BENIGN DISEASES OF THE THYROID

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BENIGN DISEASES OF THE THYROID Rivka Dresner Pollak M.D Endocrinology.

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BENIGN DISEASES OF THE THYROID. Rivka Dresner Pollak M.D Endocrinology. Thyroid gland- anatomy. Thyroid gland- anatomy. sternocleidomastoid. strap muscles. trachea. thyroid. jugular v. esophagus. carotid a. vertebra. Recommended and Typical Values for Dietary Iodine Intake. - PowerPoint PPT Presentation

Transcript of BENIGN DISEASES OF THE THYROID

Page 1: BENIGN DISEASES OF THE THYROID

BENIGN DISEASES OF THE THYROID

Rivka Dresner Pollak M.D

Endocrinology.

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Thyroid gland- anatomyThyroid gland- anatomy

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Thyroid gland- anatomyThyroid gland- anatomy

sternocleidomastoidsternocleidomastoid

thyroidthyroid

esophagus

tracheatrachea

jugular v.

carotid a.carotid a.

strap musclesstrap muscles

vertebra

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Recommended and Typical Values for Dietary Iodine Intake

Recommended Daily Intake μg I/dayAdults 150During pregnancy 200Children 90-120

Typical Iodine intakesNorth America 75-300Europe (Germany, Belgium) 50-70Switzerland 130-160Chile <50-150

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Thyroid secretion

P

ProteinBound

Thyroidhormone

Free T4, T3 Tissue actionTissue action

Hormone metabolismHormone metabolism

Fecal excretionFecal excretion

Serum thyroid hormone bindingSerum thyroid hormone binding

Feedback controlFeedback control

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TBG = thyroxine binding globulinTTR = transthyretin% binding- mostly to TBGT4 - 99.5T3- 95

DEIODINASETYPE 1 & 2

THYROXINE BINDING GLOBULIN

Estrogen

Androgen =

Glucocorticoids =

Acute illness N

Chronic illness

Liver dis.

METABOLISM

TRANSPORT

THYROID HORMONES TRANSPORT AND METABOLISM

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Serum protein binding of thyroid hormonesSerum protein binding of thyroid hormones

Total TTotal T44

TBG T4T4T4

TBG T4T4 T4 T4T4

““Pill effect”Pill effect”

BoundBound Free Free

synthesisBy liver

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Regulation of Thyroid hormone secretionRegulation of Thyroid hormone secretion

Hypothalamus

TT44, T, T33

TSHTSH(-)(-) (+)(+)

TRHTRH(+)(+)(-)(-)

PituitaryPituitary

Thyroid

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Assessment of bioactive thyroid Assessment of bioactive thyroid hormoneshormones

Check free hormone levels:Check free hormone levels:Free TFree T44

Free TFree T33

Check thyroid hormone “biosensor’:Check thyroid hormone “biosensor’:TSH TSH

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Thyroid function testsThyroid function tests

Hypo HyperHypo Hyper Hypo HyperHypo Hyper 11oo Hypo 1 Hypo 1oo Hyper Hyper

TSHTSHFTFT33nmol/Lnmol/L

FTFT44

pmol/Lpmol/L

0.15

4

3.0

1.2

21

10

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Laboratory tests in thyroid diseaseLaboratory tests in thyroid disease

Anti-thyroid antibodies:Anti-thyroid peroxidase (TPO)

Thyroid stimulating antibodies:TSI-Thyroid stimulating imunoglobulinsTSH receptor Antibody

Thyroglobulin

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2. Thyroid scanning2. Thyroid scanning

Radioactive isotopes of I (Radioactive isotopes of I (131131I, I, 123123I)I)PertechnetatePertechnetate

Generates Data on:Generates Data on:- Anatomy- Anatomy- Physiology- Physiology

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Normal thyroid scanNormal thyroid scan

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““Hot nodule”Hot nodule”

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““Cold” noduleCold” nodule

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Multinodular goiter (MNG)Multinodular goiter (MNG)

Pertechnetate scanPertechnetate scan CHEST X-RAYCHEST X-RAY

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RRadio adio AActive ctive IIodine odine UUptake ptake ((RAIURAIU))

0 6 12 18 240

10

20

30

40

50

Time (hours)

HyperthroidismHyperthroidism

NormalNormal

Hyperthyroidism withHyperthyroidism withRapid turnoverRapid turnover

HypothroidismHypothroidism

2

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Thyroid abnormalitiesThyroid abnormalities

