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Parathyroid Gland
and
Hyperparathyroidism
Anatomy of Parathyroid gland
 Small fat lobules usually bruised on
operation table may look like parathyroid
 Sink test
Sink in water parathyroid will sink – fat
lobule will float
•Small, oval in shape 0.5 to 6x3x1.5mm
•Yellowish brown colour 30 to 40 mgs
•Size and appearance resembles a ‘ Tur dal
•Exact no. of parathyroid may vary
•Gilmour (1936)
88% 4 glands
6% 5 glands
6%Glands : might be due to fusion
Position of Parathyroid
 Inferior Thyroid gland varies in position.
 Usually situated at the lower pole of thyroid
gland.
 May be found any where in this situation
downwards to the upper pole Thymus.
 5% found in upper anterior Mediastinum.
 Embryo logically Inferior. thyroid gland shows
origin with Thymus – 3rd bronchial arch
Parathyroid III
•Upper two Parathyroid glands fairly constant,
• closely embedded in thyroid at Postero Lateral border of
thyroid Gland immediately above entry of inf. thyroid artery.
•Rarely it might vary above and within substance of thyroid gland
along the of thyroid gland.
• with approximately 75% being located either cricothyroidal or juxtathyroidal,
and the remainder are located primarily behind the upper pole of the thyroid gland.
•Common embryological origin from IV th bronchial arch.Parathyroid IV
di George Syndrome – Congenital absence of parathyroid gland
Thymus and pharyngeal derivatives
Histology:
 Rich sinusoidal capillary net work with
islands of secretary cells.
 Glandular cells
 Chief (Principle cells) Small, vasicular
nuclei and poorly staining cytoplasm
 Clear cells : Found in hyperplastic
Neoplastic Tumours.
Physiology:
1.Stimulates osteoclastic activity.
increasing bone Reabsorption by
mobilizing Ca PO4 from bone.
2) Increases Reabsorption of calcium
from renal tubules Thus reducing
urinary excretion of calcium.
3) Augments absorption of Ca from gut.
4) Renal tubular PO4 increases Ca
Chief cells produce Parathormone
Released directly into circulation
Hyperparathyroidism
3) Tertiary HPT :
Persistant HPT after Renal
Transplantation in Renal
osteodystrophy.
1)Primary
•a) Hyperplasia
• Chief Cell Alone
MEN I
MEN II a
FHHH
• Water Clear Cell (WCCH)
b) Neoplasia
Carcinoma
• Adenoma
2) Secondary :
• Chronic renal failure with Renal
ostodystrophy
Serum Ca lowers leading to Compensatory
parathyroid Hyperplasia of all 4 glands
•Malabsorption syndrome
Clinical Features
Bones,
Stones,
Abdominal groans
and Psychic moans
 Rarely found in first decade of life.
 20 to 60 years.
bones; Vague bony pain and
joint pains D/D Rheumatism
Generalized decalcification of skeleton Von-
Reclinghausen’s disease
( Osteitis cystica fibrosa)
Early Skull, Phalanges
Loss of density
Sub Periosteal erosion
 Late: Generalized calcicification
 Multiple bone cyst
 Psuedo tumours of Jaw
Parathyroid fractures
Stones:
 Multiple, Recurrent Renal Stones.
 Nephrolithiasis – Nephrocalcinosis
 Ectopic Calcification.
Abdominal groans
 Dyspeptic cases : Nauseas,. vomiting,
anorexia.
 Peptic Ulcer
 Pancreatitis Not fully confirmed.
Psychic Moans
 Uncommon, Lethargy
 Tiredness, Listlessness, irrational
behaviour
 Wrongly Labeled as Neurotic
Hypercalcemic Syndrome:
 Minor mental changes, Lethargy
 Polydypsia, Polyurea
 Dehydration, Persistent Irritable GIT
Acute HPT syndrome
• Nausea, vomiting
• Abdominal pain
• Oliguria
• Coma
Asymptomatic: Detected during biochemical check up.
Laboratory Studies
 Serum Calcium : Serial reading for 3 occasions. ( 9.5 to 11
mg_
 >11 mg% Suspicious of HPT. >12 definite for HPT
- No tourniquet
- Long storage
- Low PO4 diet
- Diurnal variation 1 to 4%
Cortisone Test
150mg/day/10 days
No effect Primary HPT
Calcium levels reduced
all other causes
Secondories in bone
Carcinoma with endocrine
potential
( bronchus, kidney, ovary)
Multiple Myeloma
Sarcoidosis
Thyrotoxicosis,
Hypervitaminosis D
Laboratory Studies II
 Serum PO4 : Lower than normal (<300mg /dl)
 Alkaline PO4 : increases if there is bone involvement
 Urinary Calcium
– Low Ca+ diet
– Useful with only high Serum Ca
– Ser. Ca: Renal Stones.
