Endocrinology Board Review: Thyroid Disorders
Endocrinology Board Review: Thyroid Disorders
Endocrinology Board Review: Thyroid Disorders
BOARD REVIEW
THYROID DISORDERS
Henri Godbold, MD
General
- Thyroid produces two related hormones
thyroxine(T4) and triidothyronine (T3)
- Function is through nuclear receptors playing a
role in cell differentiation
- Maintains thermogensis, and metabolic
homeostasis
- Disorders result from autoimmune processes that
either stimulate overproduction of hormones
(thyrotoxicosis) or glandular destruction and
hormone deficiency (hypothyroidism)
- Benign nodules and various forms of thyroid
cancers
Anatomy
- Located anterior to trachea consist two lobes
- Weighs 12-20gm soft and highly vascular a
posterior region gland contain four parathyroid
gland that produce parathyroid hormone
- Lateral borders of the gland is transversed by the
recurrent laryngeal nerves
- Develops from the floor of the primitive pharynx
third week of gestation migrates from the
foramen cecum, at the base of tongue along the
thyroglossal duct to neck
- Hormonal synthesis usually begin at about 11
weeks’ gestation
Thyroid Physiology
- Thyroid releases (2) forms of hormones
- Thyroxine (T4) and triiodothyroxine (T3) ratio
14:1
- T3 is 80% derived from peripheral tissue
- T4 all within the thyroid gland
- T3 is produced from T4 in liver, kidneys,
pituitary gland and CNS
- T3 is the physiologically active in almost all
tissue binding to specific nuclear receptors
regulating the transcription of thyroid hormone
dependent genes
Drugs decreasing Peripheral
conversion of T4 to T3
Propranolol
Corticosteroids
Propylthiouracil (PTU)
Amiodarone
SYNTHESIS AND RELEASE
- TSH controls release under the influence TRH
from the hypothalamus
- TSH stimulate thyrocyte function resulting in
iodide uptake actively on the basal surface of the
thyroid follicle cell
- Iodide undergoes oxidation to iodine which
iodinates tyrosine residues catalyzed by
peroxidase
- Thyroglobulin coupling occurs to form mono-
and diiodotyrosine (MIT and DIT
- Two DITs coupling = T4
- One DIT and one MIT combine =T3
- If iodine scarce, the production of T3 is increase
- Activity is dictated by # iodines attached
Secretion
Degradation process with endocytosis of the follicular
colloid containing MIT, T3,
T4, DIT attached to thyroglobulin undergoes fusion
with lyosome resulting in proteolysis release
Deiodination occurs with the recycling iodide and
secretion of T3 and T4
Circulating thyroid hormones are more than 99%
protein bound, are thyroxine-binding globulin,
albumin, and transthyretin.
80% of circulating T3 is derived from the conversion
of T4 outside the thyroid
Serum half-life of T3 is much shorter than that T4
(1day vs 8days)
Storage
- Iodine as iodinated tyrosine of
thyroglobins 8000 micrograms total
- T4 and T3 represent 600 micrograms
each
- Enough hormone is stored in the
follicular colloid to last 2-3 months
Overveiw of Thyroid Fx Workup
1st Test 2nd Test 3rd Test
C. MICROSCOPIC
i. Nodules of varying sizes composed of colloid
follicles
ii. Calcification, hemorrhage, cystic degeneration,
and fibrosis
Treatment:
a. sedative and digitalis if needed
b. Iodide
c. Lugol (5% iodine and 10% K iodine)
d. Methimazole
Hypothyroidism
a. Clinical features
i. Fatigue
ii. Sensitivity to cold temperatures
iii. Decreased cardiac output
iv. Myxedema:
- Facial and periorbital edema
- Peripheral edema of the hands and
feet
- Deep voice
- Macroglossia
v. Constipation
vi.Anovulatory cycles
b. Lab
i. Decrease Free T4
ii. Primary hypothyroidism: elevated TSH
Iatrogenic hypothyroidism
Most common cause of hypothyroids in US
Secondary to thyroidectomy or RAI rx
Rx: Levothyroxine 12.5-50mcg PO qd adjusting
dose by 12.5-25mcg/d q4-8wks
