Pigmented Lesions of the Eyelid

Updated: Feb 12, 2024
  • Author: Donny W Suh, MD, MBA, FAAP, FACS; Chief Editor: Hampton Roy, Sr, MD  more...
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Overview

Practice Essentials

Pigmented eyelid skin lesions are those that display hues of brown, black or blue, or may be mistaken for brown or black lesions.

The pigmentation of skin lesions is caused by:

Melanin, blood, and exogenous pigment (eg, tattoo)

It is imperative to monitor any changes in size, shape or color of these lesions as they may indicate eyelid skin cancer. Early detection and treatment can save cosmetic appearance, vision, and lives.

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Background

The eyelids often are affected by a variety of lesions. Most eyelid lesions are of benign origin, but some eyelid lesions may be malignant.

Malignant melanomas are responsible for only 1% of all eyelid lesions. The importance of this lies in the fact that, although only 3% of all skin cancers are melanomas, more than two thirds of all deaths from skin cancer are attributable to malignant melanoma. Therefore, it is important to recognize benign and malignant lesions of the eyelid, especially when pigmented. See the images below.

Lentigo maligna or superficial spreading melanoma Lentigo maligna or superficial spreading melanoma of the eyelid. Courtesy of Joel Sugar, MD.
Focal melanoma of the upper lid in a patient with Focal melanoma of the upper lid in a patient with history of prior excised conjunctival melanoma. Courtesy of M Duffy, MD, PhD.
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History of the Procedure

Change in size, shape, or color of a pigmented eyelid lesion is significant in the history.

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Problem

Suspicious eyelid lesions, particularly when they are pigmented, need to be removed for purposes of a biopsy. Although a pigmented eyelid lesion may appear benign, it is wise to obtain a specimen for pathological examination because of the associated risk for mortality associated with malignant melanoma. Eyelid lesions in patients aged 76 or older are more likely to be malignant. [1]

Pigmented lesions in infants and small children are more commonly benign and related to inflammation and may pose a significant risk of vision problems. This is particularly true with capillary hemangiomas, cavernous hemangiomas, and giant hairy nevi. Pigmented lesions in infants and children also may be associated with pathology in contiguous structures or associated with systemic disease. These lesions should alert the ophthalmologist that further investigation may be needed. This is particularly true with such lesions as cavernous hemangioma, lymphangioma, and juvenile xanthogranuloma.

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Epidemiology

Frequency

The frequency of pigmented lesions of the eyelid varies according to the lesion type and patient characteristics. Certain lesions are seen only in infants and small children, whereas others are seen only in elderly persons (seborrheic keratosis). Environmental characteristics play a role, with the frequency of benign and malignant eyelid lesions increasing in areas closer to the equator. In a major study of removed eyelid growths, 59% were of epidermal origin, 1.5% were malignant, and 6% were premalignant (eg, actinic keratosis or Bowen's disease). Among the malignant growths, the majority (95%) were basal cell carcinoma and a minority (5%) were squamous cell carcinoma. In another significant study of eyelid tumors, 85.7% were benign, 1.1% premalignant, and 13.1% malignant growths. More than half (56.5%) of malignant tumors were basal cell carcinomas, 34.6% were sebaceous carcinomas, 3.8% were squamous cell carcinomas, and 1.7% were lymphoma or plasmacytoma. [2, 3]

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Etiology

Pigment-producing cells derive embryologically from the neural crest. These cells are destined to reside in the basal cell layer of the epidermis. Melanocytes are melanin-producing cells found in the basal cell layer of the epidermis. Nevus cells are incompletely differentiated melanocytes that are found in clumps in the epidermis or the dermis. Nevus cells may or may not produce pigment and, therefore, can be classified as melanotic or amelanotic.

Nevi (moles) can be congenital or acquired. Congenital nevi acquire pigmentation at puberty, at which time they slowly migrate from the epidermis to the dermis. [4]  Coincident with this descent, nevi become less active and, therefore, less capable of converting into a malignant lesion. The most active nevus is the junctional nevus. This resides at the epidermal/dermal border and is the most likely of all nevi to convert to a melanoma. As nevi descend further into the dermis (compound and intradermal nevi), they become relatively inactive and, thus, incapable of malignant transformation.

Melanomas arise from epidermal melanocytes and represent less than 1% of all eyelid tumors. It can occur in 1 of the 3 following forms: superficial spreading malignant melanoma, lentigo maligna melanoma, and nodular melanoma. Lentigo maligna is the premalignant form of lentigo maligna melanoma. This is found on the face of elderly patients and is related to exposure to the sun. Once this lesion penetrates into the dermis, it is classified as a lentigo maligna melanoma. Lentigo maligna melanoma is responsible for 90% of all head and neck tumors.

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Pathophysiology

Melanocytes produce melanin and are derived from neural crest cells. Pigmented lesions of the eyelids arise from 1 of 3 types of melanocytes, as follows: (1) epidermal or dendritic melanocytes, (2) nevus cells or nevocytes, and (3) dermal or fusiform melanocytes.

