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PARATHYROID
DISORDERS
Dr. Nilutpal Gogoi
MBBS, MS.
Assistant Professor,
Department of General Surgery
GMCH
ANATOMY
■ Endocrine glands situated behind thyroid gland
■ Four in number
■ Weight: 40-50 grams
■ Secrete: Parathormone
■ Superior glands:
– Develop from 4th pharyngeal pouch
– Behind RLN
■ Inferior glands
– Develop from 3rd pharyngeal pouch
– Infront of RLN
– Variable in position:Tracheo-oesophageal groove, Behind esophgus, Carotid sheath
■ Blood supply- inferior thyroid artery (End artery)
Parathormone
■ 84 aminoacids
■ Secretion not dependent on pitutary gland
■ Half life- 4 minutes
■ Functions :
– Converts vitamin D into 1,25- dihydrocholecalciferol in kidney
– Absorption of calcium from gut
– Mobilises calcium from bone
– Reabsorption from renal tubules
Calcium metabolism
■ Normal value: 8.5-10.2 mg/dl
■ Commonest protein part of bound calcium is Albumin (80%)
■ Level controlled by
– PTH
– Calcitonin
– Vitamin D- Acts on bone, kidney and GIT
■ Functions
1. Blood coagulation
2. Neuromuscular activity
3. Cellular activity
4. Bone integrity.
HYPERPARATHYROIDIS
M
(HPT)
Hyperparathyroidism
■ Types
1. Primary
2. Secondary
3. Tertiary
PRIMARY HPT
■ 3rd most common endocrine disease
■ Causes hypercalcemia
■ Etiology
- Parathyroid adenoma
- Familial/ genetic causes
- MEN 1 syndrome
- Therapeutic ionizing radiations
- Lithium: parathyroid hyperplasia and HPT with no bone or renal problems
Clinical features of HPT
■ Clinical vignette: “Bones, stones, abdominal groans and psychic moans”
■ Middle aged women( 3:1)
■ Incidence: 1:1000
■ Asymptomatic > 50% cases
Clinical feature contd.
■ BONES
- Raised PTH
- Increased osteoclastic activity
- Extensive decalcification of bone
- Bone pain, subosteal erosions
- Osteitis fibrosa cystica: single/ multiple cysts/ pseudotumours in the jaw, skull or
phalanges
- Osteopenia, osteoporosis and pathological fracture
Clinical feature contd.
■ STONES:
- Renal stone in 25% patients
- Recurrent stones
- Calcium phosphate and oxalate type
- Metaststic calcification, nephrocalcinosis, renal failure
- Calcification in renal vessels: renal hypertension.
Clinical feature contd.
■ ABDOMINALGROANS
- Stimulates gastrin release: peptic ulceration
- Precipitate acute pancreatitis
- Increases gall stone disease ( calcium bilirubinate)
■ PSYCHIC MOANS:
- Behavioural and neurotic problems: depression and anxiety
Acute hyperparathyroidism (Crisis)
■ Causes
- Sidden increase in PTH due to rupture od parathyroid cyst or bleeding in parathyroid
tumour
- Severe dehydration precipitates crisis
- Secondaries in bone.
Acute hyperparathyroidism (Crisis)
■ Clinical presentation
1. Abdominal pain
2. Vomiting
3. Dehysration
4. Oliguria
5. Muscular weakness
6. Death
■ Serum calcium: >12mg%
Acute hyperparathyroidism (Crisis)
■ Treatment
- Forced diuresis: 3-5 litres of saline with frusemide
- Rehydration: normal saline 300ml/hr
- Steroids: inhibit effects of vitamin D
Dose: 400/ day iv for 5 days
- Bisphosphonate:
Cloodranate sodium, pamidronate
Inhibits mobilization of calcium from bone
Dose: 4mg iv followed by 8mg
Investigations
Parameters Primary HPT Secondary HPT
parathormone High High
Calcium High Normal
Phosphate Dcreased Increased
• Increased serum PTH level: specific abd diagnositic, > 0.5
• Bone density assesment
• Vitamin D estimation
• Increased urinary calcium level: >250 mg/24 hours
• Raised al;kaline phosphate level
Investigations
■ X-ray features:
- skull: salt and pepper appearance
- Phalanges: supperiosteal bone resorption
- Jaw: osteitis fibrosa cystica
- Spine: rugger jersy spine
■ USG abdomen
■ Thallium- technetium scan: hot spotes ( diagnostic of parathyroid adenoma)
Treatment
■ Parthyroidectomy
■ Indications
1. Severe symptoms
2. Young age group
3. Markedly reduced bone density
4. Serum calcium > 11mg%
5. Urinary calculi
6. Urinary calcium > 400 mg/24 hours
Parathyoidectomy
■ Preoperative preperation:
