5/21/2018. Disclosures. Consulting: Myriad Genetics SciBase. Superficial Atypical Melanocytic Proliferations. SSM, LMM and (some of) their Simulants

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1 Disclosures Consulting: Myriad Genetics SciBase Superficial Atypical Melanocytic Proliferations SSM, LMM and (some of) their Simulants 1

2 Melanomas and Nevi. Nevi are important mainly in relation to melanoma Precursors but risk for individual lesions is low Risk markers important mainly in high risk situations Simulants important in everyday clinical decision-making Makes sense to consider attributes of melanomas before discussing nevi Low UV Pathway I Low-CSD Melanoma Supertpficial Spreading Melanoma Lentiginous junctional nevus Banal Acquired Nevus (junctional, compound, dermal) Low Grade Dysplasia High Grade Dysplasia Deep Pigmented Bap-1 penetrating Epithelioid Deficiency nevus (DPN)/ Melanocytoma Melanocytoma Melanocytoma (PEM) Compound dysplastic nevus Superficial Spreading Melanoma Melanoma in Melanoma in Melanoma in BPDM (rare) DPN (rare) PEM (rare) BRAF V600E, (BRAF or NRAS NRAS)+BAP1 TERT, CDKN2A, TP53, PTEN (BRAF, MEK1, (BRAF+PRKAR1 or NRAS) A) or PRKCA +(CBNN1 or APC) Superficial spreading or pagetoid melanoma 2

3 Criteria for Melanoma vs. Nevi Feature Melanoma Dysplastic Nevus Nevus Size larger intermediate smaller Symmetry poor good good Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed nevoid Poor circumscription common less common uncommon Nested variable predominant predominant Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous continuous discontinuous discontinuous Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform, moderate- random, mild- minimal severe (size > 1.5x) moderate (1-1.5x) (1x) Mitoses - junctional about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon uncommon Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Dermal Cells uniform atypia random atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses Superficial Melanoma and Mimics in Low CSD Skin Superficial Spreading ( Pagetoid ) Melanoma Junctional and superficial Compound nevi Dysplastic Nevi Recurrent and Traumatized Nevi Pagetoid Spitz and other pagetoid proliferatons Superficial Atypical Melanocytic Proliferations (SAMPUS) 3

4 Case 1. DEE History: M50, Lesion of Back Reason for Consultation: Is this a melanoma or a severely dysplastic nevus? Broad, moderately to highly cellular, asymmetric. Cells at periphery of lesion - predominantly in nests - predominantly near the DEJ - some nests bridging between adjacent elongated rete ridges Pattern of melanocytic dysplasia, with severe cytologic atypia and moderate architectural disorder. 4

5 Adjacent component more highly cellular. More severe uniform atypia Pagetoid scatter Diffuse fibroplasia Bandlike lymphocytic infiltrate Few clusters of immature cells in dermis Adjacent component more highly cellular. More severe uniform atypia Pagetoid scatter Diffuse fibroplasia Bandlike lymphocytic infiltrate Few clusters of immature cells in dermis Localized clusters of mature nevoid cells (precursor/associated nevus) Your Diagnosis? Melanoma? Nevus? 5

6 Criteria for Melanoma vs. Nevi Feature Melanoma Dysplastic Nevus Nevus Size larger intermediate smaller Symmetry poor good good Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed nevoid Poor circumscription common less common uncommon Distribution of Nests variable, irregular predominant predominant, regular Pattern of Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous (single cells) continuous discontinuous discontinuous Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform atypia, random atypia, minimal severe (>1.5x) mild-moderate Mitoses - junctional about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon uncommon Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Dermal Cells uniform atypia random atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses Diagnosis, Case 1, M50. Malignant melanoma, superficial spreading type, nonulcerated, nontumorigenic and nonmitogenic invasive radial growth phase only, Clark level II, greatest Breslow thickness 0.28 mm, see comment. Comment Dermal mitotic rate is zero, tumor infiltrating lymphocytes are absent (with moderate noninfiltrating lymphocytes), there is no radial growth phase regression, there is no ulcer, there are no microscopic satellites, and there is no evidence of vascular, lymphatic or neural invasion. Age < 56 Associated compound dysplastic nevus. Appears to be minimally excised. MPATH-Dx % 5 year survival Case 2. Clinical Information. Lesion of left shin with a mottled color in a 26-year-old woman. Reason for Consultation. I am enclosing for your consultation a melanocytic lesion present for many years from the right shin of a 27-year-old woman. Though the lesion had not changed (according to the patient), her clinician decided to remove it because he didn t like the mottled color. 6

7 Description. A relatively broad moderately cellular plaque-like lesion. Comprised mainly of nested large epithelioid melanocytes with abundant cytoplasm that contains finely divided dusty melanin pigment. Some bridging nests between adjacent rete - possible junctional melanocytic dysplasia of the epithelioid type. Nests somewhat haphazardly distributed along the interface Poor circumscription Patchy to bandlike lymphocytic infiltrate Diffuse fibroplasia Nests somewhat haphazardly distributed along the interface Poor circumscription Patchy to bandlike lymphocytic infiltrate Diffuse fibroplasia 7

