Russell Derm Pathology

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Can you name the Russell Derm Pathology ?

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Indurated, scaling, erythematous papules, nodules or plaques that occasionally ulcerate and bleed. Often develops in preexisting actinic keratosis
Well-defined, painless, pearlescent nodule in sun-exposed area of older people. The margin is pink with telangiectasias. The most common malignancy of the skin and the entire body.
Extension of lentigo maligna (intraepidermal) into the dermis. Long RADIAL GROWTH PHASE.
Clark's Level____: Invasive into the subcutaneous fat. High risk of metastasis.
Melanoma warning signs are Asymmetry, Border, Color, Diameter, and _____
Histological features are clusters of small, darkly staining basaloid tumor cells invade dermis. Palisading at the periphery of tumor nests. Bluish myxoid stroma.
Extreme hyperkeratosis in Actinic Keratosis may cause development of a cutaneous ______.
_____ skin: Large, singly dispersed melanosomes in keratinocytes. Many stage IV melanosomes.
Histological features are acanthosis, horn cyst, and hyperkeratosis.
Flesh-colored, pedunculated tags of skin in the neck, axilla, groin, or under a woman's breast
Spectrum of disorders characterized by increased numbers of mast cells in the skin and occasionally in other organs. Round to oval, red-brown non-scaling multiple prurituc papules
Dermal edema resembling a hive occurs in normal skin as a result of localized stroking with a pointed Instrument.
Histological features are club-shaped elongated rete ridges, basal hypermelanosis and an increased number but no nesting of melanocytes. Solar elastosis (damaged elastin fibers) in
Besides lentigines, _____ patients develop benign hamartomatous gastrointestinal polyps, mostly in the jejunum, but the entire bowel may affected.
The current lifetime risk for developing invasive melanoma in the US is 1:___, a 2000% increase since 1930
Clark's Level ___: Tumor fills the papillary dermis and pushes against the reticular dermis.
Multiple sebaceous adenomas and sebaceous carcinomas associated with hereditary nonpolyposis colorectal carcinomas.
A melanocyte-specific enzyme required for melanin synthesis
_____ blue nevus: must be biopsied to rule out melanoma
Flat, usually small (0.5cm) macule. Clinically insdistinguishable from junctional nevus.
Spitz Nevus: ______ Stain. The positively staining cells in the epidermis are Merkel cells.
Large, usually unilateral hyperpigmented, hypertrichotic (=hairy) patch on the shoulder or chest
Type of melanoma that develops on lower extremities and back. 70% of cases. Peak incidence in 4th and 5th decade.
Activation of _____ by keratinocyte-derived alpha-MSH (melanocyte stimulating hormone) stimulates melanogenesis, melanocyte differentiation and transfer of melanosomes to keratinoc
Extremely common dermal fibrous tumors. Tends to occur on exposed sites on the limbs and the upper back, especially over the scapula.
Autosomal dominant trait associated with germline activating mutations in FGFR3. Thickened, hyperpigmented skin with velvety appearance.
MUTATIONS that diminish the activity of the retinoblastoma (RB) tumor suppressor proteins and ____ tumor suppressor protein are common in both familial and sporadic melanomas
Localized area of dermal edema and erythema (wheal) that occur when lesional skin is rubbed.
White macules, 2-6mm in diameter. Idiopathic. Once formed, macules do not increase in size. Decreased number of melanocytes with decreased amount of melanin.
A pale nodule with a central pore. A sphere of epidermis gets oriented inward and buried within the skin.
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Histological features are fibrohistiocytic tumor with a storiform growth pattern, trapped subcutaneous fat, and tumor invades subcutaneous fat.
____ skin: Mostly small melanosomes. Melanosome-comples aggregates are rapidly degraded in keratinocytes. Few stage IV melanosomes.
Symmetrical cup-shaped umbilicated tumor with a central depression filled with keratin.
Excessive ___ exposure, particularly early in life, is the single most important risk factor for malignant melanoma.
Light brown pigmented macule with many dark brown small, scattered macules (2-3mm) and papules on pigmented background. May be very large >15cm. Less common than junctional or comp
Partial _____ in melanoma is an unfavorable prognostic sign.
Histologic features are lentiginous proliferation of melanocytes at the epidermal-dermal junction, single melanocytes with nuclear atypia, no upward scatter of melanocytes into the
Skin tumor with the worst prognosis.
Type of melanoma. Malignant cells only in epidermis.
Not all nevi become melanomas because of ________
The risk of malignant melanoma rises to 1:__, if melanoma in-situ is included
Benign neoplasms composed of melanocytes, which are neural crest-derived cells that migrate to the epidermis during embryogenesis. Symmetrical, well-circumscribed, small flat macul
______ Type Basal Cell Carcinoma: Locally destructive with deep invasion into the underlying stroma. Often requires repeated excisions.
The most common epithelial skin tumor; most people >50 have them. 'Stuck on' appearance. Benign tumor of keratinocytes.
