Tutorial 2- Benign Lesions/Elderly Skin Flashcards

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1
Q

Features of elderly skin (7)

A

Rhytides (wrinkles)

Skin thinning

Solar/actinic purpura

Dyspigmentation

Subcutaneous lipoatrophy

Actinic damage

Solar lentigos

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2
Q

What are rhytides?

A

Wrinkles

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3
Q

What is actinic damage, or photoaging

A

Actinic damage, or photoaging, is distinct from the changes of chronological aging of the skin.

Manifestations include: Solar elastosis, Favre-Racouchot syndrome, Poikiloderma of Civatte

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4
Q

What is solar elastosis? What does it look like histologically?

A

Solar elastosis is thickened, yellowish discolored skin with significant wrinkling. Histologically, there are increased elastin fibres in the dermis.

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5
Q

What is poikloderma of vicatte?

A

Poikiloderma of civatte is reticulated pigment and telangiectasia on the sun-exposed areas of the neck, with sparing of the submental chin.

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6
Q

What is Favre-Racouchot syndrome

A

In Favre-Racouchot syndrome, there are multiple large comedones in the lateral and inferior periorbital skin associated with significant solar elastosis.

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7
Q

T or F? 80% of a person’s lifetime risk of skin cancer occurs before the age of 18

A

False.
The importance of sunscreen in elderly skin is often minimized or overlooked.

There are benefits of sunscreen use in the adult population, with significant decreases in the number of actinic keratoses in study subjects who used sunscreen for as little as a single summer.

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8
Q

What is acne rosacea?

A

Acne rosacea is a common skin disease in adults, affecting up to 12% of elderly patients. It has both vascular and inflammatory manifestations.

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9
Q

What are key features of acne rosacea? (6)

A
facial flushing (transient erythema)
non-transient baseline erythema
papules and pustules
telangiectasias
burning or stinging of the skin
underlying soft tissue hypertrophy- can be rhinophyma
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10
Q

What is rhinophyma?

A

Soft tissue hypertrophy of the nose.

Associated with acne rosacea

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11
Q

What is the pathogenesis of acne rosacea?

A

Pathogenesis - unknown. The disease is on a clinical spectrum with acne vulgaris.

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12
Q

What are common triggers for the flushing seen in acne rosacea? (4)

A

UV light exposure, exercise, hot beverages, and spicy foods.

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13
Q

How do you treat inflammatory rosacea, including severe and most severe cases?

A

Inflammatory rosacea is treated with topical agents such as topical metronidazole, azelaic acid, precipitated sulfur, sodium sulfacetamide, or tretinoin (Retin-A). Most severe disease is treated with oral tetracycline class antibiotics. The most severe cases are treated with oral isotretinoin (Accutane).

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14
Q

How do you treat vascular rosacea?

What is the treatment of choice for telangiectasia?

A

Vascular rosacea responds minimally to topical and oral anti-inflammatory therapy. Treatments for vascular manifestations of the disease include oral beta-blockers such as nadolol or the alpha blocker clonidine. These medications help to improve flushing, though do not improve facial telangiectasia or baseline erythema.

The treatment of choice for telangiectasia is with a hemoglobin targeting laser such as a 585-595nm tunable pulsed-dye laser or the 532nm diolite laser.

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15
Q

How do you treat sebaceous and soft tissue changes in acne rosacea?

A

nasal planing

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16
Q

T of F? There is no relationship between alcohol use and acne rosacea?

A

True

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17
Q

Cutaneous growths commonly encountered during the skin exam of older patients

A
Seborrheic keratosis 
Acrochordon 
Solar lentigo 
Melanocytic nevi 
Cherry hemangioma 
Sebaceous hyperplasia 
Epidermoid cyst 
Milium 
Dermatofibroma 
Neurofibroma 
Lichen simplex chronicus and prurigo nodularis
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18
Q

What are seborrheic keratoses (SK)?

A

Seborrheic keratoses, or SKs, are very common benign skin lesion with a variety of morphologies, commonly affecting older persons, with an increasing number with increasing age.

