Malignant MelanomaMalignant Melanoma
Dr Foroogh MousaviDr Foroogh Mousavi
What is melanomaWhat is melanoma
 Skin malignancy that is the result of uncontrolledSkin malignancy that is the result of uncontrolled
multiplication of melanocytes.multiplication of melanocytes.
 Melanocytes are a group of cells in the superficialMelanocytes are a group of cells in the superficial
layer of the skin that produce melanin ( a darklayer of the skin that produce melanin ( a dark
pigment) as a response to ultraviolet light.pigment) as a response to ultraviolet light.
 Other forms: ocular , visceralOther forms: ocular , visceral
EtiologyEtiology
 Genetics : p16,p19,ras.Genetics : p16,p19,ras.
 UV exposure , by various mechanisms includingUV exposure , by various mechanisms including
damaging melanocytes DNA.damaging melanocytes DNA.
 Sunburn : intermittent, blistering sunburns.Sunburn : intermittent, blistering sunburns.
 Warning signs: changing moles, positive familyWarning signs: changing moles, positive family
history, previous history of melanomahistory, previous history of melanoma
EpidemiologyEpidemiology
 Highest incidence rate in Queensland ,Australia:Highest incidence rate in Queensland ,Australia:
57 per100,000.57 per100,000.
 Rapid increase in incidence worldwide, only secondRapid increase in incidence worldwide, only second
to lung cancer. Risk: 1 in 1500 in 1935 , 1 in 75 into lung cancer. Risk: 1 in 1500 in 1935 , 1 in 75 in
2000.2000.
 Gender demographics :M>FGender demographics :M>F
 Average age of diagnosis : 57 yrs, rare in <10 yrs.Average age of diagnosis : 57 yrs, rare in <10 yrs.
DiagnosisDiagnosis
 Clinical: checking suspicious lesion , ABCD.Clinical: checking suspicious lesion , ABCD.
 Pathology/biopsy : confirms diagnosisPathology/biopsy : confirms diagnosis
 Imaging: staging and spreadImaging: staging and spread
StagingStaging
 According to skin layers involved ( Clarke):According to skin layers involved ( Clarke):
 Level I : epidermis, Level II to IV : dermis, Level V:Level I : epidermis, Level II to IV : dermis, Level V:
subcutaneous fatsubcutaneous fat
 According to depth (Breslow): 0.75 mm, 0.76-1.5,According to depth (Breslow): 0.75 mm, 0.76-1.5,
1.51-4mm, > 4mm.1.51-4mm, > 4mm.
 TNM :Thickness and ulceration, Nodes , MetastasisTNM :Thickness and ulceration, Nodes , Metastasis
Nodal assessmentNodal assessment
 Sentinel node biopsy :Sentinel node biopsy :
 Indicated if >1mm thickIndicated if >1mm thick
 Sentinel node : the very first draining lymph nodeSentinel node : the very first draining lymph node
 Blue dye or Tc radioisotopeBlue dye or Tc radioisotope
Melanoma on medicalMelanoma on medical
imagingimaging
 Chest radiograph :Chest radiograph :
-Routinely obtained on diagnosis-Routinely obtained on diagnosis
-Usually negative on stage I and II: usually negative ,-Usually negative on stage I and II: usually negative ,
provides a baseline for future comparison.provides a baseline for future comparison.
- Important to obtain in stage III and higher : first- Important to obtain in stage III and higher : first
metastatic site are lungs.metastatic site are lungs.
Melanoma on medicalMelanoma on medical
imagingimaging
 CTCT
 Head : brain mets assessmentHead : brain mets assessment
 Chest: indicated in stage IV disease to detectChest: indicated in stage IV disease to detect
asymptomatic metsasymptomatic mets
 Abdomen : stage III, in-transit and locally recurrentAbdomen : stage III, in-transit and locally recurrent
usually low yield but provide a base line.usually low yield but provide a base line.
 Pelvis : only when primary region is below the waistPelvis : only when primary region is below the waist
58 year old female who developed left-handed weakness. A. Non-contrast melanoma
on CT, usually has a hemorrhagic appearance. B. Contrast enhanced CT , mets show
contrast enhancement due to destruction of blood-brain barrier.
AA B
Medical imagingMedical imaging
 MRI : brainMRI : brain
Only in case of known mets or symptomatic patients.Only in case of known mets or symptomatic patients.
