HMWCKs(+), p63; S100(-)
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Atypical fibroxanthoma
S100(-); CD10/CD68/CD99 (+)
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Dermatofibroma: FXIIIA/CD10 (+); S100(-)
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Dermatofibrosarcoma protuberans: CD34(+); S100(-)
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Neural tumors
S100/SOX10 (+); CD34(+) (not in DM)
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Leiomyosarcoma
Actin/desmin (+), S100(-)
TERMINOLOGY
Abbreviations
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Desmoplastic melanoma (DM)
Synonyms
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Desmoplastic/neurotropic melanoma
Definitions
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Form of invasive melanoma composed of spindle cells associated with dense stromal collagen
Resembles scar
CLINICAL ISSUES
Epidemiology
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Age
Presents in sun-damaged skin of elderly adults
Presentation
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Firm, skin-colored, tan or pink plaque or nodule
Treatment
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Surgical approaches
It is important to resect DMs with clear surgical margins
–
Needs to be done as early as possible for successful clinical management
There is increasing evidence that sentinel lymph node biopsy may not be indicated for “pure” variants
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This variant has low incidence of regional lymph node metastases
Prognosis
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Tumor thickness (Breslow depth)
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Histological subtype: Pure (longer disease-free survival) vs. combined
Pure subtype is defined as > 90% scar-like areas
Combined subtype is defined as densely cellular spindle cell collections
–
Lacks significant scar-like areas (> 10%)
MICROSCOPIC
Histologic Features
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Ill-defined spindle cell neoplasm with highly infiltrative pattern of growth
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Overlying epidermis may show melanoma in situ (usually lentigo maligna type)
•
Stromal collagen on scanning magnification resembles scar
•
Spindle cells are arranged in fascicles and merge with scar-like areas
•
Cellular density and cytologic atypia can vary based on histologic subtype
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Discrete dermal lymphoid aggregates