A. Evaluation of Dermatologic Lesions
- There are over 1000 distinct dermatologic entities
- There are <20 distinct skin lesions
- Goal is to classify major lesion(s) to limit differential diagnosis
- Consider accompanying symptoms, including systemic complaints
- Major Lesion Types
- Bullae
- Vessicles
- Purpura
- Plaques - consider psoriasis
- Waxy Lesions - seborrheic dermatitis
- Pruritic Lesions - atopic dermatitis
- Scales - type and pattern of scales
- Target Lesions
- Erythromelalgia
- Examination of hair, nails, mucous membranes is part of dermatologic evaluation
B. Definitions
- Macule: flat lesion on skin (neither elevated nor depressed)
- Papule: small solid elevation <0.5cm diameter
- Plaque: raised or depressed lesion >0.5cm diameter
- Wheal: whelt; circumscribed area of edema of skin, usually red, usually pruritic
- Nodule: a small (<0.5cm), raised, solid, circular structure, penetrates into dermis
- Vesicle: small, raised circumscribed elevation of skin (blister) containing fluid
- Bullae: a large vesicle (>0.5cm) with circumscribed area of separation from epidermis
- Erosion: shallow ulcer, generally without bleeding
- Pustule: vesicle containing dead neutrophils and bacteria (pus)
- Petechiae: due to capillary rupture/bleeding, 1-3mm purple macules
- Hyperkeratosis
- Increase in thickness of stratum corneum; seen as a scale
- May retain basketweave pattern, or become dense and compact
- Papillomatosis
- Epidermal and papillary dermal proliferation upward
- Occurs in irregular waves or spikes
- Parakeratosis: retention of keratinocytic nuclei in stratum corneum
- Squamous eddies (pearls): concetric layers of squamous cells with increasing central keratinization
- Verrucous (Verrucose): resembling a wart; roughened, irregular or filiform surface
C. Bullae
- Upper Epidermis
- Pemphigus Vulgaris
- Scalded Skin Syndrome (Staphylococcal)
- Subepidermal
- Erythema Multiforme
- Stevens-Johnson Syndrome
- Toxic Epidermal Necrolysis
- Bullous Pemphigoid
- Herpes Gestationes
- Cicatricial pemphigoid
- Lupus erythematosus
D. Vesicles
- VZV
- Chicken Pox
- Shingles
- Contact Dermatitis
- Dermatitis Herpetiformis
- Herpes simplex virus (HSV)
- Drug eruption
E. Purpura
- Definition: non-blanching erythema
- Palpable Purpura
- Rocky Mountain Spotted Fever
- Meningococcemia and Gonococcemia
- Bacterial Endocarditis
- Obliterative Vasculitis - cryoglobulinemia, hypersensitivity vasculitis, others
- Drug Reaction
- Atrial Myxoma
- Non-Palpable Purpura
- Disseminated Intravascular Coagulopathy (DIC)
- Scurvy [1]
- Purpura due to anticoagulants
- Glucocorticoid (steroid) induced purpura
- Senile purpura
- Vasculitis
- Inflammation of blood vessel walls
- Extravasation of blood and inflammatory cells into surrounding tissue
- ANCA Related: PAN, Wegener's Granulomatosis, Behcet's Disease, others
- Henoch-Schonlein Purpura and Hypersensitivity
- Infectious, associated with immune complexes: bacterial endocarditis, others
- Occlussive Disease: Cryoglobulinemia, Cholesterol Emboli,
- Most of these cause a palpable purpura
- Disseminated Intravascular Coagulopathy (DIC) often causes a non-palpable purpura
F. Common Dermatologic Findings
- Common Acne
- Rosacea
- Psoriasis
- Hives
- Nail Changes
- Xanthelasma
- Bright yellow, sharply marginated plaques
- Usually on eyelids, may also occur on external ear areas
- Usually found in patients with lipid disorders
- Seborrheic Dermatitis
- Waxy, inflammatory dermatitis
- Waxy scales, "dandruff", redness in nasolabial fold and eyebrows
- Most common in persons 30-60 years of age
- Eczematous Dermatitis
- Definition: ill defined erythematous scaly plaques ± pruritus
- Erythema with irritation and dryness
- Pruritus may be prominent; localized edema
- Actinic Keratosis (AK) [2]
- Synonyms: Solar Keratosis, Solar Elastosis, Senile Keratosis
- Types: Pigmented AK and Non-pigmented AK
- Rough, faintly erythematous, slightly raised skin lesions
- Most frequently on face and hands (sun exposed area)
- Overall very slow progression to frank invasive cancer
- ~1:1000 progress each year to squamous cell cancer
- Cafe-au-lait Spots (Macules)
- Found in ~10% of normal persons
- Neurofibromatosis (NF) - diagnostic for NF if >5 macules with diameter >1.5 cm
- Polyostotic Fibrous Dysplasia (Albright's Syndrome)
- Dermatophytosis [6]
