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response to the level of thyroid hormones in the blood by a negative feedback mechanism. The secretion of TSH is also under the influence of the hypothalamic thyrotrophin-
releasing hormone (TRH).
Pharmacological control ofsecretion
The production of thyroid hormones can be inhibited by thionamide antithyroid drugs such as carbima­zole, propylthiouracil and methimazole which block the binding of iodine but do not interfere with the uptake of iodide by the gland.
High doses of iodine (e.g. Lugol’s patients with excessive thyroid hormone produc­tion result in an increase in the amount of iodine­rich colloid, and a diminished liberation of thyroid hormones; the gland also becomes less vascular. The effects of iodide treatment are maximal after 2 weeks of treatment and then diminish. This canbe useful in preparing hyperthyroid patients for surgery when antithyroid drugs have been ineffective.
Lack of iodine in the diet prevents the formation of thyroid hormones, and excess pituitary TSH is pro­duced, which may result in an iodine- deficient goitre. Thiocyanates prevent the thyroid gland from taking up iodide.
2
) given to
which may replicate even in the absence of TSH. The difference in areas of excessive activity and other areas of regression results in a varied appearance of the gland. Some follicles are lined with hyperactive epithelium and others with flattened atrophic cells. Some contain no colloid, others an excessive amount. The thyroid interstitium is excessive, with some fibrosis and mononuclear cell infiltration. Factors which are associated with the development of a mul­tinodular goitre include female gender and elevated TSH secondary to iodine deficiency or natural goitro­gens. Nodular goitres may produce a normal amount of T4, but sometimes excessive T4 production results in hyperthyroidism in this condition (toxic nodular goitre). Radioactive iodine- 131 is the treatment of choice in such cases.
The thyroid is usually enlarged, irregular and nodular and, although one lobe often predominates at presentation, the condition does affect the entire gland.
Symptoms
The enlarging thyroid can produce a number of ‘pres­sure’ symptoms including dysphagia, breathlessness, orthopnoea, hoarseness and facial swelling.
Investigation ofmultinodular goitre
Pathology ofgoitre
The term ‘goitre’ is used to describe any enlargement of the thyroid gland irrespective of the underlying pathology. It can be diffuse or nodular and non­or toxic.
Multinodular goitre
The aetiology of multinodular goitre is unclear but several contributing factors have been identified. The principal cause is believed to be a functional hetero­geneity of follicular cells, with some having a higher growth potential than normal follicular cells, some of
2
Jean Guillaume Auguste Lugol (1788–1851), Physician, Hôpital Saint- Louis, Paris. He proposed a solution of iodine as a treatment for tuberculosis, for which it was ineective. Its use in treating thyrotoxicosis was pioneered by Henry Stanley Plummer (1874–1936).
toxic
Patients require a few specific investigations.
TSH concentration is low in the few patients with
hyperthyroidism in association with multinodular goitre.
Ultrasound of the gland to exclude any suspicious
nodules.
Computed tomography (CT) of the neck and thoracic inlet may be required to define the size of the goitre, the extent of the goitre including any retrosternal extension, and to identify the of tracheal compression (Box39.1).
presence
Complications
• Tracheal displacement or compression.
• Haemorrhage into a cyst, producing pain and increased swelling (which may produce sudden tracheal compression).
• Toxic change.
• Malignant change (rare).
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Box 39.1 Symptoms ofmultinodular goitre
Dysphagia: usually of solids, worse with certain food, for example meat.
Breathlessness: worse on exertion, bending forward (especially, retrosternal extension).
Orthopnoea: owing to the weight of the gland pressing on the trachea when lying flat.
Stridor: from significant tracheal compression.
Hoarseness: from pressure on one recurrent laryngeal nerve (rare).
Facial congestion: venous engorgement especially on raising arms (Pemberton’s sign
3
).
Clinical features inthyroid disease
Patients may present complaining of a lump in the neck and/or with symptoms due to excessive or diminished amounts of circulating thyroxine.
The thyroid swelling
The characteristics of an enlarged thyroid are a mass in the neck on one or both sides of the trachea, which moves on swallowing, since it is attached to the larynx by the pretracheal fascia.
