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7/31/2019 Smith.pdf Melanoma
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Metastatic Melanoma
Scott Hession Smith
Harvard Medical School IVGillian Lieberman, MD
Scott H. Smith
Gillian Lieberman, MD
September 2001
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Agenda for Presentation
Brief overview ofdisease & preferredsites of metastasis
Discussion ofdifferent imaging
modalities formetastatic melanoma
Patient presentation
Scott H. Smith
Gillian Lieberman, MD
Melanoma, back
Color irregularity
Asymmetry
Border
irregularityImage from J. L. Melton, MD,
Loyola Univ. Chicago
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Epidemiology
Scott H. Smith
Gillian Lieberman, MD
1999 47,000 new primary melanomas
7300 deaths
~1 in 90 Americans will develop
3% of all USA cancers
3rd most common cause of brain metastases (mets)
Affects all ages
Men 30-49: 2nd
most common CA
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Risk factors
Scott H. Smith
Gillian Lieberman, MD
RISK FACTOR RELATIVE RISKAge >15 88
Pigmented lesion 7-64;148
Caucasian 12
Previous cutaneous Melanoma 5-9
Melanoma in 1st degree relative 2-8
Immunosuppression 2-8
Excessive sun (UVB) 3-5Sun sensitivity 2-3
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Numerous classifications
Scott H. Smith
Gillian Lieberman, MD
Cutaneous melanoma Malignant melanocytes
Subtypes exist
Noncutaneous
Mucosal epithelia
Retina
Leptomeninges
Melanoma, trunk
Image from J. L. Melton, MD,
Loyola Univ. Chicago
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Skin: fundamentals
Scott H. Smith
Gillian Lieberman, MD
Image: Edward Buckingham, MD, Combined Plastics Conference, 2000
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5-yr Survival and Tumor Depth
Newer staging system
I, II- localized IA= 4.00 mm
III- limited nodal met, 30-35%
IV- advanced met,~6months
Scott H. Smith
Gillian Lieberman, MD
Clarks
Levels1 2 3 4 5
Image: Edward Buckingham, MD, Combined Plastics Conference, 2000
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Clinical symptoms & signs
Scott H. Smith
Gillian Lieberman, MD
Early: size, change in shape or color,pruritis
ABCDEFs (asymmetry, irregular border,
color variation, diameter >5mm, elevation,
enlarging, Family History)
Late: tenderness, bleeding, ulceration
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Unfavorable Prognosis
Scott H. Smith
Gillian Lieberman, MD
Histologic features Ulceration
High mitotic activity
Tumor micro-satellites Vertical growth
Consider metastatic
potential!Image: Edward Buckingham, MD, Combined Plastics Conference, 2000
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Common sites for metastasis
Skin
Lungs (70%)
Lymph nodes (23-75%)
Liver (58%)
Central nervous (50%)
Kidney (35%)Bone (11-17%)
Bowel & mesentary(8%)
Spleen (1-5%)
Diagnostic dilemma:How to detect?
1. Before known mets
2. With known mets
3. While monitoringtreatment of mets
Average latentperiod of mets:
2-5 years
Scott H. Smith
Gillian Lieberman, MD
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Before known metastasis
Patients who are asymptomatic
Initial screen with PA chest x-ray
Other imaging studies rarely reveal mets whenpatients are symptom-free
Sentinel lymph node (SLN) biopsy
First node to receive tumor drainage
Other screening: Palpate regional nodes, liver, spleen
Neuro exam
Bone pain? Liver function tests
Scott H. Smith
Gillian Lieberman, MD
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Screening chest x-ray
Hematogenousspread: favors bases
Rounded opacities
Bilateral
No cavitation
No gas-fluid levels+/- hilar adenopathy
+/- pleural effusions
Scott H. Smith
Gillian Lieberman, MD
Lung mets
Image: Robert Dunn, MD, Canberra Hospital
S H S i h
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Scott H. Smith
Gillian Lieberman, MD PA chest x-ray: looking for lung, bone mets
Image: Robert Dunn, MD, Canberra Hospital
Lung mets
S tt H S ith
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Lymph nodes
Scott H. Smith
Gillian Lieberman, MD
Melanoma
Other nodes
Possible SLN
Melanoma
Possible LN spread
Diagram from Melanoma.netDiagram from Melanoma.net
S tt H S ith
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Lymphoscintography
Tumors >1mm thick
Technetium-99 injected in or around tumor
Drainage patterns visualized with gammaprobe- mark site
Inject blue dye to identify lymphatic tracks
& sentinel node
Scott H. Smith
Gillian Lieberman, MD
Scott H Smith
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Lymphoscintography
Scott H. Smith
Gillian Lieberman, MD
SLN
(L)
Technetium-99 gamma probe blue dye identification
Diagram from Melanoma.net Diagram from Melanoma.net
Scott H Smith
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Beth Israel Deaconess Patient
33 year old man with known metastaticmelanoma, multiple risk factors
Metastases to:
Brain
Kidneys
Lungs
Scott H. Smith
Gillian Lieberman, MD
Scott H Smith
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CNS mets: MRI
Often symptomatic
