Parathyroid Pathology Singh Flashcards

1
Q

Describe histology of parathyroid gland

A
  • Chief cells
  • Oxyphil cells
  • Adipocytes
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2
Q

Function of the parathyroid gland?

A
  • calcium homeostasis
    • PTH causes direct release of calcium from bone and exerts effects on kidneys
      • Ca reabsorption and phosphate reabsoption blocking
      • Convert inactive Vit D to active
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3
Q

Low serum calcium results in ___ PTH secretion.

A

Low serum calcium results in increased PTH secretion.

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4
Q

Primary Hyperparathyroidism lab values & causes?

A
  • Parathyroids are secreting too much PTH so it is high as well as calclium
  • Adenoma (85-95%), Primar y hyperplasia (5-10%), Parathyroid carcinoma (~1%)
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5
Q

What are the sx of primary hyperparathyroidism?

A
  • Painful bones, renal stones, abdominal groans and psychic moans
  • Osteoporosis, nephrolithiasis, constipation/gallstones, depression/lethargy/seizures
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6
Q

What is Osteitis Fibrosis Cystica (von Recklinghausen’s disease of bone)

A
  • Starts as a brown tumor with osteoclast driven bone destruction that results in small fractures and hemorrhage and reactive tissues
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7
Q

What can osteitis fibrosis cystica be mistaken for?

A

Metastatic disease

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8
Q

How does hyperparathyroidism in the book comapre to real life?

A

Most primary hyperparathyroid cases are asymptomatic and discovered incidentally though routine lab work with an elevated Ca level

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9
Q

What type of scan is done to diagnose parathyroid adenoma?

A

Technetium scan, this shows an increased uptake disproportionate to other glands

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10
Q

Describe parathyroid adenoma

A
  • benign neoplasm of parathyroid chief or oxyphil cells
  • usually solitary and surrounded by rim of normal parathyorid tissue
    • can cause other glands to shrink due to the excessive PTH from the adenoma
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11
Q

Describe primary hyperplasia of parathyroids causing primary hyperparathyroidism.

A
  • Almost always in multiple glands
  • MEN sysndromes may be responsible
  • NO normal rim of parathyroid tissue → lacking normal tissue next to it as seen in an adenoma (no adipocytes)
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12
Q

Describe parathyotid carcinoma.

A
  • Metastasis is the tell tale sign
  • one of the causes of primary hyperparathyroidism
  • Has features of invasion to adjacent tissues and vascular invasion
  • Elevated PTH doesn’t go down after surgery
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13
Q

High calcium level but suppresed PTH, what causes this?

A
  • Hypercalcemia of Malignancy
  • vitamin D excess
  • excess calcium ingestion
  • medications (thiazide’s)
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14
Q

What is the difference between hypercalcemia casued by hyperparathyroidism and non paathyroid sources?

A

Hyperparathyroidism:

  • likely asx
  • commonly due to PT adenoma

Non PT sources:

  • more likely to be symptomatic → mental status changes, n/v, QT interval shortened
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15
Q

What are the mechanisms of malignant hypercalcemia?

A
  • Humoral hypercalcemia of malignancy is related to PTHrP (80%) which is analogous to PTH and related to squamous carcinomas
    • there is also Vitamin D mediated pathway which is seen in lymphomas
  • Local osteolytic hypercalcemia
    • release of ca due to osteoclastic bone resorption
      • breast carcinoma and myeloma
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16
Q

Clinical features of hypocalcemia?

A
  • Behavioral disturbances/stupor
  • numbness and parasthesias
  • muscle cramps and tetany
    • trosseau sign +
    • Chvostek sign +
  • convulsions
17
Q

Renal Osteodystrophy?

A
  • Dissecting osteitis in hyperparathyroidism
  • In secondary hyperparathyroidism renal osteodystrophy can lead to rugger jersey sign
18
Q

What is Calciphylaxis (calcific uremic ateriolopathy)?

A
  • Secondary hyperparathyroidism in assoc. with renal disease that is assoc. with extensive calcification and occlusion of blood vessels resulting in ischemia
  • Patients die from sepsis
19
Q

Describe tertiary HPT?

A
  • calcium and PTH high (same as primary HPT)
  • Tertiary HPT comes out of patient who historically had secondary hyperparathyroidism first
    • it went on for so long and eventually got cured but now body releases excess PTH
20
Q

What causes primary hypoparathyroidism and what are the lab values?

A
  • Low calcium and low PTH
  • Acquired:
    • Iatrogenic is the most common cause
    • also caused by autoimmune attack
  • can be congenital:
    • DiGeorge
    • CASR
    • Familial Isolated Hypoparathyroidism
21
Q

Describe DiGeorge syndrome in relation to the parathyroid glands.

A
  • sometimes the parathyroid glands are affected
  • can have tetany due to hypocalcemia from parathyroid hypoplasia/aplasia
22
Q

What are the two types of CaSR mutations?

A

Inactivating CaSR (loss of function):

  • body believes there isn’t enough calcium even when there is
  • turns on PTH → hypercalcemia
  • reduces renal excretion → hypocalciuria
  • Called Familial Hypocalcuric hypercalcemia

Activating CaSR (gain function):

  • body thinks there is plenty of calcium when there isn’t
  • turns off PTH → hypocalcemia
  • increases renal excretion → hypercalciuria
  • Called AD hypoPTH Hypercalciuric hypocalcemia
23
Q

What are labs seen in psuedohypoparathyroidism?

A
  • normal or elevated PTH
  • Hypocalcemia and hyperphosphatemia
  • resistance to PTH
24
Q

What is Albright’s Hereditary Osteodystrophy?

A
  • short stature and obesity
  • shortened fingers and toes
  • occasionally seizures and tetany
  • assoc. with psuedohypoparathyroidism