8 Nests somewhat haphazardly distributed along the interface Tendency to confluence of nests Patchy to bandlike lymphocytic infiltrate Diffuse fibroplasia Nests somewhat haphazardly distributed along the interface Nests in dermis not larger than largest in epidermis Tendency to confluence of nests Focal pagetoid scatter Your Diagnosis? Melanoma? Nevus? 8

9 Dermal mitotic activity in atypical cells that resemble those in epidermis. The mitosis on the right could be considered junctional; however there seems to be a wisp of collagen between the nest which is predominantly located in the dermis, and the overlying junctional nest. Non tumorigenic mitogenic VGP: Nests in the dermis are smaller than the largest nests in the epidermis. Count dermal mitoses in 1 sq. mm even if not fully occupied by tumor, express rate as a whole number Criteria for Melanoma vs. Nevi Feature Melanoma Dysplastic Nevus Nevus Size larger intermediate smaller Symmetry poor good good Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed nevoid Poor circumscription common less common uncommon Distribution of Nests variable, irregular predominant, regular predominant, regular Distribution of Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous (single cells) continuous discontinuous minimal Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform atypia, random atypia, minimal severe (>1.5x) mild-moderate Mitoses junctional/dermal about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon none Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Dermal Cells uniform atypia random atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses 9

10 Diagnosis, Case 2 F26 Skin, right shin: Malignant melanoma, superficial spreading type, nonulcerated, with non-tumorigenic but mitogenic early vertical growth phase, Clark s level II, greatest Breslow thickness 0.51 mm, see description and comment. Comment. Differential diagnosis could include severe dermal and epidermal melanocytic dysplasia, however, dermal (or even epidermal) mitotic activity essentially rules out this diagnosis. The lesion is not a Spitz nevus/tumor because it is not comprised of large spindle and/or epithelioid cells. Dermal mitotic rate: 2 per square millimeter Tumor-infiltrating lymphocytes essentially absent in the invasive component, with brisk noninfiltrating lymphocytes nearby Focal radial growth phase regression present No ulcer, no microscopic satellites, and no evidence of vascular, lymphatic, or neural invasion. Associated junctional dysplastic nevus of the epithelioid subtype Actinic elastosis in the adjacent dermis is present and mild. Lesion is completely excised with a closest border of approximately 1 mm. Superficial Melanoma and Mimics in Low CSD Skin Superficial Spreading ( Pagetoid ) Melanoma Junctional and superficial Compound nevi Dysplastic Nevi Recurrent and Traumatized Nevi Pagetoid Spitz and other pagetoid proliferations Superficial Atypical Melanocytic Proliferations (SAMPUS) Case 3. Clinical Information. A macular slightly variegated lesion from the back of a 37-year-old woman. Reason for Consultation. Is this a dysplastic nevus? 10

11 25451 Clinical Information. A 3 mm macular slightly variegated lesion from the back of a 37-year-old woman. Reason for Consultation. Is this a dysplastic nevus? Small Poorly circumscribed Nest predominate, discrete Patchy lymphocytes, scant fibroplasia, numerous melanophages (clinically atypical) 11

12 Slight/absent cytologic atypia No mitoses Your Diagnosis? Melanoma? Nevus? Your Diagnosis? Dysplastic? Nondysplastic? 12

13 Criteria for Melanoma vs. Nevi Feature Melanoma Dysplastic Nevus Nevus Size larger intermediate smaller Symmetry poor good good Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed nevoid Poor circumscription cannot assess less common uncommon Distribution of Nests variable, irregular predominant, regular predominant, regular Distribution of Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous (single cells) continuous discontinuous minimal Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform, moderate- random, mild- minimal severe (size > 1.5x) moderate (1-1.5x) (1x) Mitoses junctional/dermal about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon none Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Dermal Cells uniform atypia random or no atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses Diagnosis, Case 2-1, F37. Diagnosis. Skin, abdomen: Lentiginous junctional nevus, with mild dysplasia, see description and comment. OR Lentiginous junctional nevus Comment. Mild dysplasia is not an independent risk factor for melanoma however if this patient should have other clinically atypical nevi and/or a family or personal history of melanoma, or other melanoma risk factors, consideration of periodic surveillance may be appropriate. The lesion appears to be excised however even if this were not the case, reexcision might not be necessary if this biopsy was considered representative of the lesion and especially if the patient were to be followed. Since mild dysplasia is not an independent risk factor for melanoma, lesions of this type might be better given a descriptive name such as lentiginous junctional nevus. It is important to distinguish these lesions from nevoid lentigo maligna, which can also be characterized by slight degrees of cytologic atypia. This is an MPATH Category 1 lesion (no need for reexcision even if margins are positive). Superficial Atypical Nevi. Nevi are important mainly in relation to melanoma Precursors but risk for individual lesions is low (one in thousands) Risk markers important mainly in high risk situations (patients with multiple atypical nevi, family history, high CSD etc.) Simulants important in everyday clinical decision-making. 13

