Blue, Brown, Gray and Black Lesions Flashcards

1
Q

List the developmental lesions

A

-Physiologic pigmentation
-Peutz-Jeghers syndrome

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2
Q

List the injury lesions

A

-Amalgam tattoo
-Intentional tattoo
-Smoker’s melanosis
-Drug-related pigmentation

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3
Q

List the neoplastic lesions

A

-Melanotic macule
-Melanocytic nevus
-Blue nevus
-Melanoma

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4
Q

List the metabolic lesions

A

-Addison disease

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5
Q

Physiologic Pigmentation
-Category
-Etiology
-Demographics
-Clinical Presentation
-Diagnosis
-Tx

A

“racial pigmentation”

Category
-Developmental

Etiology
-Increase in production of melanin by melanocytes

Demographics
-Patients with a darker complexion

Clinical Presentation
-Attached gingiva most common location
-Can be seen anywhere (even tips of fungiform papilla on dorsal tongue)

Diagnosis
-Established clinically

Tx
-No tx

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6
Q

Peutz-Jeghers Syndrome
-Category
-Etiology
-Clinical Presentation
-Diagnosis
-Tx

A

Category
-Developmental

Etiology
-Autosomal dominant genetic disease

Clinical Presentation
-Oral and perioral freckles that first present during childhood and adolescence (lips and cheeks)
-Skin and mucosal freckles
-Intestinal polyps (small bowel)
-Increased risk of malignancy (GI, pancreatic, breast, ovarian)

Diagnosis
-Family history
-Genetic testing

Tx
-Oral and perioral pigmentation persists throughout life and does not require tx
-Lifelong monitoring for development of neoplasia

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7
Q

Amalgam Tattoo
-Category
-Etiology
-Demographics
-Clinical Presentation
-Radiographic Presentation
-Diagnosis
-Tx

A

Category
-Injury

Etiology
-Amalgam becomes embedded in oral mucosa

Demographics
-Patients with a history of amalgam restorations

Clinical Presentation
-Black, blue or gray macules
-Gingiva, alveolar mucosa, and buccal mucosa most common

Radiographic Presentation
-May appear as a dense radiopacity

Diagnosis
-Radiograph
-Biopsy
-MUST be distinguished from melanocytic neoplasia

Tx
-No tx

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8
Q

Smoker’s Melanosis
-Category
-Etiology
-Demographics
-Clinical Presentation
-Diagnosis
-Tx

A

Category
-Injury

Etiology
-Increased melanin production
-Protective response against noxious chemicals in tobacco smoke

Demographics
-Females affected with higher frequency

Clinical Presentation
-Anterior facial mandibular gingiva most common
-Multiple brown macules

Diagnosis
-Correlate clinical presentation with smoking history and medical history
-Biopsy if any doubt

Tx
-Pigmentation can disappear after smoking cessation

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9
Q

Drug-Related Pigmentation
-Category
-Etiology
-Demographics
-Clinical Presentation
-Diagnosis
-Tx

A

Category
-Injury

Etiology
-Different for different medications
-Some chelate with iron or melanin and deposit in lamina propria
-Some stimulate melanocytes to produce melanin

Demographics
-Patient taking medications known to cause pigmentation

Clinical Presentation
-Diffuse, painless, symmetric, bluish-gray macular pigmentation of the hard palate

Diagnosis
-Correlation between initiation of the drug and onset of pigmentation
-Biopsy

Tx
-No tx

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10
Q

What medications are known to cause pigmentation?

A

-Minocyline
-Antimalarials (chloroquine, hydroxychloroquine, quinidine, quinacrine)
-Tranquiilizers (chlorpromazine)
-Chemotherapeutic agents (imatinib)
-Estrogen
-AIDS medications (zidovudine/AZT)

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11
Q

Melanotic Macule
-Category
-Etiology
-Demographics
-Clinical Presentation
-Diagnosis
-Tx

A

Category
-Neoplastic

Etiology
-Increase in melanin and melanocytes

Demographics
-2:1 female predilection
-Average age of 42yrs

Clinical Presentation
-Solitary, uniformly tan to dark-brown
-Most common on lower lip

Diagnosis
-Biopsy (recent onset, large size, irregular pigmentation, unknown duration, or recent enlargement)

Tx
-No tx

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12
Q

Melanocytic Nevus
-Category
-Etiology
-Demographics
-Clinical Presentation
-Diagnosis
-Tx

A

“mole”

Category
-Neoplasm

Etiology
-Benign localized proliferation of nevus (melanocytic) cells derived from the neural crest

Demographics
-10-40 cutaneous nevi per white adult (common)

Clinical Presentation
-Uncommon intraorally
-Junctional nevus (brown/black macule)
-Compound nevus
(brown/tan papule)
-Intradermal/intramucosal nevus (brown/tan papule with papillomatous surface - hair may grow from center)

Diagnosis
-Clinical diagnosis can be made on skin (biopsy if any doubt)
-Biopsy necessary if intraoral
-Biopsy necessary if >6mm

Tx
-Monitor for signs of change (small % develop into melanoma)

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13
Q

Blue Nevus
-Category
-Etiology
-Demographics
-Clinical Presentation
-Diagnosis
-Tx

A

Category
-Neoplasm

Etiology
-Benign proliferation of dendritic melanocytes usually deep within CT

Demographics
-Female predilection
-Usually in children and young adults

Clinical Presentation
-Macular or dome-shaped, blue or blue-black
-Smaller than 1cm
-Any cutaneous or mucosal site
-Palate is most common oral location

Diagnosis
-Biopsy

Tx
-Surgical excision

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14
Q

Melanoma
-Category
-Etiology
-Demographics
-Clinical Presentation
-Diagnosis
-Tx

A

Category
-Neoplasm

Etiology
-Malignancy of melanocytic cells

Demographics
-Risk factors for cutaneous melanoma:
1. Acute sun damage
2. Fair complexion (blonde hair, blue eyes)
3. Multiple moles, freckling, dysplastic nevi)
4. Family history
-Oral melanoma
1. 5th-7th decade of life
2. Male predilection

Clinical Presentation
- 25% head and neck
- 40% extremities
- <1% intraoral (palate and maxillary ginigiva most common sites)
-ABCDE of melanoma:
1. Asymmetry
2. Borders - irregular
3. Color variation
4. Diameter - greater than 6mm
5. Evolving

Diagnosis
-Biopsy

Tx
-Wide surgical excision
-Radiation
-Immunotherapy
-Depth of invasion is an important prognostic factor
-Oral mucosal melanoma has worse prognosis than cutaneous melanoma (<20% 5-yr survival)

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15
Q

Addison Disease (hypoadrenocorticism)
-Category
-Etiology
-Clinical Presentation
-Diagnosis
-Tx

A

Category
-Metabolic

Etiology
-Adrenocortical insufficiency secondary to:
1. Autoimmune adrenalitis
2. Tuberculosis
3. AIDS
4. Metastatic Cancer
-Increased ACTH production by anterior pituitary

Clinical Presentation
-Generalized hyperpigmentation of the skin (bronzing)
-Diffuse of patchy, brown, macular pigmentations of the oral mucosa
-Systemic symptoms (weakness, weight loss, irritability, depression, nausea, vomiting, hypotension)

Diagnosis
-Decreased serum cortisol levels
-Increased plasma ACTH levels

Tx
-Steroid replacement therapy

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