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THYROID,
PARATHYROID,
& ADRENAL GLANDS
REI KRISTOFFER C. UBINA
Junior Intern
St. Paul University Philippines
OBJECTIVES
• Review the embryology, histology, anatomy, and
physiology of the thyroid, parathyroid, and adrenal
glands
• Approach history and physical examination of patients
with thyroid, parathyroid, or adrenal pathology
• Discuss diagnostic investigations for thyroid, parathyroid,
and adrenal diseases
• Discuss the medical and surgical approaches in the
management of patients with thyroid, parathyroid, and
adrenal diseases
THETHYROID GLAND
THYROID EMBRYOLOGY
• 3rd week – arises as an
outpouching of the
primitive foregut
• 5th week – paired lateral
anlages fuse with the
median anlage
• 8th week – thyroid
follicles initially
apparent
THYROID EMBRYOLOGY
• Medial anlage – endoderm cells
• Lateral anlages – neuroectodermal in origin
THYROID EMBRYOLOGY
• Thyroglossal duct – epithelial-lined tube
THYROID EMBRYOLOGY
• Developmental Abnormalities
• Thyroglossal duct cyst and sinus
• Lingual thyroid
• Ectopic thyroid
• Pyramidal lobe
THYROID ANATOMY
• Brown
• Firm
• Located posterior to the
strap muscles
• Weighs approximately
20 g
THYROID ANATOMY
THYROID ANATOMY
BLOOD SUPPLY
• Superior thyroid arteries
• Inferior thyroid arteries
• Thyroidea ima
VENOUS DRAINAGE
• Superior thyroid vein
• Middle thyroid vein
• Inferior thyroid vein
INNERVATION
• Recurrent laryngeal
nerve
LYMPHATIC SYSTEM
THYROID HISTOLOGY
• Divided into lobules
that contain 20 to 40
follicles
• Spherical and average
30 µm in diameter
FOLLICLES
• Lined by cuboidal
epithelial cells
• Contains a central
store of colloid
PARAFOLLICULAR CELLS
• C cells
• Contain and secrete
calcitonin
THYROID PHYSIOLOGY
• Iodine metabolism
• Thyroid hormone synthesis, secretion, and
transport
THYROID PHYSIOLOGY
THYROID PHYSIOLOGY
CASE
• A 29-year old female was referred to a Head &
Neck clinic for the evaluation of a thyroid nodule.
Patient reports that this nodule was found
incidentally while she was getting ready for work
one morning.
• She went to her private medical doctor, who
ordered a thyroid ultrasound, which
demonstrated a 2-cm nodule in the right lobe of
the thyroid.
QUESTION
• After thorough history and physical examination,
what would you order first for this patient?
A.Thyroid function tests (TSH,T4)
B. CT neck
C. MRI neck
D. Radioactive Iodine uptake scan
E. Any of the above
QUESTION
• After thorough history and physical examination,
what would you order first for this patient?
A.Thyroid function tests (TSH,T4)
B. CT neck
C. MRI neck
D. Radioactive Iodine uptake scan
E. Any of the above
TESTS OFTHYROID FUNCTION
• SerumTSH (0.5-5 µU/mL)
• T4 (55-150 nmol/L)
• T3 (1.5-3.5 nmol/L)
• TRH
• Thyroid antibodies
• Serum thyroglobulin
• Serum calcitonin (0-4 pg/ml)
QUESTION
• What would you order first for this patient?
A.Thyroid function tests (TSH,T4)
It is important to first establish the patient’s
thyroid function.
At this point, you should also obtain Fine Needle
Aspiration (FNA) with ultrasound guidance, if
necessary, to obtain cells for cytopathology.
PATIENT HISTORY
• Family history of thyroid disease or thyroid cancer?
• Familial syndromes (MEN)
• Personal history of radiation to head/neck
• Increased risk of thyroid cancer
• Hoarseness, SOB, difficulty swallowing
• Compressive symptoms of thyroid goiter
CASE
• Patient reports that her voice seems to have
become slightly more “husky” lately. She recalls
only occasional discomfort with sensation that
something is “pushing” in.