Colloid goitre
All diseases of the thyroid are more common in geo­graphical locations in which the water and diet are low in iodine. In the UK, the most notorious district historically was Derbyshire, and the frequency of goi­tres in this region gave rise to the term ‘Derbyshire neck’. Iodination of table salt has all but abolished this state of affairs. Switzerland, Nepal, Ethiopia and Peru are also areas where natural iodine is very scarce in the diet and water, and thyroid disease is more com­mon. The most common lesion of the thyroid gland due to iodine deficiency is the colloid goitre, in which the gland is enlarged and the acini are atrophic with a large amount of colloid. This can also occur in physi­ological goitres (pregnancy and puberty). This accu­mulation of colloid is probably due to over secretion of TSH from the anterior pituitary, acting on the thy­roid, which is unable to produce T4.
Hyperplasia
In primary hyperthyroidism (Graves’ disease4), the thyroid is uniformly enlarged and there is hyperactiv­ity of the acinar cells with reduplication and infolding of the epithelium. The gland is very vascular and there is little colloid to be seen. Lymphocyte infiltra­tion is usually a predominant feature.
Retrosternal goitre
Evidence of retrosternal enlargement of the thyroid should be sought by palpation and percussion with the neck fully extended. A retrosternal thyroid can block the venous return to the superior vena cava and result in engorgement of the jugular veins and their tributaries and in oedema of the upper part of the body– a cause of the superior mediastinal syndrome. In such cases, CT imaging of the thoracic inlet should be performed to assess its extent.
Tracheal displacement
The trachea should be examined to determine dis­placement or compression by the thyroid enlarge­ment; the patient should be asked to take a deep breath with the mouth open, when stridor may become apparent.
Vocal cord integrity
The vocal cords should be examined by flexible nasendoscopy or indirect laryngoscopy, as thyroid carcinoma may infiltrate the recurrent laryngeal nerves and cause vocal cord paralysis. If surgery is contemplated, it is important to know whether or not the cords are functioning normally before operation.
3
Hugh Spear Pemberton (1890–1956), Physician, Liverpool,
UK.
4
Robert Graves (1796–1853), Physician, Meath Hospital,
Dublin, Ireland.
Regional nodes
As with any other lump, the regional lymph nodes must be examined in any case of thyroid swelling. The draining nodes of the thyroid lie along the carotid
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sheath on each side. Hard enlarged nodes strongly suggest malignant disease of the thyroid.
The physiological state ofthe patient
Determine whether the patient is euthyroid, hyper­thyroid or hypothyroid. In the majority of patients, this can be determined from the clinical features.
Hyperthyroidism
Clinical features of hyperthyroidism are determined by examination of the eyes and the hands, as well as from the history and examination of the neck. Thyroxine potentiates the actions of adrenaline (epinephrine), and many of the features of hyperthyroidism represent increased activity of the sympathetic nervous system.
History
The patient is irritable and nervous, and cannot keep still. The appetite is increased and yet there is loss of weight; diabetes mellitus is the other condition in which this paradox occurs. Diarrhoea is occasionally a feature. The patient prefers cold environments rather than warm. Palpitations due to tachycardia or atrial fibrillation may occur.
Examination
The thyroid gland
The thyroid itself is usually smoothly enlarged but not invariably so. It may be highly vascular and demon­strate a bruit and thrill.
Eye signs
Exophthalmos is present in most patients with hyperthyroidism of Graves’ disease, owing to oedema and infiltration by mononuclear cells of the orbital fat and extrinsic muscles of the eye.
Lid retraction: the innervation of the levator pal­pebrae superioris is partly under sympathetic control. In hyperthyroidism, it is tonically active, retracting the upper lid, giving the appearance that the patient is staring.
Lid lag: ask the patient to follow your finger as you move it from over the head downwards – the
upper lid does not immediately drop, revealing the white sclera above the cornea.
Dilated pupils owing to increased sympathetic
pupil dilator tone.
Double vision following the examiner’s finger to
• the upper outer quadrant. This is due to infiltra­tion of the extrinsic muscles of the eye, which causes exophthalmic ophthalmoplegia.
Exophthalmos is an extremely distressing condi­tion for the patient and, if severe, the patient is unable to close the eyelids; the eyes are then susceptible to corneal ulceration and eventual blindness. This condition is difficult to treat, but may respond to high­dosage corticosteroids; surgical decompression of the orbit with suture of the eyelids across the eyeball (tarsorrhaphy) may be required.
The hands
Sweating: the hands are warm and moist.
