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Dr. Ashraful Huq (Ridoy)
FCPS
+8801811999070
Bangladesh Eye Hospital Ltd.
Dhaka, Bangladesh
o The pituitary gland, or hypophysis, is
an endocrine gland
o Produce number of hormones which control
the secretions of many other endocrine glands
o Its anatomical position is important in
ophthalmological view
 The anterior pituitary
(adenohypophysis) arises
from Rathke's pouch, an
upward growth from the
ectodermal roof of the
stomodeum
 The posterior pituitary
(neurohypophysis) arises
from a downward growth
from the floor of the
diencephalon
 Occupies a cavity of the
sphenoid bone called
sella turcica at the
middle cranial fossa
 Roof is formed by
diaphragma sellae
 The stalk of pituitary is
attached above to the
floor of third ventricle
 Size of a pea (< 8 mm)
 It weighs about 0.5 gm.
Anterior Lobe:
• FSH
• LH
• ACTH
• TSH
• Prolactin
• GH
Posterior Lobe:
• ADH
• Oxytocin
Benign tumors of pituitary gland
 Etiology is unknown
 10-15% of all primary brain tumors
 75% of adenomas are endocrinogically
secreting
 25% of those with MEN-I develop pituitary
adenomas
Hormones Clinical features
Secreting (75%) Chromophobes
(50%)
Prolactin Female: Infertility,
amenorrhea,
galactorrhea
Male :
Hypogonadism,
impotency, sterility,
↓libido,
gynecomastia,
galactorrhea
Acidophils (20%) GH Acromegaly(adult)
Gigantism(child)
Basophils(5%) ACTH, FSH & TSH Cushing disease,
FSH & TSH tumors
Nonsecreting
(25%)
Microadenoma < 10 mm diameter Secreting adenoma
Macroadenoma > 10 mm diameter Mass effects
Non secreting
Localized mass effects
• Chiasmal syndromes
• Compression of other adjacent structures
~ Cavernous sinus (paresis of 3rd, 4th or 6th CN causing
disorders of extraocular motility)
~ Hypopituitarism (direct pressure, vascular damage)
~ Papilloedema (raised ICP, very rare)
Endocrine effects
• Hypersecretion
Growth Hormone ACTH
Female
• Infertility-amenorrhea- galactorrhea
Male
• Hypogonadism, impotence, sterility, ↓ libido,
gynecomastia, galactorrhea
 Growth hormone deficit
• In children: dwarfism
• In adults: weakness, overweight , reduced cardiac output, low blood
sugar levels, and reduced exercise tolerance
 TSH deficit
• Hypothyroidism
 ACTH deficit
• Underactive adrenal gland, which causes low blood
pressure, hypoglycemia, fatigue, weight loss, vomiting, and low stress
tolerance
 ADH deficit
• Diabetes Insipidus
Blurred vision
Headache
Diplopia
Colour desaturation
Visual field defect
Optic atrophy
Post fixation blindness
Visual hallucination
See-Saw nystagmus
 Bitemporal hemianopia
 Incongruous homonymous hemianopia
 Bitemporal central scotoma
 Diffuse scotoma
 Junctional scotoma
 Classic defect in
pituitary adenoma
 Occurs in central
chiasmal defect
 Superotemporal field
affected first
↓
Lower temporal
field defect
 Occurs in optic tract
lesion
 Occurs in post.