FunctionFunctionStructureStructure

Hyperthyroidism Hypothyroidism

EtiologyEtiology

RRXX

ThyroiditisThyroiditisGoiterGoiter

NodularNodular Diffuse Diffuse

BenignBenign MalignantMalignant Function nl Function nl

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Hyperthyroidism-EtiologyHyperthyroidism-Etiology

• Diffuse toxic goiter (Graves’ disease)- most common in young people• Toxic adenoma (Plummers’ diesease)• Toxic mulitinodular goiter (MNG)• Subacute thyroiditis-Hyperthyroid phase• Hyperthyroid phase of Hashimotos’ thyroiditis• (“Hashitoxicosis)• Factitious hyperthyroidism• Rare causes: -TSHoma

-Hydatidiform mole/choriocarcinoma- Multiplex pregnancy- Struma ovarii

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Graves’ diseaseGraves’ disease• Diffuse toxic goiterDiffuse toxic goiter

• OpthalmopathyOpthalmopathy

• DermopathyDermopathy

•Acropathy Acropathy

(clubbing)(clubbing)Etiology: AutoimmuneAnti-TSH receptor antibodies (stimulating, blocking, neutral)Anti-thyroid antibodies expression of HLA-DR3 association with:

-diabetes mellitus-type 1 myasthenia gravis-Addison’s disease lupus- pernicious anemia

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• Epidemiology : incidence 0.3-1.5/1000

• Female: Male 5:1

• Most Common cause of hyperthyroidism

Graves’ diseaseGraves’ disease

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Thyroid and pituitary function in Thyroid and pituitary function in Graves’ diseaseGraves’ disease

TT44, , TT33 TSHTSH(+)(+) (-)(-)

(+)(+)

Thyroid Stimulating Thyroid Stimulating Immunoglobulins (TSI)Immunoglobulins (TSI)

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Graves’ disease- Graves’ disease- Clinical featuresClinical features

Symptoms:

Fatigue palpitationsWeight lossHeat intoleranceFrequent bowel movementsSweatinghyperkinesia

Signs:

TachycardiaMuscle wasting pulse pressureEye signsDiffuse goiterLymphadenopathySplenomegalyHyperreflexia

In the elderly: cardiovascular symptoms, myopathy

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Graves’ Disease- GoiterGraves’ Disease- Goiter

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Graves disease- Graves disease- OpthalmopathyOpthalmopathy

Extrathyroidal TSHR is present in retro-orbital adipocytes, muscle cells and fibroblasts

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Grave’s Opthalmopathy

• Class 0 — No symptoms or signs • Class I — Only signs, no symptoms (eg, lid

retraction, stare, lid lag) • Class II — Soft tissue involvement • Class III — Proptosis • Class IV — Extraocular muscle involvement • Class V — Corneal involvement • Class VI — Sight loss (optic nerve involvement)

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Graves’ disease dermopathyGraves’ disease dermopathy

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Graves disease- diagnosisGraves disease- diagnosis

• Clinical hyperthyroidism

• Biochemistry: FT4, TT3 , TSHcholesterol

• Serology: anti-TSH receptor antibodiesanti-thyroid antibodies

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Graves’ disease- therapyGraves’ disease- therapy1. Antithyroid drugs:

Thionamides- Propylthiouracil (PTU)Propylthiouracil (PTU)Methimazole (MMI)Methimazole (MMI)-blockers

3. Definitive therapy:131I- side effects:

hypothyroidism

Surgery- subtotal thyroidectomy

side effects: anesthesia morbidityhypoparathyroidismrecurrent laryngeal nerve damagehypothyroidism

Treat for 12 monthsTreat for 12 months

~30%remissionremission70%

RecurrenceOr non-remission

Follow-upFollow-up

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Anti-thyroid thionamide drugsAnti-thyroid thionamide drugs

PTU (propylthiouracil) MMI (methimazole)

Dosage: TID Once daily

Effect: T4, T3 synthesis T4, T3 synthesis

inhibits T4→T3(high dose) (slow)

Agranulocytosis*: Non-dose dependent Dose dependent

(> 40 mg/day)

> 40 yrs

Pregnancy: placental transfer placental

transfer

aplasia cutis

*occurrence 0.3-0.6%

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Treatment of Graves' Orbitopathy

• Treatment of patients with Graves' orbitopathy has three components:

• Reversal of hyperthyroidism, if present • Symptomatic treatment • Treatment with a glucocorticoid, orbital irradiation,

orbital decompression surgery to reduce inflammation in the periorbital tissues

• Anti thyroid drugs and thyroidectomy are safe; Radioactive iodine may worsen the situation.

