DD- COMMON SKIN TUMORS (BENIGN) Flashcards

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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.

A

Lipoma

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
Q

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.

A

Keloid Scar

26
Q

Keloid Scar Rx

A

Topical steroids under occlusion
Intralesional steroids
Surgical excision: works best for ear keloids
Surgery +/- Radiation

27
Q

Seborrheic Keratosis are called?

A

“Barnacles of Life”

Benign tumor of the hair follicle
Distribution- primarily head, neck, trunk

28
Q

Seborrheic Keratosis

Clinical Variants

A

Dermatosis papulosa nigra
Stucco keratosis
Inflamed seborrheic keratosis
Sign of Leser-Trélat

29
Q

Benign tumor of the hair follicle

Distribution- primarily head, neck, trunk

A

Seborrheic Keratosis

30
Q

Seborrheic KeratosisTreatment

A

Moisturizers

Cryosurgery- treatment of choice

31
Q

Infancy to adulthood
Any skin surface including mucous membranes
increased on sun-exposed skin

A

Nevocellular Nevi

32
Q

Junctional Nevus are typically?

A

Flat macules

33
Q

Compound Nevus are typically?

A

Papual/Nodule
Dark
on Trunk

34
Q

Nevocellular Nevi

Treatment Options

A

Appropriate
Shave biopsy
Punch biopsy
Excision

35
Q

Dysplastic Nevus

A

Acquired melanocytic proliferation
Round to oval to irregular
Variegation in color- tans, brown, black, reds
Margins- often indistinct

36
Q

Neurofibromatosis Type 1:

Diagnosis requires 2 or more of the following criteria

A
  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
Q

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

A

Café-au-Lait Spots