Thyroid Diseases
Thyroid Diseases
Thyroid Diseases
Inflammatory
Autoimmune
Hashimotos ds Chronic lymphocytis thyroiditis
Multinodular
Toxic
Diffuse : Graves disease Multinodular Toxic adenoma
Granulomatous
De Quervains thyroiditis
Fibrosing
Riedels thyroiditis
Infective
Acute (bacterial & viral thyroiditis) Chronic (TB, syphilis)
Neoplastic
Benign Malignant
Other
amyloid
Simple Goiter
Aetiology Iodine deficiency Dyshormogenesis Goitrogens The natural history of simple goiter Persistent growth stimulation causes diffuse hyperplasia Mixed patterns develops with areas of active and inactive lobules as result of fluctuating stimulation Active lobules become more vascular and hyperplastic until haemorrhage occurs, causing central necrosis Necrotic lobules coalesce to form nodules filled with either iodine-free colloid or a mass of new but inactive follicles Continual repetition of these processes result in a nodular goitre
Nodular Goiter
Later stage of natural history of simple goitre Multiple multinodular goitre may be colloid or cellular cystic degeneration and haemorrhage is common Can develop retrosternal goitre
dyspnea, cough, stridor, SVC obstuction
Solitary Nodule
70% are clinically isolated, 30% dominant May have risk of neoplasia 15% isolated - malignant 30-40% - follicular adenomas Remainders non neoplastic, colloid degeneration, thyroiditis, cysts Ix
TFT autoAb titres Isotope scan
Hot/cold 80% cold & only 15% malignant
Hypothyroidism
Autoimmune thyroiditis (Hashimotos ds, 1o myxodema) Iatrogenic Dyshormongenesis Goitrogens 2o to pituitary or hypothalamic disease Endemic cretinism
Hashimotos disease
destruction of thyroid cells by various celland Ab-mediated immune processes. Ab bind and blocking the TSH inadequate thyroid hormone production and secretion Middle age woman Uniformly enlarge & firm (occ asymmetrical & irregular) Thyroglobulin & microsomal Ab (90%)
Hashimotos disease
TFT
Low T4 & T3 High TSH
Treatment
levothyroxine sodium, usually for life. goal of therapy is to restore a clinically and biochemically euthyroid state. standard dose is 1.6-1.8 mcg/kg lean body weight per day
Hyperthyroidism
Diffuse toxic goitre (Graves disease) Toxic nodular goitre Acute thyroiditis Gestational thyrotoxicosis Exogenous iodine Drugs- amiodarone Thyrotoxicosis factitia TSH-secreting pituitary tumours Metastatic differentiated thyroid carcinoma Hcg-producing tumours Hyperfunctioning ovarian teratoma thyrotoxicosis factitia (rare)
1o vs 2o hyperthyroidism
1o (Graves ds)
Enlargement of thyroid and toxic features appear simultaneously
Toxic features are usually severe Nervous manifestations young Exopthalmos and eye signs are common small, diffuse, smooth
2o
Goitre appears first, toxic features develope after an interval
Toxic features are mild Cvs manifestations elderly These are absent large, nodular, irregular
Signs
Tachycardia Hot, moist palms Eye sign
Exopthalmos Lid lag/ retraction Dilated pupils Double vission
Exophtalmos
Pretibial myxoedema
Simple goiter present b4 hyperthyroidism Middle aged/elderly Many cases, nodule inactive but intranodular tissue is active Nodule activated hyperthyroidism
Investigations
Essential
Serum TSH (T3 and T4 if abnormal) Serum thyroid autoantibodies FNAC of all palpable discrete swellings
Optional
Calcium and albumin CXR and thoracic inlet if tracheal deviation/retrosternal Isotope scan if discrete swelling and toxicity coexist
Normal Undetectable
Myxoedema
Suppressive T4 therapy
High
Undetectable
Low
High
Low
High
T3 toxicity
Low/Undetectable
Normal
High
Treatment of thyrotoxicosis
Antithyroid drugs carbimazole -adrenergic blocking drugs Anti-thyroid drugs combined with subsequent thyroidectomy Radioactive iodine-131
Anti-thyroid Drugs
restore in euthyroid state and maintain for prolong period in hope of remission Carbimazole 10mg 8-hourly Continue for 12 months Aware of toxic symptoms within 2 weeks, if symptoms recur further 6 months treatment with surgery is advised High relapse rate (60%) after terminating the treatment (even in 2 or more years of tx) Medical tx alone usually confined to 1 hyperthyroidism in children and adolescents
-adrenergic blocking drugs Propanolol induces rapid symptomatic improvement of cvs features in patients with severe hyperthyroidism
Extent of resection
size of gland age of patient experience of surgeon need to minimise risk of recurrent toxicity
Hemithyroidectomy, total thyroidectomy (depends) It cures by reducing mass of overactive tissue in diffuse toxic goitre and toxic nodular goitre Advantages: the goitre removed, cure is rapid and cure rate high if surgery adequate Disadvantages: recurrence in 5% of cases and risk of surgery complications
Procedures
While the patient is deep asleep and pain-free (general anesthesia), an incision is made in the front of the neck.