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The effect of high- dose PTUThe effect of high- dose PTU

0 1 2 3 4 5 620

25

30

35

40

45

50 FT4

FT3

012345678910

Days

12001200 600600PTU dose mg/day:

Upper limit of normal

Normalrange

140

120

100

80

Pulse rate:

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Subacute thyroiditisSubacute thyroiditis

Etiology: (Post) viral inflammation of thyroid

Symptoms & signs: HyperthyroidismPainful swelling of thyroidPain irradiation to earFeverSometimes “silent”

Laboratory: ESR acute phase reactants (CRP)

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Subacute thyroiditis- therapySubacute thyroiditis- therapy

A self limited disease

Therapy depends on symptoms/signs

Non-steroid anti-inflammatory agents (NSAIDS)

-blockers

Corticosteroids

Outcome - in 6 months 90% euthytroid

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Hypothyroidism- classificationHypothyroidism- classification

1. Hashimoto’s thyroiditis2. Post 131I therapy for Grave’s disease3. Post thyroidectomy4. Excessive I intake (amiodarone-procor)

Primary - TSH↑

Secondary TSH ↓ or normal:Hypopituitarism due to adenoma, destructive lesion, ablationTSH↓

Tertiary:Hypothalamic dysfunction (rare)

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Hypothyroidism- Hypothyroidism- clinical featuresclinical features

Symptoms:

Fatigue WeaknessWeight gainCold intoleranceConstipationCrampsParesthesias (carpal tunnel)

Signs:

Coarse featuresBradycardiaMyxedemaAnemia

Laboratory: serum thyroid hormones, cholesterolanemia (iron def., megaloblastic)

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HypothyroidismHypothyroidism

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Hypothyroidism- myxedemaHypothyroidism- myxedema

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Hypothyroidism-Hypothyroidism- differential diagnosis differential diagnosis

Serum FT4 andTSH

FT4, TSH

Primary hypothyroidism

FT4, TSH normal/low

Secondary hypothyroidism

TRH test

Excessive response

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Hypothyroidism- therapyHypothyroidism- therapy

• Levothyroxine 0.05-0.3 mg/day

• Combined L-T4 and L-T3 may be beneficial with

respect to well-being

• In elderly patients (at high risk for CVD),

“go low, go slow”

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Hypothyroidism- treatmentHypothyroidism- treatment

Before After

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Thyroid Storm and Myxedema Coma – rare endocrine emergencies

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THYROID STORM

Clinical setting

History of Graves’ disease and discontinuation of medications/

previously undiagnosed hyperthyroidism.

Acute onset of hyperpyrexia (over 40 ˚C)

Sweating

Marked tachycardia, often with atrial fibrillation

Nausea, vomiting, diarrhea

Agitation, tremulousness, delirium

Occasionally “apathetic” – without restlessness and agitation, but with

weakness, confusion, and cardio-vascular dysfunction.

Acute life threatening exacerbation of thyrotoxicosis

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THYROID STORMDIAGNOSIS:

Largely based on the clinical findings and clinical suspicion.

Elevated serum FT4, FT3.

Low TSH

MANAGEMENT

1. Supportive care

Fluids, Oxygen, Cooling blanket,cetaminophen

2. Specific measuresPropranolol, 40-80 mg every 6 hours.Antithyroid drugs – PTU. Glucocorticoids - Dexamethasone, 2 mg every 6 hours (due to reduction in glucocorticoids half life)

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Myxedema ComaMyxedema ComaExtreme hypothyroidism:

• Coma• Hypothermia• Hypoventilation• Hypoglycemia• Hyponatremia• Bradycardia

Laboratory: FT4 , FT3, TSHCo2 retention

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Myxedema Coma- therapyMyxedema Coma- therapy

Treat:

Ventilation

Precipitating factors

T4 or T3 I.V.Corticosteroids-50-100mg hydrocortisoneevery 8 hours

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Subclinical Hypothyroidism

TSH FT4 AND FT3 NORMAL

Biochemical definition

WHEN TO TREAT?WHEN TSH > 10AND WHAT ABOUT 4.5<TSH<10????

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Subclinical hyperthyroidism• TSH below lower limit of normal (<0.3)

• Free T3 & Free T4 – normal

• Make sure not over treatment of hypothyroidism

• Associated with increased risk of atrial fibrillation in subjects > age 60 and accelerated bone loss in postmenopausal women

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Always repeat the test

before initiating

therapy!

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Amiodarone (Procor)-induced thyroid dysfunction

• Each Procor tablet (200 mg) has 75 mg Iodine• Procor can cause: hypothyroidism- does not require discontinue the

medication (thyroxine can be added)Hyperthyroidism- anti thyroid drugs have limited

efficacy; radioactive iodine doesn’t workThyroiditis- may require steroids

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