Path Flashcards

(39 cards)

1
Q

What cells are seen in the parathyroid?

A

Chief cells

Oxyphil cells

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2
Q

Which cells of the parathyroid contain PTH?

A

Chief cells

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3
Q

What can be seen in a normal parathyroid tissue stain?

A

Fat globules

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4
Q

What is the most important cause of hypercalcemia?

A

Primary hyperparathyroidism

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5
Q

Most frequent parathyroid lesion

A

Adenoma

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6
Q

Primary hyperparathyroidism

A
Adults, 50's or later
Women more common
Solitary adenoma, 0.5 to 5.0 grams
Soft nodule, well circumscribed
Squash surrounding tissue
Inconspicuous adipose tissue
MEN-1, MEN-2, Familial hypocalciuric hypercalcemia
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7
Q

Primary hyperplasia

A

All four glands
Component of MEN syndrome
Combined weight rarely over 1 gram
Water clear cells, islands of oxyphils

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8
Q

Parathyroid carcinomas

A
Circumscribed lesions
One gland
Can exceed 10 grams in weight
Invasion of surrounding tissues
Nephrolithiasis, nephrocalcinosis, metastatic calcification secondary to hypercalcemia
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9
Q

Symptoms of primary hyperparathyroidism

A

Painful bones
Renal stones
Abdominal groans
Psychic moans

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10
Q

Most common cause of secondary hyperparathyroidsism

A

Renal failure

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11
Q

Symptoms of secondary hyperparathyroidism

A

Symptoms of chronic renal failure

Calciphylaxis - vascular calcification, significant ischemic damage to skin and other organs

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12
Q

Causes of hypoparathyroidism

A

Acquired - inadvertent consequence of surgery
Autoimmune - LYMPHOCYTES
Congenital absence - DiGeorge syndrome

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13
Q

Hallmark of hypocalcemia

A

Tetany

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14
Q

Major clinical manifestations of hypoparathyroidism

A
Hypocalcemia - tetany
Mental status changes
Intracranial manifestations
Ocular dz
Cardio manifestations
Dental abnormalitites
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15
Q

Pseudohypoparathyroidism

A

Resistance to PTH
Serum PTH lvls normal or elevated
Hypocalcemia
Hyperphosphatemia

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16
Q

Causes of hyperthyroidism

A

Diffuse hyperplasia associated with Graves disease
Hyperfunctional multinodular goiter
Hyperfunctional adenoma

17
Q

Clinical manifestations of hyperthyroidism

A
Excessive lvls of thyroid hormone
Increase in BMR
Flushed, thin
Heat intolerance
Sweating
Tachy, palpitation, cardiomegaly (first signs)
18
Q

Dx of hyperthyroidism

A

Low TSH

Increased free T4

19
Q

Congenital hypothyroidism

A

Endemic iodine deficiency in diet

20
Q

Causes of acquired hypothyroidism

A

Sugical removal
Radiation induced ablation
Drugs like methimazole, propylthiouracil, lithium

21
Q

Circulating autoantibodies in autoimmune hypothyroidism

A

Antimicrosomal
Antithyroid peroxidase
Antithyroglobulin antibodies

22
Q

Hashimoto Thyroiditis

A
Most common cause of hypothyroidism where iodine lvls are sufficient
Intense LYMPHOCYTIC INFILTRATE
More common in women
45-65 y/o
Atrophic follicles 
Hurthle cells
23
Q

Subacute Granulomatous De Quervain Thyroiditis

A
Women more than men
40-50 y/o
Most common cause of thyroid pain
Triggered by viral infection - coxsackievirus, mumps, measles, adenovirus
Seasonal incidence peaking in summer
Multinucleate giant cells
24
Q

Subacute Lymphocytic Thyroiditis

A

PAINLESS

Circulating anti-thyroid peroxidase antibodies

25
Graves Disease
``` Most common cause endogenous hyperthyroidism Exophthalmos Pretibial myxedema Colloid is pale with scalloped margins Women more than men 20-40 y/o Over 80 grams ```
26
Cause of diffuse goiters
Dietary iodine deficiency
27
Endemic goiter
Where there is low levels of iodine | Andes and Himalayas
28
Multinodular goiter
All long standing simple goiters convert to this Weights of more than 200 grams Intrathoracic or plunging goiter
29
Hallmark of all follicular adenomas
Presence of intact, well formed capsule encircling the tumor
30
Most prominent subtype of thyroid carcinoma
Papillary carcinoma
31
Papillary carcinoma
Associated with previous exposure to ionizing radiation Fibrovascular stalk Psammoma bodies Optically clear or empty nuclei - Orphan Annie eye nuclei Intranuclear inclusion/intranuclear grooves Vascular invasion uncommon Mets to lymph nodes
32
Follicular Carcinoma
More frequent in areas with dietary iodine deficiency Psammoma bodies not present Lymphatic spread uncommon Vascular dissemination common
33
Anaplastic carcinoma
Aggressive | Undifferentiated
34
Medullary Carcinoma
Derived from parafollicular cells, or C cells, of thyroid Secrete calcitonin Amyloid deposits
35
Most consistent morphologic feature of diabetes
Diabetic microangiopathy
36
Diabetic nephropathy
THREE LESIONS - Glomerular lesions Renal vascular lesions Pyelonephritis (including necrotizing papillitis)
37
Nodular glomerulosclerosis
Kimmelstiel-Wilson Ovoid or spherical, laminated, nodules of matrix Periphery of glomerulus PAS positive Consequences - ischemia, tubular atrophy, interstitial fibrosis
38
Insulinoma
Beta cell tumor Most common pancreatic endocrine neoplasm Excess insulin Induces clinically significant hypoglycemia Precipitated by fasting or exercise High circulating insulin lvls High insulin to glucose ratio
39
Gastrinoma
Marked hypersecretion of gastrin Diarrhea ZE syndrome - pancreatic islet cell lesions, hypersecretion of gastric acid, severe peptic ulceration Intractable jejunal ulcers = ZE syndrome