– Upper Limit : 250 mg in Males 300 mg in Females
 Bone biopsy from iliac crest
 CAT Scan
 Ultra Sonogram
 X-Ray Studies.
Localization of Parathyroid Pathology:
 Preoperative:Minimum invasive:
 Barium swallow,
 Cine oesophagogram
 Neck massage PTH, urinary
cyclic AMP
 Ultra Sound
 Thyroid Scan
 Technetium Tc 99m
Sestamibi radionuclide
91% to100% accuracy
 Computer assisted isotope
scanning:Substraction scanning
 Computed tomography
 Preoperative:Invasive:
 Selective venous sampling
of PTH
 Selective anteriography
 Arterial injection of
selenomethionine 15
 Needle aspiration
Intra operative:
•Methylene blue
•0-Toludine blue,
•Urinary Cyclic AMP
•intraoperative assessment of PTH
•intraoperative gamma probes for
nuclear mapping
Parathyroidectomy:Indications
1) Primary HPT
Hyperplasia – 3.1/2
Adenoma --- one
Carcinoma – Local Radical Diss.
2) Secondary HPT
– If bone decalcifation
- Severe pain.
3) Tertiary HPT
4) Re operative.
Auto Transplantation of Parathyroid
– Primary Thyroid hyperplasia
– Secondary HPT
– Re operative HPT
– Total Thyroidectomy for Ca Thyroid
 Felix Mandl in Vienna, Austria
performed the first successful
parathyroidectomy in 1925.
 Endoscopic parathyroidectomy was
pioneered by Dr Michel Gagner at the
Cleveland Clinic in 1996
Surgical techniques
 Open Parathyroidectomy
 Minimally invasive parathyroid surgery
Deferred parathyroid Autotransplantation
 Immediately placed in to sterile saline or tissue culture
 Sliced into 1x1x3mm silvers.
 3ml Glass vials will accommodate 10 silvers
1 to 1.5 ml
– 10% DMSO dimethyl sulfoxide
– 10% autologus serum
– 80% Tissue culture media
 Frozen 1degree centigrade per minute
 Till you reach -80degree Centigrade
 -190 o C Vapour phase Liquid nitrogen freezer
 Linde BF 4/6 biological freezing system
 Thawing rapidly to 57oC
 Implant in Thigh sub cutaneously

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Parathyroid gland

  • 2. Anatomy of Parathyroid gland  Small fat lobules usually bruised on operation table may look like parathyroid  Sink test Sink in water parathyroid will sink – fat lobule will float •Small, oval in shape 0.5 to 6x3x1.5mm •Yellowish brown colour 30 to 40 mgs •Size and appearance resembles a ‘ Tur dal •Exact no. of parathyroid may vary •Gilmour (1936) 88% 4 glands 6% 5 glands 6%Glands : might be due to fusion
  • 3. Position of Parathyroid  Inferior Thyroid gland varies in position.  Usually situated at the lower pole of thyroid gland.  May be found any where in this situation downwards to the upper pole Thymus.  5% found in upper anterior Mediastinum.  Embryo logically Inferior. thyroid gland shows origin with Thymus – 3rd bronchial arch Parathyroid III •Upper two Parathyroid glands fairly constant, • closely embedded in thyroid at Postero Lateral border of thyroid Gland immediately above entry of inf. thyroid artery. •Rarely it might vary above and within substance of thyroid gland along the of thyroid gland. • with approximately 75% being located either cricothyroidal or juxtathyroidal, and the remainder are located primarily behind the upper pole of the thyroid gland. •Common embryological origin from IV th bronchial arch.Parathyroid IV di George Syndrome – Congenital absence of parathyroid gland Thymus and pharyngeal derivatives
  • 4. Histology:  Rich sinusoidal capillary net work with islands of secretary cells.  Glandular cells  Chief (Principle cells) Small, vasicular nuclei and poorly staining cytoplasm  Clear cells : Found in hyperplastic Neoplastic Tumours.