A 55 yr female with melanoma of right leg and hemorrhagic
metastasis to the brain.
T1: large hyperintense lesion left posterior parietal lobe.
Increased conspicuity of smaller lesions on post-Gad.
Melanoma on medicalMelanoma on medical
imagingimaging
 PET :PET :
 Indicated for staging of known nodal disease, in-Indicated for staging of known nodal disease, in-
transit diseasetransit disease
 Therapy responseTherapy response
 Pre-operative assessment ( excluding mets)Pre-operative assessment ( excluding mets)
A
B
82 year old male with
right knee melanoma.
A.Initial PET scan
showing intensely
FDG right knee
lesion.
B. progressive disease
, cutaneous ,
subcutaneous and
intramuscular mets.
67 year old male with
resected lip, shoulder
and scalp melanoma.
Also confirmed
duodenojejunal
junction melanoma.
Brain mets found on
staging PET
Course and prognosisCourse and prognosis
 Curable if detected early. Usual presentations are onCurable if detected early. Usual presentations are on
extreme ends of spectrum.extreme ends of spectrum.
 Depends on :Thickness, ulceration, nodal involvement,Depends on :Thickness, ulceration, nodal involvement,
metastasis.metastasis.
 If up to 1mm thick , no ulceration and no nodalIf up to 1mm thick , no ulceration and no nodal
involvement : 95 %, 5 year survival .involvement : 95 %, 5 year survival .
 If 4 mm and ulcerated: 45% 5yr survivalIf 4 mm and ulcerated: 45% 5yr survival
 If ulcerated lesion & positive node: 24-29%If ulcerated lesion & positive node: 24-29%
 Lung mets : 7% , 5 yr survivalLung mets : 7% , 5 yr survival
TreatmentTreatment
 Surgery : wide local excision, Sentile node excision,Surgery : wide local excision, Sentile node excision,
brain mets ( symptomatic )brain mets ( symptomatic )
 ChemotherapyChemotherapy
 RadiotherapyRadiotherapy
ReferencesReferences
 emedicine.comemedicine.com
 Radiopedia.orgRadiopedia.org
 Dermnetnz.orgDermnetnz.org

Melanoma

  • 1.
    Malignant MelanomaMalignant Melanoma DrForoogh MousaviDr Foroogh Mousavi
  • 2.
    What is melanomaWhatis melanoma  Skin malignancy that is the result of uncontrolledSkin malignancy that is the result of uncontrolled multiplication of melanocytes.multiplication of melanocytes.  Melanocytes are a group of cells in the superficialMelanocytes are a group of cells in the superficial layer of the skin that produce melanin ( a darklayer of the skin that produce melanin ( a dark pigment) as a response to ultraviolet light.pigment) as a response to ultraviolet light.  Other forms: ocular , visceralOther forms: ocular , visceral
  • 4.
    EtiologyEtiology  Genetics :p16,p19,ras.Genetics : p16,p19,ras.  UV exposure , by various mechanisms includingUV exposure , by various mechanisms including damaging melanocytes DNA.damaging melanocytes DNA.  Sunburn : intermittent, blistering sunburns.Sunburn : intermittent, blistering sunburns.  Warning signs: changing moles, positive familyWarning signs: changing moles, positive family history, previous history of melanomahistory, previous history of melanoma
  • 5.
    EpidemiologyEpidemiology  Highest incidencerate in Queensland ,Australia:Highest incidence rate in Queensland ,Australia: 57 per100,000.57 per100,000.  Rapid increase in incidence worldwide, only secondRapid increase in incidence worldwide, only second to lung cancer. Risk: 1 in 1500 in 1935 , 1 in 75 into lung cancer. Risk: 1 in 1500 in 1935 , 1 in 75 in 2000.2000.  Gender demographics :M>FGender demographics :M>F  Average age of diagnosis : 57 yrs, rare in <10 yrs.Average age of diagnosis : 57 yrs, rare in <10 yrs.
  • 6.
    DiagnosisDiagnosis  Clinical: checkingsuspicious lesion , ABCD.Clinical: checking suspicious lesion , ABCD.  Pathology/biopsy : confirms diagnosisPathology/biopsy : confirms diagnosis  Imaging: staging and spreadImaging: staging and spread
  • 8.
