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Skin-Melanocytic Tumors
Last major update: November 2008 - next update November 2009
Revised: 11 July 2009
Author: Nat Pernick, M.D., PathologyOutlines.com, Inc.
Copyright: (c) 2002-2009, PathologyOutlines.com, Inc.
Staging
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● Primary difference between clinical and pathologic stage grouping is whether regional lymph nodes are staged clinically (including radiologic exam) or pathologically (after excision)
● Clinical staging: perform after complete excision of tumor, microstaging (pathologic exam to determine Breslow thickness and Clark level of invasion) and assessment of metastases
● Note: significant survival differences are noted based on clinical versus pathologic staging
● Pathologic staging: uses clinical staging information plus pathologic examination of regional lymph nodes and pathologic confirmation of metastases
Primary tumor (T)
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● TX: primary tumor cannot be assessed (e.g. shave biopsy or regressed melanoma)
● T0: no evidence of primary tumor
● Tis: melanoma in situ
● T1: melanoma 1.0 mm or less in thickness with or without ulceration
● T1a: melanoma 1.0 mm or less in thickness and level II or III, no ulceration
● T1b: melanoma 1.0 mm or less in thickness and level IV or V or with ulceration
● T2: melanoma 1.01 - 2.0 mm in thickness with or without ulceration
● T2a: melanoma 1.01 - 2.0 mm in thickness, no ulceration
● T2b: melanoma 1.01 - 2.0 mm in thickness, with ulceration
● T3: melanoma 2.01 - 4.0 mm in thickness with or without ulceration
● T3a: melanoma 2.01 - 4.0 mm in thickness, no ulceration
● T3b: melanoma 2.01 - 4.0 mm in thickness, with ulceration
● T4: melanoma greater than 4.0 mm in thickness with or without ulceration
● T4a: melanoma greater than 4.0 mm in thickness, no ulceration
● T4b: melanoma greater than 4.0 mm in thickness, with ulceration
● Notes: ulceration means absence of intact epidermis overlying the primary melanoma, as assessed by histologic examination
Regional lymph nodes (N)
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● NX: regional lymph nodes cannot be assessed
● N0: no regional lymph node metastasis
● N1: metastasis in one lymph node
● N1a: clinically occult (microscopic) metastasis
● N1b: clinically apparent (macroscopic) metastasis
● N2: metastasis in 2-3 regional nodes or intralymphatic regional metastasis without nodal metastases
● N2a: clinically occult (microscopic) metastasis
● N2b: clinically apparent (macroscopic) metastasis
● N2c: satellite or in-transit metastasis without nodal metastasis
● N3: metastasis in four or more regional nodes, or matted metastatic nodes, or in-transit metastasis or satellite(s) with metastasis in regional node(s)
● Satellite metastases: defined arbitrarily as intralymphatic metastases occurring within 2 cm of the primary melanoma
● In-transit metastases: defined arbitrarily as intralymphatic metastases occurring more than 2 cm from the primary melanoma but before the first echelon of regional lymph nodes
● Regional nodal metastases: disease confined to one nodal basin or two contiguous nodal basins
● Note: HMB45 or MelanA positive isolated cells in sentinel nodes appear to have no prognostic significance, at least short term (AJSP 2007;31:1175)
Distant Metastases (M)
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● MX: distant metastasis cannot be assessed
● M0: no distant metastasis
● M1: distant metastasis
● M1a: metastasis to skin, subcutaneous tissues or distant lymph nodes
● M1b: metastasis to lung
● M1c: metastasis to all other visceral sites or distant metastasis at any site associated with an elevated serum lactic dehydrogenase (LDH)
Clinical stage grouping
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● 0 : Tis N0 M0
● IA : T1a N0 M0 ()
● IB : T1b N0 M0 or T2a N0 M0
● IIA : T2b N0 M0 or T3a N0 M0
● IIB : T3b N0 M0 or T4a N0 M0
● IIC : T4b N0 M0
● III : Any T, N1-N3, M0
● IV : Any T, any N, M1
● Note: clinical staging includes microstaging of the primary melanoma and clinical/radiologic examination for metastases, but no pathologic examination of lymph nodes
● Stages I/II: no evidence of metastases; stage I are considered low risk for metastases / mortality, and stage II are considered intermediate risk
● Stage III: regional metastases to lymph nodes, satellite metastases or in-transit metastases; no substaging is done
● Stage IV: distant metastases
Pathologic stage grouping and 5 year survival
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● 0 : Tis N0 M0
● IA : T1a N0 M0 (95%)
● IB : T1b N0 M0 or T2a N0 M0 (89-91%)
● IIA : T2b N0 M0 or T3a N0 M0 (77-79%)
● IIB : T3b N0 M0 or T4a N0 M0 (63-67%)
● IIC : T4b N0 M0 (45%)
● IIIA : T1-T4a, N1a or N2a, M0 (67%)
● IIIB : T1-T4b, N1a or N2a, M0 or T1-T4a, N1b or N2b, M0 or T1-T4b, N2c, M0 (52-54%)
● IIIC : T1-T4b, N1b or N2b, M0 or any T, N3 M0 (24-28%)
● IV : Any T, any N, M1
● Stages I/II: no evidence of metastases (regional or distant); stage I are considered low risk for metastases / mortality, and stage II are considered intermediate risk
● Stage III: regional metastases to lymph nodes, satellite metastases or in-transit metastases; stage IIIA are considered to have intermediate risk for distant metastases / survival, stage IIIB to have high risk and stage IIIC to have very high risk
● Stage IV: distant metastases
Tables
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Notes
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● Increased complexity of AJCC 2002 system did not improve its predictive ability over the simpler AJCC 1997 (Cancer 2006;106:163)
Additional references
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● CA Cancer J Clin 2004;54:131, Cancer Control 2002;9:9, Staging Tool
End of Skin-Melanocytic Tumors > Staging of melanomas
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