Dermatopathology - Entities & Features Flashcards

1
Q

Clear cell acanthoma

A

Clear demarcation from epidermis
Often neutrophils present
PAS + showing abundant glycogen

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2
Q

Poroma

A
Small monomorphic cells 
Epidermis ‘raining down’ 
Sharp demarcation of epidermis to dermis
Glandular structures in dermis
Connected to basal layer of epidermis
Forms vertically oriented columns
Ductal spaces
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3
Q

Trichilemmoma

A

Acanthosis in epidermis
Eyeliner sign / peripheral palisade
Some koilocytic like changes at edges of lesion
Clear cell change due to glycosylation of cytoplasm
Overlying hypergranulosis and hyperkeratosis

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4
Q

Fibroepithelioma of pinkus

A

Fenestrated strands off epidermis
BCC like areas in scaffold
PHLDA1 marker - less staining in basaloid areas , more staining in pink areas

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5
Q

Tumour of follicular infundibulum

A

Epidermal epithelial growth with a plate like configuration and multiple connections to the epidermis
- keratinocytes have glycogenated appearance resembling those of outer root sheath
Prominent surrounding basement membrane

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6
Q

Elastosis perforans serpinosa

A
  • extrusion of elastin fibres / transepidermal elimination
  • associated folliculitis
  • can have overlying parakeratosis with neuts
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7
Q

Folliculitis de calvans

A
Plasma cells
Polytrichia
Scarring fibrosis 
Neutrophilic abscesses 
Hair shaft granulomas 
Lymphocytes
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8
Q

Granular cell tumour

A

Overlying epidermis may show pseudoepitheliomatous hyperplasia
Proliferation of large to polygonal cells with granular eosinphilic cytoplasm in sheets
Individual cells with indistinct borders, small round centrally located nuclei
Large eosinophilic
S100 +ve
CD68 +ve

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9
Q

Syringocystadenoma papilliferum

A

CYSTIC neoplasm opening into surface
Epidermis has hyperplasia and papillomatosis
Tumour shows papillary growth pattern with papillae composed of FIBROVASCULAR CORE surrounded by 2 layers of cells — inner tall columnar cells with eosinophilic cytoplasm
Plasma cells conspicuous
Look for associated sebaceous naevus

DDx: hydrocystadenoma, hydradenoma, hidradenoma papilliferum,

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10
Q

Granuloma annulare

A
Closed off palisading granulomas
Upper third epidermis
Granulomatous inflammation 
Mucin stain positive (colloidal iron, alcian blue)
Normal dermis visible
Eosinophils
Multinucleated giant cells
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11
Q

Acantholytic acanthoma

A

Papillomatosis, epidermal hyperplasia with overlying hyperkeratosis

Prominent acantholysis throughout epidermis

Mild superficial perivascular infiltrate

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12
Q

Acute generalised exanthematous pustulosis

A

Subcorneal or superficial intraepidermal neutrophilic pustules with admixed few acantholytic keratinocytes
Background spongiosis with neutrophilic exocytosis and scattered dyskeratotic cells
Papillary dermal oedema
Perivascular mixed inflammatory infiltrate

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13
Q

Dermatofibroma aka fibrous histiocytoma

A
  • Epidermal hyperplasia with flattened rete ridges ,
  • Basal induction - induction follicles and sebaceous glands
  • Poorly circumscribed proliferation of spindled and/or epithelioid fibroblasts and histiocytes
  • Multinucleated giant cells - touton like
  • Xanthomatised histiocytes
  • Cellular dermis with collagen entrapment more prominent at periphery
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14
Q

Pilomatricoma

A
  • Multinodular tumour in dermis and/or subcutis composed of nests resembling those of the hair matrix with abrupt transition to central shadow cells
  • calcifications and foreign body granulomatous response
  • numerous mitotic figures
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15
Q

Sebaceous adenoma

A

Nodular sebaceous and basaloid proliferation
Broadly connected to epidermis
Predominance sebaceous glands
Minimal cytological atypia

Erosion overlying is commmon
More mature sebocytes over less differentiated blue cells
Lipidized cells

MMR gene mutations MSH2, MSH6, PMS2, MLH1

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16
Q

T/F viral cytopathic change going down hair follicles is more likely VZV than HSV

A

True

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17
Q

Palisaded encapsulated neuroma

A

Well circumscribed but non encapsulated
Usually cleft but no capsule
Spindled cells wavy nuclei
Mast cells present

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18
Q

Bullous arthropod bite reaction

A

Subepidermal bulla ,
eos predominate
Superficial and deep eosinophilic infiltrate

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19
Q

Cylindroma

A

Jig saw arrangements of basaloid islands
Two cell populations small basaloid cells periphery and larger pale cells centrally
Eosinophilic aggregates within nests and around nests forming stroma

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20
Q

What is a sunburn cell

A

Single or few apoptotic cells high up in epidermis

Consistent with a photodermatosis

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21
Q

Polymorphous light eruption

A

Variable epidermal spongiosis with dyskeratosis
Superficial and deep mixed inflammation (mostly lymphocytic)
Red cell extravasation
Marked papillary dermal oedema

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22
Q

Chronic cutaneous lupus erythematosus

A

Follicular plugging
BM thickening
Lichenoid reaction pattern - basal vacuolation and apoptotic keratinocytes
Superficial and deep lymphocytic infiltrate
Mucin interstitially