Congential Hypothyroidism(cretinism)
a. Etiology
i. Endemic region: iodine deficiency during intrauterine and
neonatal life ( worldwide)
ii. Non endemic regions: thyroid dysgenesis
b. Presentation
i. Failure to thrive
ii. Stunted bone growth and dwarfism
-Commonly absent distal femoral epiphysis
iii. Spasticity and motor incoordination
iv. Mental retardation
v. Goiter (endemic cretinism)
- Endemic goiter
a. Uncommon in the US
b. Etiology: dietary deficiency of iodine
Clinical Manifestation
congenital Hypothyroidism
Occurs in 1/4000 Worldwide
Most infant are asymptomatic at birth because of
transplacental passage of T4 (usu 3rd day of life)
Most common cause is thyroid dysgenesis
Presentation: hypoglycemia, jaundice
micropenis, midline facial
anomalies, enlarge posterior
fontanelle, macroglossia
Rx: Initial dose: Sodium L-tyroxine 10-15
microgrms/kg/day( should not be mixed soy
protien or iron) Then, 4 micrgms/kg/day
Thyroiditis
1. Hashimoto's thyroiditis
a. Definition: chronic autoimmune disease characterized by
immune destruction of the thyroid gland and hypothyroidism
b. Most common noniatrogenic cause of hypothyroidism and Goiter
in children > 6yo and adults in US
c. Clinical presentation
i. Females > males; age 40-65
ii. Painless goiter
iii. Hypothyroid
iv. Initial inflammation may cause transient hyperthyroidism.
d. Gross: pale enlarge gland
e. Micro:
i. Lymphocytic inflammation with germinal centers
ii. Epithelial "Harthle cell" changes
f. May be associated with other autoimmune diseases
(SLE, RA, SS [Sjogren's syndrome], etc.)
g. Complication: increased risk of non-Hodgkin‘ lymphoma (NHL)
B-cell lymphoma
2. Subacute thyroiditis
a. Synonyms: De Quervain's thyroiditis, granulomatous
thyroiditis
b. Clinical features
i. Second most common form of thyroiditis
ii. Females > males; age 30-50
iii. Preceded by a viral illness
iv. Tender, firm, enlarged thyroid gland
v. May have transient hyperthyroidism
c. Micro: granulomatous thyroiditis
d. Prognosis: typically the disease follows a self-limited course
e. Symptoms: control with analgesics, prednisone very severe
dx
Riedel's thyroiditis
a. Definition: rare disease of unknown etiology characterized by
destruction of the thyroid gland by dense fibrosis and fibrosis
of surrounding structures (trachea and esophagus)
b. Clinical features
i. Females > males; middle age
ii. Irregular, hard thyroid that is adherent to adjacent
structures
iii. May mimic carcinoma and present with stridor,
dyspnea, or dysphagia
c. Micro
i. Dense fibrous replacement of the thyroid gland
ii. Chronic inflammation
d. Associated with retroperitoneal and mediastinal fibrosis
Thyroid Neoplasia
Adenomas
a. Follicular adenomas are the most common
b. Clinical features
i. Usually painless, solitary nodules
In first 20 yrs life likely malignant than older person
ii. "Cold nodule" on thyroid scans
iii. May be functional and cause hyperthyroidism
(toxic adenoma)
2. Papillary carcinoma
a. Epidemiology
i. Account for 80% of malignant thyroid tumors
ii. Females > males; age 20-50
iii. Risk factor: radiation exposure
b. Micro
i. The tumor typically exhibits a papillary pattern.
ii. Occasional psammoma bodies
iii. Characteristic nuclear features Clear "Orphan Annie eye" nuclei Nuclear grooves
Intranuclear cytoplasmic inclusions
c. Lymphatic spread to cervical nodes is common.
d. Treatment
i. Resection is curative in most cases.
ii. Radiotherapy with iodine 131 is effective for metastases.
e. Prognosis: excellent; 20-year survival = 90%
Follicular carcinoma
a. Accounts for 15% of malignant thyroid tumors
b. Females > males; age 40-60
c. Hematogenous metastasis to the bones or lungs is common.
d. High mortality rate because most present with distant mets
Medullary carcinoma