14 Grading of atypia in nevi: correlation with melanoma risk Arumi-Uria, McNutt, Finnerty, 2003 Grading of nevi with architectural disorder (dysplastic nevi) involves architectural and cytological features. Grades of atypia are related to patient history of melanoma: personal history of melanoma present in 5.7% of 2,504 patients with mild, 8.1% of 1657 with moderate, and 19.7% of 320 patients with severe atypia. Odds ratio as a measure of association between NAD and history of melanoma: 4.08 for severe versus mild, 2.81 for severe versus moderate and 1.45 for moderate versus mild dysplasia. Melanoma risk is greater in persons whose nevi have higher grade histological atypia Dysplasia Grading Criteria. Arumi-Uria et al, Mod Pathol, 2003 Mild Moderate Severe The clinically most atypical macular nevus was biopsied from 80 newly incident cases of melanoma and spouse controls. Histological dysplasia was assigned on a subjective 0-4 point scale by a 13-member panel of dermatopathologists (International Melanoma Pathology Group) Subjects with panel ratings > 1 had increased relative risk of melanoma: Odds ratio after adjustment for confounders = 3.99, 95% CI kappa statistic was 0.28 for the panel histological diagnoses, indicating poor interobserver reproducibility. Repeating study agreed but found size to be a good surrogate/correlate for atypia Evidence-based criteria for histologic dysplasia as a risk marker 14

15 Xiong, Rabkin, Piepkorn, Rabkin, Barnhill Piepkorn, et al, JAAD, Barnhill 2014 et al JAAD Given that measuring diameter tends to be more objective than grading dysplasia, these results could provide increased consistency when assessing risk of melanoma among patients with dysplastic nevi Mild Dysplasia Poorly reproducible diagnosis (vs. nevus) Not associated with melanoma risk Not a high risk precursor Not a strong simulant of melanoma UNCERTAINTY vs. Moderate dysplasia, No dysplasia Should be considered in the spectrum of banal nevi (junctional or compound nevus, e.g. lentiginous junctional nevus) Complete excision is not necessary even when margins are positive TERM MILD DYSPLASIA SHOULD NO LONGER BE USED (Lentiginous) Junctional Nevus < 4 mm diameter minimal cytologic atypia 15

16 Moderate Dysplasia Controversial Poorly reproducible diagnosis (vs mild, severe) UNCERTAINTY vs. Mild dysplasia, MIS Associated with melanoma risk Probably not a high risk precursor A weak simulant of melanoma (at least histologically) Complete excision is a consideration; observation is an option Severe Dysplasia Reasonably reproducible diagnosis UNCERTAINTY vs. MIS Associated with melanoma risk Probably a high risk precursor A strong simulant of melanoma (at least histologically) Should be managed by complete excision and consideration of follow-up, similar to MIS Proposal for Grading Dysplasia Junctional/compound nevus Includes former mild dysplasia and Clark s nevus Low Grade Dysplasia (LGD) Former moderate dysplasia High Grade Dysplasia (HGD) Former severe dysplasia 16

17 Case 4. Part Clinical Information. Please find enclosed slides on a 36-year-old male with multiple dysplastic nevi removed. Reason for Consultation. I have also enclosed a prior pathology report of other lesions removed. My diagnosis is compound melanocytic nevus with architectural disorder and moderate cytologic atypia. However, I am concerned that this lesion may be severely dysplastic. Would you recommend a reexcision procedure? Broad Symmetric Moderately cellular Poorly circumscribed 17

18 Broad Symmetric Moderately cellular Poorly circumscribed Slight low level pagetoid scatter Moderate random atypia Nuclear size 1-1.5x Your Diagnosis? Melanoma? Nevus? Your Diagnosis? Dysplastic? Nondysplastic? 18

19 Your Diagnosis? Low Grade? High Grade? Criteria for Melanoma vs. Nevi Feature Melanoma Dysplastic Nevus Nevus Size larger intermediate smaller Symmetry poor good good Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed (nevoid to epithelioid) nevoid Poor circumscription cannot assess less common uncommon Distribution of Nests variable, irregular predominant, regular predominant, regular Distribution of Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous (single cells) continuous discontinuous minimal Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform, moderate- random, mild- minimal severe (size > 1.5x) moderate (1-1.5x) (1x) Mitoses junctional/dermal about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon none Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Dermal Cells uniform atypia random or no atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses Diagnosis (Part 2, Case 3). Skin, back (M36): Compound nevus with moderate dysplasia, completely excised, see description and comment. OR Compound dysplastic nevus, low grade Comment. Patient presents with multiple lesions, some of which are dysplastic nevi with moderate dysplasia. Benign lesions with little or no potential for recurrence and no potential for metastasis. Periodic follow-up may be appropriate for this patient, especially if there are other clinically atypical nevi and/or a family or personal history of melanoma. Although the lesion extends close to the specimen margin, there is no essential indication for reexcision, especially if the patient is to be followed. This is an MPATH DX Category 1 or perhaps Category 2 lesion, depending on clinical correlation and preference. 19

20 Case 5. Part 2-3. Clinical Information: A lesion from the back of a 54 year old man Reason for consultation: The clinician was concerned about a melanoma but I favor a dysplastic nevus. Description: Very broad Moderately cellular Reasonably symmetrical Uniformly elongated rete Patchy infiltrate in dermis 20

