Skin pathology Flashcards

1
Q

Atopic dermatitis

A
  • Pruritic, erythematous, oozing rash with vesicles and edema
  • Often involves face and flexor surfaces
  • Type I HSR, associated wit asthma and allergic rhinitis
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2
Q

Contact dermatitis

A
  • Pruritic, erythematous, oozing rash with vesicles and edema
  • Arises upon exposure to allergens
  • Irritants: poison ivy and nickel jewelry (type IV HSR), irritant chemicals (e.g., detergents), drugs (e.g., PCN)
  • Treatment: removal of offending agent, topical steroids, if needed
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3
Q

Acne vulgaris

A
  • Comedones (whiteheads and blackheads)
  • Pustules (pimples)
  • Nodules
  • Due to chronic inflammation of hair follicles and sebaceous glands
  • Hormone-related increase in sebum and excess keratin block follicles (comedones)
  • Propionibacterium acnes infection leads to inflammation (pustules or nodules)
  • Treatment: benzoyl peroxide
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4
Q

Psoriasis

A
  • Well-circumscribed salmon-colored plaques with silvery scale. Ausspitz sign
  • Usually on extensor surfaces of elbows and knees, as well as the scalp and sacral area
  • Due to excessive keratinocyte proliferation
  • Possible autoimmune etiology
  • Associated wit HLA-C allele on PSORS1 on chromosome 6
  • 30% - facility history, HLA B13, 17
  • Lesions often arises in areas of trauma (environmental trigger)
  • Treatment: corticosteroids, UVA-light with psoralen, immune-modulating therapy
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5
Q

Varicella (chickenpox)

A
  • Viral infection of childhood
  • Characterized by fever and a generalized vesicular eruption
  • The varicella-zoster virus may remain latent for years in dorsal root ganglia
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6
Q

Pemphigus vulgaris

A
  • Autoimmune destruction of desmosomes
  • Formation of severe intraepidermal bullae is characteristic
  • First lesions often occur in the oral mucosa, and extensive skin involvement follows
  • Due to IgG antibody against desmoglein
  • IF highlights IgG surrounding keratinocytes (‘fish net’)
  • Rupture easily - leaving large denuded surfaces subject to secondary infection
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7
Q

Lichen planus

A
  • Pruritic, planar, polygonal, purple papules
  • Often with reticular white lines on surface (Wickham striae)
  • Commonly involves wrists, elbows, and oral mucosa
  • Inflammatory infiltrate composed of lymphocytes at the dermal-epidermal junction (‘saw-tooth’ appearance)
  • Presence of apoptotic keratinocytes mainly in basal cell layer
  • Etiology is unknown - associated with chronic hepatitis C virus infection and vaccination against hepatitis
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8
Q

Bullous pemphigoid

A
  • Resembles pemphigus vulgaris, but is much less severe
  • Autoimmune destruction of hemidesmosome
  • IgG autoantibodies agianst epidermal BM
  • Presents as subepidermal blisters of skin filled with fluid containing eosinophils (between dermis and epidermis); oral mucosa is spared
  • Tense bullae do not rupture easily
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9
Q

Dermatitis herpetiformis

A
  • Due to autoimmune deposition of IgA at tips of dermal papillae
  • Presents as pruritic vesicles and bullae that are grouped
  • Usually involves the extensor surfaces of the knees and elbows, scalp, upper back, and sacral area
  • Dermal microabscesses with neutrophils and eosinophils at the tips of dermal papillae
  • Associated with celiac disease
  • Resolve with a gluten-free diet
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10
Q

Erythema multiforme

A
  • Presents with multiple type of lesions, including macules, papules, and vesicles
  • Characteristically associated with a ‘target’ lesion resembling an archer’s bull’s eye
  • Most commonly associated with HSV infection
  • Usually hypersensitivity to coexistent infectious agents, various drugs, a concomitant connective tissue disorder, or an associated malignancy
  • EM variants: Stevens-Johnson syndrome, Toxic epidermal necrolysis
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11
Q

Vitiligo

A
  • Localized loss of pigmentation
  • Due to autoimmune destruction of melanocytes by toxic intermediates of melanin production or by neurochemical factors
  • Associated with autoimmune disorders, such as Graves disease and Addison disease
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12
Q

Albinism

A
  • Congenital lack of pigmentation
    (1) Ocular albinism: melanin dysfunction limited to the eyes; X-linked disorder
    (2) Oculocutaneous albinism: involves eyes, skin, and hair; predisposes to actinic keratosis, basal and squamous cell carcinoma, and malignant melanoma; most often autosomal recessive
  • Tyrosine-negative albinism - failure of conversion of tyrosine to DOPA
  • Tyrosine-positive albinism - unknown etiology
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13
Q

Freckle

A
  • Increase of melanin pigment within basal keratinocytes - melanosomes
  • Darkens when exposed to sunlight
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14
Q

Lentigo

A
  • Pigmented macule caused by melanocytic hyperplasia in the epidermis
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15
Q

Melanocytic nevus

A
  • Lesion classified as a benign tumor or hamartoma
  • Nevus cells are derived from melanocytes and ordinarily occur in cluster or nests
    (1) Juntional nevus: confined to the epidermal-dermal junction, most common mole in children
    (2) Compound nevus: both at the epidermal-dermal junction and in the dermis
    (3) Intradermal nevus: cinfined to clusters within the dermis, most common mole in adults
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16
Q

Blue nevus

A
  • Pigmented nevi that are present at birth

- Characteristically include nodular foci of dendritic, highly pigmented melanocytes in the dermis

