Malignancy Flashcards
Nodular BCC
Large atypical basaloid tumor islands
Peripheral palisading retraction clefting
Pigmented- melanin pigment tumor/stroma- dendritic melanocytes
Epidermal ulceration
Bowen
Thickened epidermis
Complete replaced full thickness atypical pleomorphic cells
Numerous apoptotic keratinocytes, abnormal mitotic figures
Basement membrane intact, absent dermal invasion
Superficial BCC
Multifocal tumor islands high papillary dermis
Attached undersurface epidermis
Peripheral pallisading, retraction clefting
Morpheic
Infiltrative cords cells single-few layered thickness
Cords dissect collagen within sclerotic stroma( hyalinised- morpheic)
Perineural invasion
Squamous cell carcinoma
Hyperkeratosis papillomatosis
Tongues of squamous proliferations
invading dermis
Tumor cells large pale atypical keratinocytes, keratotic differentiation
(Single cell keratinisation, keratin cysts)
Infiltrative lower border, mixed inflammatory infiltrate
EMPD
Nested proliferation
Large Pale neoplastic Paget’s cells (with atypical nuclei)
Basal epidermis, varying levels throughout epidermis
Groups flatten basal cells. multifocal with skip areas
no dyskeratosis
Bowens stains
negative for CK7, EMA, CEA
positive for high molecular weight keratins
EMPD stains
PAS+ diastase resistant CEA EMA CK+
Alcian blue, mucicarmine
Gross cystic disease fluid protein
Clear cell acanthoma
- Scale-crust
- Neutrophils in epidermis, microabscesses stratum corneum
- Psoriasiform proliferation pale (“clear”)keratinocyte, sharp demarcation
- glycogen PAS-positive, diastase labile
- Perivascular lymphocytes, Dilated blood vessels edematous pale dermal papillae
Epidermal nevus
Hyperkeratosis, papillomatosis, acanthosis, hypergranulosis
Epidermolytic hyperkeratosis rarely
Acantholytic dyskeratosis rarely
Perivascular lymphocytes often
Epidermal nevus etiology
post-zygotic somatic mosaicism for mutations in the FGFR3 gene or PIK3CA gene
Porokeratosis
Cornoid lamella (angulated column of parakeratosis)
under which hypogranulosis
dyskeratosis keratinocytes or pale staining
Epidermis normal, hyperplastic, atrophic
Perivascular (1.109) or lichenoid (1.72) lymphocytes,
AK
-hyperkeratosis, ulceration
-Parakeratosis overlying atypical keratinocytes sparing epidermis over adnexa (“alternating” pink and blue hue in stratum corneum “flag sign”)
-Atypical keratinocytes deeper epithelium
loss maturation, hyperchromatism, pleomorphism, increased mitoses, dyskeratosis
-Multiple buds into papillary dermis
-Perivascular lichenoid lymphocytes, plasma cells
-Solar elastosis in the dermis
features of malignancy
Atypical( keratinocytes, basaloid cells) hyperchromatic, pleomorphic, atypical mitoses, dyskeratosis Loss of maturation with descent Dermis invasion, perineural
sebaceous neoplasms plus KA
Muir–Torre syndrome