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23
Q

Lupus tumidus

A

Relative sparing of epidermis
Superficial and deep lymphocytic inflammation
Mucin deposition interstitially

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24
Q

Subacute cutaneous lupus erythematosus

A
CF. DLE
- presence of more epidermal atrophy
- epidermal atrophy 
Basement membrane thickening
Mucin deposition 
Superficial and deep lymphocytic infiltrate with periappendegeal spread /peri-eccrine 
- Less hyperkeratosis
- Less Basement membrane thickening
- Less follicular plugging
- Less inflammatory infiltration
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25
Lesions with keratin horn
Seb K AK IEC SCC
26
Lichen planopilaris
Usually 8 pilosebaceous follicles in each mm of biopsy Thus 36 or more follicles normal in a 4mm scalp biopsy - lichenoid band like infiltrate with interface changes involving follicular infundibulum, concentric lamellar fibroplasia - interfollicular epidermis usually spared - loss of sebaceous glands and follicles - DIF nonspecific cytoid bodies positive for IgM - fusion of hair follicles - in LPP not lupus
27
Traumatic neuroma
- Proliferation of small bundles of well delineated nerve fascicles in a fibrotic stroma STAIN: S100 for Schwann cells
28
Blastomycosis like pyoderma
Hyperplasia Neutrophils No evidence fungal/hyphae/
29
Sebaceous adenoma
Sebaceous lobule like structures Peripheral basaloid cells (germinative cells) not more than >50% need DNA mismatch repair markers Cf. Sebaceoma - more disorganised, do not always retain the architecture; sebaceous duct like structures more prominent in sebaceoma
30
Mixed tumour of the skin | Chondroid syringoma
Circumscribed nodule Clear cut cartilage with bluish appearance Myxochondroid change, looks like cells are sitting in lacunae Elongated , curved atubular structures Rounded ductal structures / sometimes cystic structures
31
Lichen sclerosus
``` Hyperkeratosis Epidermal atrophy Some lichenoid change Follicular plugging Homogenised collagen [papillary dermis Underlying band like infiltrate ```
32
Adamantinoid trichoblastoma
Small nests with peripheral palisade — clear cells in middle not sebaceous origin
33
Warty dyskeratoma
Solitary cup shaped focus with acantholysis and dyskeratosis DDx: Acantholytic acanthoma — no dyskeratosis Old lesions of Grover’s - can be proliferative/atypical Comedonal Darier
34
Palisaded encapsulated neuroma
Fascicular arrangement of Schwann cells- often separated by small clefts with neural/wavy nuclei with pointed polar ends - no dysplasia - can see some nuclear palisading - often has artefactual change like BCC where tumour separates from dermis - no clear capsule or thin capsule only s100 positivity Ddx: NF, Pilar leiomyomas
35
Verruca (deep plantar wart)
Church spire like hyperkeratosis | See inclusion like keratohyalin
36
Diameter of microscope field Olympus microscope
11mm at x2 power
37
Secondary syphilis
Numerous plasma cells, superficial and deep Lichenoid reaction pattern or psoriasiform reaction pattern with long thin rete Endothelial cell swelling
38
Halo naevus
Regression in naevus Lichenoid reaction centrally Dense admixed lymphocytes in the upper dermis
39
Venous lake
Large dilated channel containing erythrocytes with thin endothelial lining with thin fibrosis Dilated capillary/venule Can be thrombosed secondary to trauma
40
Thrombophlebitis
Thrombosis within a thick walled lumen within the subcutaneous fat Ddx: erythema induratum Polyarteritis nodosa
41
Clear cell acanthoma
Well demarcated acanthotic epidermis with pale/clear cells, overlying parakeratosis and may co-exist with a prurigo nodule —> PAS, followed by PAS-diastase to remove glycogen
42
Blue naevus
- Dendritic melanophages and spindled melanocytes - Spindled cell proliferation, spindled melanocytes look like angulated cells with processes - Often arranged around a follicular structure - Pigment throughout lesion
43
Spitz naevus
Plump epithelioid nests Vertical orientation of nests in papillary dermis Doesn’t always have Kamino bodies
44
Juvenile xanthogranuloma
Sheet like nodular aggregates of lymphocytes histiocytes and eosinophils with admixed touton giant cells - admixed xanthomatous cells / foam change
45
Syringoma
- Tadpole shaped eccrine structures in dermis forming tadpole-like structures
46
Phototoxic drug eruption
Intraepidermal blister with neutrophils | Epidermal necrosis
47
Pyogenic granuloma
Exophytic vascular nodule Lobulated capillary network Epidermal collarette Neutrophils correlate with degree of ulceration
48
Polymorphic eruption of pregnancy
Nonspecific findings — eosinophils with lymphocytic inflammation — perivascular — dermal oedema
49
Sebaceoma
Nodular sebaceous and basaloid proliferation
50
Nodular melanoma
- Prominent vertical growth phase - few mitotic figures - check peripheries in case arising in melanoma in situ
51
Ashy dermatosis
Lichenoid reaction pattern Pigment incontinence Upper dermal inflammation (lymphocytes/eosinophils)
52
Angioleiomyoma
- Discrete nodule in dermis of smooth muscle spindle cells arranged into fascicles -