Tachycardia: a rapid pulse is almost invariable
and typically the sleeping pulse is also raised. There may be atrial fibrillation and indeed the patient may present with heart failure. A rapid sleeping pulse rate permits differentiation of hyperthyroidism from an acute anxiety state; such patients when sleeping will have a normal pulse rate whereas, in patients with hyperthyroidism, the sleeping pulse rate will remain elevated.
Fine tremor of the outstretched hands is present
and reflects the increased sympathetic activity.
Finger clubbing, more accurately termed ‘thyroid
acropachy’.
Onycholysis: the nail lifts off the nail bed, a condi-
tion also seen in psoriasis and with some fungal infections.
Pretibial myxoedema, thickening of the subcuta-
neous tissues in front of the tibia, is a rare feature.
Aetiology
Patients with hyperthyroidism fall into two groups: primary (Graves’ disease) and secondary.
Primary hyperthyroidism (Graves’ disease)
This occurs usually in young women with no preceding history of goitre. The gland is smoothly enlarged and exophthalmos common. Symptoms are primarily
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those of irritability and tremor; exophthalmos and ophthalmoplegia are often quite marked. Primary hyperthyroidism is due to the action of autoanti which bind to, and stimulate, the TSH receptor. These thyroid­longed stimulatory effect compared with TSH; hence the traditional name of ‘long­stimulators’.
stimulating antibodies have a pro-
acting thyroid
Secondary hyperthyroidism
Secondary hyperthyroidism is overactivity develop­ing in an already diseased and hyperplastic gland. It is a disease of middle age, occurring in patients with a
existing non- toxic (euthyroid) goitre. The gland is
pre­nodular and there are no eye changes. Symptoms fall more on the cardiovascular system, the patient often presenting in heart failure with atrial fibrillation, although nervousness, irritability and tremor may also be present.
bodies
Hashimoto’s disease
Hashimoto’s disease5 is an uncommon thyroid disease that was the first of the autoimmune diseases to be elucidated. The patient is usually a middle­woman with clinical evidence of hypothyroidism. The gland is uniformly enlarged and firm, although it may occasionally be asymmetrical and irregular.
Macroscopically, its cut surface is lobulated and greyish yellow. Microscopically, there is diffuse infil­tration with lymphocytes, increased fibrous tissue and diminished colloid. It is an autoimmune disease in which the patient has developed both a humoral and cell­within their own thyroid. Thyroglobulin and micro­somal antibodies can be demonstrated in about 90% of patients.
by demonstrating the presence of thyroid antibodies and, if necessary, by biopsy, because thyroidectomy will precipitate severe hypothyroidism in these cases. Occasionally, lymphoma occurs in such glands.
mediated autoimmune reaction to elements
It is important to diagnose the condition correctly
aged
Hypothyroidism
Congenital hypothyroidism
Congenital hypothyroidism (or cretinism) is a condi­tion in which the child is born with little or no function­ing thyroid. The infant is stunted and mentally subnormal, with puffy lips, a large tongue and protu­berant abdomen, often surmounted by an umbilical hernia.
Adult hypothyroidism
In adults, hypothyroidism (or myxoedema) usually affects women, and most often occurs in the middle aged or elderly. These patients have a slow, deep voice and are usually overweight and apathetic, with dry, coarse skin and thin hair, especially in the lat­eral third of the eyebrows. In contrast with hyperthy­roidism, myxoedematous patients usually feel cold in hot weather, have a bradycardia and are consti­pated. They are often anaemic and may suffer from heart failure owing to myxoedematous infiltration of the heart.
Treatment
Thyroxine replacement therapy with levothyroxine will shrink the gland and treat the symptoms of myxoedema.
Riedel’s thyroiditis
Riedel’s thyroiditis6 is an extremely rare disease of the thyroid in which the gland may be only slightly enlarged, but is woody hard with infiltration of adja­cent tissues. It is a chronic inflammatory condition that is associated with elevated IgG4levels and IgG4­positive plasma cell infiltrates, supporting an autoim­mune aetiology.
It may be mistaken clinically for a thyroid carci­noma due to its hard texture and apparent infiltration of the neighbouring muscles, but histologically the
5
Hakaru Hashimoto (1881–1934), Surgeon, Kyushu
University, Kyushu, Japan.
6
Bernhard Riedel (1846–1916), Professor of Surgery, Jena,
Germany.
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Box 39.2 IgG4- related diseases
The following conditions are increasingly being recognized to be part of a spectrum of conditions associated with elevated IgG4levels and plasma cell infiltrates.
