CIS Flashcards
Wickham striae and lichen planus
pruritic, purple, polygonal, planar, papules, and plaques
associated with Hep C
seboerreic keratosis-
never need to biopsy
white things coming out
What structure is most likely to have a different appearance in axillary skin?
Eccrine/apocrine sweat glands
Spongiosis seen in eczematous dermatitis develops in which area?
Stratum spinosum
Allergic atopic
“spongiotic dermatitis”
food, insect, light, drug, allergen testing
humoral mediation type I*
eosinophils prominent in inflammation
responds to topical steroids
history to differentiate from allergic contact
- family history of eczema, hay fever or asthma
Allergic contact “spongiotic dermatitis”
poison ivy, nickel, other metals, rubber compounds
T-cell mediated type IV*
lymphocyte rich inflammation
Will not respond to topical steroids
no inflammation until 2nd exposure; > 24 hr delay
Often topically applied antigens
Primary irritant “spongiotic dermatitis”
chemicals
no prior exposure as direct damage to epidermis
necrosis and ulceration with neutrophil response
- localized mechanical or chemical irritants (nonimmunologic)
drug-related eczematous dermatitis
- infiltrate ofen deeper with *abundant eosinophils
Temporal relationship to drug administration
photoeczematous eruption “spongiotic dermatitis”
occurs at sites of sun exposure, may require associated exposure to systemic or topical antigen
eczematous insect bite reaction
spongiotic dermatitis
wedge-shaped infiltrate; many eosinophiles
A 25 y/o female has been using lip balm continuously for months and the changes seen in the image are not improving. Presumptive dx? what to do?
Presumptive Diagnosis?
Allergic or irritant contact exfoliative cheilitis
What to do?
Stop using the lip balm and substitute moisturizer with limited ingredients and/or topical corticosteroid. Could consider cultures for S. aureus or C. albicans.
A 34 year old female developed a pruritic rash that involved the skin. Her dentist also noted bluish and reddish white lesions in the mouth.
Wickham striae and lichen planus
Topical steroids were used to control itching
and problems resolved after a few months.
Test to order for definitive diagnosis?
None, biopsy can be done for difficult cases.
What clinical entities are associated with this disorder and what is the pathophysiology?
Hepatitis C, ulcerative colitis, alopecia areata, vitiligo, dermatomyositis, morphea, lichen sclerosis and myasthenia gravis
It is a cell-mediated immune response of unknown origin.
Atrophy of which structure leads to “dry skin”?
Sebaceous gland
old skin?
Aging and chronic actinic skin damage
Sunburn
acute inflammation with pain, desquamation, blistering with secondary infections, chronic actinic skin damage including wrinkles, solar elastosis, solar lentigos, actinic keratoses, squamous cell carcinomas, basal cell carcinomas and melanomas
A 52 year old male presents with a new skin rash not responding to topical cortisone and moisturizers. During the physical examination the rash is diffuse and there is also axillary and cervical lymphadenopathy. Presumptive dx?
Presumptive Diagnosis?
Ichthyosis
What subtype?
** Ichthyosis vulgaris (autosomal dominant or acquired)
other types:
Acquired associated with hypothyroidism, sarcoidosis, lymphoma, visceral or generalized cancer, HIV or medications (e.g. nicotinic acid and hydroxyurea)
Congenital ichthyosiform erythroderma (recessive)
Lamellar ichthyosis (recessive)
X-linked ichthyosis
Test(s) to order for definitive diagnosis?
Search for underlying etiology and continue
topical treatment until underlying cause
is found and treated - CBC with diff, lymph node biopsy in this case of probable lymphoma
Newborn with blistering skin disease. Presumptive Diagnosis?
Epidermolysis bullosa
Supportive care with treatment of infections and contractions as they occur
Test to order for definitive diagnosis?
Skin biopsy to exclude other blistering disorders and electron microscopy to sub-classify the disease if epidermolysis bullosa is the diagnosis
I. Simplex type: keratin 14 or 5 mutation
Intraepidermal (suprabasilar) blisters
II. Junctional type: defect at lamina lucida (laminin or BPAG2 defects)
Intra-lamina lucida subepidermal blisters