- Superficial fungal infections - erythematous and scaly
- Fungal mycelia detected by exam of material from border of rash
- Diagnosis made with KOH (potassium hydroxide) preparation of skin scarping
- Athlete's Foot - Tinea pedis
- Jock Itch - Tinea cruris
- Scalp Infection - Tinea capitis
- Tinea versicolor (pityriasis versicolor) - pigmentary disorder, usually in tropics
- Piedra - asymptomatic fungal infection of hair shaft
- Tinea nigra - common in tropical regions outside of US and Europe
- Melasma (Chloasma)
- Hyperpigmentation usually on face
- Associated with pregnancy and/or taking progestational agents
- Pigment is light tan to very dark brown
- Milia
- Collection of 1-2mm white, hard, rounded, superficial papules
- Usually occur on the face
- Lesions contain keratinous contents (can be found by lancing)
- Senile Angioma
- Also called "cherry red spot"
- Usually occurs in persons age 20-30
- Found on lip or trunk
- Usually 2-3 mm bright red, globular papules
- Senile Lentigo ("liver spots")
- Single or group of well circumscribed macules
- Usually light yellowish brown due to increase in melanocyte numbers
- May gradually develop, over many years, into melanoma
- Therefore, lentigos which change in shape or color should be evaluated
- Spider Nevus
- Central, punctate, bright red macule or papule
- Fine red lines radiate out (similar to spider legs)
- On compression, central body pulsates (blanches)
- Most commonly found in patients with portal hypertension (usually cirrhosis)
- Dermatofibroma
- Isolated, slightly elevated, hard, button-like nodules
- Usually discolored and <1cm in diameter
- Lateral compression leads to dimpling or depression of dermatofibroma
- May be confused with melanoma (lateral compression raises melanoma)
- Skin Ulcers
- Pressure ulcers
- Lower extremity - common in diabetes mellitus
- Venous stasis - particularly in patients with congestive heart failure
- Keloids and Hypertrophic Scars [4]
- Very common abnormalities in wound healing
- Due to excess accumulation of collagen in scar
- Fibroblasts do not regulate collagen synthesis properly
- Fibroblast proliferation is abnormally increased
- Increased levels of and/or responses to IGF-1, TGFß, and IL-1 have been noted
- Fetal wounds heal rapidly without scarring and express little or no TGFß
- Therefore, TGFß is believed to play a central role in scar formation
MISCELLANEOUS DERMATOLOGIC CONDITIONS |
G. Erythromelalgia- Characteristics
- Intense burning pain, increased cutaneous temperature of skin
- Intesne, diffuse, erythema of skin, usually lower extremities, no arterial compromise
- Precipitation of symptoms by heat and gravity
- Relief of symptoms by cooling and elevation
- Very uncommon disease
- Associated Diseases
- Myeloproliferative disease with thrombocytosis
- Rheumatologic: systemic lupus, rheumatoid arthritis, vasculitis
- Pregnancy
- Idiopathic
- Treatment - single dose of aspirin 500mg
H. Ichthyosis
- Dry, scaly skin
- Hereditary and acquired forms
- May be paraneoplastic (usually acquired type)
- Very uncommon disease
I. Sweet's Syndrome [5]
- Acute febrile neutrophilic dermatosis
- Associated Conditions
- Malignancy - acute myelocytic leukemia (AML) most common
- Infection - Yersinia, Chlamydia, Mycoplasma, Toxoplasma
- Drug reaction
- Neutrophil overproduction - as with granulocyte stimulating factor (G-CSF, Neopogen®)
- Autoimmune disease
- Symptoms
- Erythematous rash - well demarkated papules and plaques, dense white cell infiltrates
- Sudden onset fever
- Neutrophilia
- Endomyocarditis including valve insufficiency and cardiomyopathy can occur
- Diagnosis
- Neutrophilia
- Rash with neutrophilic infiltrates
- Fever must be present
- Cardiac assessmentwith echocardiograqphy and/or endomyocardial biopsy
- Treatment
- Antibiotics - to cover above organisms; doxycycline 100mg po bid
- Glucocorticoids - prednisone 40mg qd or equivalent
- Continue treatment for ~14 days or until symptoms fade
- Glucocorticoid taper as required
References
- Meisel JL and Mark EJ. 1995. NEJM. 333(25):1695 (Case Record)
- Fluorouracil. 1993. Med Let. 35(907):97
- Chren MM and Landefeld S. 1994. JAMA. 272(24):1922
- Singer AJ and Clark RAF. 1999. NEJM. 341(10):738
- Dorenkamp M, Weikert U, Meyer R, et al. 2003. Lancet. 362(9393):1374 (Case Report)
- Schwartz RA. 2004. Lancet. 364(9440):1173