- Vocal cords assesed
- Treatment of high calcium levels preoperatively
1. Diuresis
2. Steroids: prednisolone 20mgTDS for 5 days
3. Phosphate infusion: 100mmol infusion in 6 hours
4. Calcitonin subcutaneous injection: 200 units BD for 5 days
5. Biphosphate- Etiodronate disodium: 7-5 mg/kg slow iv infusion for 3 days
6. Mithramycin: 25 microgram/kg single dose.
Parathyoidectomy
■ Total parathyroidectomy
- For parathyroid hyprplasia
- All four glands removed
- 1/3 rd of one gland autotransplanted into forearm muscle (brachioradia;is) or
sternocleidomastoid with marker stitch
- Transplamted gland slice in 1mm pieces
- 18 pieces embedded
Parathyoidectomy
■ Adenoma in gland with normal other glands: Removal of single gland
■ Carcinoma: parathyroidectomy plus hemithyroidectomy with postoperative
radiotherapy
■ All 4 glands diseased:Transcervical thymectomy added.
Parathyoidectomy
■ Surgical approaches;
1. Classical approach
2. Minimally invasive parathyroidectomy
3. Median sternotomy extension
4. Video- assisted parathyroidectomy
5. Endosopic parathyroidectomy
6. Remedial parathyoidectomy
7. Subtotal parathyroidectomy
8. Subtotal parathyroidectomy
9. Total parathyroidectomy with parathyroid sutotransplantation.
Parathyoidectomy
■ Complications:
- Haemorrhage, RLN palsy, hypocalcaemia.
- Persistent HPT: Serum calcium does not normalise immediately after surgery.
- Recurrent HPT: Serum calcium after surgery becomes normal but again increases in 6-
12 months.
- Hypoparathyoidism with devere hypocalcaemia- whwn all glands arec removed
- Hungry bone syndrome: In patients with npreop hypethyoidism,Thyroid hormone
level drops acutely after surgery, stimulus to break down bone is removed,
Bones remove calcium from plasma rapidly
Parathyoidectomy
- Presentation
Hypocalcaemia
Hypophosphatemia
Hypomagnesemia
Hyperkalemia
■ Vitamin D supplementation and elemental calcium: for 6 months
■ Ca;citriol with 2gm calcium supplement.
MEN SYNDROME
MEN Syndrome
■ Autosomal dominant.
■ Types
- Type 1 (Werner’s syndrome)- 3P’s
1. Parathyroid hyperplasia/ adenoma
2. Pitutary tumour- Prolactinoma
3. Pancreatic tumour- Gastrinoma, Insulinoma,Glucoganoma,VIP’oma
Chromosome 11
MEN syndrome
■ Type II A ( Sipple syndrome): chromosome 10
- Medullary carcinoma thyroid
- Pheochromocytoma
- Parathyroid hyperplaisa
■ Type II B
- Medullary carcinoma thyroid
- Pheochromocytoma
- Neuroma
HYPOPARATHYROIDIS
M
Hypoparathyoidism
■ PTH level < 10pg/ml
■ Types
1. Temporary:
– More common (2-50%)
– Lasts for 2 months maximum upto 6 months
– Decrease in calcium
– Increase in phosphorous
Hypoparathyoidism
2. Permanent:
– Less common (0.4%)
– Continues beyond 6 months
– Decreased calcium
– Increase in phosphorous.
3. Hungry bone syndrome:
– Common (5-13%)
Hypoparathyoidism
■ Causes-:
- Direct trauma to parathyroid glands
- Devascularization of glands
- Removal of gland during surgery
Hypoparathyoidism
■ Clinical features:
- Circumoral tingling, numbness and paresthesia
- Carpopedal spasm, laryngeal stridor
- Respiratory musckle spasm, suffocation
- Cataract formation
- Convulsion.
Hypoparathyoidism
■ Treatment :
- IV calcium gluconate: 10ml, 10% solution oveer 10 minutes
- Ssymptoms not resolve: Calcium infusion at 1-2 mg/kg/hr
- 1-2 gm oral calcium per day.
(Calcium carbonate: 1250 mg= 500mg elemental calcium)
-Vitamin D supplementation: 0.25- 1 microigram/day.