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19
Q

Where do seborrheic keratoses occur and what do they look like?

A

The lesions occur on hair-bearing skin, with a sharply marginated “stuck-on”, waxy appearance. They are commonly light brown macules, papules, or plaques, though they can range from flesh-colored to black in color.

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20
Q

T of F: Seborrheic keratoses may be inherited in an autosomal dominant fashion

A

True

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21
Q

T or F: There is no association with HPV and seborrheic keratoses

A

True

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22
Q

What histological sign is seen in SK?

A

String of beads: SK lies on a flat horizontal plane surrounded by normal epidermis.

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23
Q

What histological signs can be seen in SK?

A

Proliferation of benign-appearing squamous and basaloid cells without cytologic atypia. There is hyperkeratosis, acanthosis, papillomatosis, and the presence of horn pseudocysts.

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24
Q

What is acanthosis?

A

Acanthosis is diffuse epidermal hyperplasia (thickening of the skin). It implies increased thickness of the stratum basale and stratum spinosum

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25
Q

What is hyperkeratosis?

A

thickening of the stratum corneum

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26
Q

What is Papillomatosis?

A

Papillomatosis is skin surface elevation caused by hyperplasia and enlargement of the dermal papillae

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27
Q

How do you treat SKs?

A

these lesions are benign so usually you don’t need treatment. But they can become traumatized, inflamed, erythematous, painful, or pruritic. In that case–> treat.

Destructive treatment methods include cryotherapy, electrodessication, and shave removal

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28
Q

What are acrochordons?

A

A skin tag or soft fibroma.

Acrochordons are soft, flesh-colored to tan-brown pedunculated papules. Lesions range in size from 1mm to 2cm. Acrochordons are asymptomatic, but may be painful secondary to torsion, irritation or infarction.

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29
Q

Where are acrochordons most commonly found?

A

in skin fold areas such as the lateral aspects of the next, breast creases, and groin folds.

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30
Q

What do acrochordons look like histologically?

A

Histologically, lesions are polypoid growths dense collagenous stroma containing blood vessels with a relatively normal-appearing overlying epidermis.

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31
Q

How do you treat acrochordons?

A

Unless irritated or infarcted, acrochordons are a cosmetic concern.
Irritated or infarcted lesions may be treated with cryotherapy or electrodessication for smaller lesions, or with scissor snip excision or shave removal for larger lesions.

32
Q

What are solar lentigos?

A

Also known as liver spots or senile freckles.
Solar lentigos are well-circumscribed, round, oval, or irregularly tan to brown macules. Pigmentation may be homogeneous or mottled. Multiple lesions are usually present. Solar lentigos are classically described as multiple sharply demarcated tan brown macules with uniform, reticulated pigmentation on sun-exposed skin.

33
Q

Where are solar lentigos most likely to be found?

A

sun-exposed skin such as dorsal hands, forearms, and the face.

34
Q

Which of these is not seen histologically when looking at solar lentigos?

elongated, club-shaped rete ridges
reticulated pattern of rete ridges
Papillomatosis
basal layer hyperpigmentation 
thinning of the epidermis
A

Papillomatosis- it is the rete ridges that become elongated, not the papillary dermis

35
Q

How do you treat solar lentigos?

A

Solar lentigos are benign lesions, and are therefore a cosmetic concern only.
Treatment with cryotherapy and melanin-targeting lasers such as the Q-switched alexandrite laser are effective. Bleaching agents such as topical hydroquinone are not useful.
Patients should be counseled to use sunscreens and practice sun-avoidance.

36
Q

What are melanocytic nevi and what do they look like?

A

Moles
are well-circumscribed, round or oval flat macules or elevated papules, 2 to 6mm in diameter. There may be slight asymmetry or color variation, though nevi should have clear borders.

37
Q

Apart from congenital nevi that are present at birth, when do acquired nevi appear?

A

1st-3rd decade of life

38
Q

What are the 3 kinds of acquired nevis and how are they classified?

