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46 Cards in this Set

  • Front
  • Back
Skin Phototypes
I - Pure white - tender sunburn, no tan
II - Pure white - tender sunburn, light tan
III - White - non-tender sunburn, dark tan
IV - Beige - No sunburn, dark tan
V - Brown - no sunburn, dark tan
VI - Black - no sunburn, dark tan
Common Melanocytic Nevus

AKA, when appears
AKA - Mole
Appear - early childhood, disappear by age 60
Junctional Common Melanocytic Nevus
macular, brown, pigment is in epidermis
Compound Common Melanocytic Nevus
elevated, tan to brown color, pigment is epidermal & dermal
Dermal nevus
flesh-colored as pigment is in the dermis, elevated
Congenital Nevus
pigmented lesion present at birth, rare varieties become apparent within first 12 months of life
Congenital Nevus

Management (Small CN <1.5 cm)
Should be excised as soon as possible
Congenital Nevus

Management (Large CN >1.5 cm)
Excise before age 12 even if not obviously dysplastic
Congenital Nevus

Management (Giant)
Prognosis
remove as soon as possible

Prognosis: poor if melanoma develops
ABCDE of Moles
A - Asymmetry - in shape
B - Borders - are irregular
C - Color - is mottled, shades of brown, black, gray, red & white
D - Diameter - usually large (>6 mm)
E - Enlargement -
Dysplastic Nevus Syndrome
-arise in childhood, before puberty
-increased number of moles in sun-exposed areas
-moles also present in non sun-exposed areas
Dysplastic Nevus Syndrome

Incidence
-Almost all patients with familial cutaneous melanoma
-30-50% of patients with sporadic primary melanoma
5% of general white population
Familial Atypical Mole & Malignant Melanoma
(FAMMM)
Essentially dysplastic nevus syndrome with 2 blood relatives with melanoma
Benign pigmented nevi

Treatment
monitoring, excision if cosmetically undesired, laser
Dysplastic nevi

Treatment
-Surgical excision (do not laser or freeze)
-Monitoring by patient monthly and provider annually
Predisposing Factors for Melanoma
-Prescence of precursor lesions
-Family history
-Phenotype (Blonde or red hair, blue or green eyes, lighter skin type, freckling tendency(
-hx of blistering sunburns
-increased sun exposure
Halo nevi
synonymous with Sutton's nevus or Leukoderma acquisitum centrifugum
Halo nevi

Etiology
due to circulating cytotoxic antibodies
Superficial Spreading Melanoma
-Account for 70% of all melanomas
-Evolves over a period of 1-5 years
-2% occur in phototypes V & VI
Nodular Melanoma
-Accounts for 16% of all melanomas
-Age - Median 50 years
-Prognosis -- worse than superficial spreading melanoma
Nodular Melanoma

Evolves when
Evolves over 6-18 months

Rarely associated with nevus remnant
Lentigo Maligna
Flat, macular, intraepidermal neoplasm and the precursor or evolving lesion of Lentigo Maligna Melanoma (LMM)
Lentigo Maligna

AKA
Hutchinson's nevus,
Hutchinson's freckle,
Melanoma in situ
Lentigo Maligna

Age affected, who affected
-Median age is 65
- = in males & females
-older population with increased sun exposure
Lentigo Maligna Melanoma
-5% of all melanomas
-Age = 7th decade
-Occur on head and neck
-May take 20 years to evolve from Lentigo maligna
Acral Lentiginous Melanoma
-2-8% of all melanomas
-Age - 65 years old
-Males > Females
Acral Lentiginous Melanoma
very common in American & African blacks & Japanese
Acral Lentiginous Melanoma

Evolution & Prognosis
Evolves over 2-5 years

Prognosis - survival rates for volar type are less than 50%
-Subungual (nail) type has 5 year survival rate of 80%
Stages of Melanoma
Stage 1 - localized dz with no clinically palpable nodes
Stage 2 - palpable regional lymph nodes
Stage 3 - presence of distant metastasis
Metastatis Melanoma
Local - within 5 cm of primary site
Intransit metastases - >5cm from primary site
Metastaic Melanoma

Melanogenuria
generalized blue-gray cutaneous discoloration, may be accentuated in sun-exposed areas of skin
Oral Leukoplakia
sharply defined, white, macular, slightly raised area, cannot be rubbed off, remains after irritant removed
Oral Leukoplakia

Predisposing Factors
-tobacco
-alcohol
-HPV Types 11 & 16
Oral Leukoplakia

Prognosis
-10% progress to malignancy
-on the floor of mouth, more likely to progress to squamous cell carcinoma
Actinic Keratosis
single or multiple, discrete, dry, rough, adherent, scaly lesions on habitually sun-exposed skin
Actinic Keratosis

Common in....
-middle age men
-skin types I, II, III
-outdoor workers, sportspersons
Basal Cell Carcinoma

Predisposing Factors
-Most common type of skin cancer

Predisposing Factors
-Phototypes I & II
-Prolonged sun exposure
Basal Cell Carcinoma

Treatment
-Excision with primary closure, skin flaps or grafts
-Cryosurgery, curettage, electrosurgery
-Imipuimod
Squamous Cell Carcinoma
Malignant tumor of skin & mucous membranes
Squamous Cell Carcinoma

Predisposing factors
HPV
Immunosuppression
PUVA
Scars
Chronic ulcers
Discoid Lupus
Bowen's Disease
Usually a solitary lesion on exposed skin
Bowen's Disease

Description
Slowly enlarging, erythematous macule, sharp border, little or no infiltration, slight scaling
Bowen's Disease

Treatment
-Excision
-Moh's surgery in difficult sites
-Cryotherapy
-Efudex
-Imiquimod
Erythoplasia of Queyart
Clinically & histologically resembles Bowen's disease but occurs on penis
Invasive Squamous Cell Carcinoma
Fleshy, granulating, friable, crusted nodules

-Has capacity to metastasize
Invasive Squamous Cell Carcinoma

Treatment & Prognosis
Excision
Accutane

Prognosis -- SCC has remission rate after therapy of 90%