Riedel’s thyroiditis.
Mikulicz syndrome glands).
Mediastinal fibrosis.
Retroperitoneal fibrosis.
Peri- aortitis and peri- arteritis.
Inflammatory aortic aneurysm.
gland is replaced by fibrous tissue containing a dense lymphoplasmacytic infiltrate. It is associated with other IgG4-
Treatment with high- dose steroids may be effective, but resection of a portion of the gland may be required if symptoms of tracheal compression develop.
related conditions (Box39.2).
7
(affecting salivary and lacrimal
De Quervain’s thyroiditis
De Quervain’s thyroiditis8 is a rare condition usually affecting young women. It often follows a viral infec­tion of the upper respiratory tract. The gland is slightly enlarged, firm and tender. It is generally self­and rarely leads to hypothyroidism.
limiting,
Investigations inthyroid disease
Serum free T4 and free T3. Measurement of the bio-
logically active unbound fraction is more accurate than measurement of total T3 and T4; elevation suggests hyperthyroidism.
7
Jan Mikulicz- Radecki (1850–1905). Professor of Surgery in
Krakow and Königsberg.
8
Fritz de Quervain (1868–1940), Professor of Surgery, Bern,
Switzerland.
TSH concentration: raised in myxoedema; suppress ed in hyperthyroidism, in which the gland secretes T4 autonomously.
Thyroid scintigram: radioiodine studies of the
thyroid gland can provide very useful information. A small tracer dose of γ­injected intravenously and the gland scanned with
ray detector to map areas of high uptake
a γ­reflecting high activity. A nodule in the thyroid gland that is hyperactive can be pinpointed by this method, a so­ nodule that is not producing T4will not take up the radioiodine, for example a cyst or tumour (‘cold nodule’).
Thyroid antibodies, anti- thyroglobulin antibodies
or antithyroid peroxidase antibodies, indicate an autoimmune pathology such as Hashimoto’s thyroiditis, or primary hyperthyroidism; other autoantibodies are often present.
Ultrasound of the thyroid gives valuable informa­tion as to whether a mass is solid or cystic, unifocal or multifocal. Certain radiological features can be markers of increased risk for malignancy and there are now grading systems to aid the identification of nodules which should have a needle biopsy.
Fine- needle aspiration and core biopsy allow
• material to be obtained for cytological and histo­logical examination. It is now the principal investi­gation for all solitary nodules, often under ultrasound guidance.
Serum cholesterol is usually raised in myxo-
edema and may be normal or a little low in hyperthyroidism.
Electrocardiogram (ECG): in myxoedema, cardiac
• involvement will show low electrical activity with small complexes. Atrial fibrillation complicating hyperthyroidism will be confirmed.
CT scan: allows definition of size and extent of goi­tre, particularly any retrosternal extension and the presence of tracheal compression.
called ‘hot nodule’. Similarly, a
ray- emitting iodine- 131 is
Clinical classification ofthyroid swellings
The clinical assessment of a patient with a thyroid swelling has two components.
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1 The physical characteristics of the gland itself. Is it
smoothly enlarged? Is there a single nodule present? Is it multinodular?
2
The endocrine state of the patient. Is the patient
euthyroid, hyperthyroid or hypothyroid?
A synthesis of these two observations gives a simple clinical classification of the vast majority of thyroid swellings, as follows.
Smooth, euthyroid enlargement of the thyroid
gland: this is the ‘physiological’ goitre, which tends to occur at puberty and pregnancy.
Nodular, euthyroid gland: this is the common nod-
ular goitre, there being either a solitary nodule or multiple nodules.
Smooth, hyperthyroid goitre: primary hyperthy-
roidism (Graves’ disease).
Nodular hyperthyroid goitre: toxic nodular goitre.
The less common findings are as follows.
Smooth, firm enlargement with myxoedema:
Hashimoto’s disease. Usually in a middle­woman, and the gland is sometimes asymmetrical and irregular.
Invasive enlargement, hard: carcinoma.
Riedel’s thyroiditis and acute thyroiditis are uncommon.
aged
Outline oftreatment ofgoitre
Euthyroid nodular enlargement
T4 replacement (levothyroxine) may be effective by reducing TSH secretion, and so suppressing further enlargement. It is best given following thyroidectomy to suppress enlargement of the remaining gland tissue.