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22 Description: Very broad Moderate pagetoid scatter, low level Moderately cellular Mild to moderate cytologic atypia Reasonably symmetrical Mild to moderate solar elastosis Uniformly elongated rete Patchy infiltrate in dermis Your Diagnosis? Melanoma? Nevus? Your Diagnosis? Dysplastic? Nondysplastic? 22

23 Your Diagnosis? Low Grade? High Grade? Compound nevus with severe dysplasia (Severe architectural disorder, moderate cytological atypia) Feature Melanoma Dysplastic Nevus Nevus Size larger intermediate smaller Cellularity high intermediate lower Symmetry poor good good Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed (nevoid to epithelioid) nevoid Poor circumscription common less common uncommon Nested variable predominant predominant Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous continuous discontinuous discontinuous Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform atypia, random atypia, minimal, moderate-severe mild-moderate (1-1.5X) mild Mitoses - junctional about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon uncommon Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Dermal Cells Absent uniform atypia random or no atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses Diagnosis, Case 5 Junctional nevus with severe melanocytic dysplasia, completely excised, see note vs. Junctional dysplastic nevus, high grade vs Intraepidermal atypical melanocytic proliferation (IAMPUS), cannot r/o MIS Diagnosis is based on severe architectural features (single cell predominance, low level pagetoid scatter), with mild to moderate cytologic atypia. MPATH-Dx Category III (consider excision with up to 5 mm margins, if present at the margin) 23

24 Next Case. Part Clinical Information. An irregular pigmented lesion on the back of a 59 year old man Reason for Consultation. Is this a nevoid melanoma? Broad, focally highly cellular, asymmetric diffuse fibroplasia and variably sized nests in dermis 24

25 Only minimal pagetoid scatter Moderate cytologic atypia No mitoses Cells in dermal nests are small, nevoid No confluent sheetlike growth HMB46 staining is top-heavy (stratified) Ki-67 proliferation is minimal in dermis 25

26 p16 staining is positive in a checkerboard pattern, with nuclear and cytoplasmic positivity Helpful Markers in Nevus vs. Melanoma HM45 stratification J Invest Dermatol Mar;100(3):313S-317S. Immunophenotyping of compound and spitz nevi and vertical growth-phase melanomas using a panel of monoclonal antibodies reactive in paraffin sections. Lazzaro B1, Elder DE, Rebers A, Power L, Herlyn M, Menrad A, Johnson B. Low Ki-67 proliferation rate A zonal comparison of MIB1-Ki67 immunoreactivity in benign and malignant melanocytic lesions. Li LX, Crotty KA, McCarthy SW, Palmer AA, Kril JJ. Am J Dermatopathol Dec;22(6): Preservation of p16 protein expression More problematical; presence in an atypical tumor at least precludes homozygous loss of 9p21 and is therefore reassuring but does not preclude diagnosis of melanoma 9p21 Locus Contains p16, p14 and p15, all suppressor genes Presumably all lost together in cases of homozygous 9p21 loss Appears to have special significance in Spitzoid lesions 26

27 Your Diagnosis? Melanoma? Nevus? Your Diagnosis? Dysplastic? Nondysplastic? Your Diagnosis? High Grade? Low Grade? 27

28 Case 5, M59, back Feature Melanoma Dysplastic Nevus Nevus Size larger intermediate smaller Cellularity high intermediate lower Symmetry poor good good Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed (nevoid to epithelioid) nevoid Poor circumscription common less common uncommon Nested variable predominant predominant Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous continuous discontinuous discontinuous Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform atypia, random atypia, minimal, moderate-severe mild-moderate (1-1.5X) mild Mitoses - junctional about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon uncommon Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive or focal rare, minimal absent Dermal Cells Absent uniform atypia random atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses Diagnosis. Case 6, M59. Skin, right, mid back: Compound nevus with severe dermal and epidermal dysplasia and dermal fibrosis ( sclerosing atypical nevus, fibrosing dysplastic nevus"), extending close or to specimen base and margins, see description and final comment. OR - Dysplastic nevus, high grade, with a sclerosing dermal component Overall Comment. The presence of p16 staining rules out the possibility of 9P21 loss, which has been associated with aggressive behavior in a recent fluorescence in situ hybridization (FISH) study of atypical lesions, most of which were variants of Spitz tumors. Despite reassuring findings from special stains (and lack of mitoses), this is objectively an atypical lesion, and complete excision would be recommended, or perhaps alternatively, careful follow-up of the lesional site (MPATH DX Category 2 or 3). Especially if this patient should have other clinically atypical nevi and/or a family or personal history of melanoma, consideration of periodic surveillance of his skin would also be appropriate. 19 Lesions with no recurrence (all completely excised) 28

29 Papillomatous naevoid melanoma Papillomatous epithelial strands; dense proliferation; lack of maturation; atypia; mitoses In-transit or lymph node metastases occurred in 33% of patients Maturing naevoid melanoma Change from epithelioid, pleomorphic melanocytes in the junctional component to smaller but still atypical cells arranged in nests surrounded by dense collagen no disease progression was seen in those with maturing naevoid melanomas (including two with measured thicknesses of 3.0 and 3.5 mm, respectively) Significance of Nevi. Nevi are important mainly in relation to melanoma Precursors but risk for individual lesions is low Risk markers important mainly in high risk situations Simulants important in everyday clinical decision-making Case 7. Clinical Information. Pigmented lesion on the back of a 40 year old woman Reason for Consultation. Rule out melanoma? 29

