Feature | Spitz naevus | Atypical Spitz tumour | Spitzoid melanoma |
Clinical | |||
Age | Any age (2/3 < 20 years) | No difference | No difference |
Location | Any location (extremities and trunk preferred; H&N in children) | No difference | No difference |
Colour | Red–brown; occasionally pigmented | No difference | No difference |
Silhouette | |||
a. Size | Small (most <6 mm) | Variable | Large (>10 mm) |
b. Symmetry | Present | Variable | Asymmetrical |
c. Circumscription | Present | Variable | Poor |
Evolution/clinical course | Stable | May metastasise to regional LNs; natural history uncertain | Variable malignant course: regional LN mets but favourable outcome to widely metastatic disease and death |
Architectural | |||
Epidermis | |||
Silhouette | |||
a. Size | Small | Variable | Large |
b. Symmetry | Present (must evaluate fully excised lesion) | Variable | Asymmetrical |
c. Circumscription | Present (must evaluate fully excised lesion) | Variable | Poor |
Epidermal hyperplasia | Present | No difference | May be atrophic/ulcerated |
Artifactual clefting | Present | No difference | Variable |
Kamino bodies | May be present (∼50% of cases—multiple levels increase detection) | No difference | No difference |
Pagetoid spread | Often present | Variable | Prominent; present at edge of lesion or upper half of epidermis |
Dermis/subcutis | |||
Cellular density | Variable (low–moderate) | Moderate– dense | Dense (confluent growth) |
Pattern of growth | Organised, nested and interstitial growth | Variable | Confluent, destructive |
Architectural maturation | Present | Variable | Absent |
Deep front of lesion | Infiltrative with outlier cells | Variable | Expansile or infiltrative |
Involvement of subcutis | Rare—may be minimal | Variable | May be pronounced |
Stromal/inflammatory response | Variable (usually mild) | Variable | Inflammation or regression may be noted |
Cytological | |||
Nuclear size | Moderate–large | No difference | Large |
Nuclear shape | Normal–angulated | No difference | Pleomorphic |
Cytoplasm | Abundant, eosinophilic ‘ground-glass’ | No difference | Variable |
N/C ratio | Low | No difference | Variable |
Multinucleation | Present | No difference | No difference |
Hyperchromasia | Low–moderate | Variable | High |
Nucleoli | Present (small–moderate sized) | Variable | Present (large) |
Nuclear membrane | Normal | Variable | Irregular |
Chromatin pattern | Dispersed | Variable | Coarse |
Cytological maturation | Present | Variable | Absent |
Other | |||
Mitotic activity | Absent–moderate (up to 6 per 10hpf); confined to junction or superficial dermis | Variable | High (often >6 per 10hpf); abnormal or deep forms |
Perineural or angiolymphatic invasion | Absent | Absent | May be present |
Sentinel lymph node | Negative | May be positive | May be positive |
Necrosis | Absent | Absent | May be present |
Immunohistochemistry | |||
HMB-45 | Variable (typically stratified) | Variable | Variable (often diffuse) |
MIB-1 | Low proliferative index (<10%) | Variable (<15%) | High (>15%) |
Cytogenetics | Normal or isolated gain of 11p | Intermediate–often complex aberrations | Complex chromosomal aberrations |
H&N, head and neck; LN, lymph node.