53
Lichen striatus
Combination of 2 reaction pattern in epidermis - spongiosis and lichenoid — peri-eccrine lymphocytic infiltration
54
Clear cell hidradenoma
- solid and cystic areas with scattered ducts DDx. poro-hidradenoma , many poroid cells
55
Mastocytosis
— Increase in mast cells | — look at proportion of mast cells to lymphocytes
56
Cellular Dermatofibroma
DF - CD13a positive, CD34 neg | Vs. DFSP - CD34 positive, CD 13a neg
57
Erythrasma
Corynebacterium - gram pos bacilli in s. Corneum | Pagetoid dyskeratosis
58
Urticaria
Neuts in vessel wall Dermal oedema Polymorphous infiltrate
59
Epidermolytic acanthoma
Hyperkeratosis Slightly endophytic Coarse granules VACUOLATED cytoplasm with eosinophilic globules
60
Granulomatous pigmented purpuric dermatosis
Granulomas in upper papillary dermis Haemosiderin deposition Papillary dermis filled with lymphocytes and histiocytes
61
Hypertrophic lichen planus
Lichenoid reaction in rete ridges
62
Extramammary Paget’s disease
Intraepidermal proliferation with predominantly single cells with admixed nests throughout the epidermis - individual cells are large with amphophilic cytoplasm, large nucleus and prominent nucleoli CK7, CEA, Cam5.2, S100 - likely primary EMPD - CK20, CEA, CAM5.2 positive, CK7, S100 CK20 positive == urothelial origin
63
VZV blister
More likely to have associated folliculitis
64
Warty dyskeratoma
Cup shaped invagination with overlying hyperkeratosis and parakeratosis - acantholytic dyskeratosis of the invaginating epidermis with scattered corp ronds and grains is noted - dermal papillae lined by basal cells resemble villi and project into the invagination
65
Glomus tumour
Solid, well circumscribed nodular proliferation of small monotonous cells with round central nucleus and eosinophilic cytoplasm around dilated blood vessels - no atypic - cell positive for SMA
66
Actinic keratosis
Variable keratinocytic atypia in lower layers of epidermis with overlying focal parakeratosis - alternating ortho and parakeratosis - “sail sign”
67
Lichen striatus
Lichenoid reaction pattern Mixed spongiotic reaction pattern with lichenoid - peri eccrine distribution
68
Sarcoidosis
Non caseating epithelioid granulomas in dermis and /or subcutaneous tissue with minimal lymphocytic infiltrate - Schumann bodies or asteroid bodies present
69
Alopecia areata
Decreased anagen/telogen ratio (INCREASED TELOGEN HAIRS) MORE CATAGEN HAIRS (AT LEAST 50% — R. MORTIMORE) - sparse lymphocytic infiltrate around hair bulbs (swarm of bees) with admixed eos - fibrous tracts seen with pigment incontinence +/- pigment casts
70
Traumatic fat necrosis
Lobular panniculitis | Fat necrosis , suppurative and granulomatous response
71
Erythema elevatum diutinum
NODULAR DENSE MIXED INFILTRATE WITH PREDOMINANT NEUTROPHILS AND LYMPHOCYTES, PLASMA CELLS, LCV. Fibrosis and lipid deposits in late lesions. May or may not have grenz zone
72
Trichotillomania
``` Peripilar haemorrhage Trichomalacia Pigment casts Lymphocytic infiltrate Increased catagen hairs ```
73
FOLLICULITIS DE CALVANS
Dense infiltrate of neutrophils and plasma cells surrounding ruptured follicular units - follicular plugging and intra/perifollicular neutrophilic infiltrates - neutrophilic abscesses and hair shaft granulomas in dermis with admixed lymphocytes, histiocytes
74
Acne keloidalis nuchae
Perifollicular lymphoplasmacytic infiltrate with neuts - follicle rupture, hair shaft granulomas assoc. with suppurative inflammation and dermal fibrosis Sinus tracts common
75
Deep penetrating naevus
Symmetric compound melanocytic proliferation , extends to lower reticular dermis and SC fat in wedge shaped pattern . Nuclei small with hyperchromasia —> extend down adnexae —> stains with cyclin D1 - has had mutation in common with melanoma pathway
76
Desmoplastic trichoepithelioma
Cords and strands forming dermal proliferation , Angiomyxoid stroma Dystrophic calcification
77
Microcystic adnexal carcinoma
- narrow, deeper islands with ductal differentiation - stratified growth pattern with microcyst in upper portion and smaller nests and single cells at base - invasion deep into subcutis (less likely syringoma) - when around eye, have more prominent hyalinised stroma - aka sclerosing sweat duct carcinoma Polyclonal CEA stain - around eccrine ducts
78
Spindle cell SCC
- composed of partially or predominantly Atypical spindled cells in whorls or intersecting fascicles - prominent mitoses
79
Angiokeratoma
Intermixed dilated vessels with acanthotic epidermis | Hyperkeratosis
80
Pseudoxanthoma elasticum
Wavy shortened elastic fibres in dermis Stain: VVG, von kossa for calcium Pseudo-PXE induced by penicillamine does not have calcium
81
Chondrodermatitis nodularis helicus
- narrow ulceration - fibrin and necrosis above level of cartilage - surrounding acanthosis Granulation tissue, fibrosis in dermis below the ulceration - sometimes transepidermal elimination of cartilage - cartilage if seen - can show degenerative changes
82
Morphoea profunda
Sclerotic collagen diffusely Extending down to SC fat - septal panniculitis Eccrine glands high riding Loss of peri-eccrine fat
