Pre-cancerous skin lesions Flashcards

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1
Q

What are the clinical features of actinic keratoses?

A
  • A flat or thickened papule or plaque
  • White or yellow; scaly, warty or horny surface
  • Skin coloured, red or pigmented
  • Tender or asymptomatic
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2
Q

What sort of patients get actinic keratoses?

A

Actinic keratoses affect people that have often lived in the tropics or subtropics and have predisposing factors such as:

  • Other signs of photoageing skin
  • Fair skin with a history of sunburn
  • History of long hours spent outdoors for work or recreation
  • Defective immune system
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3
Q

Are actinic keratoses considered pre-cancerous?

A

It is considered precancerous or an early form of cutaneous squamous cell carcinoma.

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4
Q

How is a diagnosis of actinic keratosis made?

A

Actinic keratosis is usually easy to diagnose clinically or by dermoscopy (see actinic keratosis dermoscopy). Occasionally, a biopsy is necessary, for example, to exclude SCC, or if treatment fails.

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5
Q

What are the physical treatment options of actinic keratoses?

A

Cryotherapy using liquid nitrogen

Liquid nitrogen spray is required to ensure adequate depth and duration of the freeze. This varies according to lesion location, width and thickness. Healing varies from 5–10 days on the face, 3–4 weeks on the hands, and 6 weeks or longer on the legs. A light freeze for a superficial actinic keratosis usually leaves no mark, but longer freeze times result in hypopigmentation or scar.

Shave, curettage and electrocautery

Shave, curettage (scraping with a sharp instrument) and electrocautery (burning) may be necessary to remove a cutaneous horn or hypertrophic actinic keratosis. Healing of the wound takes several weeks or longer, depending on the body site. A specimen is sent for pathological examination.

Excision

Excision ensures the actinic keratosis has been completely removed, which should be confirmed by pathology. The surgical wound is sutured (stitched). The sutures are removed after a few days, the time depending on the size and location of the lesion. The procedure leaves a permanent scar.

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6
Q

What are the non-physical removal treatment options available for actinic keratoses?

A

Diclofenac is more often used as an anti-inflammatory drug. Applied as a gel twice daily for 3 months, it is fairly well tolerated in the treatment of actinic keratoses, but less effective than the other options listed here.

5-Fluorouracil is a cytotoxic agent. The cream formulation is applied once or twice daily for 2 to 8 weeks. 5-fluorouracil cream is sometimes combined with salicylic acid. Its effect may be enhanced by calcipotriol ointment.

Imiquimod cream is an immune response modifier. It is applied 2 or 3 times weekly for 4 to 16 weeks.

Photodynamic therapy (PDT) involves applying a photosensitiser (a porphyrin chemical such as methyl aminolevulinic acid) to the affected area prior to exposing it to a source of visible light.

Ingenol mebutate gel is effective after only 2–3 applications.

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7
Q

What is the definition of Bowen’s disease?

A

Squamous cell carcinoma in situ, often called Bowen’s disease, is a growth of cancerous cells that is confined to the outer layer of the skin.

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8
Q

What does Bowen’s disease look like?

A

A patch of Bowen’s disease starts as a small red scaly area, which grows very slowly. It may reach a diameter of a few centimetres across. It commonly occurs on sun-exposed skin, especially the face, scalp and neck, as well as the hands and lower legs. More than one area may be present. The development of an ulcer or lump on a patch of Bowen’s disease may indicate the formation of invasive squamous cell cancer.

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9
Q

How can Bowen’s disease be treated?

A

Freezing with liquid nitrogen. This is done in the clinic. It causes redness, puffiness, blistering or crusting, and may be slow to heal. It can be done in stages for large patches.

Curettage. This involves scraping off the abnormal skin under a local anaesthetic. The area then heals with a scab, like a graze.

Excision. The abnormal skin can be cut out,under local anaesthetic, provided it is not too large. This involves cutting around the lesion and stitching the skin which will leave a scar. If this method of treatment is chosen, you will be informed about the type of surgery planned and any other potential complications.

5-fluorouracil cream. This is a cream that may control or eradicate the disorder. There are different ways of using it, and, if it is felt to be the best treatment, the doctor who sees you will explain these to you. It works by killing the abnormal skin cells. This means that the skin will become red and look worse during treatment, and will then heal after the end of the course of treatment, once the abnormal cells have gone (see Patient Information Leaflet on 5-Fluorouracil Cream).

Imiquimod (Aldara) cream. This was originally developed for the treatment of genital warts, but imiquimod cream has been found useful in treating Bowen’s disease. It also causes inflammation of the skin during treatment (see Patient Information Leaflet on Imiquimod Cream).

Photodynamic therapy. A chemical is applied to the skin that makes the cells in the patch of Bowen’s disease sensitive to particular wavelengths of light. Light from a specially designed lamp is then shone onto the patch. This treatment can be painful and cause inflammation; however any inflammation should disappear within a few days (see Patient Information Leaflet on Photodynamic Therapy).

Radiotherapy and laser are other therapies occasionally used for the treatment of Bowen’s disease, although radiotherapy is not used for patches on the lower leg.