30 A Lesion of the Back in a 40 Year Old Woman shave biopsy under the left arm has caused consternation two of us believing that we are dealing with a melanoma two others believing that although worrisome not yet melanoma 30

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33 Your Diagnosis? Melanoma? Nevus? Your Diagnosis? Dysplastic? Nondysplastic? 33

34 Your Diagnosis? High Grade? Low Grade? Clark s Dysplastic Nevus vs. Melanoma in Situ vs. Nevus Feature Melanoma Dysplastic Nevus Nevus Size tend to be larger intermediate smaller Symmetry poor good good Keratinocytes irregular uniform elongated rete uniform Melanocytes epithelioid mixed nevoid Nested variable predominant predominant Nests coalescent bridging discrete Lentiginous continuous discontinuous discontinuous Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform atypia, random atypia, minimal severe (> 1.5x) mild-moderate Mitoses about 1/3 of cases almost always absent absent Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Diagnosis Rendered malignant melanoma, probably lentigo maligna type, showing Clark level III invasion with early tumorigenic but nonmitogenic vertical growth phase, at a greatest Breslow thickness of 0.30 mm associated nevus with congenital pattern features 34

35 New Information! I received a call from the primary care physician of this patient asking me to review a biopsy from June of 2004, which I had signed out as a compound congenital melanocytic nevus. She told me that the lesion had developed repigmentation in the previous biopsy site I think it is almost certain that the subsequent biopsy is a pseudomelanoma based on the fact that there was no atypia in the original shave biopsy specimen, the interval between biopsy and repigmentation is only three months, and the re-pigmentation is in the previous biopsy site. The lack of this additional information at the time you received the biopsy was a handicap 35

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37 New Report! superficial atypical melanocytic proliferation, c/w recurrent nevus phenomenon, extending to specimen margins I would make only one reservation, and that is that this lesion should be reexcised again with a margin of normal skin around the scar and any residual lesion 37

38 RECURRENT MELANOCYTIC NEVUS Pseudomelanoma (Ackerman) pigmented patch at site of prior shave biopsy of a benign compound or dermal nevus repigmentation occurs quickly (6 weeks) pigment does not extend beyond scar's borders Histology RECURRENT MELANOCYTIC NEVUS variably sized and shaped sometimes confluent nests single cells & nests above DEJ usually not beyond mid-spinous layer occasional lesional cells or nests in dermis slight cytologic atypia ( reactive? ), rare mitoses proliferation does not extend beyond scar original nevus should be reviewed 38

39 Lessons Atypia in recurrent nevi can be severe, yet is reactive. Mitoses can be present Dermal atypia can be present A superficial scar can mimic diffuse fibroplasia seen in many melanomas Keep a high index of suspicion Consider a full differential diagnosis Call for history if necessary 39

40 Significance of Nevi. Nevi are important mainly in relation to melanoma Precursors but risk for individual lesions is low Risk markers important mainly in high risk situations Simulants important in everyday clinical decision-making Conclusions Former mild dysplasia is a benign lentiginous nevus (the commonest type of nevus) Low grade dysplasia (former moderate dysplasia) can be observed clinically or by patients, looking for evidence of changing lesions High grade dysplasia is difficult to distinguish from melanoma in situ (UNCERTAINTY), may have competence for local persistence, recurrence and progression, and should be completely excised All of these are melanocytic neoplasms of low (or no) malignant potential which have little or no competence for metastasis Lake Wakatipu and Queenstown, New Zealand, from the Top of The Remarkables (Mountains of Mordor in the distance) 40

41 Session II. High CSD Melanomas and Simulants. Lentigo maligna melanoma Atypical lentiginous nevi/proliferations High CSD: Lentiginous Nevi and Lentigo Maligna Melanoma and Simulant(s) Lentiginous Melanoma of Sun-Damaged Skin LMM in situ LMM invasive Distinction from Dysplastic Nevi (Dysplastic Nevuslike Melanoma/Nevoid Lentigo Maligna Lentiginous Nevi of the Elderly (i.e. CSD Skin) Solar (actinic) lentigo, pigmented AK, SK High UV Pathway II Pathway III High-CSD Melanoma (LMM)? IMP? IMP Desmoplastic Melanoma? IAMP? IAMP Lentigo maligna melanoma in situ Melanoma in situ Lentigo Maligna Melanoma Desmoplastic Melanoma NRAS, BRAFnon- V600E, KIT, NF1 NF1, ERBB2, MAP2K1, MAP3K1, BRAF, EGFR, MET, TERT, CDKN2A, TERT, NFKBIE, NRAS PIK3CA TP53, PTEN, RAC1 PTPN11 41

42 Case F64 Lesion of back 42

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44 Your Diagnosis? Dysplastic Nevus - IAMP? Melanoma? Criteria for Melanoma vs. Nevi Feature Melanoma Dysplastic Nevus Superficial Nevus Size larger intermediate smaller Symmetry poor good good Elastosis moderate-severe mild-moderate minimal- mild Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed (nevoid /epithelioid) nevoid Poor circumscription often less common uncommon Distribution of Nests variable, irregular predominant, regular predominant, regular Distribution of Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous continuous discontinuous minimal Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform atypia, random atypia, minimal severe ( > 1.5x) mild-moderate Mitoses junctional about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon none Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Dermal Cells uniform atypia random or no atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses Our Diagnosis Case Lentigo maligna melanoma in situ 44

