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IMAGING OF ENDOCRINE DISEASES
Presented By :
Dr. Seham Adam
The pituitary gland (or hypophysis cerebri), together with its
connections to the hypothalamus, acts as the main endocrine
interface between the central nervous system and the rest of
the body.
Gross anatomy
The pituitary gland sits atop the base of the skull in a
concavity within the sphenoid bone called the sella turcica
(pituitary fossa), immediately below the hypothalamus and
optic chiasm.
The pituitary is usually divided (in practice) into anterior and
posterior parts
ANATOMY OF PITUTARY GLAND
OPTIC CHIASMA
INFUNDIBULUM
PITUTARY GLAND
CAVERNOUS SINUS
ANATOMY OF PITUTARY GLAND
ANATOMY OF PITUTARY GLAND
ANATOMY OF PITUTARY GLAND
ANATOMY OF PITUTARY GLAND
Normal Pituitary
IMAGING TECHNIQUES
High resolution (2 to 3mm thick slices)
• Sagittal T1-WI pre & post Gadolinium
• Coronal T1-WI pre & post Gadolinium
• Axial T2-WI
•Dynamic Gadolinium enhanced coronal T1-WI for small microadenoma.
MRI OF PITUITARY GLAND
IMAGING SEQUENCES
Pituitary Microadenomas are a minority of all pituitary
adenomas.
By definition, a microadenoma is less than 10 mm in size.
If the same tumor is greater than 10 mm in size, it is then
considered a pituitary macroadenoma. Differences in
presentation and imaging merely represent a difference in
size rather than any fundamental difference in biology.
MRI OF PITUITARY GLAND
IMAGE INTERPRETATION
Pituitary Macroadenomas are the most common
suprasellar mass in adults, They are defined as pituitary
adenomas greater than 10 mm in size and are
approximately twice as common as pituitary
microadenomas.
On imaging, they usually present as a solid tumor with
attenuation similar to the brain (30-40 HU) and demonstrate
moderate contrast enhancement. The same is observed on
MRI, where they are isointense to the grey matter both on T1-
and T2-weighted images. However, attenuation and signal
characteristics can significantly vary depending on tumor
components such as hemorrhage, cystic transformation, or
necrosis
MRI OF PITUITARY GLAND
IMAGE INTERPRETATION
Pituitary Adenoma
PITUITARY GLAND
DISEASES
Prolactinoma (high secretion of prolactin).
Acromegaly (high secretion of G.H. after 18 yrs).
Cushing Syndrome (high secretion of ACTH).
PITUITARY HYPOPLASIA
Failure of hypothalamic axons & surrounding
Venous plexus to connect with (anterior lobe ) adenohypophysis
• Global adenohypophyseal dysfunction.
• Preserved (posterior lobe )neurohypophyseal function
Imaging Findings:
• Small shallow sella turcica
• Small adenohypophysis.
• Ectopic Neurohypophysis.
• Midline facial & cranial anomalies
PITUITARY ADENOMAS:
Clinical Presentation
►Hormone hypersecretion
Acromegaly
Cushing’s Disease
Amenorrhea / Galactorrhea
►Symptoms from mass effect
Headaches
Vision loss
Pituitary gland dysfunction
Pituitary Adenoma
Prolactinoma
High serum Prolactin
1.Pregnancy
2.Stress
3.Lactation
4.Wet nursing reflex
1.Prolactinoma
2.Pituitary tumor
3.Polycystic ovaries
4.Primary hypothyroidism
5.Post herpes zoster
Prolactinoma
Clinical presentaion
Most Common Functional Pituitary adenoma (30-40%)
 Female : Male Prevalence-10:1, median age of diagnosis-34 yrs
Prolactinoma
Serum Prolactin level (ng/ml)
Acromegaly
• Most commonly due to pituitary adenoma
• Clinical Presentation
• enlargement of the hands, feet, nose, tongue, lips and ears
• general thickening of the skin with moist hands
• Organomegaly (especially thyroid, heart and liver)
• Characteristic thick, deep voice and slowing of speech
• Mandible: prognathism with gaping teeth
Acromegaly
Pituitary MRI-macroadenomas are detected in >80% of acromegaly.