83
Collagenous and Elastotic marginal papules and plaques of the hand
- Thickened, vertically oriented collagen bundles with foci of calcification -
84
Stains for sebaceous neoplasm
Adipophilin, EMA, MSH2, MSH6, MSH1, PMS2,
85
Lesions with pagetoid spread
``` Melanoma Merkel cell ca IEC SCC AK EMPD ```
86
Amyloidosis
Melanophages Globular deposits of eosinophilic material with clefting STAINS: crystal violet aka methyl violet - changes to magenta (metachromatic stain), Congo red, thioflavin T
87
Pityriasis versicolor
Distinct cell wall rather than artefact with poor edges Spores and hyphae PAS+ Does not enter the epidermis, only the stratum corneum
88
Photoaggravated drug eruption
- Dendritic cells in the dermis - mild spongiosis due to acute on chronic reaction - sunburn cells in the epidermis
89
Granular cell tumour
Can have malignant subtype - proliferation of large to round polygonal cells with granular eosinophilic cytoplasm in sheets - individual cells show indistinct borders, small round centrally located nuclei - large eosinophilic cytoplasmic granules —> pustulo-ovoid bodies of Milan, positive Stains: s100 positive, Cal-ritinene positive Malignant subtype has Ki67
90
Pyogenic granuloma
- Significant cellularity around the vessels | - lobulated collection of dilated capillaries
91
Trichilemmoma
Endophytic proliferation of lobules with clear squamous cells
92
Angiosarcoma
Poorly demarcated proliferation of anatomising blood vessels (cracked collagen pattern) - and solid areas. Vessels show atypical spindled or epithelioid endothelial cells with multilayering and papillary structures - solid areas show sheets of spindled cells
93
EMPD STAINS
CEA, EMA, CK7 - mucicarmine - CAM5.2 - CK20, GCDFP-15
94
PROGNOSTIC FEATURES OF SCC
- distance from tumour margin - PNI - LVI - Clark level - diameter >2mm - site Depth 2mm - recurrence
95
Syringocystadenoma papilliferum
Cystic neoplasm opening onto surface. Epidermis shows hyperplasia and papillomatosis. Double cell wall layer
96
Trichoepithelioma
CD34 positive stroma | Mesenchymal papillary body
97
Eccrine spiradenoma
Basophilic circular populations with eosinophilic aggregates, two cell population, lymphocytes percolating through nests
98
Pigmented spindle cell naevus of Reed
Junctional or compound (usually limited to papillary dermis) plaque like growth pattern with spindled melanocytes running parallel to epidermis - conspicuous melanin pigment - symmetrical configuration with sharp lateral borders no significant nuclear atypia
99
Stains for sebaceous neoplasm
Adipophilin, EMA, MSH2, MSH6, MSH1, PMS2,
100
Lesions with pagetoid spread
``` Melanoma Merkel cell ca IEC SCC AK EMPD ```
101
Amyloidosis
Melanophages Globular deposits of eosinophilic material with clefting STAINS: crystal violet aka methyl violet - changes to magenta (metachromatic stain), Congo red, thioflavin T
102
Pityriasis versicolor
Distinct cell wall rather than artefact with poor edges Spores and hyphae PAS+ Does not enter the epidermis, only the stratum corneum
103
Photoaggravated drug eruption
- Dendritic cells in the dermis - mild spongiosis due to acute on chronic reaction - sunburn cells in the epidermis
104
Granular cell tumour
Can have malignant subtype - proliferation of large to round polygonal cells with granular eosinophilic cytoplasm in sheets - individual cells show indistinct borders, small round centrally located nuclei - large eosinophilic cytoplasmic granules —> pustulo-ovoid bodies of Milan, positive Stains: s100 positive, Cal-ritinene positive Malignant subtype has Ki67
105
Pyogenic granuloma
- Significant cellularity around the vessels | - lobulated collection of dilated capillaries
106
Trichilemmoma
Endophytic proliferation of lobules with clear squamous cells
107
Angiosarcoma
Poorly demarcated proliferation of anatomising blood vessels (cracked collagen pattern) - and solid areas. Vessels show atypical spindled or epithelioid endothelial cells with multilayering and papillary structures - solid areas show sheets of spindled cells
108
EMPD STAINS
CEA, EMA, CK7 - mucicarmine - CAM5.2 - CK20, GCDFP-15
109
PROGNOSTIC FEATURES OF SCC
- distance from tumour margin - PNI - LVI - Clark level - diameter >2mm - site Depth 2mm - recurrence
110
Syringocystadenoma papilliferum
Cystic neoplasm opening onto surface. Epidermis shows hyperplasia and papillomatosis. Double cell wall layer
111
Trichoepithelioma
CD34 positive stroma | Mesenchymal papillary body
112
Eccrine spiradenoma
Basophilic circular populations with eosinophilic aggregates, two cell population, lymphocytes percolating through nests
113
Pigmented spindle cell naevus of Reed
Junctional or compound (usually limited to papillary dermis) plaque like growth pattern with spindled melanocytes running parallel to epidermis - conspicuous melanin pigment - symmetrical configuration with sharp lateral borders no significant nuclear atypia
114
Sweet syndrome
Epidermis normal Marked papillary Dermal oedema Florid neutrophilic inflammatory infiltrate with karyorrhexis - true vasculitis can present focally — Gossamer strands DDx: pustular vasculitis Rheumatoid neutrophilic dermatosis, BADAS, Behcet’s
