Pathology: Thyroid II Flashcards

1
Q

What is a thyroglossal duct cyst?

A

Cystic dilation of thyrogossal duct remnant

  • Presents as anterior neck mass
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2
Q

Wha is lingual thyroid?

A
  • *Persistence of thyroid tissue at base of tongue**
  • Don’t get embryological descent of thyroid through thyroglossal duct
  • Presents as a base of tongue mass
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3
Q

What is Hyperthyroidism?

A

Increased level of circulating thyroid hormone

  • Increase basal metabolic rate by increasing synthesis of Na/K ATPase
  • Increases sympathetic nervous sytem activity due to expression of B1 adrenergic receptors
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4
Q

What are clinical features of hyperthyroidism?

A
  • Weight loss despite increased appetite
  • Heat intolerance and sweating
  • Tachycardia with increased cardiac output
  • Arrhythmia (esp. in elderly)
  • Tremor, anxiety, insomnia, and heightened emotions
  • Staring gaze with lid lag
  • Diarrhea with malabsorption
  • Oligomenorrhea
  • Bone resorption with hypercalcemia (can lead to osteoporosis)
  • Decreased muscle mass with weakness
  • Hypocholesterolemia
  • Hyperglycemia
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5
Q

What is most common cause of hyperthyroidism?

A

Graves Disease

  • Autoantibody (IgG) that stimulates TSH receptors
  • Leads to increased synthesis and release of thyroid hormone
  • Occurs in women of childbearing age
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6
Q

What are clinical features of Graves Diseaes?

A

Hyperthyroidism

Diffuse Goiter

Exophthalmos and pretibial myxedema (due to IgG activation of TSH receptors at these sites causing production of excess glycosaminoglycans)

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7
Q

What are lab features of Graves Disease?

A

- Increased total and free T4

- Decreased TSH (T4 down regulates TRH receptors on anterior pituitary)

- Hypocholesterolemia

- Increased serum glucose

- “Scalloping” histology of thryoid follicles

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8
Q

What is the treatment for Graves disease?

A

Beta-blockers

Thioamide (blocks production of T4)

Radioiodine ablation

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9
Q

What is thyroid storm?

A

Feared Complication of Graves Disease

  • Elevated catecholamines and massive hormone excess (stress)
  • Arrhythmia, hyperthermia, and vomiting with hypovolemic shock
  • Treted with PTU, Beta-blockers, and steroids
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10
Q

What is a multinodular goiter?

A

Enlarged thyroid gland with multiple nodules

  • Due to relative iodine deficiency
  • Usually nontoxic (euthyroid)
  • Rarely, regions become TSH-independent (“toxic goiter”)
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11
Q

What is Cretinism? What are its symptoms?

A

Hypothyroidism in neonates and infants

Clinical Features:
Mental Retardation
Short Stature with skeletal abnormalities
Coarse facial features
Enlarged tongue
Umbilical hernia

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12
Q

What are causes of Cretinism?

A
  • Maternal hypothyroidism during early pregnancy
  • Thyroid agenesis
  • Dyshormonogenetic goiter
  • Iodine deficiency
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13
Q

What is myxedema? Clinical features?

A

Hypothyroidism in older children or adults

  • *Clinical Features:**
  • Myxedema (edema has “dough-like” consistency)
  • Larynx –> deepening of voice
  • Enlarged tongue
  • Weight gain despite normal appetite
  • Slowing of mental activity
  • Muscle weakness
  • Cold intolerance with decreased sweating
  • Bradycardia with decreased cardiac output
  • Oligomenorrhea
  • Hypercholesterolemia
  • Constipation
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14
Q

What are causes of Myxedema?

A

Iodine Deficiency

Hashimoto Thyroiditis (autoimmune destruction of thryoid gland

Drugs (i.e. lithium)

Surgical removal or radioablation of thyroid

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15
Q

What is Hashimoto Thyroiditis?

A

Autoimmune destruction of thyroid gland

  • Associated with HLA-DR5
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16
Q

What are clinical features of Hashimoto Thyroiditis?

A

Initially may present as hyperthyroidism (due to initial destruction of cells and abundant release of T4)

  • Passes a point of normal thyroid regulation then:

- Progresses to hypothyroidism (decreased T4 and Increased TSH)

- Antithyroglobulin and antimicrosomal antibodies are often present (signs of thyroid damage)

- Chronic inflammation with formation of germinal centers and hurthle cells, histologically

17
Q

What is Subacute (deQuervain) Granulomatous thyroiditis?

A
  • Granulomatous thyroiditis that follows a viiral infection
  • Presents as tender thyroid with transient hyperthyroidism
  • Self-limited; does not progress to hypothyroidism
18
Q

What is Reidel Fibrosing Thyroiditis?

A
  • Chronic inflammation with extensive fibrosis of thyroid
  • Presents as hypothyroidism with ‘hard as wood’ nontender thyroid gland
  • Fibrosis may extend to local structures (i.e. airway)

–> Classically a young female

19
Q

What is a 131I radioactive uptake study?

A

Completed to help diagnose thyroid nodules

  • Increaed uptake of 131I seen in Graves or nodula goiter
  • Decreased uptake of 131I seen in adenoma and carcinoma (warrants FNA - fine needle aspiration - biopsy)
20
Q

What is a follicular adenoma?

A

Benign proliferation of follicles surrounded by a fibrous capsule

  • Usually nonfunctional; rarely may secrete thyroid hormone
21
Q

What are the four types of thyroid carcinomas?

A

Papillary Carcinoma (*Most Common* = 80%)

Follicular Carcinoma

Medullary Carcinoma

Anaplastic Carcinoma

22
Q

What is a major risk factor for papillary carcinoma?

A

Exposure to ionizing radiation in childhood

23
Q

What are histological signs of papillary carcinoma?

A

Production of papillary structures

  • Presence of “orphan annie-eyed” nuclei
  • Presence of nuclear grooves
  • Calcification of papillary architecture leads to psammoma bodies
24
Q

Where does papillary carcinoma of the thyroid spread?

A

Cervical lymph nodes

  • however, even with lymph node spread, there is an excellent prognosis
25
Q

What is follicular carcinoma? Where does it metastesize to?

A

Malignant proliferation of follicles in the thyroid

  • Surrounded by a fibrous capsule with invasion through capsule –> FNA cannot distinguish between follicular adenoma and follicular carcinoma
  • Generally goes into blood (hematogenous metastesis)
26
Q

What is medullary carcinoma?

A

- Malignant proliferation of parafollicular C cells

- High levels of calcitonin produced by tumor may lead to hypocalcemia

- Calcitonin often deposits within tumor as amyloid (localized amyloidosis)

27
Q

What are familial cases of medullary carcinoma associated with?

A

Multiple Endocrine Neoplasia (MEN) 2A and 2B

–> RET oncogene

Detection of RET mutation warrants prophylactic thyroidectomy

28
Q

What is anaplastic carcinoma?

A

Undifferentiated malignant tumor of thyroid

  • Usually seen in elderly
  • Often invades local structures leading to dysphagia or respiratory compromise
  • poor prognosis
  • Clinically similar to Reidels thyroiditis (which is seen in younger patients)