45 Case 2. Part Clinical Information. A large pigmented lesion of the back in a 74-year-old man. Reason for Consultation. I called this lesion a dysplastic nevus. The clinician then calls back to inform us that this is a 2.2 cm irregular pigmented lesion. Now looking at the deepers we think this might be a lentiginous melanoma. Description Shave biopsy of a broad lesion with a dermal component and a moderately cellular junctional component. Lesion is ill-defined (poorly circumscribed) at each periphery, with features overlapping with those of actinic lentigo. Subtle increase of melanocytes along the dermal-epidermal junction, with mild to moderate but relatively uniform cytologic atypia. Pagetoid scatter is minimal. Focally there are elongated rete ridges, overlapping with features of dysplastic nevus, however these changes are focal within the lesion rather than being symmetrically distributed at shoulders adjacent to a dermal component. Lentiginous nevus versus lentiginous melanoma Poorly circumscribed at each periphery 45

46 JunctionaI IAMP Patchy lymphocytic infiltrate Solar elastosis Bridging rete 46

47 Your Diagnosis? Melanoma? Nevus? Criteria for Melanoma vs. Nevi Feature Melanoma Dysplastic Nevus Superficial Nevus Size larger intermediate smaller Symmetry poor good good Elastosis moderate-severe mild-moderate minimal- mild Rete ridges irregular uniformly elongated uniform Junctional Melanocytes epithelioid mixed (nevoid /epithelioid) nevoid Poor circumscription often less common uncommon Distribution of Nests variable, irregular predominant, regular predominant, regular Distribution of Nests coalescent (confluent) bridging discrete Size of Nests variable uniform uniform Lentiginous continuous discontinuous minimal Pagetoid high, extensive low, focal, minimal minimal Nuclear atypia uniform atypia, random atypia, minimal moderate-severe mild-moderate Mitoses junctional about 1/3 of cases almost always absent absent Pyknosis/necrosis common uncommon none Fibroplasia diffuse concentric minimal Lymphocytes bandlike, lichenoid patchy, perivascular minimal Regression frequent, extensive rare, minimal absent Dermal Cells uniform atypia random or no atypia no atypia limited maturation maturation maturation mitoses no mitoses no mitoses Lentiginous nevus versus lentiginous melanoma Diagnosis. Case 2, M74 Skin, mid back: Superficial atypical melanocytic proliferation of uncertain significance, most consistent with melanoma in situ, lentiginous type (nevoid lentigo maligna), versus atypical lentiginous nevus of the elderly, see comment. (i.e. SAMPUS ) 47

48 Diagnosis. Case 2, M74 Overall Comment. There are overlapping features among atypical actinic lentigines, lentiginous junctional nevi with and without atypia, and lentiginous or nevoid lentigo maligna. Lesions in a high CSD environment must be interpreted with circumspection. Overdiagnosis should be avoided as even atypical lentiginous junctional nevi of the elderly seem to be biologically low grade (non-metastasizing but perhaps locally recurring potential). It is judicious to completely excise these lesions in order to be sure that they have been completely examined histologically and also to minimize any possibility of local persistence, recurrence or future progression. Nevoid Lentigo Maligna/Lentiginous Melanoma (Lentiginous Nevus) Kossard Aust J Dermatol Nevoid lentigo maligna King, Page, Googe & Mihm. Modern Pathology 2005 Lentiginous melanoma Ferrahi, Egbert & Swetter J Cutan Pathol 2005 Dysplastic nevus-like LMM Clinical diagnosis may vary e.g. lentigo maligna, atypical nevus, pigmented basal cell carcinoma, seborrheic keratosis and lentigo. Biopsies may mimic junctional nevus or dysplastic nevus, at least focally Lentiginous proliferation of melanocytes at the dermo-epidermal junction both as single cells and as small nests with areas of confluent growth, extending to the edges of the biopsy. Rete ridges maintained Pagetoid spread of melanocytes was not prominent in H&E - stained sections. Diagnosis of melanoma more easily recognized in the complete excision specimens; similar atypical melanocytic proliferation occurring over a broad area flanking the prior biopsy sites. Stains for MITF and Mart-1 highlight continuous basal melanocytic proliferation as well as foci of pagetoid scatter. Lentiginous Melanoma King, Page, Googe, Mihm. Mod Pathol 2005 Initial biopsies mimicked lentiginous nevus or dysplastic nevus Lentiginous proliferation of melanocytes at DEJ both as single cells and as small nests with areas of confluent growth, extending to the edges of the biopsy. Retiform epidermis was maintained and pagetoid spread of melanocytes was not prominent in H&E sections. Immunohistochemical stains for MITF and Mart-1 highlighted the extent of the basalar melanocytic proliferation as well as foci of pagetoid spread by melanocytes. Mart 1 UNCERTAINTY IS COMMON! PROGNOSIS IS GOOD IF LESION IS SUPERFICIAL IMPORTANT TO COMPLETELY EXCISE FOR FULL EXAMINATION AND TO MINIMIZE ANY POTENTIAL FOR LOCAL PERSISTENCE, RECURRENCE AND PROGRESSION MITF 48