115
Sebaceoma
Nodular Basaloid nests with sebaceous differentiation Minimal cytologic atypia Basaloid cells predominant >50% STAINS: MSH2, MSH6, PMS2, MLH1 , adipophilin
116
Digital myxoid cyst
Localised deposit of mucin in cystic space Cyst without any specific lining — mucin stains: colloidal iron , alcian blue
117
Porokeratosis
normal basket-weave stratum corneum No neutrophils Vertical column of parakeratosis - cornoid lamella Underlying hypogranulosis, focal thinning of epidermis with scattered dyskeratotic cells
118
Desmoplastic trichoepithelioma
Well demarcated discrete dermal lesion Narrow cords and strands of compact epithelial cells and keratinous microcyst in a background of dense and collagenous sclerotic stroma - BCC has high + staining for BCl-2 - BCl-2 also good for differentiating between inflamed Seb K and SCC (more positive in inflamed SebK) - TE is positive for CK20 whilst a BCC is negative for CK20
119
Blue naevus
pigmented spindle cell proliferation | Dendritic melanophages in setting of sclerotic stroma
120
Lentigo maligna melanoma
Proliferation of atypical melanocytes at DEJ as confluent proliferation of single cells and nests - extends along adnexal structures - pagetoid spread within epidermis throughout the lesion - eosinophilic stroma displaces solar elastosis
121
Bullous pemphigoid
Subepidermal cellular bullae —.eosinophils, neutrophils , lymphocytes DDx: EBA, bullous arthropod bite reaction, bullous drug Cf. EBA - 1. vesiculation can involve adnexae unlike BP 2. More neutrophils
122
Keratoacanthoma
- Large glassy keratinocytes forming sheets - Associated with pseudohorn cysts - Chronic inflammation and scarring - associated with multilayering of sweat ducts - syringometaplasia
123
Neurofibroma
Variably circumscribed, non encapsulated proliferation of spindle cells with wavy nuclei, arranged haphazardly in a loose myxoid stroma Scattered mast cells Stains: s100 for Schwann cells positive, tryptase for mast cells m CD34 positive stroma
124
Inverted follicular keratosis
Endophytic proliferation of squamous epithelium and basaloid cells with finger like projections into the dermis Squamous eddies characteristically present at base Mild lymphohistiocytic infiltrate in dermis
125
Trichofolliculoma
Large central primary dilated follicular infundibulum with multiple small secondary hair follicles emptying into mother follicle - cellular fibrous stroma in close approximation to the hair follicle
126
Schwannoma
Encapsulated lesion in dermis and/or subcutis Cellular areas composed of closely packed spindle cells with tapered wavy nuclei - producing a palisading pattern (Antoni A) Intermixed less cellular areas showing scattered spindle cells No neurofilament - no axons Positive neurofibromin
127
Apocrine hydrocystoma
Unilocular or multilocular cystic cavity lined by TWO layers of epithelial cells with decapitate secretions in lumen
128
Dermatofibroma
``` Basal induction Acanthotic and hyperpigmented basal layer Spindled cell proliferation papillary mesenchymal bodies Sclerotic entrapment of collagen ```
129
Mixed tumour of the skin
Well circumscribed biphasic tumour with admixed epithelial and mesenchymal components Plasmacytoid Dyscohesive solid masses of cells - myoepithelial cells
130
Atypical genital naevus
Large atypical junctional nests - Stromal fibrosis/lamellar fibrosis - can be confused with melanoma
131
PITYRIASIS VERSICOLOR
Spores and hyphae in stratum corneum - COMPARED TO DERMATOPHYTE INFECTION —> LESS SPONGIOTIC —> NO NEUTROPHILS —> no sandwich sign
132
Atrophic epidermis only ~3 cells thick with lichenoid ddx
Dermatomyositis Lupus Porokeratosis
133
Trichoadenoma
Small doughnut like proliferation of keratolytics composed of eosinphilic squamous cells with large central horn cysts. Fibroblastic stroma Epidermal type keratinisation with granular layer
134
HSV folliculitis
- Sebaceous gland necrosis | - Neutrophilic debris
135
Digital myxoid cyst
Localised deposit of mucin in cystic space | - cyst without specific lining
136
Interface obscuring lichenoid dermatitis
Erythema multiforme (reticulated degenerative changes in late biopsy) SJS/TEN FDE (pigment incontinence, neutrophils in infiltrate) PLEVA (parakeratosis, erythrocyte extravasation) SCLE (follicular involvement, BM thickening, mucin) GVHD Adjacent herpes blister paraneoplastic pemphigus (suprabasal acantholysis) Acute lupus erythematosus
137
Desmoplastic melanoma
SUBTLE proliferation of spindle cells in dermis with scattered atypical cells - spindle cells may form fascicles in a fibrotic stroma Perineural invasion often seen S100 best, SOX-10 good too HMB-45 , Melan-A can often be negative
138
Fibroepithelioma of pinkus
Anastomosing thin strands of epidermis with fenestrated appearance In setting of fibroblastic stroma
139
Flegel disease