Magnetic resonance imaging (MRI) best
Gadolinium-enhanced MRI- most sensitive
Most mets are T2 bright and enhance Edema common
CT+ may miss small mets & leptomeningeal spread
Ddx of primary tumor: Bronchogenic carcinoma (ca) (50%)
Breast ca (20%)
Colon, rectal ca (15%) Melanoma, Renal ca (10%)
Scott H. Smith
Gillian Lieberman, MD
Scott H Smith
T2 i h d MRI
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Scott H. Smith
Gillian Lieberman, MD T2-weighted MRI
Large right frontal met:
heterogeneous hyper-intensity
Large left occipital met:heterogeneous hyperintensity
BIDMC PACS system, courtesy of Dr. M. Spencer
CSF bright
(T2)
Generalized edema wit
slight shift ofseptum
Scott H Smith
T1 i h d MRI f d li i
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Scott H. Smith
Gillian Lieberman, MD T1-weighted MRI after gadolinium
Large right frontal met
hypointense with ringenhancement
Large left occipital met:
hypointense with ring enhancement BIDMC PACS system, courtesy of Dr. M. Spencer
CSF dark
(T1)
Enhancement of
choroid plexus
Scott H. Smith
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Computed Tomography (CT)
Best for abdominal viscera and peritoneumLiver: mets will enhance with contrast, best
during portal-venous phase
Kidneys: may see hemorrhage, parenchyma willenhance- can follow ureters to bladder
Abdominal cavity: +/- malignant ascites,
hemoperitoneum
Stomach: see target lesion with oral contrast
Bowel: see irregularities of lumen
Scott H. Smith
Gillian Lieberman, MD
Scott H. Smith
CT ith l t t ith t IV t t
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Scott H. Smith
Gillian Lieberman, MD CT with oral contrast, without IV contrast
BIDMC PACS system, courtesy of Dr. M. Spencer
Bilateral renal mets with massive hemorrhage
Low density lesion with hemorrhage
Scott H. Smith
CT ith l t t ith t IV t t
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Gillian Lieberman, MD CT with oral contrast, without IV contrast
BIDMC PACS system, courtesy of Dr. M. Spencer
Extravasation of left renal hemorrhage
Left iliopsoas muscle
Scott H. Smith
CT ith l t t IV t t
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Gillian Lieberman, MD CT with oral contrast, + IV contrast
Lower attenuation lesion, compressingthe renal (enhancing) parenchyma
BIDMC PACS system, courtesy of Dr. M. Spencer
Enhancing renal parenchyma
Scott H. Smith
CT ith l t t ith IV t t
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Gillian Lieberman, MD CT with oral contrast, with IV contrast
BIDMC PACS system, courtesy of Dr. M. Spencer
Scott H. Smith
CT ith oral contrast itho t IV contrast
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Gillian Lieberman, MD CT with oral contrast, without IV contrast
Courtesy of Dr. M. Spencer
Stomach with mets projecting into lumen
Scott H. Smith
CT with oral contrast without IV contrast
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Gillian Lieberman, MD CT with oral contrast, without IV contrast
Duodenum with mets projecting into lumen
Courtesy of Dr. M. Spencer
Scott H. Smith
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Gillian Lieberman, MD
Positron Emission Tomography (PET)
Future of imaging metastatic
melanoma?
Use of glucose analog (FDG-glucose)
Advantages: melanoma has high FDG uptake= high
sensitivity in detecting mets early
Able to distinguish between recurrent
disease & radiation necrosis Single test for entire body
Limitations:
CT is better for small pulmonarylesions
Image from Kiran Mehta, MD
Increased
uptake by
mets
Scott H. Smith
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Gillian Lieberman, MD
Positron Emission Tomography (PET)
Malignant melanomaof the right shoulder(bright white spotsnear crossed yellow
lines)
Mets involving theright upper lobeperipherally as well asthe right hilum andmediastinum
Image from Lyndon Gritters, Univ. of Iowa
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Gillian Lieberman, MD
References
Allan, R. Sentinel node localization: do or dye alone? The British Journal of
Radiology, 74 (2001), 475-77. Buckingham, Edward.Melanoma. Combined Plastics Conference, September 6, 2000.
Carvahlo, Paulo.Metastatic Melanoma. Atlas of Brain Perfusion SPECT, case 2, June
1998.
Gritters, Lyndon S., Francis, Isaac R., Zasadny and Wahl, Richard L., "Initial
Assessment of Positron Emission Tomography Using 2-Flourine-18-Fluoro-2Deoxy-
D-Glucose in the Imaging of Malignant Melanoma" The Journal of Nuclear Medicine
(Sept 1993) 1420-1427.
Mehta, Kiran.Melanoma and lymphomas: PET scan applications. SFJM Vol. 4, no. 2:
1-5. Mehta, Sheila. CNS Melanoma. eMedicine Journal, August 20, 2001; Vol.2, #8:1-11.
Terhune, Margaret H., Swanson, Neil, Johnson, Timothy. Use of Chest Radiography in
the Initial Evaluation of Patients with Localized Melanoma. Archives of Dermatology,
May 1998; Vol 134, no. 5: 569-72.
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Acknowledgements
Special thanks to: Gillian Lieberman, MD
Matthew Spencer, MD
Pamela Lepkowski
Larry Barbaras and Cara Lyn Damour
David Quinlan
Gillian Lieberman, MD