Cushing`s
Disease
• pituitary Adenoma 60%(Cushing’s Disease)
• Ectopic source 15% (ACTH/CRH tumors)
ACTH-Dependent
75%
• Adrenal Adenomas
• Adrenal Carcinoma
• Nodular Hyperplasia (micro or macro)
ACTH-Independent
25%
Cushing’s Syndrome
Symptom of mass effect
• Headache
• Vision loss
• Pituitary hormone dysfunction
• Cranial Nerve Abnormality.
 Lipoma
 Pars intermedia cyst (Rathk’s Cleft cyst )
 Meningioma
 Craniopharyngioma
 Arachnoid cyst
 Apoplexy
 Sheehans` syndrome
 Aneurysm
Differential Diagnosis
Lipoma
Meningioma
Rathk`s Cleft Cyst
•A benign growth found on the pituitary gland in the brain, specifically a
fluid-filled cyst in the posterior portion of the anterior pituitary gland. It
occurs when the Rathke's pouch does not develop properly
Cranio-pharyngioma
Arachnoid Cyst
Apoplexy
acute clinical syndrome caused by either
hemorrhagic or non-hemorrhagic necrosis
of the pituitary gland. Although variable, it
typically comprises headache, visual
deficits, ophthalmoplegia, and altered
mental status. An existing pituitary
macroadenoma is usually present (60-
90%), but it has occurred with healthy
glands in a few isolated cases.
Sheehan’s Syndrome
Sheehan syndrome is a rare cause of pituitary
apoplexy and hypopituitarism. It only occurs in
postpartum females who experience large volume
hemorrhage and hypovolemic shock during
delivery
Clinical presentation
pituitary failure
may be silent and present with delayed hypopituitarism
• agalactorrhoea
• amenorrhea
• oligomenorrhea
• adrenal insufficiency
• hyponatremia (diabetes insipidus) in the acute setting
of extreme hypovolemia
• hypothyroidism
• growth hormone deficiency
• optic chiasm compression
• visual field loss
• headache
• ophthalmoplegia
Aneurysm
The Thyroid Gland
Thyrotoxicosis
Graves disease
Normal Ultrasound Appearance of the Thyroid
Gland
Ultrasound Appearance of Diffuse Thyroid
Enlargement (Goiter)
Thyrotoxicosis
Graves disease
Hypothyroidism
Thyroiditis
Ultrasound appearance of thyroid Ultrasound appearance of thyroiditis
Thyroid nodules
Suspicious sonographic features :
 Hypoechoic
 Micro calcification
 Infiltrative margin
 Taller than wider
 Abnormal cervical lymph node.
The radioactive iodine uptake test
The thyroid uptake is performed to evaluate the function of the
gland.
Low uptake suggests thyroiditis while high uptake suggests Graves
disease
Radionuclide imaging is unreliable in excluding or confirming the
presence of cancer.
The Parathyroid Gland
Parathyroid Imaging
1.Sonography
2.99mTc-sestamibi Scintigraphy
are the dominant imaging techniques for
preoperative location of parathyroid adenomas
Numerous studies comparing these techniques suggest
similar sensitivities and specificities for solitary adenoma
detection.
Localization accuracy is also improved when both
studies are obtained preoperatively
Ultrasound
Ultrasound is one of the most commonly used initial imaging modalities.