Hyperkeratosis with focal parakeratosis / papule has a discrete zone of ortho-hyperkeratosis contrast with normal epithelium - in the periphery the epidermis is acanthotic with colarette-like elongated rete ridges, - lymphocytic lichenoid infiltrate in early lesions - EM membrane coated granules (Odland bodies) - slight degree of hyperchromatic mood or nuclear infoldings - resembling Sezary cells, have been described in some cases of Flegel disease
140
Schwannoma
Circumscribed encapsulated dermal nodule Antoni A and B areas Palisaded nuclei Thickened vessel walls
141
Vitiligo
Absence of melanocytes (halo cells) Sparse inflammatory infiltrate Epidermal atrophy \STAINS: SOX-10, Melan-A, HMB-45, s100
142
Discoid eczema
``` Stratum corneum serum crust Spongiosis of epidermis Epidermotropism of lymphocytes Eosinophils Drug induced spongiotic dermatitis - pityrisiaform spongiosis according to KC Chong ```
143
HSV infection
Margination of chromatin Steel gray nuclei Nuclear dust Intraepidermal vesicles - mixed inflammatory infiltrate: variable in HSV infection according to KC Chong (can have neuts, eos, or be monomorphic)
144
Actinic keratosis
Parakeratotic changes in stratum corneum - compact hyperkeratosis, nuclear dysplasia Sometimes acantholysis
145
Pigmented spindle cell naevus of Reed
Spindled melanocytes run parallel to the epidermis Junctional or compound plaque like growth pattern Symmetrical configuration with sharp lateral borders Younger patient — no solar elastosis
146
Mycosis fungoides
Atypical lymphocytes giving rise to Pautrier microabscesses Exocytosis of lymphocytes/epidermotropism (more atypical and larger than lymphocytes in the dermis) Wiry collagen fibres Single lymphocytes lining up against the Basement membrane zone Atypical lymphocytes are surrounded by halos
147
Mixed tumour of the skin/choroid syringoma
Circumscribed dermal nodule with two cell populations | Fibromyxoid stroma
148
Mastocytosis
Cf normal mast cells —> in mastocytosis, hypertrophic and clustered, more spindled —> stains: tryptase is the most specific - CD117, toluidine blue (metachromatic change blue to purple)
149
Trichilemmoma
- Eosinophilic lobules with eyeliner sign - palisaded - has some incr pink cuticle/basement membrane surrounding lobules - clear cells centrally - can have scattered mitoses DDx: clear cell IEC, clear cell SCC, clear cell acanthoma, sebaceous differentiation
150
Inverted follicular keratoma
Endophytic , somewhat bulbous, lobular proliferation with squamous eddies - keratinocyte proliferation seems to surround one or several follicular canals opening onto the surface
151
Tumour of follicular infundibulum
Fenestrated and plate like structures | - pale pink cells
152
Melanoma in situ | - superficial spreading
Symmetry/poor peripheral circumscription (but cannot comment on this on a partial biopsy specimen)/pagetoid/ Nested though Scatter of single cells throughout all levels of epidermis Mitoses Variable stromal reaction Fibrosis within the dermis Scatter of cells above basal layer
153
Angiofibroma /fibrous papule of the nose
Concentric fibrosis around follicle Angioma OPD stroma Fibroblasts - can be multinucleated
154
Superficial multifocal BCC
need to Comment on regression or evidence of tumour beyond scar
155
IEC
Comment on solar elastosis, whether has an underlying epidermal lesion eg. Actinic keratosis - look for dermal invasion -
156
Hydrocystoma
- apocrine snouting | - Unilocular
157
Blue naevus | - common sclerotic
Spindled dendritic melanocytes in dermis Melanophages - histiocytes containing excess melanin pigment Thickened collagen associated with lesion
158
Neurofibroma
Spindle cell proliferation in dermis with wavy nuclei Loose stroma with fibrillary architecture Mast cells No cytological atypia Neurofibrosarcoma only really seen in context of neurofibromatosis
159
Porphyria cutanea tarda
Caterpillar bodies - PAS positive Dermal festooning Paucicellular subepidermal blister
160
Granuloma annulare
Closed off granulomas with necrobiosis - Mucin, presence of eosinophils , less likely plasma cells - perivascular lymphocytes Usually upper portion of dermis (upper 1/3) - areas of dermal dermis also present - multinucleated giant cells
161
Proliferating trichilemmal cyst
Abrupt keratinisation —> transition to keratin - can have cytological atypia Akermann considered this a form of SCC
162
Lichen sclerosus /balanitis xerotica obliteraans
Homogenisation of collagen in papillary dermis Can have eosinophils Can see smooth muscle and nerves in specimen of this area
163
Mucocoele
Myxoid stroma Pseudo cystic structure containing mucin Glandular structures on lip
164
Warty dyskeratoma
;Cup shaped invagination with acantholysis - acantholytic dyskeratotis at the base and sides of a cup like epidermal invagination Flattened parakeratosis = grains Shrunken nuclear bodies with perinuclear halo
165
Eccrine poroma
Monomorphous cell population individual cells trying to form a duct Connecting to epidermis Raining down(classic)
166
MF stains
CD2 - rarely lost CD5 , 2 — both reliable T cell markers CD4 , 8 — for clonality CD30 — exclude LyP, ALCL
167
Deep penetrating naevus
B-catenin positive | Extend down adnexal structures
168
Clonal naevus
Small discrete nests of large pigmented epithelioid melanocytes
169
DARIER VS. GROVER DISEASE