THANKYOU

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Parathyroid disorders final.pptx

  • 1. PARATHYROID DISORDERS Dr. Nilutpal Gogoi MBBS, MS. Assistant Professor, Department of General Surgery GMCH
  • 2. ANATOMY ■ Endocrine glands situated behind thyroid gland ■ Four in number ■ Weight: 40-50 grams ■ Secrete: Parathormone ■ Superior glands: – Develop from 4th pharyngeal pouch – Behind RLN
  • 3. ■ Inferior glands – Develop from 3rd pharyngeal pouch – Infront of RLN – Variable in position:Tracheo-oesophageal groove, Behind esophgus, Carotid sheath ■ Blood supply- inferior thyroid artery (End artery)
  • 4. Parathormone ■ 84 aminoacids ■ Secretion not dependent on pitutary gland ■ Half life- 4 minutes ■ Functions : – Converts vitamin D into 1,25- dihydrocholecalciferol in kidney – Absorption of calcium from gut – Mobilises calcium from bone – Reabsorption from renal tubules
  • 5. Calcium metabolism ■ Normal value: 8.5-10.2 mg/dl ■ Commonest protein part of bound calcium is Albumin (80%) ■ Level controlled by – PTH – Calcitonin – Vitamin D- Acts on bone, kidney and GIT ■ Functions 1. Blood coagulation 2. Neuromuscular activity 3. Cellular activity 4. Bone integrity.
  • 8. PRIMARY HPT ■ 3rd most common endocrine disease ■ Causes hypercalcemia ■ Etiology - Parathyroid adenoma - Familial/ genetic causes - MEN 1 syndrome - Therapeutic ionizing radiations - Lithium: parathyroid hyperplasia and HPT with no bone or renal problems
  • 9. Clinical features of HPT ■ Clinical vignette: “Bones, stones, abdominal groans and psychic moans” ■ Middle aged women( 3:1) ■ Incidence: 1:1000 ■ Asymptomatic > 50% cases
  • 10. Clinical feature contd. ■ BONES - Raised PTH - Increased osteoclastic activity - Extensive decalcification of bone - Bone pain, subosteal erosions - Osteitis fibrosa cystica: single/ multiple cysts/ pseudotumours in the jaw, skull or phalanges - Osteopenia, osteoporosis and pathological fracture
  • 11. Clinical feature contd. ■ STONES: - Renal stone in 25% patients - Recurrent stones - Calcium phosphate and oxalate type - Metaststic calcification, nephrocalcinosis, renal failure - Calcification in renal vessels: renal hypertension.
  • 12. Clinical feature contd. ■ ABDOMINALGROANS - Stimulates gastrin release: peptic ulceration - Precipitate acute pancreatitis - Increases gall stone disease ( calcium bilirubinate) ■ PSYCHIC MOANS: - Behavioural and neurotic problems: depression and anxiety
  • 13. Acute hyperparathyroidism (Crisis) ■ Causes - Sidden increase in PTH due to rupture od parathyroid cyst or bleeding in parathyroid tumour - Severe dehydration precipitates crisis - Secondaries in bone.
  • 14. Acute hyperparathyroidism (Crisis) ■ Clinical presentation 1. Abdominal pain 2. Vomiting 3. Dehysration 4. Oliguria 5. Muscular weakness 6. Death ■ Serum calcium: >12mg%
  • 15. Acute hyperparathyroidism (Crisis) ■ Treatment - Forced diuresis: 3-5 litres of saline with frusemide - Rehydration: normal saline 300ml/hr - Steroids: inhibit effects of vitamin D Dose: 400/ day iv for 5 days - Bisphosphonate: Cloodranate sodium, pamidronate Inhibits mobilization of calcium from bone Dose: 4mg iv followed by 8mg
  • 16. Investigations Parameters Primary HPT Secondary HPT parathormone High High Calcium High Normal Phosphate Dcreased Increased • Increased serum PTH level: specific abd diagnositic, > 0.5 • Bone density assesment • Vitamin D estimation • Increased urinary calcium level: >250 mg/24 hours • Raised al;kaline phosphate level
  • 17. Investigations ■ X-ray features: - skull: salt and pepper appearance - Phalanges: supperiosteal bone resorption - Jaw: osteitis fibrosa cystica - Spine: rugger jersy spine ■ USG abdomen ■ Thallium- technetium scan: hot spotes ( diagnostic of parathyroid adenoma)
  • 18. Treatment ■ Parthyroidectomy ■ Indications 1. Severe symptoms 2. Young age group 3. Markedly reduced bone density 4. Serum calcium > 11mg% 5. Urinary calculi 6. Urinary calcium > 400 mg/24 hours
  • 19. Parathyoidectomy ■ Preoperative preperation: - Vocal cords assesed - Treatment of high calcium levels preoperatively 1. Diuresis 2. Steroids: prednisolone 20mgTDS for 5 days 3. Phosphate infusion: 100mmol infusion in 6 hours 4. Calcitonin subcutaneous injection: 200 units BD for 5 days 5. Biphosphate- Etiodronate disodium: 7-5 mg/kg slow iv infusion for 3 days 6. Mithramycin: 25 microgram/kg single dose.