Greyscale
most nodules need to be >1 cm to be confidently seen on ultrasound
parathyroid adenomas tend to be homogeneously hypoechoic vs the overlying thyroid gland
an echogenic thyroid capsule separating the thyroid from the parathyroid may be seen
Doppler ultrasound
Can commonly show a characteristic extrathyroidal feeding vessel (typically a branch off the
inferior thyroidal artery 1,6), which enters the parathyroid gland at one of the poles. Internal
vascularity is also commonly seen in a peripheral distribution. This feeding artery tends to
branch around the periphery of the gland before penetration. This feature can give a
characteristic arc or rim of vascularity. The overlying thyroid gland may also show an area of
asymmetric hypervascularity that may help to locate an underlying adenoma
Parathyroid Adenoma
Parathyroid Adenoma
99mTc-sestamibi Scintigraphy
Is used to localize parathyroid adenoma that cannot be localized
with other imaging modalities as ultrasound or MRI. Localization of
parathyroid
adenoma allows the surgeon to use a minimally
invasive surgical approach
Adrenal gland
Adrenal Gland
 The adrenal gland is named for it is location adjacent to the kidney : ad-renal .
 Also known as supra adrenal glands.
 Characteristic inverted Y,V or T shape.
 Situated on the posterior abdominal wall over the upper pole of the kidneys behind
the peritoneum.
 Each gland is enclosed in the peri-renal fascia and have body and two limbs.
Histology
Adrenal cortex-90% of adrenal composed of three
zones.
1.zona glomerulosa –outermost secretes
mineralocorticoids(aldosterone)
2.zona fasciculate- 80%-secretes cortisol.
3. zona reticulate-5-10%-secretes androgens.
Histology
Adrenal medulla- 10% of adrenal made up of
chromaffin cells , secretes- epinephrine or nor
-epinephrine
Part of sympathetic autonomic nervous
system
Normal Gland / CT , MRI
Anatomical landmarks:
 Right Adrenal Gland :
Superior to right kidney , medial to right lobe of liver lateral to crus of right
hemidiaphragm , posterior to IVC.
 Left Adrenal Gland :
Superior to upper pole of left kidney in triangle formed by left lateral margin of aorta,
posterior surface of body and tail of pancreas and upper pole of left kidney.
Imaging Modalities
Ultrasound .
Computed tomography.
Magnetic resonance imaging.
Nuclear medicine imaging.
Adrenal Adenoma
• most common adrenal mass lesion and are often found incidentally during abdominal imaging
• The most common disease states caused by functioning adenomas are Cushing syndrome (due
to excess cortisol production), Conn syndrome (due to excess aldosterone production)
Thus, tissues containing lipid and water have signal loss (i.e.,
appear darker) on out-of phase images.
Thus, on out-of phase images, the adenoma appears darker than
on in-phase images.
CT in Differentiating Benign from Malignant Adrenal Masses
certain imaging findings are helpful in differentiating benign from
malignant lesions.
•Larger lesions
•Change in lesion size
•The shape .
•Intracellular lipid content of the adrenal mass
represents the histologic difference between adenomas and metastases
•Differences in vascular enhancement patterns represent the physiologic
difference.
•Adenomas vigorously enhance and exhibit early washout of contrast
material compared with metastases
out-of phase images in-phase images
Benign lesion
Malignant lesion
in-phase images
out-of phase images
Adrenal Hyperplasia
nonmalignant growth (enlargement) of the adrenal glands and is a rare
cause of ACTH-independent Cushing syndrome, with unilateral adrenal
cortical adenomas being the commonest
Adrenal Hyperplasia
 enlarged limbs of one or both adrenal glands >10 mm thick
 normal adrenal morphology maintained
Adrenal Hemorrhage
Causes
 Anticoagulant therapy
 Stress
 Sepsis ( waterhouse friderichsen)
 Surgery
 Tumor
 Blunt abdominal trauma
Adrenal Hemorrhage
Adrenal Cyst
Adrenal Myelolipomas
 Rare benign and usually asymptomatic tumors of the adrenal gland characterized by predominant
amount of fat.
 The amount of fatty component according to soft tissue is variable
Adrenal Myelolipomas
The CT appearance is usually characteristic. The typical adrenal myelo-
lipoma appears as an adrenal lesion with fat-containing components with
soft tissue and punctate calcification.