Chiasmal lesion
 Compressing only the
macular fibers
Bitemporal central
scotoma
 Central scotoma in one
eye with superotemporal
visual field loss in the
other eye
 Caused by compression
to anterior loop to the
decussating nasal fibers
in posterior optic nerve
(Von Wilbrand's knee)
Bow tie atrophy Diffuse atrophy
 Large adenoma leading to haemorrhage or
infarction of pituitary gland
 Occur in pregnancy
 Compresses hypophysial portal vessels
 Presentation: hyperacute chiasmal syndrome
 Treatment : high dose steroid / surgery
 Visual acuity
 RAPD
 Color vision
 Ocular motility
 Fundus examination
Endocrinological evaluation
• Serum prolactin
• FSH
• TSH
• GH
• Insulin stress test
Ocular investigation
• Visual Field Analysis
• Hess / Lees chart
Imaging
• MRI / CT scan of brain
• X-ray skull (Ant. & Lat. view)
 Referral to Endocrinologist & Neuro-surgeon
 Observation
 Medical therapy
• Dopamine agonists – Cabergoline/Bromocriptine
 Surgery
• When mass causing severe compression
• Endoscopic - Transphenoidal, transfrontal
• Craniotomy
• Visual recovery is tri-phasic
Transfrontal
Trans-
sphenoidal
Surgery
Radiotherapy
Observation
Medical therapy
Radiotherapy
• Following incomplete removal of tumour
• Primary treatment
Gamma knife stereotactic radiotherapy
• Close proximity to the optic nerve
• Cavernous sinus invasion
Surgery Radiotherapy Medical
Non-functioning
adenoma
1st line 2nd line -
Prolactinoma 2nd line 2nd line 1st line
Acromegaly 1st line 2nd line 2nd line
Cushing’s
disease
1st line 2nd line -
Medical therapy –
• Monthly for large tumors or during pregnancy for
tumors of any size
• 6 month intervals in microadenoma for 1 year,
then yearly
Surgery –
• Immediately postoperatively
• 4-6 weeks postoperatively
• 4 months intervals for a year
• Yearly for 5 years
• Every 2 years
Radiotherapy –
• At the midpoint and end of radiotherapy
• 3 months interval for a year
• 6 months interval for a year
• Yearly
Evaluation -
• Visual acuity
• Fundoscopy
• Visual field
• Imaging
 Pituitary adenomas occurs with a wide
spectrum of clinical features
 Should be managed between different
specialists
 Neuro-ophthalmological manifestations are
frequent and varied
 Physicians must be aware about these in order
to refer patients to ophthalmologist for early
diagnosis and treatment
Pituitary adenoma

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Pituitary adenoma

  • 1. Dr. Ashraful Huq (Ridoy) FCPS +8801811999070 Bangladesh Eye Hospital Ltd. Dhaka, Bangladesh
  • 2. o The pituitary gland, or hypophysis, is an endocrine gland o Produce number of hormones which control the secretions of many other endocrine glands o Its anatomical position is important in ophthalmological view
  • 3.  The anterior pituitary (adenohypophysis) arises from Rathke's pouch, an upward growth from the ectodermal roof of the stomodeum  The posterior pituitary (neurohypophysis) arises from a downward growth from the floor of the diencephalon
  • 4.  Occupies a cavity of the sphenoid bone called sella turcica at the middle cranial fossa  Roof is formed by diaphragma sellae  The stalk of pituitary is attached above to the floor of third ventricle  Size of a pea (< 8 mm)  It weighs about 0.5 gm.
  • 5. Anterior Lobe: • FSH • LH • ACTH • TSH • Prolactin • GH Posterior Lobe: • ADH • Oxytocin
  • 6.