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10
Q

How will Bowen’s disease be diagnosed?

A

A patch of Bowen’s disease can look rather like other scaly skin conditions, such as psoriasis. For this reason a biopsy (a small sample of skin) may be needed to make the diagnosis.

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11
Q

What is lentigo maligna?

A

Lentigo maligna is an early form of melanoma in which the malignant cells are confined to the tissue of origin, the epidermis, hence it is often reported as ‘in situ’ melanoma. It occurs in sun damaged skin so is generally found on the face or neck, particularly the nose and cheek. It grows slowly in diameter over 5 to 20 years or longer.

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12
Q

What are the clinical features of lentigno maligna?

A

Lentigo maligna appears as a long-standing brown patch, most commonly on the face, which slowly enlarges and develops darker areas. Most in situ (very early) melanomas do not cause any symptoms.If a lentigo maligna is not treated promptly, it could become hard and lumpy, bleed, ooze or crust.

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13
Q

How is a diagnosis of lentigo maligna made?

A

A Dermatologist will examine the area carefully, usually with a magnifying device called a Dermatoscope, which is placed on the skin. This will help the Dermatologist decide whether the area needs to be looked at more closely under the microscope. This may involve removing the whole area under local anaesthetic (a procedure known as an excision) and the tissue is sent to the laboratory to be examined. If the area is too large to remove easily, a sample of it (an incisional biopsy) may be taken. If a lentigo maligna is found, the pathology report will provide information that will help to plan the next step in treatment.

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14
Q

What is the treatment of lentigo maligna?

A

The main treatment for lentigo maligna is surgical. There is no other treatment of proven benefit and usually no other tests are needed.

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15
Q

What distinguishes lentigo maligna on dermatoscope?

A

Facial pigmented lesions are characterised dermoscopically by pseudonetwork – this is pigmentation arising around prominent facial hair follicles, and several types of skin lesion may appear rather similar to lentigo maligna. However, lentigo maligna shows greater variation in the thickness of the lines making up the network, often forming an atypical rhomboid pattern associated with greyish dots, the structure tends to be irregular, and there is variation in colour.

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16
Q

What is a seborrhoeic keratosis?

A

A seborrhoeic keratosis is a harmless warty spot that appears during adult life as a common sign of skin ageing. Some people have hundreds of them.

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17
Q

What are the clinical features of seborrhoeic keratoses?

A
  1. Flat or raised papule or plaque
  2. 1 mm to several cm in diameter
  3. Skin coloured, yellow, grey, light brown, dark brown, black or mixed colours
  4. Smooth, waxy or warty surface
  5. Solitary or grouped in certain areas, such as within the scalp, under the breasts, over the spine or in the groin
  6. STUCK ON APPEARANCE
18
Q

What dermatoscope signs are there for diagnosing a seborrheic keratosis?

A

Dermatoscopy often shows a disordered structure in a seborrhoeic keratosis, as is also true for a skin cancer. There are diagnostic dermatoscopic clues to seborrhoeic keratosis, such as multiple orange or brown clods (due to keratin in skin surface crevices), white “milia-like” clods, curved thick ridges and furrows forming a brain-like or cerebriform pattern.

19
Q

What is the treatment for seborrhoeic keratoses?

A

An individual seborrhoeic keratosis can easily be removed if desired. Reasons for removal may be that it is unsightly, itchy, or catches on clothing.

Methods used to remove seborrhoeic keratoses include:

Cryotherapy (liquid nitrogen) for thinner lesions (repeated if necessary)

Curettage and/or electrocautery

20
Q

What is a viral wart?

A

A viral wart is a very common growth of the skin caused by infection with human papillomavirus (HPV). A wart is also called a verruca, and warty lesions may be described as verrucous.

21
Q

How do common warts present?

A

Common warts present as papules with a rough, papillomatous and hyperkeratotic surface ranging in size from 1 mm to larger than 1 cm. They arise most often on the backs of fingers or toes, around the nails—where they can distort nail growth—and on the knees. Sometimes they resemble a cauliflower; these are known as butcher’s warts.

22
Q

What creams can be used to treat viral warts?

A
  • Topical retinoids, such as tretinoin cream or adapalene gel
  • The immune modulator, imiquimod cream
  • Fluorouracil cream
23
Q

What is a dermatofibroma?

A

A dermatofibroma is a common benign fibrous nodule that most often arises on the skin of the lower legs.

24
Q

What causes dermatofibroma?

A

It is not clear if dermatofibroma is a reactive process or if it is a neoplasm. The lesions are made up of proliferating fibroblasts. Histiocytes may also be involved.

They are sometimes attributed to an insect bite or rose thorn injury, but not consistently. They may be more numerous in patients with altered immunity.

25
Q

What are the clinical features of dermatofibromas?

A
  1. People may have 1 or up to 15 lesions.
  2. Size varies from 0.5–1.5 cm diameter; most lesions are 7–10 mm diameter.
  3. They are firm nodules tethered to the skin surface and mobile over subcutaneous tissue.
  4. The skin dimples on pinching the lesion.
  5. Colour may be pink to light brown in white skin, and dark brown to black in dark skin; some appear paler in the centre.
  6. They do not usually cause symptoms, but they are sometimes painful or itchy.
26
Q

How are dermatofibromas managed?

