Benign Neoplasms of the Skin Flashcards

1
Q

What are vascular tumors? What cell they arise from?

A
  1. Cherry angioma, endothelial cells

2. Infantile hemangioma, endothelial cells (from embolized placental cells or angioblasts)

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2
Q

What is an example of a vascular malformation?

A

Port wine stain

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3
Q

What tumors are from sebaceous glands?

A

Sebaceous Hyperplasia and Nevus sebaceous

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4
Q

What skin growths arise from melanocytes?

A

nevi, melanoma, ephelides (freckles), lentigo (sunspots), café au lait macule

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5
Q

What are clinical features of cherry angiomas?

A
  • mostly on the trunk
  • bright red, smooth-topped papules
  • can have 100’s
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6
Q

What are clinical features of infantile hemangioma?

A

-Most common soft tissue tumor of infancy (10-12%); benign endothelial cell neoplasm
-usually resolve by age 9
-

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7
Q

What are clinical features of a port-wine stain?

A
  • vascular malformations
  • they do not resolve spontaneously
  • Over time, the vascular malformation may worsen, changing from a pink patch to a thicker purple plaque with nodularity
  • Port wine stains may be associated with systemic abnormalities like Sturge Weber syndrome (SWS)
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8
Q

What is a Nevus sebaceus?

A
  • A hamartoma that most commonly presents as a papillomatous, yellow-orange linear plaque on the face or scalp.
  • Rapid growth at puberty
  • Lesions on the scalp are associated with ALOPECIA
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9
Q

What are clinical features of sebaceous hyperplasia?

A
  • Common benign tumor of oil gland.
  • Increases frequency after middle age
  • Distributes face >trunk> extremities.
  • Primary lesions 1-6mm yellowish-white papule with central dell.
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10
Q

What are acrochordons?

A

Little worm-like benign “skin tags”

-commonly occur in areas of rubbing including the neck, axilla and infra-mammary area in women

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11
Q

What cells do dermatofibromas arise from?

A

Fibroblasts

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12
Q

Clinical characteristics of dermatofibromas

A

-second most common fibrohistocytic tumor of the skin
(skin tags #1)
-Brown, firm papule usually 3-10mm.
-Typically acquired in adults and most common in legs.
-Dimple sign: pinch lesion and should see slight downward movement of tumor

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13
Q

What skin growths arise from keratinocytes? (hint: age spots)

A

Seborrheic keratosis

Yes these are the age spots, aka “barnacles of life”

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14
Q

What is the clinical appearance of Seborrheic keratosis?

A
  • oval, slightly raised, light brown to black papules or plaques.
  • most commonly located on the chest and back.
  • They are also commonly found on the scalp, face, neck and extremities
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15
Q

Are there three subtypes of seborrheic keratosis?

A

Yes
a. Dermatosis Papulosa Nigra: in black people

b. Stucco keratosis: found around the ankles, feet, forearms and dorsal hands
c. Sign of Leser-Trelat: Paraneoplastic syndrome reported to occur with the sudden onset of multiple seborrheic keratoses, associated with adenocarcinoma of the stomach in 60% and also associated with other common malignancies.

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16
Q

What is a compound nevi?

A

=when melanocyte nests are in DEJ and dermis

intradermal: exclusively in dermis
junctional: just at DEJ above basement membrane

17
Q

Name 3 types of nevus (not based on location)

A

Blue nevus
Congenital nevus:
Dysplastic nevus

18
Q

What is the criteria for diagnosing FAMM?

A
  • The occurrence of malignant melanoma in 1 or more first- or second-degree relatives
  • The presence of numerous (often >50) melanocytic nevi, some of which are clinically atypical
  • Many of the associated nevi showing certain histologic features
19
Q

What causes Café au lait macules?

A

Subtle increase in number of melanocytes with increased melanin production
•Distribution- trunk and proximal extremities

20
Q

What skin growths arise from neural cells? What do they look like?

A

Neurofibromas

•Soft flesh colored papules characterized by the “button hole sign”

21
Q

How is neurofibromatosis inherited?

A

•AD inheritance

  • 50% of cases due to spontaneous mutations
  • Defect in neurofibromin gene, a tumor suppressor, on chromosome 17 for NF-1
22
Q

How do you diagnose Neurofibromatosis?

A

2 or more of the following criteria:

  1. Six or more café au lait macules more than 1.5 cm in diameter
  2. Two or more neurofibromas, or 1 plexiform neurofibroma
  3. Axillary or inguinal freckling (Crowe’s sign)
  4. Optic glioma
  5. Two or more Lisch nodules
  6. Distinctive osseous lesion, such as sphenoid wing dysplasia or thinning of the long bone cortex
  7. A first degree relative (parent, sibling or child) with the disorder