Pheochromocytoma
• ~ 10% are extra-adrenal
• ~10% are bilateral
• ~10% are malignant
• ~10% are found in children
• ~10% are familial
• ~10% are not associated with
hypertension
• ~10% contain calcification
Polycystic ovaries
• Hairsutism - 70%
• Secondary Amenorrhea - 50%
• Obesity - 40%
• Abnormal uterine bleeding - 30%
• Normal menstruation - 20%
• Risk of DM2, breast and endometrial Ca
• Infertility

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IMAGING OF ENDOCRINE DISEASES بعد التعديل .pptx

  • 1. IMAGING OF ENDOCRINE DISEASES Presented By : Dr. Seham Adam
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  • 3. The pituitary gland (or hypophysis cerebri), together with its connections to the hypothalamus, acts as the main endocrine interface between the central nervous system and the rest of the body. Gross anatomy The pituitary gland sits atop the base of the skull in a concavity within the sphenoid bone called the sella turcica (pituitary fossa), immediately below the hypothalamus and optic chiasm. The pituitary is usually divided (in practice) into anterior and posterior parts
  • 4. ANATOMY OF PITUTARY GLAND OPTIC CHIASMA INFUNDIBULUM PITUTARY GLAND CAVERNOUS SINUS
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  • 12. IMAGING TECHNIQUES High resolution (2 to 3mm thick slices) • Sagittal T1-WI pre & post Gadolinium • Coronal T1-WI pre & post Gadolinium • Axial T2-WI •Dynamic Gadolinium enhanced coronal T1-WI for small microadenoma.
  • 13. MRI OF PITUITARY GLAND IMAGING SEQUENCES
  • 14. Pituitary Microadenomas are a minority of all pituitary adenomas. By definition, a microadenoma is less than 10 mm in size. If the same tumor is greater than 10 mm in size, it is then considered a pituitary macroadenoma. Differences in presentation and imaging merely represent a difference in size rather than any fundamental difference in biology.
  • 15. MRI OF PITUITARY GLAND IMAGE INTERPRETATION
  • 16. Pituitary Macroadenomas are the most common suprasellar mass in adults, They are defined as pituitary adenomas greater than 10 mm in size and are approximately twice as common as pituitary microadenomas. On imaging, they usually present as a solid tumor with attenuation similar to the brain (30-40 HU) and demonstrate moderate contrast enhancement. The same is observed on MRI, where they are isointense to the grey matter both on T1- and T2-weighted images. However, attenuation and signal characteristics can significantly vary depending on tumor components such as hemorrhage, cystic transformation, or necrosis
  • 17. MRI OF PITUITARY GLAND IMAGE INTERPRETATION
  • 19. PITUITARY GLAND DISEASES Prolactinoma (high secretion of prolactin). Acromegaly (high secretion of G.H. after 18 yrs). Cushing Syndrome (high secretion of ACTH).
  • 20. PITUITARY HYPOPLASIA Failure of hypothalamic axons & surrounding Venous plexus to connect with (anterior lobe ) adenohypophysis • Global adenohypophyseal dysfunction. • Preserved (posterior lobe )neurohypophyseal function Imaging Findings: • Small shallow sella turcica • Small adenohypophysis. • Ectopic Neurohypophysis. • Midline facial & cranial anomalies
  • 21. PITUITARY ADENOMAS: Clinical Presentation ►Hormone hypersecretion Acromegaly Cushing’s Disease Amenorrhea / Galactorrhea ►Symptoms from mass effect Headaches Vision loss Pituitary gland dysfunction
  • 23. Prolactinoma High serum Prolactin 1.Pregnancy 2.Stress 3.Lactation 4.Wet nursing reflex 1.Prolactinoma 2.Pituitary tumor 3.Polycystic ovaries 4.Primary hypothyroidism 5.Post herpes zoster
  • 24. Prolactinoma Clinical presentaion Most Common Functional Pituitary adenoma (30-40%)  Female : Male Prevalence-10:1, median age of diagnosis-34 yrs
  • 26. Acromegaly • Most commonly due to pituitary adenoma • Clinical Presentation • enlargement of the hands, feet, nose, tongue, lips and ears • general thickening of the skin with moist hands • Organomegaly (especially thyroid, heart and liver) • Characteristic thick, deep voice and slowing of speech • Mandible: prognathism with gaping teeth
  • 27. Acromegaly Pituitary MRI-macroadenomas are detected in >80% of acromegaly.