    StagingStaging  According toskin layers involved ( Clarke):According to skin layers involved ( Clarke):  Level I : epidermis, Level II to IV : dermis, Level V:Level I : epidermis, Level II to IV : dermis, Level V: subcutaneous fatsubcutaneous fat  According to depth (Breslow): 0.75 mm, 0.76-1.5,According to depth (Breslow): 0.75 mm, 0.76-1.5, 1.51-4mm, > 4mm.1.51-4mm, > 4mm.  TNM :Thickness and ulceration, Nodes , MetastasisTNM :Thickness and ulceration, Nodes , Metastasis
  • 9.
    Nodal assessmentNodal assessment Sentinel node biopsy :Sentinel node biopsy :  Indicated if >1mm thickIndicated if >1mm thick  Sentinel node : the very first draining lymph nodeSentinel node : the very first draining lymph node  Blue dye or Tc radioisotopeBlue dye or Tc radioisotope
  • 11.
    Melanoma on medicalMelanomaon medical imagingimaging  Chest radiograph :Chest radiograph : -Routinely obtained on diagnosis-Routinely obtained on diagnosis -Usually negative on stage I and II: usually negative ,-Usually negative on stage I and II: usually negative , provides a baseline for future comparison.provides a baseline for future comparison. - Important to obtain in stage III and higher : first- Important to obtain in stage III and higher : first metastatic site are lungs.metastatic site are lungs.
  • 13.
    Melanoma on medicalMelanomaon medical imagingimaging  CTCT  Head : brain mets assessmentHead : brain mets assessment  Chest: indicated in stage IV disease to detectChest: indicated in stage IV disease to detect asymptomatic metsasymptomatic mets  Abdomen : stage III, in-transit and locally recurrentAbdomen : stage III, in-transit and locally recurrent usually low yield but provide a base line.usually low yield but provide a base line.  Pelvis : only when primary region is below the waistPelvis : only when primary region is below the waist
  • 14.
    58 year oldfemale who developed left-handed weakness. A. Non-contrast melanoma on CT, usually has a hemorrhagic appearance. B. Contrast enhanced CT , mets show contrast enhancement due to destruction of blood-brain barrier. AA B
  • 15.
    Medical imagingMedical imaging MRI : brainMRI : brain Only in case of known mets or symptomatic patients.Only in case of known mets or symptomatic patients.
  • 16.
    A 55 yrfemale with melanoma of right leg and hemorrhagic metastasis to the brain. T1: large hyperintense lesion left posterior parietal lobe. Increased conspicuity of smaller lesions on post-Gad.
  • 17.
    Melanoma on medicalMelanomaon medical imagingimaging  PET :PET :  Indicated for staging of known nodal disease, in-Indicated for staging of known nodal disease, in- transit diseasetransit disease  Therapy responseTherapy response  Pre-operative assessment ( excluding mets)Pre-operative assessment ( excluding mets)
  • 18.
    A B 82 year oldmale with right knee melanoma. A.Initial PET scan showing intensely FDG right knee lesion. B. progressive disease , cutaneous , subcutaneous and intramuscular mets.
  • 19.
    67 year oldmale with resected lip, shoulder and scalp melanoma. Also confirmed duodenojejunal junction melanoma. Brain mets found on staging PET
  • 20.
    Course and prognosisCourseand prognosis  Curable if detected early. Usual presentations are onCurable if detected early. Usual presentations are on extreme ends of spectrum.extreme ends of spectrum.  Depends on :Thickness, ulceration, nodal involvement,Depends on :Thickness, ulceration, nodal involvement, metastasis.metastasis.  If up to 1mm thick , no ulceration and no nodalIf up to 1mm thick , no ulceration and no nodal involvement : 95 %, 5 year survival .involvement : 95 %, 5 year survival .  If 4 mm and ulcerated: 45% 5yr survivalIf 4 mm and ulcerated: 45% 5yr survival  If ulcerated lesion & positive node: 24-29%If ulcerated lesion & positive node: 24-29%  Lung mets : 7% , 5 yr survivalLung mets : 7% , 5 yr survival
  • 21.
    TreatmentTreatment  Surgery :wide local excision, Sentile node excision,Surgery : wide local excision, Sentile node excision, brain mets ( symptomatic )brain mets ( symptomatic )  ChemotherapyChemotherapy  RadiotherapyRadiotherapy
  • 22.