Eyelid melanoma shares similarities with cutaneous melanoma and has similar risk factors such as excessive sun exposure, dysplastic nevi, personal history of melanoma, older age, and Fitzpatrick skin types I-II. Additionally, there are systemic conditions that may increase the likelihood of developing eyelid melanoma, including familial atypical multiple mole melanoma syndrome, familial melanoma, and xeroderma pigmentosum. [1, 3]

 

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Presentation

A careful history is important when a patient presents with a pigmented lesion of the eyelid. A patient should be asked when the lesion was first noticed; whether it was present at birth; if it has changed in size, shape, or color; and whether there are any associated symptoms, such as discharge, irritation, or bleeding. Benign lesions tend to maintain a uniform appearance, while malignant melanomas tend to be asymmetric, have irregular borders, and often are associated with changes in color. This has been taught to medical students as the ABCs of melanoma. [5]

Benign lesions

Freckles: These lesions are small (1-3 mm in diameter) tan-to-brown macules originating from epidermal melanocytes. They occur more commonly in light-skinned individuals and darken with sun exposure. These lesions reflect melanocyte overactivity, not proliferation.

Lentigo simplex: These lesions arise from epidermal melanocytes and may appear on skin and mucous membranes as brown macules. They usually appear in childhood, are unaffected by sun exposure, and are associated with Peutz-Jeghers syndrome.

Solar lentigo: These tan-to-brown macules are found commonly in sun-exposed areas of older individuals and in patients with xeroderma pigmentosum. Lesions usually have irregular borders and slowly increase in size.

Melasma: Melasma is a skin condition that is characterized by the development of irregularly shaped skin areas containing varying shades of brown pigmentation. It most commonly occurs on the sides of the face, the forehead, the upper lip, the chin, and the sides of the neck. Frequently, melasma is associated with pregnancy or the use of oral contraceptives, but melasma can occur in men. Most pregnancy-associated cases fade away following delivery, eventually clearing within a few months.

Melanocytic nevus: They frequently occur on the eyelid skin and on the eyelid margins. The clinical appearance often is predictive of histologic type (see Histologic Findings). Lesions typically present in childhood as small, flat tan macules that increase in size. As the lesion increases in diameter, a nest of cells drops off into the dermis; then, a compound nevus is formed. They are elevated slightly and pigmented. Intradermal nevus are dome-shaped, pedunculated, or papillomatous and usually are less pigmented or amelanotic.

Congenital melanocytic nevus: These lesions occur in 1% of newborns and may be single or multiple and usually are deeply pigmented. Their border is irregular, and the surface may be covered with hair. The challenges of management of facial congenital melanocytic nevi (CMN) are the balance of the risk of malignant transformation, surgical management, and long-term evaluation of functional and cosmetic outcomes. [6]

Spindle-epithelioid cell nevus: Also termed juvenile melanoma or Spitz nevus, spindle-epithelioid cell nevus is a pink-to-orange dome-shaped nodule occurring in children and young adults.

Balloon cell nevus: They are lightly pigmented, elevated lesions that usually are less than 5 mm in diameter. No clinical features are used to make the differential diagnosis with the other nevocellular nevi.

Nevus of Ota: These nevi are blue-to-purple lesions with mottled discoloration of the skin in the distribution of the ophthalmic and maxillary divisions of the trigeminal nerve. Nevus of Ota frequently is associated with ipsilateral ocular melanocytosis involving the conjunctiva, sclera, and uveal tract.

Blue nevus: These nevi are solitary, blue nodules that are less than 1 cm in diameter.

Malignant lesions

Cutaneous malignant melanoma: Lentigo maligna is a tan or brown macular lesion with irregular borders and is the premalignant stage of lentigo maligna melanoma. [7]  Superficial spreading melanomas present as a brown, irregularly shaped macule. Nodular melanomas typically are dark brown or black nodules or plaques (rare on eyelids). See the image below.

Lentigo maligna or superficial spreading melanoma Lentigo maligna or superficial spreading melanoma of the eyelid. Courtesy of Joel Sugar, MD.

Basal cell carcinoma are pigmented about 5% of the time; 13 (5.06%) of 257 cases were found to have pigment in a recent study by Kirzhner and Jakobiec. [8]

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Indications

Any pigmented lesion that shows growth is suggestive of malignancy, and a biopsy should be performed. Particular characteristics that are suggestive of malignant transformation are irregular borders, changes in color, asymmetry, ulceration, or bleeding.

Pigmented lesions in childhood that cause disruption of images to the retina and are amblyogenic should be treated surgically.

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Relevant Anatomy

Eyelid skin, although thinner, is continuous with and, therefore, histologically identical to skin in other parts of the body. The dermis contains a collagen matrix with vascular channels and dermal appendages. The epidermis contains a basal cell layer where melanocytes reside. The eyelid margin is continuous with the palpebral conjunctiva.

Pigmented lesions can arise on the eyelid or eyelid margin. Margin tumors should arouse the suspicion of a conjunctival neoplasm. The propensity of pigmented lesions to arise on the eyelid is related to the actinic exposure of the area.

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Contraindications

No contraindications to surgery are known.

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