DD- COMMON SKIN TUMORS (BENIGN) Flashcards

(37 cards)

1
Q

Typically arise in middle age
MOST common vascular tumor in adults
Generally no association with underlying disease
Usually on the trunk

A

Cherry HemangiomasSENILE CHERRY ANGIOMAS

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2
Q

Cherry Hemangiomas Treatment

A

Superficial electrodesiccation

Liquid nitrogen followed by curettage

Shave biopsy

Pulse dye laser- best for small lesions

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3
Q

The most common soft tissue tumor of infancy (10-12% of infants)
Benign endothelial cell neoplasm

A

Infantile Hemangioma
CAPILLARY HEMANGIOMA

other names:STRAWBERRY HEMANGIOMA, CAPILLARY HEMANGIOMA

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4
Q

Infantile Hemangioma- Complications

A
Ulceration 
Size- may obstruct vision or feeding 
Congenital syndromes (PHACES)
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5
Q

Infantile Hemangioma- Treatment Options

A

Observation

Local wound care

Pulsed dye laser

Topical, intralesional and systemic steroids

Beta-blockers

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6
Q

Stain with Glut-1, a placental antigen
More common in:
Girls
Premature infants

A

Infantile Hemangioma

STRAWBERRY HEMANGIOMA, CAPILLARY HEMANGIOMA

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7
Q
Vascular malformation
Present at birth
Persists into adulthood
Often irregular vascular channels that do NOT stain with Glut-1
Somatic mutation in GNAQ
A

Port Wine Stain

CAPILLARY MALFORMATION

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8
Q

Port Wine Stain- Complications

A

Overgowth of an extremity covered by a large port wine stain

Varicose veins, venous stasis, edema, ulceration

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9
Q

Port Wine Stain Treatment

A

Pulsed dye laser

Why treat?
Persist into adulthood
Get worse with time
Dark purple, nodular, bleeding blebs

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10
Q

Often only a precursor lesion is noted at birth, occasionally fully formed
Rapid proliferation in the first 1-3 months of life
Spontaneous involution over years

A

Infantile Hemangioma

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11
Q

Stain with Glut-1

A

nfantile Hemangioma

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12
Q

do NOT stain with Glut-1

A

Port Wine Stain

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13
Q

Hemangioma vs Port Wine gender

A

Hemangioma - girls

Port Wine- none

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14
Q

Klippel-Trenaunay syndrome

A

Port Wine on legs

may cause edema

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15
Q

Sturge Weber Syndrome

A

Port Wine on face

ocular and neurologic abnormalities including glaucoma, seizures and developmental delay

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16
Q

hamartoma
presents as a papillomatous yellow-orange plaque on face/scalp

Somatic mutations in HRAS and KRAS

A

Nevus Sebaceus

17
Q

Nevus Sebaceus

A

enlargement of sebaceous glands

18
Q

Nevus Sebaceus Treatment Options

A

Observation

Surgical excision

19
Q

Common benign tumor of oil gland
Increasing frequency after middle age

Distribution- face>trunk>extremities

A

Sebaceous Hyperplasia

20
Q

Sebaceous Gland HyperplasiaTreatment

A

No treatment

cosmetic issue only

21
Q

Acrochordon

SKIN TAGS, FIBROEPITHELIAL POLYPS

A

Common- ¼ of all adults have at least one
Solitary or multiple

Soft, flesh-colored tan to brown exophytic papule (1-4 mm) with narrow base

22
Q

benign tumor of adipose tissue.
It is the most common form of soft tissue tumor.
oft to the touch, usually movable, and are generally painless.

23
Q

Lipoma Treatment options

A

No treatment

Surgical excision

24
Q

Positive dimple (Fitzpatrick) sign
Complications- pain, pruritus
Distribution- legs
Typically solitary

A

Dermatofibroma

25
It is a result of an overgrowth of granulation tissue (collagen type 3) at the site of a healed skin injury which is then slowly replaced by collagen type 1.
Keloid Scar
26
Keloid Scar Rx
Topical steroids under occlusion Intralesional steroids Surgical excision: works best for ear keloids Surgery +/- Radiation
27
Seborrheic Keratosis are called?
“Barnacles of Life” Benign tumor of the hair follicle Distribution- primarily head, neck, trunk
28
Seborrheic Keratosis | Clinical Variants
Dermatosis papulosa nigra Stucco keratosis Inflamed seborrheic keratosis Sign of Leser-Trélat
29
Benign tumor of the hair follicle | Distribution- primarily head, neck, trunk
Seborrheic Keratosis
30
Seborrheic Keratosis Treatment
Moisturizers | Cryosurgery- treatment of choice
31
Infancy to adulthood Any skin surface including mucous membranes increased on sun-exposed skin
Nevocellular Nevi
32
Junctional Nevus are typically?
Flat macules
33
Compound Nevus are typically?
Papual/Nodule Dark on Trunk
34
Nevocellular Nevi | Treatment Options
Appropriate Shave biopsy Punch biopsy Excision
35
Dysplastic Nevus
Acquired melanocytic proliferation Round to oval to irregular Variegation in color- tans, brown, black, reds Margins- often indistinct
36
Neurofibromatosis Type 1: Diagnosis requires 2 or more of the following criteria
1. 6+ café au lait macules > 1.5 cm 2. 2+ neurofibromas, or 1 plexiform neurofibroma 3. Axillary or inguinal freckling 4. Optic glioma 5. 2+ more Lisch nodules 6. osseous lesion or thinning of the long bone cortex 7. FDR with the disorder
37
Subtle increase in number of melanocytes with increased melanin production Congenital or early childhood Distribution- trunk and proximal extremities Typically solitary Multiple lesions associated with NF
Café-au-Lait Spots