49 Case 3. Part Clinical Information. Left posterior shoulder, F81. Reason for Consultation. Favor a junctional Clark s nevus (see enclosed report). Broad lesion, poorly circumscribed, sparse cellularity, single and nested melanocytes. Mainly near the dermal-epidermal junction, focal pagetoid scatter Moderate chronic CSD. Some bridging, few nests that hang down in a droplet-like pattern. Cytologic atypia mild but relatively uniform. 49

50 Your Diagnosis? Melanoma? Nevus? Diagnosis Case 3, F81 Difficult to interpret. Cytologic atypia is mild to moderate rather than severe, with somewhat concerning architectural changes One is somewhat more concerned about a lesion in chronically sun-damaged skin of older subjects. Skin, left posterior shoulder, shave biopsy: Intraepidermal atypical melanocytic proliferation of uncertain significance (IAMPUS), most consistent with atypical lentiginous junctional nevus (of the elderly/csd skin), cannot r/o evolving or early established melanoma in situ. Complete excision recommended (MPATH-Dx 2 or 3) Case 4. Part Clinical Information. Left posterior shoulder, F84. Reason for Consultation. Favor a junctional Clark s (mildly dysplastic) melanocytic nevus (see enclosed report). There is mild melanocytic atypia, and that the peripheral and deep margins of the specimen were negative in the plane of sectioning. 50

51 Your Diagnosis? Melanoma? Nevus? Diagnosis Case 4, F81 Recurrence of Case 8 Shave biopsy of similar sun-damaged skin Somewhat more cellular proliferation of nevoid and nevoid to epithelioid melanocytes, focally exhibiting severe and uniform cytologic atypia. Some of these cells are confined to the epidermis above the scar, while others appear to extend some distance beyond the periphery of the scar. This latter feature raises some concern for evolving melanoma in situ extending beyond the scar. 51

52 Skin, left posterior shoulder, shave biopsy (recurrence): Intraepidermal atypical melanocytic proliferation of uncertain significance, extending to specimen margins, see description and comment. Comment: Cannot rule out an evolving more significant lesion, suggest complete excision Case 5. Part Clinical Information. Biopsy from posterior shoulder of an 85 year old female. Reason for Consultation. This specimen, in my opinion, has histologic features concerning for melanoma because of the architectural symmetry, ill-defined borders, contiguous proliferation of atypical solitary melanocytes, and some pagetoid spread of melanocytes within the epidermis. I do not see definitive features of a scar consistent with a prior biopsy site. 52

53 Broad Moderately cellular Moderate to severe CSD Poorly circumscribed Few bridging nests Diffuse fibroplasia Cells in dermis Moderately cellular Moderate to severe CSD Nests hanging down Diffuse fibroplasia (not a scar) Moderately cellular Moderate to severe CSD Nests hanging down Diffuse fibroplasia (not a scar) Nests in dermis No maturation 53

54 Melan-A Stain Moderately cellular Continuous basal proliferation Nests hanging down Low level pagetoid scatter Nests in dermis No maturation Your Diagnosis? Melanoma? Nevus? Our Diagnosis Malignant melanoma, lentigo maligna type ( lentiginous melanoma, Clark level II, Breslow thickness 0.85 mm 54

55 Updated History Cases 3-5. Clinical Information. Three separate biopsies from left posterior shoulder of an 85-year-old female over a period of three years. The biopsies were performed 4 years and 1 year ago, and recently. The original biopsy was called a junctional Clark s (mildly dysplastic) melanocytic nevus, might have been better interpreted as a lentiginous nevus of the elderly/sundamaged skin, with mild to moderate atypia. The peripheral and deep margins of the specimen were said to be negative in the plane of sectioning. The next biopsy at presumably the same anatomic location was signed out as an atypical melanocytic proliferation consistent with a persistent/recurrent Clark s (dysplastic) nevus, involving the peripheral edge of the biopsy. It was mentioned that the differential diagnosis included early melanoma in situ evolving within a pre-existing nevus, and a reexcision was recommended. The most recent specimen was concerning for melanoma because of the architectural symmetry, ill-defined borders, contiguous proliferation of atypical solitary melanocytes, and some pagetoid spread of melanocytes within the epidermis. Additional procedure warranted to ensure that the lesion has been completely removed.` Broad lesion, poorly circumscribed, sparse cellularity, single and nested melanocytes. Mainly near the dermal-epidermal junction, focal pagetoid scatter Moderate chronic CSD. Cytologic atypia mild but relatively uniform. POTENTIAL PRECURSOR (low risk) VS ACTUAL PRECURSOR (hindsight bias) Manage by excision or follow-up Case 5 Second recurrence of a lesion that originally had only mild atypia (but moderate to severe architectural disorder) Diagnosis of dysplastic nevus should be made with caution in elderly/csd skin Complete excision is appropriate for atypical lentiginous nevus of elderly/sundamaged skin. 55

