Skin Lumps Flashcards

1
Q

Sebaceous cyst

  • two types
  • pathophysiology of these types
A

Sebaceous cysts is a general term which encompasses both:

  • epidermoid cyst
  • pilar cyst

Epidermoid cysts → proliferation of epidermal cells within the dermis

Pilar cysts (also known as trichilemmal cysts or wen) derive from the outer root sheath of the hair follicle

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2
Q

Inspection of Sebaceous cyst

  • location
  • what’s often seen
A
  • Occur @ sites of hair growth
  • Scalp, face, neck, chest and back
  • NOT soles or palms
  • Central Punctum
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3
Q

How does sebaceous cyst feel on palpation?

A
  • Firm
  • Smooth
  • Intradermal
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4
Q

Complications of Sebaceous cyst

A

Complications

  • Infection: pus discharge
  • Ulceration
  • Calcification
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5
Q

Two conditions associated with sebaceous cysts

A

Cock’s Peculiar Tumour

  • Large ulcerating trichilemmal cyst on the

scalp

  • Resemble an SCC

Gardener’s Syndrome: FAP + TODE

  • Thyroid tumours
  • Osteomas
  • Dental abnormalities
  • Epidermal cysts
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6
Q

Management of sebaceous cyst

A
  • generally do not require medical treatment
  • if they continue to grow → may become unsightly, painful, infected, or all of the above.

Surgical excision of a sebaceous cyst → a simple procedure to completely remove the sac and its contents

There are three general approaches used: traditional wide excision, minimal excision, and punch biopsy excision

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7
Q

What’s lipoma?

A

Lipoma → is a common, benign tumour of adipocytes

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8
Q

Lipoma

  • location
  • can they become malignant?
A
  • Occur anywhere fat can expand
  • i.e. NOT scalp or palms
  • can occur even on spermatic cord, submucosa
  • rarely, they may also occur in deeper adipose tissues
  • malignant transformation to liposarcoma is very rare
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9
Q

Palpation of lipoma

A
  • Soft
  • Subcutaneous
  • Imprecise margin
  • Fluctuant
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10
Q

Conditions associated with Lipoma

A

Dercum’s Disease / Adiposis dolorosa

  • Multiple, painful lipomas
  • Assoc. peripheral neuropathy
  • Obese postmen women

Familial Multiple Lipomatosis

Madelung’s Disease

Bannayan-Zonana Syndrome

  • Multiple lipomas
  • Macrocephaly
  • Haemangiomas
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11
Q

Management of lipoma

A

Management

  • may be observed
  • if diagnosis uncertain, or compressing on surrounding structures then may be removed
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12
Q

What’s ganglion?

A

A ganglion presents as a ‘cyst’ arising from a joint or tendon sheath

  • Myxoid degeneration of fibrous tissue
  • Contain thick, gelatinous material
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13
Q

Ganglion

  • common location
  • common gender
A
  • They are most commonly seen around the back of the wrist
  • 3 times more common in women
  • Ganglions often disappear spontaneously after several months
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14
Q

Inspection of ganglion

A
  • Can be found anywhere → 90% on dorsum of hand or wrist or dorsum of ankle
  • May be scar from recurrence
  • Weakly transilluminable
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15
Q

Management of ganglion

A

Ganglions often disappear spontaneously after several months

Non-Surgical

  • Aspiration followed by 3wks of immobilisation

Surgical Excision

  • Recurrence can be 50%
  • Neurovascular Palpation damage
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16
Q

What is Seborrhoeic keratoses?

  • pathophysiology
A

Seborrhoeic keratoses are benign epidermal skin lesions seen in older people

Pathophysiology:

  • Benign hyperplasia of basal epithelial layer
  • Hyperkeratosis: keratin layer thickening
  • Acanthosis: prickle layer thickening
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17
Q

Features (on inspection/palpation) of seborrhoeic keratosis

A
  • large variation in colour from flesh to light-brown to black
  • have a ‘stuck-on’ appearance
  • keratotic plugs may be seen on the surface
  • Greasy
18
Q

Management of Seborrhoeic keratosis

A
  • reassurance about the benign nature of the lesion is an option
  • options for removal include curettage, cryosurgery and shave biopsy
19
Q

What’s neurofibroma?

Pathophysiology

A

Benign nerve sheath tumour arising from schwann cells

20
Q

Inspection and palpation in neurofibroma

A

Inspection

  • Solitary or multiple
  • Pedunculated nodules

Palpation:

  • Fleshy consistency
  • Pressure can → paraesthesia
21
Q

What else to inspect/examine if neurofibroma is present?

