Malignancy Flashcards

0
Q

Nodular BCC

A

Large atypical basaloid tumor islands
Peripheral palisading retraction clefting
Pigmented- melanin pigment tumor/stroma- dendritic melanocytes
Epidermal ulceration

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1
Q

Bowen

A

Thickened epidermis
Complete replaced full thickness atypical pleomorphic cells
Numerous apoptotic keratinocytes, abnormal mitotic figures
Basement membrane intact, absent dermal invasion

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2
Q

Superficial BCC

A

Multifocal tumor islands high papillary dermis
Attached undersurface epidermis
Peripheral pallisading, retraction clefting

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3
Q

Morpheic

A

Infiltrative cords cells single-few layered thickness
Cords dissect collagen within sclerotic stroma( hyalinised- morpheic)
Perineural invasion

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4
Q

Squamous cell carcinoma

A

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

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5
Q

EMPD

A

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

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6
Q

Bowens stains

A

negative for CK7, EMA, CEA

positive for high molecular weight keratins

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7
Q

EMPD stains

A

PAS+ diastase resistant CEA EMA CK+
Alcian blue, mucicarmine
Gross cystic disease fluid protein

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8
Q

Clear cell acanthoma

A
  • 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
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9
Q

Epidermal nevus

A

Hyperkeratosis, papillomatosis, acanthosis, hypergranulosis
Epidermolytic hyperkeratosis rarely
Acantholytic dyskeratosis rarely
Perivascular lymphocytes often

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10
Q

Epidermal nevus etiology

A

post-zygotic somatic mosaicism for mutations in the FGFR3 gene or PIK3CA gene

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11
Q

Porokeratosis

A

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,

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12
Q

AK

A

-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

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13
Q

features of malignancy

A
Atypical( keratinocytes, basaloid cells) 
hyperchromatic, pleomorphic, 
atypical mitoses, dyskeratosis
Loss of maturation with descent 
Dermis invasion, perineural
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14
Q

sebaceous neoplasms plus KA

A

Muir–Torre syndrome

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15
Q

KA

A
  • Dome shaped lesion -Keratin-filled crater btw epidermal lips
  • Thickened epidermis Pale, eosinophilic, glassy, well-differentiated epithelial proliferation
  • squamous eddies or keratin pearls
  • microabscesses neutrophils within epithelium
  • mild Cytologic atypia of keratinocytes
  • Elastic fibers within epithelium base
  • Perivascular or lichenoid infiltrate of lymphocytes, eosinophils, plasma cells