Week 1 - Disorders of Cutaneous Pigmentation & Cutaneous Neoplasms Flashcards
Neoplasms usually arise from. . .
the epidermis & the dermis
Dermis
Consists of collage/elastic fibers, peripheral nerves, muscle, fat, cartilage
Vitiligo
Partial or complete loss of melanocytes, well demaracated macules/patches, hand/wrist, axillae, perioral/periorbital, anogenital
Pathogenesis: autoimmune - T cells attack melanocytes of skin & destroy them - then you get hypopigmented cells
Neoplasia
Proliferation of genetically abnormal cells - clonal population or proliferation of cells that can escape the normal cell checkpoints
Cancer
Malignant Neoplasm
Benign vs. Malignant
Benign = can't metastasis Malignant = has potential (does not have to) metastasize
Albinism
No melanin produced (or decreased melanin)
Inherited defect in tyrosinase!! (normal number of melanocytes)
-Congenital absence of enzyme and melanin is not made or is decreased
Stromal Neoplasms
Neoplasms involving connective tissue
Nevus (mole)
Benign neoplasms of melanocytes, congenital or acquired - most have mutations (BRAF most common)
How do we predict the probability of melanoma to metastasize?
Depth of invasion
What is Breslow’s depth?
It is the probability to metastasize that is predicted by depth of invasion of the melanoma
- Measured in millimeters
- Best indicator of probability to metastasize
Breslow’s depth
How deep melanoma invades into the dermis (measure from the granular layer to the lowest melanocyte)
-Best prognostic indicator!!
Sentinel lymph node biopsy:
Usually for melanomas > 1 mm in thickness - melanomas like to go to lymph nodes (they usually go here first - so if melanoma isn’t here, it usually hasn’t metastasized)
Breslow depth & Survival:
4 mm: 5 yr sur. is 37-50%
Next most imp. prognostic indicator (after Breslow depth for melanoma):
Ulceration (usually growing very fast), mitotic rate of cells