Dysplastic nevus

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Dysplastic nevus
Diagnosis in short

Dysplastic nevus. H&E stain.
LM "bridges" between sides of rete ridges, draping fibrous tissue/fibrous tissue wraps around the rete ridges ("lamellar fibrosis"), nuclear atypia - see grading section, +/-junctional component (cells in the epidermis at the DE junction) larger than the intradermal component - shoulder phenomenon
Subtypes junctional, compound
LM DDx melanoma in situ, malignant melanoma, compound melanocytic nevus, atypical lentiginous nevus
Stains Fontana-Masson stain +ve
IHC S-100 +ve, HMB-45 +ve, MART-1 +ve, MITF +ve
Gross "ugly duckling sign" - lesion looks different than the rest, ABCD criteria of melanoma, usually greater than 5 mm
Site skin - see melanocytic lesions
Syndromes dysplastic nevus syndrome
Signs ABCDEs of melanoma (asymmetry, border, colour, diameter, evolution)
Prevalence common
Prognosis benign, increased risk of melanoma
Clin. DDx melanoma in situ, other pigmented lesions

Dysplastic nevus, abbreviated DN, is a common melanocytic lesion that is closely associated with malignant melanoma.

It is also known as dysplastic melanocytic nevus, Clark nevus, and nevus with architectural disorder.

The term nevus with architectural disorder is recommended by the American National Institutes of Health (NIH); however, it is not widely adopted.[1] Also, it is the prefered term by only 15% of dermatologists.[2]

General

  • Benign.
  • Dysplastic nevi are considered a risk factor for melanoma and may be a precursor of melanoma, as the name dysplastic nevus suggests.[3]
    • Most melanoma cases do not have evidence of a pre-existing (dysplastic) nevus.[4]
  • Large numbers of these nevi (10-100) are seen in dysplastic nevus syndrome.[5]
    • Individuals with this syndrome have an increased risk of melanoma and approximately one third of their melanomas arise from a Clark nevus. The other two thirds arise de novo.

Clinical:[6]

  • Associated with sun exposure.

Treatment:

  • Dysplastic nevi with severe nuclear atypia are typically treated like melanoma in situ - complete excision with a 5 mm margin.[7]
  • Dysplastic nevi with moderate nuclear atypia with margin involvement are re-excised.[7]

Gross

Features:[6]

Note:

  • † Size matters - things smaller than 4 mm are usually not a dysplastic nevus.

Microscopic

Features:[9]

  • Melanocytes "bridges" between sides of rete ridges.
    • Joining of three or more adjacent rete ridges = suspicious for melanoma.[7]
  • Draping fibrous tissue - "lamellar fibrosis" - collagen deep to epidermis.
  • Usually moderate nuclear atypia (small nucleoli present) - see grading section.
  • +/-Junctional component (cells in the epidermis at the DE junction) larger than the intradermal component - shoulder phenomenon.

DDx:

Images

  • Dysplastic nevus - low mag. (WC/Nephron)

  • Dysplastic nevus - intermed. mag. (WC/Nephron)

  • Dysplastic nevus - high mag. - shows bridging and lamellar fibrosis. (WC/Nephron)

  • Dysplastic nevus - very high mag. - shows bridging and lamellar fibrosis. (WC/Nephron)

Grading

These lesions are often graded § :[12]

Grade Size of nucleus Other features
Mild 1x keratinocyte nucleus no nucleoli/very small nucleoli †,[13] slight hyperchromasia
Moderate 1-2x keratinocyte nucleus small nucleoli †, irregular nuclear contours
Severe >2x keratinocyte nucleus prominent nucleoli †‡

† The sizes "very small", "small" and "prominent" are not defined; it is suggested that "very small" is visible with the 40x objective, "small" with the 20x objective and "prominent" with the 10x objective. Focal, rare small nucleoli are not significant; they can be seen in benign melanocytic nevi.
‡ Prominent nucleoli (alone) is considered enough to call "severe".[12]

Notes:

  • § There is no consensus on this and practise (embarrassingly) is all over the map.[1]
    • A two-tier grading system also exists (low-grade (leave it alone) / high-grade (cut it out)).
    • Some pathologists do not grade dysplastic nevi.

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Compound

SKIN LESION, BACK, EXCISION:
- DYSPLASTIC COMPOUND NEVUS WITH MILD CYTOLOGIC ATYPIA AND MILD ARCHITECTURAL ATYPIA,
  COMPLETELY EXCISED IN THE PLANE OF SECTION (2 MM CLEARANCE).

SKIN LESION, CENTRAL BACK, EXCISION:
- DYSPLASTIC COMPOUND NEVUS WITH MILD CYTOLOGIC ATYPIA.
- NEAREST MARGIN (LATERAL MARGIN) 6 MM.