17
Q

Spitz nevus

A
  • Most often occurs in children
  • Generally benign, although an atypical variant with borderline behavior exists
  • Often characterized by spindle-shaped cells and can be confused with malignant melanoma
18
Q

Dysplastic nevus

A
  • Atypical, irregular pigmented lesion with disorderly proliferation of melanocytes, dermal fibrosis, and often subjacent dermal lymphocytic infiltration
  • May transform into malignant melanoma
  • Familial in some cases - autosomal dominant inheritance
19
Q

Lentigo maligna

A
  • Nonfamilial precursor to lentigo maligna melanoma
  • Irregular macular pigmented lesion on sun-exposed skin
  • Characterized by atypical melanocytes at the epidermal-dermal junction
20
Q

Molluscum contagiosum

A
  • Contagious viral disorder that occurs most often in children and adolescents
  • Firm, pink, umbilicated, dome-shaped papules due to a DNA poxvirus
  • Transmitted by direct contact
21
Q

Verruca vulgaris

A
  • Common wart
  • Benign papilloma caused by certain strain of HPV (3 and 10?) infection of keratinocytes
  • Flesh-colored papules with rough surface
  • Vacuolated cells (kilobytes) in the granular cell layer of the epidermis are characteristic
  • Hands and feet are common locations
22
Q

Cellulitis

A
  • Deeper (dermal) infection
  • Usually due to S. aureus or S. pyogenes
  • Presentss as a red, tender, swollen rash with fever
  • Risk factors: recent surgery, trauma, insect bite
  • Can progress to necrotizing fasciitis
23
Q

Staphylococcal scalded skin syndrome

A
  • Sloughing of skin with erythematous rash and fever
  • Leads to significant skin loss
  • Due to S. aureus infection
  • Exfoliative A and B toxins result in epidermolysis of stratum granulosum
24
Q

Actinic keratosis

A
  • Premalignant epidermal lesion caused by chronic excessive exposure to sunlight
  • Characterized by roughness, scaling, poorly demarcated plaques on the face, neck, upper trunk, or extremities
25
Q

Acanthosis nigricans

A
  • Epidermal hyperplasia with darkening of skin (‘velvet-like’ skin)
  • Sometimes a marker for visceral malignancy (stomach, lung, breast, uterus) and is often seen in the setting of diabetes and other endocrinopathies
  • Characterized by acanthosis and hyperpigmentation
26
Q

Xanthoma

A
  • Most often associated with hypercholesterolemia
  • Characterized by yellowish papules or nodules composed of focal dermal collections of lipid-laden histiocytes
  • Occurs most frequently on the eyelids
27
Q

Hemangioma

A
  • Capillary hemangioma: small, blood-filled capillaries lined with a single layer of endothelium
    (1) Port-wine stain - purple-red area on the face or neck
    (2) Strawberry hemangioma - bright-red raised lesion
    (3) Chery hemangioma - small, domed-shaped red papule
  • Cavernous hemangioma: large, endothelium-lined spaces in the dermis and subdermis
28
Q

Squamous cell carcinoma (skin)

A
  • Common malignant skin tumor
  • Most often locally invasive; fewer than 5% of tumors metastasize
  • Associated most often with excessive exposure to sunlight
  • Other risk factors: albinism, xeroderma pigmentosum, immunosuppressive therapy, arsenic poisoning, chronic inflammation
  • Usually involves sun-exposed areas - face and back of hands, lower part of face - lower lip
  • Presents as scaling, indurated, ulcerated nodule
  • Invasion of dermis by sheets and islands of neoplastic epidermal cells, often with keratin “pearls”, is characteristic
29
Q

Basal cell carcinoma (skin)

A
  • Most common of all malignant skin tumors
  • Risk factors: exposure to sunlight (UVB), albinism, and xeroderma pigmentosum
  • Presents as pearly papule, often with overlying telangiectatic vessels
  • Characterized by clusters of darkly staining basaloid cells with a typical palisade arrangement of the nuclei of the cells at the periphery of the tumor cell clusters
  • Tends to involve the upper part of face - upper lip
  • Can be locally aggressive, ulcerate, and bleed
  • Matastasis is rare
30
Q

Malignant melanoma

A
  • Malignant neoplasm of melanocytes
  • Most common cause of death from skin cancer
  • Risk factors: exposure to sunlight, albinism, xeroderma pigmentosum
  • Recognized as mole-like growth with ‘ABCD’: Asymmetry, Borders are irregular, Color is not uniform, Diameter>6mm
  • Characterized by two growth phases:
  • Radial growth horizontally along epidermis and superficial dermis
  • Vertical growth into deep dermis (higher risk of metastasis)
  • Four major subtypes of melanoma:
    (1) Lentigo maligna melanoma - radial growth
    (2) Superficial spreading melanoma - most common subtype, radial growth
    (3) Nodular melanoma - vertical growth, push the epidermis up; poorest prognosis of the subtypes
    (4) Acral-lentiginous melanoma - arises on palms or soles, often i dark-skinned persons. Not related to UV-light exposure
31
Q

Dermatomyositis

A
  • Skin and muscle inflammatory disorder
  • Skin rash - liliac discoloration of the upper eyelids with periorbital edema
  • Grotton lesions - scaling red patches over the knuckles, elbows, knees
  • Muscle weakness (proximal parts)
  • Interstial lung disease, dysphagia, vasculitis, etc.
  • 40% of adult patients have cancer