  • 20. Parathyoidectomy ■ Total parathyroidectomy - For parathyroid hyprplasia - All four glands removed - 1/3 rd of one gland autotransplanted into forearm muscle (brachioradia;is) or sternocleidomastoid with marker stitch - Transplamted gland slice in 1mm pieces - 18 pieces embedded
  • 21. Parathyoidectomy ■ Adenoma in gland with normal other glands: Removal of single gland ■ Carcinoma: parathyroidectomy plus hemithyroidectomy with postoperative radiotherapy ■ All 4 glands diseased:Transcervical thymectomy added.
  • 22. Parathyoidectomy ■ Surgical approaches; 1. Classical approach 2. Minimally invasive parathyroidectomy 3. Median sternotomy extension 4. Video- assisted parathyroidectomy 5. Endosopic parathyroidectomy 6. Remedial parathyoidectomy 7. Subtotal parathyroidectomy 8. Subtotal parathyroidectomy 9. Total parathyroidectomy with parathyroid sutotransplantation.
  • 23. Parathyoidectomy ■ Complications: - Haemorrhage, RLN palsy, hypocalcaemia. - Persistent HPT: Serum calcium does not normalise immediately after surgery. - Recurrent HPT: Serum calcium after surgery becomes normal but again increases in 6- 12 months. - Hypoparathyoidism with devere hypocalcaemia- whwn all glands arec removed - Hungry bone syndrome: In patients with npreop hypethyoidism,Thyroid hormone level drops acutely after surgery, stimulus to break down bone is removed, Bones remove calcium from plasma rapidly
  • 24. Parathyoidectomy - Presentation Hypocalcaemia Hypophosphatemia Hypomagnesemia Hyperkalemia ■ Vitamin D supplementation and elemental calcium: for 6 months ■ Ca;citriol with 2gm calcium supplement.
  • 26. MEN Syndrome ■ Autosomal dominant. ■ Types - Type 1 (Werner’s syndrome)- 3P’s 1. Parathyroid hyperplasia/ adenoma 2. Pitutary tumour- Prolactinoma 3. Pancreatic tumour- Gastrinoma, Insulinoma,Glucoganoma,VIP’oma Chromosome 11
  • 27. MEN syndrome ■ Type II A ( Sipple syndrome): chromosome 10 - Medullary carcinoma thyroid - Pheochromocytoma - Parathyroid hyperplaisa ■ Type II B - Medullary carcinoma thyroid - Pheochromocytoma - Neuroma
  • 29. Hypoparathyoidism ■ PTH level < 10pg/ml ■ Types 1. Temporary: – More common (2-50%) – Lasts for 2 months maximum upto 6 months – Decrease in calcium – Increase in phosphorous
  • 30. Hypoparathyoidism 2. Permanent: – Less common (0.4%) – Continues beyond 6 months – Decreased calcium – Increase in phosphorous. 3. Hungry bone syndrome: – Common (5-13%)
  • 31. Hypoparathyoidism ■ Causes-: - Direct trauma to parathyroid glands - Devascularization of glands - Removal of gland during surgery
  • 32. Hypoparathyoidism ■ Clinical features: - Circumoral tingling, numbness and paresthesia - Carpopedal spasm, laryngeal stridor - Respiratory musckle spasm, suffocation - Cataract formation - Convulsion.
  • 33. Hypoparathyoidism ■ Treatment : - IV calcium gluconate: 10ml, 10% solution oveer 10 minutes - Ssymptoms not resolve: Calcium infusion at 1-2 mg/kg/hr - 1-2 gm oral calcium per day. (Calcium carbonate: 1250 mg= 500mg elemental calcium) -Vitamin D supplementation: 0.25- 1 microigram/day.