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__NOTOC__
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{{Hyperparathyroidism}}


{{CMG}}; {{AE}} {{Anmol}}
{{CMG}}; {{AE}} {{Anmol}}


== Classification ==
==Tables==
{| class="wikitable"
{| class="wikitable"
! colspan="4" |Classification of hyperparathyridism
|+
!Diagnosis
!Lab findings
!
!
|-
|-
|Features
!
|'''Primary hyperparathyroidism'''
!
|'''Secondary hyperparathyroidism'''
!
|'''Tertiary hyperparathyroidism'''
!
|-
|-
|Pathology
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|Hyperfunction of parathyroid cells due to hyperplasia, adenoma or carcinoma.
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|Physiological stimulation of parathyroid in response to hypocalcaemia.
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|Following long term physiological stimulation leading to hyperplasia.
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|-
|-
|Cause
|
|
|
|
|
|
|
|-
|-
|Associations
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|May be associated with multiple endocrine neoplasia.
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|Usually due to chronic renal failure or other causes of Vitamin D deficiency.
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|Seen in chronic renal failure.
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|-
|Serum calcium
|High
|Low/Normal
|High
|-
|Serum phosphate
|Low/Normal
|High
|High
|-
|Management
|Usually surgery if symptomatic. Cincacalcet can be considered in those not fit for surgery.
|Treatment of underlying cause.
|Usually cinacalcet or surgery in those that don't respond.
|}
|}
=Causes=
==Overview==
Hyperparathyroidism is caused by an increase in concentration of parathyroid hormone in serum.
There are three type of hyperparathyroidism including primary, secondary and tertiary hyperparathyroidism.
The causes of all hyperparathyroidism is different.
==Causes of Primary hyperparathyroidism==
Causes of primary hyperparathyroidism are as follows:
===Common causes===
*Parathyroid adenoma
**Usually single gland affected
**Sometimes multiple gland affected
===Less common causes===
*Parathyroid hyperplasia
*Parathyroid carcinoma
*Radiation exposure (due to development of parathyroid adenoma or parathyroid hyperplasia)
===Genetic causes===
*HRPT2 gene mutations:
**HRPT2 gene code for parafibromin protein.
**HRPT2 gene mutations are found in a type of familial hyperparathyroidism, hyperparathyroidism-jaw tumor (HPT-JT) syndrome.
**HRTP2 gene mutations increases risk of parathyroid carcinoma.
*Cyclin D1 gene (CCND1)/PRAD1 gene:
**PRAD1 (parathyroid adenoma 1) is a protooncogene located on chromosome 11q13.
**Cyclin D1 gene translocation and oncogene action observerd in 8% of adenomas
**Cyclin D1 gene overexpression is pbserved in 20% to 40% of parathyroid adenomas
*MEN1 gene:
**MEN1 is a tumor supressor gene on chronosome 11q13.
**Somatic loss of single MEN1 allele is observed in  25% to 40% of sporadic parathyroid adenomas.
==Causes of secondary hyperparathyroidism==
Causes of secondary hyperparathyroidism are as follows:
===Common causes===
*Chronic kidney disease (leading to parathyroid hyperplasia)<ref name="pmid15507543">{{cite journal| author=Rodriguez M, Nemeth E, Martin D| title=The calcium-sensing receptor: a key factor in the pathogenesis of secondary hyperparathyroidism. | journal=Am J Physiol Renal Physiol | year= 2005 | volume= 288 | issue= 2 | pages= F253-64 | pmid=15507543 | doi=10.1152/ajprenal.00302.2004 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15507543  }}</ref>
*Vitamin D deficiency
===Less common causes===
*Severe calcium deficiency
==Causes of tertiary hyperparathyroidism==
Causes of tertiary hyperparathyroidism are as follows:
===Common causes===
*Chronic renal failure


==References==
==References==
<references />
{{reflist|2}}

Latest revision as of 17:32, 14 January 2019


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]

Tables

Diagnosis Lab findings

References