  • 28. Cushing`s Disease • pituitary Adenoma 60%(Cushing’s Disease) • Ectopic source 15% (ACTH/CRH tumors) ACTH-Dependent 75% • Adrenal Adenomas • Adrenal Carcinoma • Nodular Hyperplasia (micro or macro) ACTH-Independent 25%
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  • 31. Symptom of mass effect • Headache • Vision loss • Pituitary hormone dysfunction • Cranial Nerve Abnormality.
  • 32.  Lipoma  Pars intermedia cyst (Rathk’s Cleft cyst )  Meningioma  Craniopharyngioma  Arachnoid cyst  Apoplexy  Sheehans` syndrome  Aneurysm Differential Diagnosis
  • 35. Rathk`s Cleft Cyst •A benign growth found on the pituitary gland in the brain, specifically a fluid-filled cyst in the posterior portion of the anterior pituitary gland. It occurs when the Rathke's pouch does not develop properly
  • 38. Apoplexy acute clinical syndrome caused by either hemorrhagic or non-hemorrhagic necrosis of the pituitary gland. Although variable, it typically comprises headache, visual deficits, ophthalmoplegia, and altered mental status. An existing pituitary macroadenoma is usually present (60- 90%), but it has occurred with healthy glands in a few isolated cases.
  • 39. Sheehan’s Syndrome Sheehan syndrome is a rare cause of pituitary apoplexy and hypopituitarism. It only occurs in postpartum females who experience large volume hemorrhage and hypovolemic shock during delivery Clinical presentation pituitary failure may be silent and present with delayed hypopituitarism • agalactorrhoea • amenorrhea • oligomenorrhea • adrenal insufficiency • hyponatremia (diabetes insipidus) in the acute setting of extreme hypovolemia • hypothyroidism • growth hormone deficiency • optic chiasm compression • visual field loss • headache • ophthalmoplegia
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  • 44. Normal Ultrasound Appearance of the Thyroid Gland Ultrasound Appearance of Diffuse Thyroid Enlargement (Goiter)
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  • 49. Ultrasound appearance of thyroid Ultrasound appearance of thyroiditis
  • 50. Thyroid nodules Suspicious sonographic features :  Hypoechoic  Micro calcification  Infiltrative margin  Taller than wider  Abnormal cervical lymph node.
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  • 52. The radioactive iodine uptake test The thyroid uptake is performed to evaluate the function of the gland. Low uptake suggests thyroiditis while high uptake suggests Graves disease Radionuclide imaging is unreliable in excluding or confirming the presence of cancer.
  • 54. Parathyroid Imaging 1.Sonography 2.99mTc-sestamibi Scintigraphy are the dominant imaging techniques for preoperative location of parathyroid adenomas Numerous studies comparing these techniques suggest similar sensitivities and specificities for solitary adenoma detection. Localization accuracy is also improved when both studies are obtained preoperatively
  • 55. Ultrasound Ultrasound is one of the most commonly used initial imaging modalities. Greyscale most nodules need to be >1 cm to be confidently seen on ultrasound parathyroid adenomas tend to be homogeneously hypoechoic vs the overlying thyroid gland an echogenic thyroid capsule separating the thyroid from the parathyroid may be seen Doppler ultrasound Can commonly show a characteristic extrathyroidal feeding vessel (typically a branch off the inferior thyroidal artery 1,6), which enters the parathyroid gland at one of the poles. Internal vascularity is also commonly seen in a peripheral distribution. This feeding artery tends to branch around the periphery of the gland before penetration. This feature can give a characteristic arc or rim of vascularity. The overlying thyroid gland may also show an area of asymmetric hypervascularity that may help to locate an underlying adenoma
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  • 59. 99mTc-sestamibi Scintigraphy Is used to localize parathyroid adenoma that cannot be localized with other imaging modalities as ultrasound or MRI. Localization of parathyroid adenoma allows the surgeon to use a minimally invasive surgical approach
  • 61. Adrenal Gland  The adrenal gland is named for it is location adjacent to the kidney : ad-renal .  Also known as supra adrenal glands.  Characteristic inverted Y,V or T shape.  Situated on the posterior abdominal wall over the upper pole of the kidneys behind the peritoneum.  Each gland is enclosed in the peri-renal fascia and have body and two limbs.