Both have acantholytic dyskeratosis DARIER = more serum crust , more inflammation GROVER = less serum crust, less inflammation
170
PLEVA
Parakeratosis, lymphocytic vasculitis, erythrocytes extravasation, Vacuolar damage, apoptotic keratinocytes
171
Dermal oedema seen in?
``` Sweet syndrome Id reaction Urticaria PMLE Arthropod bite Phytodermatitis Perivascular oedema in perniosis ```
172
Acral fibrokeratoma
Thick collagen bundles surrounded by bloods vessels, oriented perpendicular to the epidermis DDx: ungal fibroma, supernumerary digit
173
Desmoplastic melanoma
pauciceullar atypical Spindled cell proliferation - atypical, spindled, malignant melanocytes - separated by fibrocollagenous stroma within the dermis or SC fat - often overlying melanoma in-situ, typically of LM type Areas that look like nerve Lymphocytic aggregates Do not stain positive for HMB-45 or Melan-A, Can stain + for PRAME IHC stain
174
Kaposi sarcoma
Haemosiderin and plasma cells at edges Can have Polypoid appearance Slit like spaces
175
Angiosarcoma stains
ERG | C-MYC
176
ALOPECIA AREATA
Terminal to vellus hair ratio 1:1 Prominent sebaceous glands Fibrous streamers and miniaturisation can be seen Swarm of bees lymphocytic inflammation Can see pigmented casts Large numbers of catagen and telogen hairs
177
Granular parakeratosis
Retained keratohyalin granules | Can have epidermal necrosis and exocytosis of neutrophils
178
Idiopathic scrotal calcinosis
Amorphous basophilic granular material Giant cell granulomatous reaction at edges
179
Dermato fibrosarcoma protuberans
Storiform configuration of spindled cells Depth of involvement with honey combing Fairly monomorphous cytology although invasive - CD34 - Factor VIII
180
Interface obscuring lichenoid reaction pattern
``` EM PLEVA Fixed drug eruption SJS / TEN LE ```
181
What can shadow keratinisation/cells be found in:
Pilomatricoma Pilomatricarcinoma BCC Follicular adnexal neoplasms
182
Sarcoidal granulomas can be seen in:
``` FIGS RC Sarcoidosis Infections Foreign body granulomatous reaction pattern Granuloma annulare Rosacea Cutaneous Crohn’s disease ```
183
Endophytic squamous proliferation - as a term rather than pseudoepitheliomatous hyperplasia
Favour reactive aetiology
184
Sporothrix
—> can resemble asteroid body
185
Suppurative granuloma
- Contains abundant neutrophils | - subtle granulomas
186
Gout
Fibrillar/Shieves of wheat appearance Can ask to process in alcohol so crystals do not dissolve Gout vs. pseudogout —> basophilic look to pseudogout as more calcified, gout with more pointy ends (soft sign)
187
Perifollicular granulomatous reaction pattern
- ruptured folliculitis —> can see flakes of keratin —> can see some necrosis though slightly unusual in folliculitis (see this in acne necrotica) - annular elastolytic giant cell granuloma
188
Chalazion
Prominent plasma cells | Granulomatous reaction pattern
189
Intravascular papillary endothelial hyperplasia / Masson’s tumour
Reactive proliferation of endothelial cells with papillary formations related to a thrombus - can be mistaken for angiosarcoma
190
Pityriasis rosea
Mild spongiosis and focal parakeratotic mounds Superficial perivascular lymphocytic infiltrate with extravasated RBC, sometimes admixed eos - DDx: EAC
191
Keratoacanthoma
``` Crateriform architecture with glassy eosinophilic atypia, Neutrophilic microabscesses, eosinophils and elastic trapping - acantholysis never present PNI can be present Lymphovascular invasion unlikely SCC can be present in the base of KA ```
192
Angiokeratoma
Acanthotic epidermis with hyperkeratosis | Intermixed dilated vessels surrounded by epidermis giving appearance of intraepidermal vessels
193
Tumour of follicular infundibulum
Superficial distinct plate-like epithelial proliferation MULTIPLE connections to epidermis - slender epidermal connections with basaloid or pale cells Less hyperkeratosis than SebK
194
Lichenoid keratosis
Lichenoid infiltrate composed primarily of lymphocytes with scattered histiocytes - eosinophils and plasma cells are sometimes present - see basal vacuolation, colloid bodies and melanin incontinence
195
Epidermolytic acanthoma
FOUR COMPONENTS IN THIS HISTOLOGIC PATTERN: 1 - clear spaces of varying size surrounding nuclei in the stratum spinosum and stratum granulosum . Large cytoplasmic vacuolation of cells above basal layer with indistinct cell borders 2 - indistinct cellular boundaries consisting of reticulated, lightly staining material 3 - a markedly thickened granular zone containing an incr number of small and large, irregularly shaped, basophilic keratohyalin-like bodies 4 - compact hyperkeratosis The basal layer is normal. Epidermolytic acanthomas generally demonstrate more papillomatosis than seen in other conditions with EHK.
196
Angioleiomyoma
Well circumscribed, subcutaneous or dep dermal nodule. Large interfacing bundles of plump spindle cells with ample eosinophilic cytoplasm, cigar-shaped nuclei and paranuclear vacuoles arranged around slit like Calcification very uncommon - can happen on acral sites
197
Dermatofibrosarcoma protuberans