A

A dermatofibroma is harmless and seldom causes any symptoms. Usually, only reassurance is needed. If it is nuisance or causing concern, the lesion can be removed surgically.

Cryotherapy, shave biopsy and laser treatments are rarely completely successful.

27
Q

What is a lipoma?

A

A lipoma is a non-cancerous tumour that is made up of fat cells. It slowly grows under the skin in the subcutaneous tissue. A person may have a single lipoma or may have many lipomas. They are very common.

28
Q

Who gets lipomas?

A

Lipomas can occur in people of all ages, however, they tend to develop in adulthood and are most noticeable during middle age. They affect both sexes equally, although solitary lipomas are more common in women whilst multiple lipomas occur more frequently in men.

29
Q

How is the diagnosis of lipoma made?

A

Diagnosis of lipoma is usually made clinically by finding a soft lump under the skin. However, if there is any doubt, a deep skin biopsy can be performed which will show typical histopathological features of lipoma and its variants.

30
Q

How are lipomas managed?

A

Most lipomas require no treatment. Most lipomas eventually stop growing and remain indefinitely without causing any problems. Occasionally, lipomas that interfere with the movement of adjacent muscles may require surgical removal. Several methods are available:

Simple surgical excision

Squeeze technique (a small incision is made over the lipoma and the fatty tissue is squeezed through the hole)

Liposuction

31
Q

What is the cause of epidermoid cysts?

A

Epidermoid cysts (infundibular cysts) are thought to be derived from the infundibular portion of the hair follicle. Some are derived from implantation of the epidermis. Rarely eccrine glands can be the source.

32
Q

What do epidermoid cysts look like?

A

They are round, sometimes dome-shaped bumps, lying just under the skin surface. Some are yellow or whitish. A small dark plug is often present, through which it may be possible to squeeze out some of the cyst’s contents. The cysts range in size from those that are smaller than a pea to those that are several centimeters across.

33
Q

How are epidermoid cysts managed?

A

Your doctor may give you an antibiotic if your cyst becomes infected. Both types of cyst are easy to remove under a local anaesthetic but this does leave a sca

34
Q

What is pyogenic granuloma?

A

Pyogenic granuloma is a relatively common, reactive proliferation of capillary blood vessels. It presents as a shiny red lump with a raspberry-like or minced meat-like surface. Although they are benign, pyogenic granulomas can cause discomfort and profuse bleeding.

35
Q

What are 5 triggers for pyogenic granuloma formation?

A
  1. Trauma: some cases develop at the site of a recent minor injury, such as a pinprick.
  2. Infection: Staphylococcus aureus is frequently present in the lesion.
  3. Hormonal influences: they occur in up to 5% of pregnancies and are sometimes associated with an oral contraceptive.
  4. Drug-induced; multiple lesions sometimes develop in patients on an oral retinoid (acitretin or isotretinoin) or a protease inhibitor.
  5. Viral infection is possible but not proven.
36
Q

What are the clinical features of pyogenic granuloma?

A

Pyogenic granuloma usually first appears as a painless red, brownish-red or blue-black spot. It grows rapidly over a period of a few days to weeks to a final size of 1–2 cm (rarely up to 5 cm). It typically bleeds easily and may ulcerate to form a crusted sore. Usually a single lesion is present but in rare cases multiple lesions may develop.

37
Q

What are the treatment options for pyogenic granuloma?

A
  • Surgical excision
  • Curettage and cauterisation: the lesion is scraped off with a curette and the feeding blood vessel cauterised to reduce the chances of re-growth.
  • Laser surgery can be used to remove the lesion and burn the base, or a pulse dye laser may be used to shrink small lesions.
  • Cryotherapy may be suitable for small lesions.
  • Chemical cauterisation using silver nitrate is effective for small lesions.
  • Imiquimod cream has been reported to be effective and may be particularly useful in children.
38
Q

What are melanocytic naevi?

A

Melanocytic naevi are pigmented moles. The word ‘melanocytic’ means that they are made up of the cells (melanocytes) which produce the dark pigment (melanin) that gives the skin its colour. Melanocytes clustered together form naevi. This type of moles vary in colour in different skin tones and they are easier to see on pink skins.

39
Q

What do melanocytic naevi look like? What are the 3 types of naevi?

A

Those that are present at birth(congenital melanocytic naevi) can be small (less than 1.5cm in diameter), medium (1.5- 20cm) and large or giant (over 20 cm in diameter). Multiple giant congenital naevi have greater risk of developing melanoma.

There are three main types of acquired melanocytic naevi:

  1. Junctional melanocytic naeviare flat, and usually circular. Their colour is usually even, and ranges from mid to dark brown.
  2. Compound melanocytic naeviare raised brown bumps, most of which are hairy. Some have a slightly warty surface.
  3. Intradermal melanocytic naeviare raised, often hairy, bumps, similar to compound naevi, but more pale coloured (often skin-coloured).
40
Q

What is the difference between the 3 types of naevi?

A