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  • 63. Histology Adrenal cortex-90% of adrenal composed of three zones. 1.zona glomerulosa –outermost secretes mineralocorticoids(aldosterone) 2.zona fasciculate- 80%-secretes cortisol. 3. zona reticulate-5-10%-secretes androgens.
  • 64. Histology Adrenal medulla- 10% of adrenal made up of chromaffin cells , secretes- epinephrine or nor -epinephrine Part of sympathetic autonomic nervous system
  • 65. Normal Gland / CT , MRI
  • 66. Anatomical landmarks:  Right Adrenal Gland : Superior to right kidney , medial to right lobe of liver lateral to crus of right hemidiaphragm , posterior to IVC.  Left Adrenal Gland : Superior to upper pole of left kidney in triangle formed by left lateral margin of aorta, posterior surface of body and tail of pancreas and upper pole of left kidney.
  • 67. Imaging Modalities Ultrasound . Computed tomography. Magnetic resonance imaging. Nuclear medicine imaging.
  • 68. Adrenal Adenoma • most common adrenal mass lesion and are often found incidentally during abdominal imaging • The most common disease states caused by functioning adenomas are Cushing syndrome (due to excess cortisol production), Conn syndrome (due to excess aldosterone production)
  • 69. Thus, tissues containing lipid and water have signal loss (i.e., appear darker) on out-of phase images. Thus, on out-of phase images, the adenoma appears darker than on in-phase images.
  • 70. CT in Differentiating Benign from Malignant Adrenal Masses certain imaging findings are helpful in differentiating benign from malignant lesions. •Larger lesions •Change in lesion size •The shape . •Intracellular lipid content of the adrenal mass represents the histologic difference between adenomas and metastases •Differences in vascular enhancement patterns represent the physiologic difference. •Adenomas vigorously enhance and exhibit early washout of contrast material compared with metastases
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  • 73. out-of phase images in-phase images Benign lesion Malignant lesion in-phase images out-of phase images
  • 74. Adrenal Hyperplasia nonmalignant growth (enlargement) of the adrenal glands and is a rare cause of ACTH-independent Cushing syndrome, with unilateral adrenal cortical adenomas being the commonest
  • 75. Adrenal Hyperplasia  enlarged limbs of one or both adrenal glands >10 mm thick  normal adrenal morphology maintained
  • 76. Adrenal Hemorrhage Causes  Anticoagulant therapy  Stress  Sepsis ( waterhouse friderichsen)  Surgery  Tumor  Blunt abdominal trauma
  • 79. Adrenal Myelolipomas  Rare benign and usually asymptomatic tumors of the adrenal gland characterized by predominant amount of fat.  The amount of fatty component according to soft tissue is variable
  • 80. Adrenal Myelolipomas The CT appearance is usually characteristic. The typical adrenal myelo- lipoma appears as an adrenal lesion with fat-containing components with soft tissue and punctate calcification.
  • 81. Pheochromocytoma • ~ 10% are extra-adrenal • ~10% are bilateral • ~10% are malignant • ~10% are found in children • ~10% are familial • ~10% are not associated with hypertension • ~10% contain calcification
  • 82. Polycystic ovaries • Hairsutism - 70% • Secondary Amenorrhea - 50% • Obesity - 40% • Abnormal uterine bleeding - 30% • Normal menstruation - 20% • Risk of DM2, breast and endometrial Ca • Infertility