- Dermal and SC proliferation of spindle cells in distinct storieform pattern; spindle cells are uniform with minimal atypia. - Involvement of subcutis imports a layered and honeycomb pattern. - No epidermal induction - Not necessarily extending to fat - CD34 stain positive - factor XIIa negative (unlike dermatofibroma)
198
Morphoea
Dermal sclerosis with thick closely packed hyalinised collagen bundles. Loss of periadnexal fat, atrophy of adnexal structures, especially pilosebaceous units. Blood vessels appear narrowed with thickened walls. Sparse lymphoplasmacytic infiltrate.
199
Chondroid syringoma
Benign tumour of sweat glands with a mucoid stroma showing cartilaginous metaplasia - chondromyxoid stroma Can be apocrine or eccrine
200
Clonal naevus
Conventional compound naevus and naevus with large epithelioid melanocytes - similar to deep penetrating naevus which has mutation in beta-catenin gene (but clonal naevus does not have mutation)
201
Lichen striatus
``` Focal parakeratosis Mild acanthosis, sometimes psoriasiform Spongiosis Dyskeratotic keratinocytes sometimes Focal basal layer liquefaction sometimes Perivascular or lichenoid lymphocytes , often around follicles and ESPECIALLY AROUND SWEAT DUCTS (syringocentricity) ```
202
Microcystic adnexal carcinoma
Infiltrative , poorly circumscribed eccrine neoplasm with focal Pilar differentiation - stratified growth pattern with microcyst in upper portion and small nests and single cells at the base - SUPERFICIAL: more squamous - INTERMEDIATE: Strands and small nests - DEEP: Cystic - nests of squamoid cells with minimal cytological atypia and duct form
203
Traumatic neuroma
Proliferation of small bundles of well delineated nerve fascicles in a fibrotic stroma
204
Angiosarcoma
Proliferation of Vessels surrounded by Enlarged endothelial cells Surrounded by inflammatory infiltrates CD31, CD34
205
Perniosis
Superficial and deep lymphocytic Fluffy perivascular oedema Eccrine (peri eccrine) inflammation
206
Desmoplastic melanoma
Often little in situ component Spindled cell proliferation Lymphoid aggregates at the edges
207
Acral compound naevus
Larger irregularly shaped pigmented junctional nests Sometimes pagetoid spread Predominance of nests over lentiginous pattern A lack of confluent lentiginous component Usually well circumscribed and asymmetrical Usually not inflamed
208
Inverted follicular keratoma
Endophytic proliferation of squamous epithelium and basaloid cells with finger like projections into the dermis. Squamous eddies characteristically present, particularly at the base. Mild lymphohistiocytic infiltrate in dermis
209
Dilated pore of winer
Keratin plugged dilated follicular infundibulum with small radiating epithelial projections
210
Dilated pore of winer
Keratin plugged dilated follicular infundibulum with small radiating epithelial projections
211
Granular cell tumours
``` Proliferation of large round to polygonal cells with granular eosinphilic cytoplasm in sheets Necrosis Pleomorphism Mitoses Perineural activity No invasion ```
212
Chronic radiation dermatitis
Hyperkeratosis with epidermal atrophy Hyalinised stroma and oedema of papillary dermis Hyalinised vessel walls and intimate hyperplasia Large stellate radiation fibroblasts with atypical changes Loss of adnexa
213
Proliferating trichilemmal cyst
Multilobulated tumour composed of lobules of squamous epithelium showing abrupt trichilemmal keratinisation. Peripheral palisading and thickened BM ma be noted. Focal keratinisation with squamous edges.
214
Merkel cell carcinoma stains
CK20, CK7 chromogranin A Synaptophysin CD31 -for extension to lymph node /lymphatic invasion Negative: - s100, - Common leukocyte antigen - TTF1 (small cell lung ca less likely to form sheets and trabeculae)
215
Chronic cutaneous lupus erythematosus
- BM thickening - Epidermal atrophy - Follicular plugging - Mucin DEPOSITION - Superficial and deep lymphocytic inflammation, periappendageal and peri-eccrine
216
Glomus tumour
Proliferation of rounded, homogeneous, hyperchromatic glomus cells surrounding vascular lumina Positive smooth muscle active Negative CD31, 34
217
Calcinosis cutis
Deeply basophilic brittle deposits in the dermis Occasionally surrounded by foreign body reaction Positive for von kossa and alizarin red
218
Trichoadenoma
Multiple small doughnut like proliferation of keratolysis composed of eosinophilic squamous cells with large central horn cysts - epidermal type keratinisation with granular layer - fibroblastic stroma
219
Large cell acanthoma
Acanthotic epidermis with cells showing large nuclei, almost twice the size of normal keratinocytes. Occasional verrucous pattern with papillomatosis or hyperkeratotic pattern may be seen.
220
Stain for naevus vs. melanoma
P16 - positive in naevi | Negative in melanoma
221
Hailey hailey disease
Extensive acantholysis usually at mid epidermis resembling dilapidated brick wall. Follicle sparing (unlike Darier) Focal dyskeratosis (eosinphilic band surrounding nucleus) Perivascular lymphocytes DIF -
222
Atypical fibroxanthoma
- CD10, CD99 | Can stain positive for SMA
223
Epithelial marker
P40 positive | In SCC