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  • 6. Physiology: 1.Stimulates osteoclastic activity. increasing bone Reabsorption by mobilizing Ca PO4 from bone. 2) Increases Reabsorption of calcium from renal tubules Thus reducing urinary excretion of calcium. 3) Augments absorption of Ca from gut. 4) Renal tubular PO4 increases Ca Chief cells produce Parathormone Released directly into circulation
  • 7. Hyperparathyroidism 3) Tertiary HPT : Persistant HPT after Renal Transplantation in Renal osteodystrophy. 1)Primary •a) Hyperplasia • Chief Cell Alone MEN I MEN II a FHHH • Water Clear Cell (WCCH) b) Neoplasia Carcinoma • Adenoma 2) Secondary : • Chronic renal failure with Renal ostodystrophy Serum Ca lowers leading to Compensatory parathyroid Hyperplasia of all 4 glands •Malabsorption syndrome
  • 9.  Rarely found in first decade of life.  20 to 60 years. bones; Vague bony pain and joint pains D/D Rheumatism Generalized decalcification of skeleton Von- Reclinghausen’s disease ( Osteitis cystica fibrosa) Early Skull, Phalanges Loss of density Sub Periosteal erosion  Late: Generalized calcicification  Multiple bone cyst  Psuedo tumours of Jaw Parathyroid fractures
  • 10. Stones:  Multiple, Recurrent Renal Stones.  Nephrolithiasis – Nephrocalcinosis  Ectopic Calcification.
  • 11. Abdominal groans  Dyspeptic cases : Nauseas,. vomiting, anorexia.  Peptic Ulcer  Pancreatitis Not fully confirmed.
  • 12. Psychic Moans  Uncommon, Lethargy  Tiredness, Listlessness, irrational behaviour  Wrongly Labeled as Neurotic
  • 13. Hypercalcemic Syndrome:  Minor mental changes, Lethargy  Polydypsia, Polyurea  Dehydration, Persistent Irritable GIT Acute HPT syndrome • Nausea, vomiting • Abdominal pain • Oliguria • Coma Asymptomatic: Detected during biochemical check up.
  • 14. Laboratory Studies  Serum Calcium : Serial reading for 3 occasions. ( 9.5 to 11 mg_  >11 mg% Suspicious of HPT. >12 definite for HPT - No tourniquet - Long storage - Low PO4 diet - Diurnal variation 1 to 4% Cortisone Test 150mg/day/10 days No effect Primary HPT Calcium levels reduced all other causes Secondories in bone Carcinoma with endocrine potential ( bronchus, kidney, ovary) Multiple Myeloma Sarcoidosis Thyrotoxicosis, Hypervitaminosis D
  • 15. Laboratory Studies II  Serum PO4 : Lower than normal (<300mg /dl)  Alkaline PO4 : increases if there is bone involvement  Urinary Calcium – Low Ca+ diet – Useful with only high Serum Ca – Ser. Ca: Renal Stones. – Upper Limit : 250 mg in Males 300 mg in Females  Bone biopsy from iliac crest  CAT Scan  Ultra Sonogram  X-Ray Studies.
  • 16. Localization of Parathyroid Pathology:  Preoperative:Minimum invasive:  Barium swallow,  Cine oesophagogram  Neck massage PTH, urinary cyclic AMP  Ultra Sound  Thyroid Scan  Technetium Tc 99m Sestamibi radionuclide 91% to100% accuracy  Computer assisted isotope scanning:Substraction scanning  Computed tomography  Preoperative:Invasive:  Selective venous sampling of PTH  Selective anteriography  Arterial injection of selenomethionine 15  Needle aspiration Intra operative: •Methylene blue •0-Toludine blue, •Urinary Cyclic AMP •intraoperative assessment of PTH •intraoperative gamma probes for nuclear mapping
  • 17. Parathyroidectomy:Indications 1) Primary HPT Hyperplasia – 3.1/2 Adenoma --- one Carcinoma – Local Radical Diss. 2) Secondary HPT – If bone decalcifation - Severe pain. 3) Tertiary HPT 4) Re operative.
  • 18. Auto Transplantation of Parathyroid – Primary Thyroid hyperplasia – Secondary HPT – Re operative HPT – Total Thyroidectomy for Ca Thyroid
  • 19.  Felix Mandl in Vienna, Austria performed the first successful parathyroidectomy in 1925.  Endoscopic parathyroidectomy was pioneered by Dr Michel Gagner at the Cleveland Clinic in 1996
  • 20. Surgical techniques  Open Parathyroidectomy  Minimally invasive parathyroid surgery
  • 21. Deferred parathyroid Autotransplantation  Immediately placed in to sterile saline or tissue culture  Sliced into 1x1x3mm silvers.  3ml Glass vials will accommodate 10 silvers 1 to 1.5 ml – 10% DMSO dimethyl sulfoxide – 10% autologus serum – 80% Tissue culture media  Frozen 1degree centigrade per minute  Till you reach -80degree Centigrade  -190 o C Vapour phase Liquid nitrogen freezer  Linde BF 4/6 biological freezing system  Thawing rapidly to 57oC  Implant in Thigh sub cutaneously