Parathyroid adenoma usually give rise to excess secretion of PTH, this condition is recognised as primary hyperparathyroidism.
Dhaka Medicine
Friday, September 27, 2019
Wednesday, September 25, 2019
Abdominal pain, nausea, polyuria, lathergy, hematuria
Hypercalcemia:
Grading:
It can ne graded as mild, moderate & severe hypercalcemia.
Causes:
with normal or elevated PTH level:
.primary or tertiary hyperparathyroidism
.Lithium induced hyperparathyroidism
. Familial hypocalciuric hypercalcemia
With low PTH level
.Malignancy ( lung, breast, renal, lymphoma)
.Multiple myeloma
.Sarcoidosis
.Hypervotaminosis D
.Thyrotoxicosis
.Thiazide diuretics
.Glaucocorticoid deficiency
.Paget's disease
Clinical Features:
Clinical features of hypercalcemia include polyuria, polydipsia, dyspepsia, anorexia, nausea, lathargy, constipation, depression, drowsiness, impaired cognition, PUD, renal colic
Investigations:
Elevated PTH level along with hypercalcemia indicate primary hyperparathyroidism is the most possible diagnosis. Elevated plasma phosphate & alkaline phosphatase along with renal failure indicate tertiary hyperparathyroidism. Familial hypocalciuric hypercalcemia can be confirmed by screening family members for hypercalcemia.
Grading:
It can ne graded as mild, moderate & severe hypercalcemia.
Causes:
with normal or elevated PTH level:
.primary or tertiary hyperparathyroidism
.Lithium induced hyperparathyroidism
. Familial hypocalciuric hypercalcemia
With low PTH level
.Malignancy ( lung, breast, renal, lymphoma)
.Multiple myeloma
.Sarcoidosis
.Hypervotaminosis D
.Thyrotoxicosis
.Thiazide diuretics
.Glaucocorticoid deficiency
.Paget's disease
Clinical Features:
Clinical features of hypercalcemia include polyuria, polydipsia, dyspepsia, anorexia, nausea, lathargy, constipation, depression, drowsiness, impaired cognition, PUD, renal colic
Investigations:
Elevated PTH level along with hypercalcemia indicate primary hyperparathyroidism is the most possible diagnosis. Elevated plasma phosphate & alkaline phosphatase along with renal failure indicate tertiary hyperparathyroidism. Familial hypocalciuric hypercalcemia can be confirmed by screening family members for hypercalcemia.
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