56 Last Case. Part Clinical Information. Lesion of right shoulder, r/o melanoma versus nevus in a 76 y.o. man Reason for Consultation. Is this anything other than a moderately atypical neurotized compound nevus? A relatively broad lesion with irregular thickening and thinning of rete ridges and a sparsely cellular infiltrate in the dermis. Generally sparsely cellular Moderate to severe CSD Poorly circumscribed 56

57 Pigmented melanophages in the dermis Increased number of melanocytes in the epidermis, many of them suprabasal Cells in the papillary dermis are delicate spindle cells and there is a sprinkling of lymphocytes Cells in the papillary dermis are delicate spindle cells and there is a sprinkling of lymphocytes 57

58 S100 stain highlights the increased cellularity in the epidermis and also labels the spindle cells in the papillary dermis Melan-A stain highlights the junctional component but the dermal spindle cells are negative. Case 6 Skin, right superior shoulder: Malignant melanoma, lentigo maligna type, nonulcerated, with pure desmoplastic vertical growth phase, Clark level IV, Breslow thickness not < 0.64 mm, extending close to the specimen base, see Comment 3. Comment Changes extend close to the base and to a peripheral margin of the specimen. It is unusual to see a small desmoplastic melanoma at this early stage of its evolution. S Should be excised locally in order to prevent any possibility of persistence, recurrence, or future progression of it. Based on its microstaging attributes, the prognosis for this lesion should be excellent. The prognosis for pure desmoplastic melanoma is if anything better than that for melanomas of similar thickness. This lesion could be managed with a relatively generous wide local excision MPATH DX Category 4 (or 5). 58

59 Take Home Messages Early/evolving LMM IS can be subtle Changes at periphery and at margins can be subtle Confluence or continuous proliferation of uniformly atypical cells Nests in epidermis overlying elastotic dermis (LeBoit) Focal areas in LMM IS can mimic dysplastic nevus Diagnosis of dysplastic nevus in sun-damaged skin of elderly is fraught with hazard Diagnosis is often based more on architectural disorder(including size) than on severe cytologic atypia. High CSD Lesions Cautious approach beware of nests of melanocytes in epidermis above solar elastosis Caution in diagnosis of dysplastic nevus in CSD skin Do not overcall actinic atypia in re-excision specimens (more of a risk marker than a precursor) Beware of subtle spindle cells in dermal component of CSD melanomas 59

60 2018 Proposed Classification of Melanoma, Precursors and Simulants 2 Melanocytic Tumours 2-5 Melanoma arising from blue naevus, and simulants/precursors 2-0 Introduction to melanocytic tumours 2-6A Melanoma arising from blue naevus 2-1A Pathway concept 2-6B Blue naevus, cellular blue naevus 2-1B Genomic landscape of melanoma 2-6C Pigmented epithelioid melanocytoma 2-1 Nodular, nevoid, and metastatic melanomas 2-6D Mongolian spot 2-2A Nodular melanoma 2-6E Naevus of Ito and Ota 2-2B Nevoid melanoma 2-6F Combined naevus 2-2C Metastatic melanoma 2-6 Melanoma arising in congenital naevi and simulants/precursors 2-2 Melanoma in Intermittently sun-exposed skin, and simulants/precursors 2-7A Melanoma arising in a giant congenital naevus 2-3A Superficial spreading melanoma 2-7B Congenital melanocytic naevus, junctional naevus, compound naevus 2-3B Simple lentigo, junctional naevus, compound naevus, dermal naevus 2-7C Proliferative nodules in congenital naevi 2-3C Speckled lentiginous naevus and naevus spilus 2-7 Spitz Tumours 2-3D Dysplastic nevi 2-8A Malignant Spitz tumour 2-3E Special site nevi breast, axilla, scalp, ear 2-8B Spitz naevus / tumour 2-3F Halo naevus 2-3G Meyerson nevus 2-8C Pigmented spindle cell naevus/tumour (Reed) 2-3H Deep penetrating naevus 2-8 Genital and mucosal melanomas, and precursors/simulants 2-3I Recurrent naevus 2-9A Mucosal melanoma (genital, oral, sinonasal) 2-3 Melanoma in chronically sun-exposed skin, and simulants/precursors 2-9B Genital naevi 2-4A Lentigo maligna melanoma 2-9 Ocular melanoma 2-4B Desmoplastic melanoma 2-10A Uveal melanoma 2-4C Lentiginous naevus 2-10B Conjunctival melanoma 2-4 Melanoma in acral skin and simulants/precursors 2-5A Acral melanoma 2-5B Acral naevus 2018 Proposed Classification of Melanoma, Precursors and Simulants 2 Melanocytic Tumours 2-3 Melanoma in chronically sun-exposed skin, and simulants/precursors 2-4A Lentigo maligna melanoma 2-4B Desmoplastic melanoma 2-4C Lentiginous naevus Bastian 2014 Epithelium associated Site High UV Low UV Glabrous Mucosa Benign Borderline Acquired nevus Dysplastic nevus Spitz nevus Atypical Spitz tumor Malignant BRAF NRAS Fusions HRAS KIT CSD Desmopl. melanoma Non-CSD melanoma Spitzoid melanoma Acral melanoma Mucosal melanoma 60