naevus, from a diffuse pigment change called primary acquired melanosis, or directly. It is rare, but because it can spread, early diagnosis matters.

Squamous cell carcinoma and its precursor lesions arise from the surface epithelium. Ultraviolet exposure, smoking and immune suppression are the main risk factors. It appears near the corneal edge as a gelatinous, vascular or whitish thickening and is often mistaken for chronic redness.

Lymphoma appears as a soft, flat, salmon-coloured elevation on the white of the eye. It is painless. Because it can be part of a systemic lymphoma, a whole-body assessment follows the diagnosis.

Spread of sebaceous cell carcinoma: this tumor of the eyelid glands can spread across the conjunctival surface and mimic stubborn one-sided lid inflammation. Unilateral blepharitis that does not respond to treatment therefore deserves caution; the subject is covered under eyelid tumors.

Which Findings Raise Suspicion?

Not every lump on the eye is a concern, but the following features call for assessment:

Growth or thickening of the lesion over recent months.

Darkening colour, irregular pigment distribution or new areas of pigment.

Prominent feeding vessels developing over and around the lesion.

A lesion fixed to the underlying tissue that cannot be moved.

Gelatinous or whitish thickening at the corneal edge.

Spontaneous bleeding or ulceration of the surface.

Persistent one-sided redness or lid inflammation that does not respond to treatment.

A palpable mass on the inner lid surface or behind the eyelid.

Diagnosis: Examination and Biopsy

Slit-lamp examination of size, borders, colour, vascularity and fixation to underlying tissue. The lids are always everted so the posterior surface is inspected too.

Photographic documentation, the most reliable way of following change objectively and the mainstay of naevus surveillance.

Anterior segment imaging, where high-resolution imaging shows the depth of the lesion and any extension into deeper tissue.

Ultrasound for thick lesions and where intraocular extension is suspected.

Biopsy and pathology, which give the definitive diagnosis. Small lesions are removed entirely, while for extensive lesions a sample is taken first. Every excised specimen goes to pathology.

Systemic assessment in melanoma and lymphoma, carried out together with the relevant specialties.

Treatment Options

Observation

Small lesions with regular borders that have not changed for years, such as naevi and pingueculae, need no surgery. They are followed with periodic examination and photographs. I also explain to my patients what to watch for so they can notice change themselves.

Surgical excision

This is the foundation of treatment. Where malignancy is possible, the lesion is removed whole with a margin of healthy tissue and without touching the lesion itself, a technique that matters because it prevents tumor cells being spread into the surrounding tissue. After excision the surface at the corneal edge is smoothed, and the tumor bed may be treated with freezing to destroy any residual cells.

Closing the defect

Wide excisions leave a bare area that has to be covered, using an autograft from the patient's own conjunctiva or amniotic membrane. Very large defects may need an oral mucous membrane graft. Covering the surface properly both speeds healing and prevents adhesions forming between lid and globe, a subject covered on the symblepharon page.

Additional treatments

Chemotherapy and immune-stimulating agents given as drops onto the surface are used in diffuse superficial disease and where surgical margins are not sufficient. In selected cases radiotherapy can be delivered through a plaque placed on the ocular surface. Melanoma and lymphoma with systemic spread are managed together with medical oncology.

Follow-Up, Prevention and When to Seek Help

The type of lesion removed determines how closely a patient is followed. Recurrence is not expected with benign tumors, though review in the first year is still advised. Squamous cell carcinoma and melanoma can recur, so follow-up continues for years and is not confined to the eye. Recurrences caught early are far simpler to treat, and that is the real reason for regular review.

The most effective preventive step is reducing ultraviolet exposure: ultraviolet-filtering sunglasses that also shield from the side, and a wide-brimmed hat, matter particularly for outdoor workers. Stopping smoking lowers the risk of squamous cell carcinoma.

If you notice a growing lump on the eye, a mole that is darkening or spreading, tissue that bleeds on its own, persistent one-sided redness or a palpable mass on the inner surface of the lid, I would advise an examination. Related conditions are collected under ocular surface diseases.

Ayşe Dolar Bilge MD, FEBOphth.
Ophthalmologist, Oculoplastic Surgery

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As an Ophthalmologist, Dr. Ayşe Dolar Bilge, I provide diagnosis and treatment services with my experienced team.

Frequently Asked Questions

Is a lump on the white of the eye dangerous?

Most lumps on the white of the eye are benign, chiefly pinguecula, naevus and cyst. A lesion that has grown or darkened over recent months, developed prominent vessels, become fixed to the underlying tissue or bled spontaneously should be assessed. Deciding on appearance alone is not sound; the distinction is made by examination and, where needed, pathology.

What should be done if a mole on the eye grows?

Conjunctival naevi usually stay unchanged for life, and slight darkening during adolescence or pregnancy is expected. Increasing size, irregular spread of pigment, new areas of pigment and the development of prominent feeding vessels are the findings that call for follow-up. Photographic surveillance is used, and where doubt persists the lesion is excised and examined pathologically.

How is conjunctival tumor surgery performed?

Where malignancy is possible, the mass is removed whole with a margin of healthy tissue and without touching the lesion directly. The tumor bed may be treated with freezing to destroy residual cells. After wide excision the bare area is covered with a patch of the patient's own conjunctiva or with amniotic membrane. The excised tissue is always sent for pathology.

Can conjunctival growths turn into cancer?

Most benign lesions do not become cancerous. There are exceptions: melanoma arising within a conjunctival naevus is rare but possible, and the diffuse pigment change called primary acquired melanosis can give rise to melanoma. Similarly, precursor lesions of the surface epithelium can progress over time to squamous cell carcinoma. That is why lesions that change deserve follow-up.

Does sun exposure increase the risk of conjunctival tumors?

Yes. Ultraviolet exposure is a leading risk factor, particularly for squamous cell carcinoma, and it also contributes to pterygium and pinguecula. Rates are higher in outdoor workers and in people living in sunny climates. Ultraviolet-filtering sunglasses that shield from the side, together with a wide-brimmed hat, are the most effective protection. Stopping smoking also lowers the risk.

Can the tumor come back after surgery?

Recurrence is not expected with benign tumors, though I still advise review during the first year. Squamous cell carcinoma and melanoma can recur, so follow-up continues for years and is not limited to the eye. Because recurrences caught early are far simpler to treat, regular review counts as part of the treatment in these conditions.

What does a salmon-coloured patch on the conjunctiva mean?

A soft, painless salmon-coloured elevation on the white of the eye suggests a lesion arising from lymphoid tissue, which may be benign lymphoid hyperplasia or a lymphoma. Biopsy makes the distinction. When lymphoma is diagnosed, a whole-body assessment follows, since it may be part of a systemic disease.

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