Week 1 - Disorders of Cutaneous Pigmentation & Cutaneous Neoplasms Flashcards

1
Q

Neoplasms usually arise from. . .

A

the epidermis & the dermis

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2
Q

Dermis

A

Consists of collage/elastic fibers, peripheral nerves, muscle, fat, cartilage

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3
Q

Vitiligo

A

Partial or complete loss of melanocytes, well demaracated macules/patches, hand/wrist, axillae, perioral/periorbital, anogenital
Pathogenesis: autoimmune - T cells attack melanocytes of skin & destroy them - then you get hypopigmented cells

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4
Q

Neoplasia

A

Proliferation of genetically abnormal cells - clonal population or proliferation of cells that can escape the normal cell checkpoints

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5
Q

Cancer

A

Malignant Neoplasm

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6
Q

Benign vs. Malignant

A
Benign = can't metastasis
Malignant = has potential (does not have to) metastasize
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7
Q

Albinism

A

No melanin produced (or decreased melanin)
Inherited defect in tyrosinase!! (normal number of melanocytes)

-Congenital absence of enzyme and melanin is not made or is decreased

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8
Q

Stromal Neoplasms

A

Neoplasms involving connective tissue

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9
Q

Nevus (mole)

A

Benign neoplasms of melanocytes, congenital or acquired - most have mutations (BRAF most common)

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10
Q

How do we predict the probability of melanoma to metastasize?

A

Depth of invasion

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11
Q

What is Breslow’s depth?

A

It is the probability to metastasize that is predicted by depth of invasion of the melanoma

  • Measured in millimeters
  • Best indicator of probability to metastasize
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12
Q

Breslow’s depth

A

How deep melanoma invades into the dermis (measure from the granular layer to the lowest melanocyte)
-Best prognostic indicator!!

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13
Q

Sentinel lymph node biopsy:

A

Usually for melanomas > 1 mm in thickness - melanomas like to go to lymph nodes (they usually go here first - so if melanoma isn’t here, it usually hasn’t metastasized)

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14
Q

Breslow depth & Survival:

A

4 mm: 5 yr sur. is 37-50%

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15
Q

Next most imp. prognostic indicator (after Breslow depth for melanoma):

A

Ulceration (usually growing very fast), mitotic rate of cells

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16
Q

Squamous cell carcinomas

A

Almost all are sun-related (sometimes related to radiation)

17
Q

Basal cell carcinoma

A

Most common human malignancy - rarely metastasizes - risk factors include sun exposure, XP, light pigment - can be ulcerated, large papules on the nose

18
Q

Cowden’s syndrome & Muir Torre Syndrome - common symptom:

A

Adnexal neoplasms/proliferations: differentiate toward hair follicle/glands, benign and malignant types

19
Q

Cowden’s Syndrome:

A

Hereditary condition prone to multiple hamartomas and malignancy
Skin: multiple trichilemmomas (face- benign proliferation of hair follicle epithelium), benign keratoses on acral skin
-Mucosal papules, cobblestoning tongue
-Internal: breast, endometrial and thyroid carcinoma
-Cerebellar lesions
-Mutation in PTEN (tumor suppressor gene) <– KNOW!

20
Q

Adenoma

A

Benign tumor of epithelial tissue

21
Q

carcinoma

A

Malignant tumor of epithelial tissue

22
Q

Multi-Torre Syndrome:

A
  • Hereditary syndrome: germline mutations in DNA mismatch repair proteins: MLH1, MSH2, MSH6, PMS2
  • These repair errors in base pairing during replication, especially in 1-2 bp repeats (microsatellites)
  • Skin: sebaceous adenoma and carcinoma, keratoacanthomas
  • Internal carcinomas: Colon/rectal, endometrial, ovarian
  • Represents subset of hereditary non-polyposis colorectal carcinoma syndrome (HNPCC)
23
Q

Merkel Cells

A

Touch, tactile cells

24
Q

What should you do when biopsying a lesion to send the pathologist?

A

(1) Have to get a good sample & have a good description (history) sent to the pathologist
(2) Be overly descriptive for pathologist
- Never use terms like rash or lesion
- Be as descriptive as possible

THINK ABOUT DEPTH -take angriest looking biopsy sample - use punch biopsy if in doubt

25
Q

What type of biopsy should you do on a rash?

A

Punch biopsy!