Melanoma & Skin Cancer Flashcards

1
Q

What is a melanoma?

A
  • Melanoma is a malignant tumor of
    melanocyte origin
  • often occurs on the skin
  • primarily due to the highest concentration
    of melanocytes in all other parts of the
    body, and is most often described in skin
    tumors
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2
Q

What are the localisation of Melanoma and Clinical types of melanoma?

A

Localisation:
- skin
- ocular
- submucosa = oral, GIT, vagina, urethra
- Melanoma of unknown primary (MUP syndrome)

Clinical types:
- superficial
- nodular
- lentigo melanoma and lentigo maligna
- Acral lentiginous melanoma
- Amelanotic and desmoplastic melanoma

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3
Q

What are the risk factors?

A

hereditary:
- familial nevus dysplastic syndrome
- increased no.of moles (>120)
- > 6mm mole size
- FHx of + melanoma

Acquired:
- excess exposure to sun
- skin freckles

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4
Q

What is the ABCDE detection of melanoma?

A

Asymmetry
Border
Colour
Diametre
Evolving

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5
Q

PTH immunoprofile for melanoma?

A

Typical imunoprofile: S100+, HMB45+, MelanA+

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6
Q

What are the stages of Breslow scale?

A

STAGE 1: < 1mm

STAGE 2: 1-2mm

STAGE 3: 2.01-4mm

STAGE 4: > 4mm

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7
Q

Where does ocular melanoma metastasise?

A

Ocular melanoma metastasizes exclusively in liver (80%), rarely in CNS, while other sites are extremely rare (almost never)

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8
Q

-What is the treatment for unresectable/metastatic?

A
  • anti-PD 1 monotherapy
    pembrolizumab
  • BRAF mutation
    Dabrafenib
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9
Q

What are some prognostic parameters in Melanoma?

A

Histological:
- Breslow scale (or Clark Scale)
- ulceration
- pigmentation
- melanoma regression
- TILS (Non-BRISK & BRISK)
- Cell type (epitheloid, spindle)

Clinical:
- LDH levels
- early vs advanced clinical stage
- number of metastatic sites

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10
Q

Local disease treatment for melanoma?

A

Excision margin based on depth in Breslow (mm)

Wide Local Excision Margins

Melanoma iS = 0.5cm margin

< 2mm (T1-T2) = 1 cm margin

> 2mm (T3-T4) = 2 cm margin

*done alongside sentinel lymph node biopsy

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11
Q

What is the ESMO treatment guideline for stage I-III melanoma?

A
  • assess in SLN is positive or negative

Negative:
- FU, if relapse, then complete LN dissection (CLND)
- adjuvant tx

Positive:
- Adj Tx
or US based FU, assess for relapse, then CLND

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12
Q

When is RT recommended in melanoma?

A
  • Post op RT incase of at least 1 of the following:
  • 3 pathological LN
  • Extracapsular spreading
  • LN metastasis > 3 cm
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13
Q

Significance of adjuvant treatment in melanoma?

A
  • beneficial to administer adj tx of high risk primary cutaneous melanoma (stage III and resectable IV)

Immune Checkpoint Inhibitor (ICI) e.g. pembrolizumb

Target Therapy e.g. dabrafenib for BRAF mutation

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14
Q

ESMO treatment of inoperable stage III-IV BRAF mutated melanoma?

A

1st line is immunotherapy
pembrolizumab

2nd line is targeted therapy
Dafrafenib

*if LDH elevated this can be 1st line due to high tumour burden

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15
Q

What are the types of basocellular carcinoma (BCC)?

A
  • nodular
  • superficial
  • Morfeaform
  • pigmentous
  • fibroepithelial
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16
Q

Basic treatment for skin BCC?

A
  • small dimension: surgery
  • larger dimension: surgery, RT
  • locally advanced: Neoadj hedgehog inhibitors, salvage surgery and RT
  • metastatic: hedgehog inhibitor e.g. vismodegib
17
Q

What is skin SCC and its basic treatment?

A
  • ulcerative or exophytic lesion of skin
  • metastatic potential > BCC, frequently in regional LN

First line treatment is surgery

18
Q

What is Merkell Cell Carcinoma (MCC)

A
  • high aggressive neuroendocrine skin carcinoma with high metastatic potential
  • pink papula appearance with 20% from polyoma virus
  • Pink papula (≈ 65% local, 26% in lymph nodes, 8% distant metastases)
  • local disease treated by surgery
  • advanced stage ICI e.g. pembrolizumab
  • chemotherapy (Etopozid+Cisplatin)
19
Q

What is Kaposi Sarcoma? (KS)

A
  • indolent vascular tumour of endothelian origin
  • caused by human herpes virus 8 (HH8)
  • AIDS related
  • mostly indolent but may be aggressive
  • described as skin cancer, but histologically not
20
Q

Types of KS?

A
  • Classic: purple slow-growing macula (lower extremity, nose, ears)
    Indolent disease course
  • Endemic: benign lymphadenopathy and children with fulminant lymphadenopathy (no HIV)
  • Iatrogenic: immunosuppressive patients in SOLID organ tx or autoimmune disease
  • Epidemic: HIV infection, in homosexuals, most aggressive form with M in LN and viscera
21
Q

Diagnosis of KS?

A
  • Pathohistological verification
  • HIV status
  • Lung, abdomen, pelvis CT
  • Endoscopy
  • PET-CT
22
Q

Localised KS treatment?

A
  • surgical excision
  • cryotherapy
  • laser ablation
  • vincristine as a cytotoxic agent for intralesional application
23
Q

Systemic KS treatment?

A
  • cART for HIV/AIDS
  • Doxorubicin, Paclitaxel
24
Q

Is secondary skin cancer rare?

A

Yes

Although rare, it is still possible e.g. via haematological cancer

Biopsy and PH verification for diagnosis

25
Q

Hematological cutaneous infiltration (leukomid)?

A
  • Leukomid = skin myeloid sarcoma
  • AML which infiltrates skin in a form of leukemid
  • Presents as M4 and M5, FAB subtype of AML
  • cutaneous infiltration as first sign of AML or AML relapse
  • Tx same as for AML
  • poor prognosis