Skin Flashcards

1
Q

what is the pathophysiology of melanoma?

A
  • acquired mutations = BRAF and NRAS which mutate due to UV affecting MAPK pathway leading to uncontrolled proliferation

-uncontrolled division of melanocytes which become invasive and metastasise

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2
Q

what are the phases of melanoma?

A
  • melanomas have 2 growth phases, radical and vertical
    • most superficial confined to epidermis with horizontal growth phase remaining in situ, slow growing
    • further genetic changes may cause vertical growth in which malignant cells breach basement membrane invading deep tissue becoming invasive
    • once reached dermis may spread via lymphatics or blood into lungs or brain
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3
Q

what are some risk factors for melanoma?

A
  • UV exposure
  • age
  • previous skin cancer
  • many moles 5<
  • first degree relatives with melanoma
  • Parkinson’s
  • Fitzpatrick
  • immunocompromised
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4
Q

what are the clinical key features of melanoma?

A
  • unusual looking mole or freckle which may itch or bleed, in radial or vertical phase
  • superficial melanomas consider ABCDE (more common)
    • Asymmetry of shape and colour
    • Border irregularity, smudgy or ill-defined margin
    • Colour variation and change
    • Diameter
    • Evolving, enlarging
  • Nodular consider EFG
    • Elevated
    • Firm to touch
    • Growing
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5
Q

how might melanoma present in those with skin of colour?

A
  • Thicker melanomas at diagnosis and highermortalityrates
  • Significantly higher rates of melanomas in areas not exposed to the sun, including thesubungual,palmar,andplantarsurfaces (eg, acral lentiginous melanomain Pacific Islanders, blacks, and Asians)
  • Non-cutaneousmelanomas (eg: mucosal melanoma, ocular melanoma)
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6
Q

what are some subtypes of melanoma?

A

superficial - most common
nodular
lentigo maligna melanoma
aural lentigous melanoma

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7
Q

what are some investigations of melanoma?

A
  • dermoscopy
  • Excisional biopsy of the lesion with a 2mm margin
  • Sentinel lymph node biopsy if the Breslow thickness is >1mm
  • PET or CT scans may be necessary in the presence of clinical suspicion for metastases- clinical with or without dermoscopy
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8
Q

how is melanoma managed?

A
  • wide local excision
  • lymphadenectomy
  • targeted therapy like BRAF inhibition
  • immunotherapy with MAB
  • radiation - unfit for surgery, adjuvant or combo
  • radiation for bony metastases, for symptom relief
  • follow up!!
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9
Q

how might melanoma complicate?

A
  • metastasis and systemic effects
  • side effects from systemic or radiation therapy
  • possible death
  • surgical - infection, dehiscence, skin necrosis, incomplete resection
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10
Q

what is squamous cell carcinoma?

A

locally invasive, malignant, epidermal keratinocytes (protein that makes up skin, hair and nails) with potential to metastasise

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11
Q

what is the pathophysiology of SCC?

A
  • combination of risk factors and UV radiation
  • leads to signature gene mutation which affects cell signalling pathways
  • causing increased epidermal growth factor release
  • epidermal hyperplasia as a result leading to SCC
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12
Q

what are some risk factors for developing SCC?

A
  • age
  • heavy UV exposure
  • smoking
  • Fitzpatrick skin type 1,2
  • chronic skin inflammation
  • pre-malignant conditions like actinic keratosis
  • previous skin cancer
  • immunosuppression
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13
Q

how might you describe the features of an SCC?

A
  • may be ulcerated, keratinocytes with crusted lesions
  • They grow over weeks to months
  • They are often tender or painful
  • Located on sun-exposed sites, particularly the face, lips, ears, hands, forearms and lower legs
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14
Q

what are some conditions that predispose the occurence of SCC?

A

bowens disease - SCC in situ
actinic keratosis
marjolin ulcer

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15
Q

what are some high risk features of a SCC lesion?

A

size of lesion, metastases, health and fitness, proximity to major structures

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16
Q

how might you investigate SCC?

A
  • clinical diagnosis
  • incisional biopsy for histology
  • excisional biopsy
  • sentinel LN biopsy
  • high risk - USS, XR, CT, MRI, LN biopsy
17
Q

how might you manage an SCC?

A

may require flap or skin graft

  • surgical excision with 3-10mm margin of normal tissue removal
  • shave, curettage and electrocautery for small, thin and low risk
  • Moh’s micrographic surgery
  • radiotherapy

metastatic

  • MDT with combo of surgery, radiotherapy, Cemiplimab, experimental targeted epidermal growth factor receptor inhibitors
18
Q

what is Bowen disease?

A

common superficial form of keratinocyte cancer - aka intraepidermal SCC

  • derived from squamous cells - flat epidermal cells that make keratin, the horny protein that makes up skin, hair and nails
  • but ‘in situ’ meaning malignant cells confined to tissue of origin ie epidermis
19
Q

how might Bowens disease present and what is the significance?

A
  • irregular scaly plaques
  • 5% may turn into invasive SCC
20
Q

what is basal cell carcinoma?

A

Slow growing, locally invasive malignancy involving the basal skin layer

21
Q

what is the pathophysiology of BCC?

A

exposure of UV radiation
leading to reduced cell mediated immunity, oxidative damage
PTCH - hedgehog signalling pathway damages

22
Q

what are some risk factors of BCC?

A
  • Fitzpatrick skin type 1,2 - “always burns, never tans”
  • sun exposure
  • P53 gene
  • previous skin cancer
  • family history
  • age + UV exposure
  • immunosuppression
23
Q

what are some types of BCC?

A

nodular
superficial
mophoeic
basosquamous

24
Q

how does BCC classically present?

A

nodular - ulcerated centre, shiny pearly edges, telangiectasia

superficial - scaly , irregular plaque, thin rolled translucent border, seen on younger, upper trunk and shoulders

25
Q

what are some high risk signs of BCC?

A

fast growing, symptomatic, eye/nose/lip involving, young, immunocompromised, non-nodular, poorly differentiated

26
Q

how might you investigate a BCC?

A
  • clinical diagnosis - use dermascope to visualise better
  • excision biopsy if unsure
  • more investigations if metastases suspected - neglected for long
27
Q

how is BCC managed?

A

excision biopsy - 3 to 5mm margin
Moh’s micro graphically controlled excision
superficial skin shaving, curettage
cryotherapy
photodynamic is low risk
topical chemo for superficial
radiotherapy
mets - combo

28
Q

what are some complications of BCC?

A
  • recurrent BCC
    • Incompleteexcisionor narrow margins at primary excision
    • Morphoeic, micronodular, and infiltrative subtypes
    • Location on head and neck
  • local invasion - bone involvement
  • metastasis rare but 1% (regional lymph nodes to bones or lungs?)