A

Junctional nevi, compound nevi, and dermal nevi, based upon the histologic location of the melanocyte nests in the epidermis and underlying dermis.

39
Q

What do congenital nevi look like?

A

Congenital melanocytic nevi are typically slightly raised at birth. They are light tan in color, often with speckling. Only large (>20cm diameter) congenital nevi have consistently demonstrated an elevated risk of malignant melanoma.

40
Q

Is the presence of hair in a congenital nevi prognostic?

A

No, although increased hair growth is quite common in congenital nevi

41
Q

T of F

Large 10 cm or more congenital melanocytic nevi have consistently demonstrated an elevated risk of malignant melanoma

A

F

20 cm

42
Q

What do junctional nevi look like clinically?

A

Clinically: junctional nevi are uniformly pigmented, well-circumscribed flat macules.

43
Q

What do junctional nevi look like histologically?

A

Histology: round balls, or nests, of nevomelanocytes are present at the tips of the epidermal rete ridges. There are no nests present in the dermis.

44
Q

What do compound nevi look like clinically?

A

Clinically: compound nevi are uniformly pigmented tan or brown well-circumscribed, sharply-demarcated papule.

45
Q

What do compound nevi look like histologically?

A

Histologically, nests of nevomelanocytes are present in both the basal layer of the epidermis as well as interspersed among collaged fibres in the dermis.

46
Q

What do dermal nevi look like clinically?

A

Clinically: dermal nevi are well-demarcated, uniformly pigmented 2-6mm papule. Dermal nevi and compound nevi may appear clinically identical.

47
Q

What do dermal nevi look like histologically?

A

Histology: nests and cords of uniform nevomelanocytes contained entirely within the dermis. Though the Melanocytes may extend deep into the dermis, there is no atypia or mitotic figures characteristic of melanoma.

48
Q

T or F: Melanocytic nevi are related to melanoma

A

True

Approximately one-third of melanomas are histologically adjacent to a nevus.

49
Q

T or F: Patients with greater than 25-50 melanocytic nevi are at greater risk than the general population for the development of malignant melanoma.

A

False

50-100 melanocytic nevi

50
Q

What are indications for excision of melanocytic nevi?

A

changing lesions, atypical clinical appearance, and irritated lesions. Some patients wish to have nevi removed for cosmetic reasons.

51
Q

What are cherry angiomas and what do they look like?

A

Also known as cherry hemangioma or senile angioma.
These benign lesions are round or ovoid few milimeter red dome-shaped papules. Very small lesions may resemble petechiae.
They are most often seen on the trunk and proximal extremities. Most individuals over the age of 60 have cherry angiomas. It is not uncommon for elderly persons to have over 100 cherry angiomas on the trunk.

52
Q

What do cherry angiomas look like histologically?

A

lesions contain congested, ectatic (dilated) capillaries and small venules in the papillary dermis

53
Q

What is sebaceous hyperplasia and what do they look like?

A

proliferations of one to multiple yellowish papules with a central dell, or depression.
Fine overlying vessel telangiectasias may be evident.

54
Q

What can sebaceous hyperplasia be confused with?

A

Clinically, the lesions can be confused with basal cell carcinoma, given their location on the face, shiny surface, and overlying telangiectasia.

55
Q

How can you treat sebaceous hyperplasia?

A

Treatment, which is cosmetic, consists of light electrodessication.

56
Q

What are epidermoid cysts and what do they look like?

A

Epidermoid cysts are the most common cutaneous cysts, usually found on the face and upper trunk. They are well-demarcated dermal nodules, often times with a central punctum.
Lesions may have a history of drainage of keratinaceous contents, or drainage may be elicited during clinical examination. Cysts are most often asymptomatic, however rupture of the cyst wall may be extremely painful.

57
Q

What are epidermoid cysts incorrectly called?

A

Epidermoid cysts are often incorrectly called sebaceous cysts. There are no sebaceous glands contained within the cyst wall, and therefore this terminology is incorrect.

58
Q

Where are epidermoid cysts derived from?