  • 7. Benign tumors of pituitary gland
  • 8.  Etiology is unknown  10-15% of all primary brain tumors  75% of adenomas are endocrinogically secreting  25% of those with MEN-I develop pituitary adenomas
  • 9. Hormones Clinical features Secreting (75%) Chromophobes (50%) Prolactin Female: Infertility, amenorrhea, galactorrhea Male : Hypogonadism, impotency, sterility, ↓libido, gynecomastia, galactorrhea Acidophils (20%) GH Acromegaly(adult) Gigantism(child) Basophils(5%) ACTH, FSH & TSH Cushing disease, FSH & TSH tumors Nonsecreting (25%)
  • 10. Microadenoma < 10 mm diameter Secreting adenoma Macroadenoma > 10 mm diameter Mass effects Non secreting
  • 11. Localized mass effects • Chiasmal syndromes • Compression of other adjacent structures ~ Cavernous sinus (paresis of 3rd, 4th or 6th CN causing disorders of extraocular motility) ~ Hypopituitarism (direct pressure, vascular damage) ~ Papilloedema (raised ICP, very rare) Endocrine effects • Hypersecretion
  • 13. Female • Infertility-amenorrhea- galactorrhea Male • Hypogonadism, impotence, sterility, ↓ libido, gynecomastia, galactorrhea
  • 14.  Growth hormone deficit • In children: dwarfism • In adults: weakness, overweight , reduced cardiac output, low blood sugar levels, and reduced exercise tolerance  TSH deficit • Hypothyroidism  ACTH deficit • Underactive adrenal gland, which causes low blood pressure, hypoglycemia, fatigue, weight loss, vomiting, and low stress tolerance  ADH deficit • Diabetes Insipidus
  • 15. Blurred vision Headache Diplopia Colour desaturation Visual field defect Optic atrophy Post fixation blindness Visual hallucination See-Saw nystagmus
  • 16.  Bitemporal hemianopia  Incongruous homonymous hemianopia  Bitemporal central scotoma  Diffuse scotoma  Junctional scotoma
  • 17.  Classic defect in pituitary adenoma  Occurs in central chiasmal defect  Superotemporal field affected first ↓ Lower temporal field defect
  • 18.  Occurs in optic tract lesion  Occurs in post. Chiasmal lesion  Compressing only the macular fibers Bitemporal central scotoma
  • 19.  Central scotoma in one eye with superotemporal visual field loss in the other eye  Caused by compression to anterior loop to the decussating nasal fibers in posterior optic nerve (Von Wilbrand's knee)
  • 20. Bow tie atrophy Diffuse atrophy
  • 21.
  • 22.  Large adenoma leading to haemorrhage or infarction of pituitary gland  Occur in pregnancy  Compresses hypophysial portal vessels  Presentation: hyperacute chiasmal syndrome  Treatment : high dose steroid / surgery
  • 23.  Visual acuity  RAPD  Color vision  Ocular motility  Fundus examination
  • 24. Endocrinological evaluation • Serum prolactin • FSH • TSH • GH • Insulin stress test Ocular investigation • Visual Field Analysis • Hess / Lees chart
  • 25. Imaging • MRI / CT scan of brain • X-ray skull (Ant. & Lat. view)
  • 26.  Referral to Endocrinologist & Neuro-surgeon  Observation  Medical therapy • Dopamine agonists – Cabergoline/Bromocriptine  Surgery • When mass causing severe compression • Endoscopic - Transphenoidal, transfrontal • Craniotomy • Visual recovery is tri-phasic
  • 28. Radiotherapy • Following incomplete removal of tumour • Primary treatment Gamma knife stereotactic radiotherapy • Close proximity to the optic nerve • Cavernous sinus invasion
  • 29. Surgery Radiotherapy Medical Non-functioning adenoma 1st line 2nd line - Prolactinoma 2nd line 2nd line 1st line Acromegaly 1st line 2nd line 2nd line Cushing’s disease 1st line 2nd line -
  • 30. Medical therapy – • Monthly for large tumors or during pregnancy for tumors of any size • 6 month intervals in microadenoma for 1 year, then yearly Surgery – • Immediately postoperatively • 4-6 weeks postoperatively • 4 months intervals for a year • Yearly for 5 years • Every 2 years
  • 31. Radiotherapy – • At the midpoint and end of radiotherapy • 3 months interval for a year • 6 months interval for a year • Yearly Evaluation - • Visual acuity • Fundoscopy • Visual field • Imaging
  • 32.  Pituitary adenomas occurs with a wide spectrum of clinical features  Should be managed between different specialists  Neuro-ophthalmological manifestations are frequent and varied  Physicians must be aware about these in order to refer patients to ophthalmologist for early diagnosis and treatment