The thyroid gland is removed. Either one lobe of the thyroid gland, or the entire gland, is removed, depending on the disease process being treated
Complications of thyroidectomy
Hormonal disturbances
Tetany (parathyroid) Thyroid crisis Hypothyroidism (due to extensive removal of thyroid tissue) Late recurrence of hyperthyroidism (d2 inadequate operation in toxic gland)
Radioactive Iodine
destroys thyroid cells reduces the mass of functioning thyroid tissue to below a critical level Swallow a glass of water containing radioiodine Useful in recurrence of hyperthyroidism after thyroidectomy (takes 2-3 months) high incidence of late hypothyroidism (75-80%) after 10 years Contraindicated in pregnant women (affecting infants thyroid) No evidence therapeutic radioiodine is carcinogenic or teratogenic
Neoplasms
Classification
Follicular epit diff Follicular benign adenoma
malign
1o
papillary (60%)
follicular (20%) Follicular epit undiff anaplastic (10%) Parafollicular cells medullary (5%) Lymphoid cells lymphoma (5%)
2o
Thyroid carcinoma
F:M = 3:1 (incidence 3.7 in 100 000) Arising in pre-existing goitres Reported following radiation of the neck in childhood Clinical features
Goiter LN (papillary ca) recurrent laryngeal nerve paralysis (locally advanced dis.) usually euthyroid
Papillary carcinoma
Commonest (60%) Young adults, adolescents or children Slow growing tumour Spread
lymphatic (late and common) Blood-born (uncommon)
Occult carcinoma- enlarged lymph node in the jugular chain with no palpable abnormality of thyroid (good prognosis) Tx
combination of surgery (total lobectomy or thyroidectomy), thyroid suppression by T4 and radioiodine
numerous papillae having a fibrovascular stalk covered by a single to multiple layers of cuboidal epithelial cells
Follicular carcinoma
Young and middle-aged adults Common in area of endemic goiter Spreads
Blood stream (common)
worsen the prognosis mortality rate twice fr papillary ca
Lymphatic rare
Invasion of capsule and the vascular spaces in the capsular region in follicular carcinoma.
Male incidence LN mets Blood vessel invasion Recurrence Mortality rate Distant mets Nodal mets
22 35 40 19 11 45 34
35 13 60 29 24 75 12
Medullary carcinoma
Arises from parafollicular C cells may secrete calcitonin (tumour marker) any age F=M associated with other cancers in MEN syndrome (type II) Deposits of amyloid between the nests of tumour cells Lymph node and blood-borne involvement are common Tx: total thyroidectomy and lymph node clearance (if involved)
Anaplastic carcinoma
elderly Rapid local spread takes place with compression and invasion of the trachea Early dissemination to the regional lymphatics and blood-stream spread to the lung, skeleton and brain Tx
radical thyroidectomy palliative radiotherapy temporary relieve (tracheostomy for obstructed airway)
TNM staging
Primary tumor (T) TX: Primary tumor cannot be assessed T0: No evidence of primary tumor T1: Tumor 1 cm or less in greatest dimension limited to the thyroid T2: Tumor more than 1 cm but not more than 4 cm in greatest dimension limited to the thyroid T3: Tumor more than 4 cm in greatest dimension limited to the thyroid T4: Tumor of any size extending beyond the thyroid capsule
Regional lymph nodes (N) NX: Regional lymph nodes cannot be assessed N0: No regional lymph node metastasis N1: Regional lymph node metastasis
N1a: Metastasis in ipsilateral cervical lymph node(s) N1b: Metastasis in bilateral, midline, or contralateral cervical or mediastinal lymph node(s)
Distant metastases (M) MX: Distant metastasis cannot be assessed M0: No distant metastasis M1: Distant metastasis
Prognosis
Well differentiated tumours
Long survival even with presence of LN deposits
Anaplastic tumours
Pt dead within a year (due to local invasion or widespread dissemination)
Thyroiditis
Granulomatous thyroiditis
subacute thyroiditis, de Quervains thyroiditis virus infection Features pain in the neck Fever Malaise firm, irregular enlargement of one or both thyroid lobes Raised ESR absent thyroid antibodies serum T4 is high or slightly raised radioiodine uptake of gland is low Self limiting, goitre subsides in few months Dx - confirmed by FNAC & radioactive iodine uptake - rapid symptomatic response to prednisolone in acute case of severe pain
Riedels thyroiditis
Rare slightly enlarged but is woody hard with infiltration of adjacent tissues represent late stage of Hashimotos disease or inflammatory origin Mistaken for thyroid ca (histologically gland is replaced by
fibrous tissue containing chronic inflammatory cells)
a/w other conditions such as retroperitoneal fibrosis, sclerosing cholangitis, and fibrosing mediastinitis Wedge resection of portion of gland if tracheal compression symptoms develop