A

Hair follicle infundibulum

59
Q

What do epidermoid cysts look like histologically?

A

The cyst wall has an epidermal lining which contains a granular layer, unlike pilar cysts. The cyst contains homogeneous eosinophilic laminated keratin.

60
Q

How do you treat milium?

A

Milium removal most commonly consists of incision of the overlying epidermis with a needle of #11 scalpel blade. The milium contents are then expressed with lateral pressure or a comedone extractor.
Topical tretinoin is a useful adjunct in cases of multiple facial milia. Treatment reduces the number of milia and improves the ease of removal of existing lesions.

61
Q

What do dermatofibromas (DF) look like? Where are they most commonly seen?

A

Brown to pink firm papules.

They are most commonly seen on the lower extremities of adults, though they may arise in any location.

62
Q

What can be correlated with the “dimple sign”?

A

A dermatofibroma. This lesion may adhere to the deeper subcutaneous tissue, resulting in a downward movement of the tumor on lateral pressure, known as the “dimple sign”.

63
Q

What do dermatofibromas look like histologically?

A

Slightly thickened epidermis. The superficial, or papillary dermis appears normal, though the deep reticular dermis contains a well-defined nodule of fibroblasts and thickened collagen bundles. The overlying epidermis is thickened.

64
Q

What are neurofibromas and what do they look like?

A

Neurofibromas are common solitary flesh-colored, soft, rubbery, mildly elevated to pedunculated papules.
Approximately 10% of patients with common neurofibromas have multiple lesions.

65
Q

Where can you find the “button-hole” sign

A

Neurofibromas- lesions are easily invaginated by direct overlying pressure

66
Q

What dz is associated with multiple cutaneous neurofibromas?

A

Neurofibromatosis type 1, or Von Recklinghausen’s disease. Autosomal Dominant. Characterized by multiple cutaneous neurofibromas, café-au-lait macules, ocular lisch nodules, and neurologic impairment. One of the diagnostic criteria for neurofibromatosis is the presence of two or more neurofibromas. Though not all patients with multiple cutaneous neurofibromas have neurofibromatosis.

67
Q

What do neurofibromas look like histologically?

A

Neurofibromas are typically well-circumscribed, non-encapsulated nodular tumors located in the dermis or subcutis. The nodule is comprised of haphazardly arranged spindle cells with tapered ends. Rare scattered axons may be seen with special stains.

68
Q

How are neurofibromas treated?

A

Solitary neurofibromas are treated with simple excision. Completely excised lesions to not recur.

69
Q

What is lichen simplex chronicus (LSC)?

A

Lichen simplex chronicus, or LSC, is a lichenification of focal areas of skin due to chronic rubbing.

70
Q

What are small papules of LSC, due to rubbing or picking called?

A

prurigo nodules
These lesions are extremely pruritic. Patients often state that they cannot keep themselves from rubbing, scratching, or picking at these lesions.

71
Q

How do you treat LSC or prurigo nodules?

A

Treatment of LSC and prurigo nodules may include any combination of the following modalities:

High-potency topical corticosteroids
Cryotherapy
Oral antihistamines
Occlusive dressings to prevent picking or rubbing

72
Q

What is pruritis?

A

itching

It occurs in up to 30% of the elderly.

73
Q

What can pruritis be due to?

What are examples of the most common systemic causes of pruritis? (5)

A

a primary skin disease, a systemic disease, medications, or as a result of the aging process itself. Once primary cutaneous causes and medication causes of pruritis have been excluded, systemic causes should be considered. The most common systemic causes of generalized pruritis include anemia, renal disease and uremia, cholestasis and hepatic disease, hypothyroidism, and lymphoma.

74
Q

What is the pathogensis of pruritis?

A

Over time, the stratum corneum loses its ability to retain water due to decreased levels of ceramides, leading to xerosis and often associated pruritis.

75
Q

What should a work-up of generalized pruritis include?

A

A work-up of generalized pruritis should include a TSH, liver enzymes, hepatitis serologies, CBC, BUN, and serum creatinine.