Amboss thyroid ca Flashcards

1
Q

40–60 years of age
Well differentiated
Hematogenous metastasis especially to Bone (lytic lesions)
Vascular and capsular invasion
Good prognosis

A

Follicular thyroid carcinoma

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2
Q

30–50 years of age
Well differentiated
Most common type of thyroid cancer
Palpable lymph nodes due to metastatic spread (often detected before primary tumor

Very good prognosis

A

Papillary thyroid carcinoma

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3
Q

After 60 years of age
Rapid local growth
Symptoms of compression of the structures of the neck (e.g. dysphagia, dyspnea)
Lymphatic and hematogenous metastasis
Poorly differentiated
Very poor prognosis

A

Anaplastic thyroid carcinoma

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4
Q

50–60 years of age
Sometimes a genetic predisposition → multiple endocrine neoplasia type 2 (MEN2)
Produces calcitonin
Diarrhea and facial flushing

A

Medullary carcinoma

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5
Q

Painless cervical lymphadenopathy

A

More common in papillary thyroid cancer and anaplastic thyroid cancer
Less common in follicular thyroid cancer

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6
Q

Signs of distant metastasis

A

More common in follicular thyroid cancer and anaplastic thyroid cancer
Less common in papillary thyroid cancer

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7
Q

Paraneoplastic syndrome

A

: diarrhea and facial flushing (typically seen in advanced medullary carcinoma) [8]

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8
Q

Medullary carcinoma thyroid cancer tumor markers

A

Calcitonin: A hormone secreted by parafollicular cells, which is the tissue of origin of medullary carcinoma

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9
Q

Psammoma bodies is seen in ____________

A

Morphology: concentric lamellar calcifications
Occurrence: seen in diseases associated with calcific degeneration
Papillary thyroid carcinomas (evidence of psammoma bodies in thyroid tissue should always raise suspicion of malignancy)
Serous papillary cystadenocarcinoma of ovary and endometrium
Meningiomas
Mesotheliomas

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10
Q

“Orphan Annie” eyes nuclei
Morphology: empty-appearing large oval nuclei with central clearing
Occurrence
Papillary thyroid carcinomas
Autoimmune thyroiditis (e.g., Hashimoto disease, Grave disease)
Nuclear grooves

A

Papillary thyroid cancer

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11
Q

Follicular carcinoma histo

A

Uniform follicles; vascular and or capsular invasion

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12
Q

Medullary carcinoma histo

A

Ovoid cells of C cell origin and therefore without follicle development
Amyloid in the stroma (stains with Congo red)

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13
Q

Anaplastic thyroid carcinoma

A

Undifferentiated giant cell (i.e., osteoclast-like cell)
Areas of necrosis and hemorrhage

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14
Q

Complications thyroid ca

A

Hypocalcemia
Dysphonia (hoarseness) and/or dysphagia:
Vocal cord function should be assessed preoperatively with laryngoscopy.

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15
Q

Etiology Medullary carcinoma:

A

associated with MEN2 (RET gene mutations) or familial medullary carcinoma

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16
Q

Etiology Papillary carcionma

A

Papillary carcinoma: associated with RET/PTC rearrangements and BRAF mutations

Ionizing radiation (particularly during childhood): mostly associated with papillary carcinoma

17
Q

Etiology Follicular carcinomaend

A

Follicular carcinoma: associated with PAX8-PPAR-γ rearrangement and RAS mutation

18
Q

Etiology Undifferentiated/anaplastic carcinoma:

A

Undifferentiated/anaplastic carcinoma: associated with TP53 mutation