• Denies shortness of breath
• Denies family history of thyroid cancer
• Denies personal history of radiation therapy or
thyroid or any other type of cancer
PHYSICAL EXAMINATION
What components of the physical examination are
critical for this patient?
PHYSICAL EXAMINATION
What components of the physical examination are
critical for this patient?
• Full head and neck exam to look for any
“lumps or bumps”
• Palpate for lymphadenopathy
• Palpate thyroid for nodularity, firmness, or
hard masses
• Fiberoptic or direct laryngoscopy to evaluate
vocal cord function
CASE
• On physical examination, you palpate a grossly
enlarged thyroid gland with a 2-cm dominant
nodule on the right thyroid lobe.
• You discover the following findings on fiberoptic
exam:
Upon inspiration:
symmetric bilateral
vocal fold abduction
Vocal folds
(true cords)
False vocal folds
Base of tongue/lingual tonsil
trachea
Epiglottis
Opening of esophagus
View on laryngoscopy
anterior
QUESTION
• Patient is sent for labs as well as FNA. Patient
returns to the clinic the following week with FNA
report reading “follicular cells, cannot rule out
follicular neoplasm”. Is surgery indicated for this
patient at this time?
• Yes
• No
QUESTION
• Patient is sent for labs as well as FNA. Patient
returns to the clinic the following week with FNA
report reading “follicular cells, cannot rule out
follicular neoplasm”. Is surgery indicated for this
patient at this time?
• Yes
• No
EXPLANATION
• Surgery is indicated. Follicular cells on FNA can be a
benign finding or may indicate follicular carcinoma.
DIAGNOSTIC INVESTIGATION
ETIOLOGIES OFTHYROID NODULES
• Benign
• Benign thyroid cysts (degenerated nodules)
• Colloid nodules
• Multinodular goiter
ETIOLOGIES OFTHYROID NODULES
• Malignant
• Papillary carcinoma
• Follicular carcinoma
• Hurthle cell tumor
• MedullaryThyroid Carcinoma
• Anaplastic Carcinoma
• Lymphoma of thyroid
MALIGNANTTHYROID DISEASES
TESTS
• CBC, Chemistry
• Thyroid function (TSH, freeT4)
• Parathyroid hormone (PTH)
• Coagulation studies (INR, PTT)
• FNA of nodule (+/- Ultrasound guidance)
• CT Neck for surgical planning, if appropriate
THYROID IMAGING
• Radionuclide Imaging
• Iodine 123 (123I)
• Iodine 131 (131I)
• TechnetiumTc 99m
pertechnetate
(99mTc)
THYROID IMAGING
• Ultrasound
• Computed tomography
• Magnetic resonance
imaging
CT scan demonstrating large right thyroid
mass causing tracheal deviation to left
BENIGNTHYROID DISORDERS
• Hyperthyroidism
• Hypothyroidism
• Goiter
HYPERTHYROIDISM
HYPOTHYROIDISM
GOITER
TREATMENT
Medical Management
• Involve endocrinology early to assist in
management
• Thyroid hormone replacement
(Levothyroxine) for hypothyroidism
• Thyroid suppression for hyperthyroidism
• I-131 for medical thyroid ablation
• Observation for benign nodules
TREATMENT
Surgery
• Failure of medical management
• Malignancy or concern for malignant
potential
• Symptom management
INDICATIONS FORTHYROIDECTOMY
• Hyperthyroidism (Grave’s) not
responsive to medical therapy with
ophthalmic symptoms
• Malignancy (confirmed or high
suspicion based on history and/or
FNA)
• Goiter with compressive symptoms
• Large thyroid nodule (>2cm) that is
unable to be adequately sampled by
FNA (sampling error due to large area
of nodule and risk of combination of
benign and malignant cells)
THYROID SURGERY
THYROID SURGERY
THYROID SURGERY
THYROID SURGERY
THYROID SURGERY
THYROID SURGERY
THYROID SURGERY
TREATMENT
Post-surgical therapy
• I-131 : Radioactive iodine ablation may be
indicated postoperatively for any residual
malignancy