Micro

The sections show hair-bearing skin with a compound melanocytic lesion. The epidermal component extends at least three rete ridges further than the dermal component (shoulder phenomenon). There is bridging between the sides of the rete ridges and lamellar fibrosis. The melanocyte nuclei are approximately the size of the keratinocyte nuclei, and do not have a prominent nucleolus (mild cytologic atypia).

There is no upward scatter of melanocytes and melanocytes in the dermis are mature. No mitotic activity is appreciated.

Junctional

SKIN LESION, LOWER BACK, EXCISION:
- DYSPLASTIC JUNCTIONAL MELANOCYTIC NEVUS WITH MILD NUCLEAR ATYPIA.
- NEAREST MARGIN (LATERAL MARGIN) 1 MM.

Micro

The sections show hair-bearing skin with a junctional melanocytic lesion. There is bridging between the sides of the rete ridges and lamellar fibrosis. The melanocyte nuclei are approximately the size of the keratinocyte nuclei, and do not have a prominent nucleolus (mild nuclear atypia).

There is no upward scatter of melanocytes. No mitotic activity is appreciated.

See also

References

  1. ↑ 1.0 1.1 Elston, D. (Jul 2012). "Practical advice regarding problematic pigmented lesions.". J Am Acad Dermatol 67 (1): 148-55. doi:10.1016/j.jaad.2012.04.006. PMID 22703907.
  2. ↑ Fung, MA. (Oct 2003). "Terminology and management of dysplastic nevi: responses from 145 dermatologists.". Arch Dermatol 139 (10): 1374-5. doi:10.1001/archderm.139.10.1374. PMID 14568850.
  3. ↑ Rezze, GG.; Leon, A.; Duprat, J. (Dec 2010). "Dysplastic nevus (atypical nevus).". An Bras Dermatol 85 (6): 863-71. PMID 21308311.
  4. ↑ Longo, C.; Rito, C.; Beretti, F.; Cesinaro, AM.; Piñeiro-Maceira, J.; Seidenari, S.; Pellacani, G. (Sep 2011). "De novo melanoma and melanoma arising from pre-existing nevus: in vivo morphologic differences as evaluated by confocal microscopy.". J Am Acad Dermatol 65 (3): 604-14. doi:10.1016/j.jaad.2010.10.035. PMID 21715047.
  5. ↑ Online 'Mendelian Inheritance in Man' (OMIM) 155600
  6. ↑ 6.0 6.1 Dediol, I.; Bulat, V.; Zivković, MV.; Marković, BM.; Situm, M. (Sep 2011). "Dysplastic nevus--risk factor or disguise for melanoma.". Coll Antropol 35 Suppl 2: 311-3. PMID 22220461.
  7. ↑ 7.0 7.1 7.2 Culpepper, KS.; Granter, SR.; McKee, PH. (Nov 2004). "My approach to atypical melanocytic lesions.". J Clin Pathol 57 (11): 1121-31. doi:10.1136/jcp.2003.008516. PMID 15509670.
  8. ↑ Barnhill, RL.; Hurwitz, S.; Duray, PH.; Arons, MS. (Feb 1988). "The dysplastic nevus: recognition and management.". Plast Reconstr Surg 81 (2): 280-9. PMID 3275948.
  9. ↑ Humphrey, Peter A; Dehner, Louis P; Pfeifer, John D (2008). The Washington Manual of Surgical Pathology (1st ed.). Lippincott Williams & Wilkins. pp. 502. ISBN 978-0781765275.
  10. ↑ Farrahi, F.; Egbert, BM.; Swetter, SM. (Jul 2005). "Histologic similarities between lentigo maligna and dysplastic nevus: importance of clinicopathologic distinction.". J Cutan Pathol 32 (6): 405-12. doi:10.1111/j.0303-6987.2005.00355.x. PMID 15953373.
  11. ↑ Edwards, SL.; Blessing, K. (Jun 2000). "Problematic pigmented lesions: approach to diagnosis.". J Clin Pathol 53 (6): 409-18. PMID 10911797.
  12. ↑ 12.0 12.1 Busam, Klaus J. (2009). Dermatopathology: A Volume in the Foundations in Diagnostic Pathology Series (1st ed.). Saunders. pp. 447-8. ISBN 978-0443066542.
  13. ↑ Arumi-Uria, M.; McNutt, NS.; Finnerty, B. (Aug 2003). "Grading of atypia in nevi: correlation with melanoma risk.". Mod Pathol 16 (8): 764-71. doi:10.1097/01.MP.0000082394.91761.E5. PMID 12920220.
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