Type of melanoma with no radial growth and invades the dermis directly. 15-30% of cases. Poor prognosis
Type of melanoma located on the palm, sole, or under the nail. Differential diagnosis: subungual hematoma.
_____ nevus: Histologic features are similar to acquired compound nevus.
Melanoma and nonmelanoma skin cancers. Defective Nucleotide Excision Repair (NER) leads to an inability of cells to repair DNA damage induced by exposure to UV light and some chemi
The most common benign sun-induced lesion
Lifetime risk of developing melanoma approaches 80-100%
Most common melanoma in patients of African, Hispanic, and Asian descent. Mortality rate is 80-90% within 3-4 years.
Histologic features are non-nested proliferation of highly dendritic heavily pigmented melanocytes surrounded by fibrosis.
Small, 1 to several mm in diameter, tan-red or light brown macules. The most common pigmented lesions in fair-skinned and/or red haired individuals.
Name a feature used to estimate the probability of metastatic spread of melanoma.
angiofibromas; mental retardation
Autosomal recessive disorder with a defect in nucleotide excision repair
Intensely pruritic, polygonal papular eruption with violaceous color and sometimes fine scales
Present at birth. Often much larger than acquired nevi, measuring more than 1.5cm in diameter, occasionally greater than 20cm.
An autoimmune inflammatory response to an unknown antigen in a nevus results in the disappearance of the nevus. The usual patient is less than 20 years old. Back is the typical loc
Larger than most acquired nevi, often larger than 6mm in diameter. Important signs are size, irregular pigmentation, irregular borders, and accentuated surface.
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Encodes a regulator of melanocortin receptor signaling
Brown-black pigment, Absorbs UV light at 200-1200nm. Protects from UV damage.
Firm solid nodule arising most frequently on the trunk. Often develop as aggregated 'protuberant' tumors with a firm indurated plaque or nodule that may sometimes ulcerate.
Multiple, small, hyperpigmented, asymptomatic papules on the face of >35% of adult African Americans. Appear at puberty. Histologically resembles seborrheic keratosis. Benign.
Associated with genomic instability including imbalance of telomere-telomerase complex and dicentric chromosomes (2 centromeres). Causes Cardiac Myxomas.
Yellow-red pigment. More photolabile than eumelanin. Causes photosensitivity.
Histologic features are elongated rete ridges, increased number of melanocytes in the basal layer. Increased amount of pigment in the keratinocytes.
Heavily pigmented, blue black nodule with smooth surface. Often confused with nodular melanoma.
Benign follicular appendage tumors (trichilemmomas); internal adenocarcinoma (often breast)
Histological features are epithelial collarette, central keratin filled 'crater' and prominent dermal inflammatory reaction. Keratinocytes with glassy, keratinized cytoplasm.
Histological features are hyperkeratosis, acanthosis, and benign fibrohistiocystic proliferation.
Clinically indistinguishable from junctional nevus.
multiple basal cell carcinomas; jaw cysts, etc.
Histological features are hyperkeratosis, prominent rete ridges, basal hyperpigmentation, and no melanocyte hyperplasia.
_____ growth phase: invasion of malignant cells into the dermis and vessels.
Cutaneous or subcutaneous, usually solitary pink, red, violet, or reddish- brown dome-shaped papule, nodule, or tumor (0.5-5 cm) . Head and extremities (sun-damaged skin) are the m
______ Tumors: Apocrine carcinoma, Cylindroma, Pilomatrixoma, Trichilemmoma, Trichoepithelioma, Sebaceous adenoma and carcinoma.
Pinching causes depression in the center. More common in women.
_____ growth phase: lateral spread of malignant cells in epidermis and papillary dermis
Hard, spiky, white keratosis on sun- exposed skin often accompanied by telangiectasia
_____ syndrome is the leukemoid form of mycosis fungoides with CD4+ T-helper tumor cells in the peripheral blood.
1-12 mm lentigines around the mouth, on the lips, and on the buccal mucosa, and also on fingers and toes on both the palmar and volar surfaces; absent from the flexor and extensor
Small, skin colored dome-shaped nodule. Benign.
Histological features are hyper and parakeratosis, inflammatory infiltrate in dermis, acanthotic, dysplastic epidermis, and solar elastosis in dermis.
_______ blue nevus: if present for a long time, does not need to be biopsied.
Mutation of _____ gene causes phenotype of red hair, light skin, inability to tan.
______ Measurement of Melanoma: Ocular micrometer is used to measure the thickness of the lesion from the stratum granulosum to the greatest depth of tumor invasion.
Histological features are intercellular bridges, keratin, and atypical mitosis.
Usually large, more than 6mm. Most are 10mm at diagnosis. Upward infiltration into the upper epidermis may not be conspicuous.

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Created Apr 21, 2012ReportNominate
Tags:pathology, russell