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 36 YO F with primary hyperparathyroidism
 During a routine parathyroid exploration - an
enlarged inferior parathyroid gland is found.
it appears to be adhered to the thyroid gland
and surrounding soft tissue.
parathyroid carcinoma.
 Parathyroid glands are located behind the
thyroid gland and control the amount of
calcium in our blood and bones
 Parathyroid carcinoma is a rare malignancy
of the parathyroid glands. These tumors
usually secrete parathyroid hormone,
thereby producing hyperparathyroidism,
which is usually severe.
 Primary hyperparathyroidism is the
unregulated overproduction of parathyroid
hormone (PTH) resulting in abnormal
calcium homeostasis.
 hyperparathyroidism -high serum calcium
levels, severe bone disease, and renal
stones
 Untreated, parathyroid carcinoma leads to
nephrocalcinosis, pathologic fractures, and
neuropsychiatric symptoms
 it can be difficult to diagnose parathyroid cancer
preoperatively due to clinical features shared with
benign causes of hyperparathyroidism.
 Imaging techniques such as neck ultrasound can help
localize the disease, but they are not useful in the
assessment of malignancy potential.
 Fine needle aspiration (FNA) prior to initial operation is
not recommended due to technical difficulty in
differentiating benign and malignant disease on
cytology specimens and the possible associated risk of
tumor seeding from the needle track.
 Complete surgical resection with microscopically
negative margins is the recommended treatment
 Blood tests-
› calcium levels are even more increased as
compared to benign primary
hyperparathyroidism.
› Increased PTH
 Imaging-
› radiography
› CT
 No effective medical therapy for parathyroid
carcinoma is known
 therapy is primarily geared toward
management of the hypercalcemia that is
often quite severe. Treatment is similar to
hypercalcemia due to other causes.
 Pre operative
› medical intervention to control hypercalcemia
› Volume expansion with isotonic saline and
diuresis with furosemide.
› any volume contraction should be corrected
before the operation.
 Operative
› The goal of the initial operation -remove the
tumor and any adherences to tissue, the
ipsilateral thyroid lobe, and any enlarged lymph
nodes.
 Postoperative
› same as for benign hyperparathyroidism.
› substantial doses of postoperative calcium
› Recurrences may happen
› Long-term cure after a recurrence is virtually
unknown.
 https://emedicine.medscape.co
m/article/280908-treatment#d8
 https://www.ncbi.nlm.nih.gov/p
ubmed/22327883
 https://emedicine.medscape.co
m/article/280908-workup#c3
 https://emedicine.medscape.co
m/article/280908-workup#c3
 https://emedicine.medscape.co
m/article/127351-overview#a4

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Hyperparathyroidism

  • 1.  36 YO F with primary hyperparathyroidism  During a routine parathyroid exploration - an enlarged inferior parathyroid gland is found. it appears to be adhered to the thyroid gland and surrounding soft tissue. parathyroid carcinoma.
  • 2.  Parathyroid glands are located behind the thyroid gland and control the amount of calcium in our blood and bones
  • 3.
  • 4.  Parathyroid carcinoma is a rare malignancy of the parathyroid glands. These tumors usually secrete parathyroid hormone, thereby producing hyperparathyroidism, which is usually severe.  Primary hyperparathyroidism is the unregulated overproduction of parathyroid hormone (PTH) resulting in abnormal calcium homeostasis.
  • 5.  hyperparathyroidism -high serum calcium levels, severe bone disease, and renal stones  Untreated, parathyroid carcinoma leads to nephrocalcinosis, pathologic fractures, and neuropsychiatric symptoms
  • 6.
  • 7.  it can be difficult to diagnose parathyroid cancer preoperatively due to clinical features shared with benign causes of hyperparathyroidism.  Imaging techniques such as neck ultrasound can help localize the disease, but they are not useful in the assessment of malignancy potential.  Fine needle aspiration (FNA) prior to initial operation is not recommended due to technical difficulty in differentiating benign and malignant disease on cytology specimens and the possible associated risk of tumor seeding from the needle track.  Complete surgical resection with microscopically negative margins is the recommended treatment
  • 8.  Blood tests- › calcium levels are even more increased as compared to benign primary hyperparathyroidism. › Increased PTH  Imaging- › radiography › CT
  • 9.  No effective medical therapy for parathyroid carcinoma is known  therapy is primarily geared toward management of the hypercalcemia that is often quite severe. Treatment is similar to hypercalcemia due to other causes.
  • 10.  Pre operative › medical intervention to control hypercalcemia › Volume expansion with isotonic saline and diuresis with furosemide. › any volume contraction should be corrected before the operation.
  • 11.  Operative › The goal of the initial operation -remove the tumor and any adherences to tissue, the ipsilateral thyroid lobe, and any enlarged lymph nodes.
  • 12.  Postoperative › same as for benign hyperparathyroidism. › substantial doses of postoperative calcium › Recurrences may happen › Long-term cure after a recurrence is virtually unknown.
  • 13.  https://emedicine.medscape.co m/article/280908-treatment#d8  https://www.ncbi.nlm.nih.gov/p ubmed/22327883  https://emedicine.medscape.co m/article/280908-workup#c3  https://emedicine.medscape.co m/article/280908-workup#c3  https://emedicine.medscape.co m/article/127351-overview#a4