• Thyroid hormone replacement after total
thyroidectomy
• Calcium replacement
• Surgery to thyroid/parathyroid bed
THE PARATHYROID GLAND
PARATHYROID EMBRYOLOGY
• Superior parathyroid
glands – derived from
the fourth branchial
pouch
• Inferior parathyroid
glands – arise from the
third branchial pouches
PARATHYROID EMBRYOLOGY
PARATHYROIDANATOMY
• Four parathyroid glands
• Gray
• Semitransparent in newborns
• Golden yellow to light brown in adults
• Ovoid
• 7 mm
• 40-50 mg each
PARATHYROID PHYSIOLOGY
• Chief cells –
produce PTH
• Oxyphil cells
• Water-clear cells
PARATHYROID PHYSIOLOGY
• Calcium homeostasis
PARATHYROID
PHYSIOLOGY
• Parathormone
• Calcitonin
• Vitamin D
PARATHYROID DISORDERS
• Hyperparathyroidism
• Hypoparathyroidism
• Parathyroid carcinoma
• Parathyromatosis
DIAGNOSTIC INVESTIGATION
PARATHYROID SURGERY
PARATHYROID SURGERY
PARATHYROID SURGERY
Care of Patients with
Adrenal Gland Problems
Adrenal Cortex: Steroid Hormone
Production
Adrenal Gland Hypofunction
• Adrenocortical steroids may decrease as a result of
inadequate secretion of ACTH
• Dysfunction of the hypothalamic-pituitary control
mechanism
• Direct dysfunction of adrenal tissue
Effect of Insufficiency of
Adrenocortical Steroids
• Loss of aldosterone and cortical action
• Decreased gluconeogenesis
• Depletion of liver and muscle glycogen
• Hypoglycemia
• Reduced urea nitrogen excretion
• Anorexia and weight loss
• Potassium, sodium, and water imbalances
Addison’s Disease
• Primary
• Secondary:
• Sudden cessation of long-term high-dose glucocorticoid therapy
Acute Adrenal
Insufficiency/Addisonian Crisis
• Life-threatening event in which the need for cortisol and
aldosterone is greater than the available supply
• Usually occurs in a response to a stressful event
Patient-Centered Collaborative
Care
• Assessment
• Clinical manifestations
Assessment
• Psychosocial assessment
• Laboratory tests
• Imaging assessment
Adrenal Gland Hyperfunction
• Hypersecretion by the adrenal cortex results in Cushing’s
syndrome/disease, hypercortisolism, or excessive
androgen production
Pheochromocytoma
• Hyperstimulation of the adrenal medulla caused by a
tumor
• Excessive secretion of catecholamines
Hypercortisolism (Cushing’s
Disease)
• Etiology
• Incidence/prevalence
• Patient-centered collaborative care
• Assessment:
• Clinical manifestations—skin changes, cardiac changes,
musculoskeletal changes, glucose metabolism, immune changes
Hypercortisolism
Cushing’s Disease
• Psychosocial assessment
• Laboratory tests—blood, salivary and urine cortisol levels
• Imaging assessment
Hypercortisolism: Nonsurgical
Management
• Patient safety
• Drug therapy
• Nutrition therapy
• Monitoring
Hypercortisolism: Surgical
Management
• Hypophysectomy
• Adrenalectomy
Hyperaldosteronism
• Increased secretion of aldosterone results in
mineralocorticoid excess.
• Primary hyperaldosteronism (Conn's syndrome) is a result
of excessive secretion of aldosterone from one or both
adrenal glands.
Patient-Centered Collaborative
Care
• Assessment
• Most common issues—hypokalemia and elevated blood
pressure
Interventions
• Adrenalectomy
• Drug therapy
• Glucocorticoid replacement
• When surgery cannot be performed—spironolactone
therapy
Pheochromocytoma
• Catecholamine-producing tumors that arise in the
adrenal medulla
• Tumors produce, store, and release epinephrine and
norepinephrine
Patient-Centered Collaborative
Care
• Assessment
• Interventions:
• Surgery is main treatment.
• After surgery, assess blood pressure.

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