A

Examine for neurofibromatosis:

  • Examine the eyes
  • Examine the axilla
  • Examine the cranial nerves (esp. 8)
  • BP
22
Q

Features of NF1

A

NF 1: von Recklinghausen’s

  • AD, Chr 17
  • Cafe-au-lait spots (>6)
  • Freckling
  • Neurofibromas
  • Lisch nodules (iris)
23
Q

Management of neurofibroma

A
  • Surgical excision only indicated if malignant growth suspected
  • Local regrowth is common
24
Q

What’s papilloma?

A

Overgrowth of all layers of the skin with a central vascular core

25
Q

Appearance of skin papilloma

A
  • Skin tag / fibroepithelial polyp
  • Pedunculated
  • Flesh coloured
26
Q

Management of papilloma / skin tag

A

(Like moles) removal of skin tags poses a threat of exacerbation of the tumorous site.

Though rare, it is possible to develop a malignant tumor by removal

27
Q

What’s Pyogenic granuloma?

A
  • Benign skin lesion → rapidly growing capillary haemangioma
  • Neither pyogenic, nor a granuloma → neither true granulomas nor pyogenic in nature
28
Q

Cause of pyogenic granuloma

A

The cause of pyogenic granuloma is not known but a number of factors are linked:

  • trauma
  • pregnancy
  • more common in women and young adults
29
Q

Features of Pyogenic Granuloma

- common locations

  • lesion progression
  • appearance
A
  • most common sites: are head/neck, upper trunk and hands. Lesions in the oral mucosa are common in pregnancy
  • initially small red/brown spot → rapidly progress within days to weeks forming raised, red/brown lesions which are often spherical in shape
  • the lesions may bleed profusely or ulcerate
30
Q

Management of pyogenic granuloma

A
  • lesions associated with pregnancy often resolve spontaneously post-partum
  • other lesions usually persist
  • Removal methods include: curettage and cauterisation, cryotherapy, excision
31
Q

What’s a dermoid cyst?

  • where do they develop?
A

Epidermal-lined cyst deep to the skin

  • develop at sites of embryonic developmental fusion
  • may develop at other sites such as the ovary and in these sites are synonymous with teratomas
32
Q

(2) types of dermoid cyst

A

Congenital / Inclusion Cysts

  • Developmental inclusion of

epidermis along lines of skin fusion

  • Midline of neck and nose
  • Medial and lateral ends of eyebrows

Acquired / Implantation Cyst

  • Implantation of epidermis in dermis
  • Often secondary to trauma (e.g. piercing)
33
Q

Inspection and Palpation signs of dermoid cyst

A

Inspection

  • Smooth spherical swelling
  • Sites of embryological fusion
  • Scar from recurrence

Palpation

  • Soft
  • Non-tender
  • Subcutaneous
34
Q

Management of dermoid cyst

A

Congenital

  • CT to establish extent
  • Surgical excision

Acquired

  • Surgical excision
35
Q

What’s dermatofibroma?

A

Benign neoplasm of dermal fibroblasts → overgrowth of fibrous tissue in the dermis

36
Q

Inspection and palpation of dermatofibroma

A
  • Can occur anywhere
  • Mostly on the lower limbs of young to middle-aged women
  • Small, brown pigmented nodule

Palpation

  • Firm, woody feel: characteristic
  • Intradermal: mobile over deep tissue
  • may feel larger than they appear on a visual inspection
37
Q

Management of dermatofibroma

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

38
Q

What’s Karatocanthoma?

A

Keratoacanthoma

  • benign epithelial tumour → overgrowth of hair follicle cells
  • Cytologically similar to well-differentiated
    SCCs
  • more common with advancing age and rare in young people
39
Q

Features of keratoacanthoma

  • progression
  • appearance
A

Progression

  • initially a smooth dome-shaped papule
  • rapidly grows to become a crater centrally-filled with keratin

Appearance

  • Said to look like a volcano or crater
  • Dome-shaped with a keratin plug
  • Intradermal
40
Q

Management of keratoacanthoma

A
  • Spontaneous regression of keratoacanthoma within 3 months is common ⇒ often resulting in a scar
  • should however be urgently excised as it is difficult clinically to exclude squamous cell carcinoma
  • Removal also may prevent scarring