1. |
Clinical presentation |
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a. |
Lesion appearance |
Presents as a darkly pigmented, well-circumscribed lesion with variable coloration, including shades of brown, black, gray, and sometimes blue. |
Presents as a darkly pigmented, asymmetrical lesion with irregular borders and variable coloration with shades of brown and black. They are usually evolving lesions which change in size, shape or color |
b. |
Size and Growth |
Typically smaller in size and tend to grow slowly over time |
Can vary in size and often exhibit rapid growth. |
2. |
Histopathology: |
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a. |
Cellular Architecture |
Proliferation of epithelioid melanocytes with abundant eosinophilic cytoplasm, vesicular nuclei, and prominent nucleoli. No atypia/pleomorphism noted. |
May show a wider range of cytologic atypia and pleomorphism. |
b. |
Mitotic Activity |
Lower mitotic rate |
Usually higher mitotic rate |
c. |
Pagetoid Spread |
Less common |
Often display pagetoid (single cell) spread within the epidermis |
d. |
Junctional activity |
Less common |
More common |
e. |
Lymphovascular Invasion |
Less common |
More common |
3. |
Immunohistochemistry |
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a. |
S100 |
Both PEM and melanoma cells may stain positive for S100 protein, but PEM cells typically show a more diffuse and strong staining pattern. |
b. |
HMB-45 |
Positive staining for HMB-45 is common in both PEM and melanoma, but PEM cells may show a more consistent and diffuse staining |
c. |
SOX10 |
Positive staining for SOX10 is often seen in both PEM and melanoma, with stronger and diffuse staining in PEM. |
4. |
Genetic and Molecular Features: |
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|
a. |
BRAF Mutation |
Less frequent |
More common |
b. |
KIT Mutations |
Some cases have been associated with KIT mutations |
Less common |
c. |
Cytogenetic Abnormalities |
Less prevalent |
More prevalent in melanomas |
5. |
Clinical Behaviour |
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a. |
Metastasis |
Less aggressive and can metastasize |
More aggressive and have a higher potential for metastasis |
b. |
Prognosis |
Indolent clinical course with good prognosis |
Poor prognosis |