Single euthyroid nodule
In the patient with a single nodule in the thyroid, this may be a solitary benign adenoma, a malignant tumour or, most likely of all, a cyst or nodule in a thy­roid showing the histological changes of a nodular goitre. Half of all solitary nodules are in fact promi­nent areas of multinodular goitres.
Historically all solitary nodules were excised to make a diagnosis. Nowadays, ultrasound combined with fine­ferentiate nodules that should be excised from benign lesions. Cysts are aspirated and checked at an interval to ensure that they do not re­distinguish benign follicular adenomas from follicu­lar carcinomas, so these are often excised to provide definitive histology.
needle aspiration cytology can usually dif-
collect. Cytology cannot
Hyperthyroidism
The available therapy comprises:
• Antithyroid drugs, of which carbimazole is the
drug of choice.
β- adrenergic blocking drugs.
• Antithyroid drugs combined with subsequent
thyroidectomy.
• Radioactive iodine- 131.
Multinodular goitre
Thyroidectomy is advised in patients with an enlarged, euthyroid, nodular goitre when there are symptoms of tracheal compression and dyspnoea. In addition, in younger patients, it is reasonable to advise surgery because of the danger of haemorrhage into a thyroid cyst with the risks of acute tracheal compression. If there is retrosternal extension in a younger patient, then surgery should be advised as delay will only make surgery more challenging. The patient may also be concerned with the cosmetic appearance of the swollen neck.
In elderly patients with a long- standing goitre that is symptomless, it is good practice to pursue a non- operative approach.
Antithyroid drugs
Carbimazole and propylthiouracil are the most com­monly used antithyroid drugs in the UK. Carbimazole is used as the first- line treatment with propylthioura­cil being used in pregnancy or in patients intolerant to carbimazole. There is rapid regression of symptoms, the patient beginning to feel better and to gain weight with reduction of tachycardia within 1–2 weeks. Treatment is continued for 12 months and may be combined with levothyroxine (so- called ‘block and replace therapy’). If symptoms recur, a further 6 months’ treatment is given, after which surgery is advised. Unfortunately, a high relapse rate (up to 60%) occurs after terminating the treatment, even if
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this is prolonged for 2 or more years. Medical treat­ment alone is, therefore, usually confined to the treat­ment of primary hyperthyroidism in children and adolescents.
The toxic effects of carbimazole include a rash, fever, arthropathy, lymphadenopathy and agranulo­cytosis; the last is a dangerous and potentially lethal complication but occurs in well under 1% of patients. The first symptom is a sore throat and patients on carbimazole must be warned to discontinue treat­ment immediately if this occurs and to report to hos­pital. Granulocyte colony­required.
stimulating factor may be
β- Adrenergic blocking drugs
In patients with severe hyperthyroidism, propranolol induces rapid symptomatic improvement of the car­diovascular features by blocking sympathetic overac­tivity, while the hyperthyroidism comes under control with specific antithyroid therapy.
Drugs andsurgery combined
The majority of adult patients in the UK are treated with preliminary carbimazole until euthy­roid; relapse after medical therapy is an indica­tion for radioactive iodine or thyroidectomy. Most patients will be euthyroid following a course of drug therapy although 50% will relapse and require further drug treatment at a later stage. Radioiodine is associated with a higher relapse rate than surgery, and a high incidence of late­onset hypothyroidism, but may be more suitable for treating older patients. It is not associated with increased malignancy.
The surgical management of primary hyperthy­roidism (Graves’ disease) is now usually limited to younger patients in their late teens or early twenties who have relapsed following their second course of drug treatment and who are looking for a long­cure for their disease. The historical operation for pri­mary hyperthyroidism had been subtotal thyroidec­tomy in an attempt to render the patient euthyroid with no need for exogenous thyroxine. Unfortunately, most patients will require thyroxine replacement in time, and, by leaving too much thyroid tissue in situ, there is a risk of recurrence. As a result, total thyroid­ectomy has become the operation of choice for these patients in the same way as for patients with multi­nodular goitre.
term
Radioactive iodine
From the patient’s point of view, this is the most pleasant treatment, as all the patient has to do is swallow a glass of water containing the radioiodine. There is no need for prolonged treatment with drugs or the risk of operation; it is particularly useful in recurrence of hyperthyroidism after thyroidectomy. It usually takes 2–3 months before the patient is ren­dered euthyroid. Antithyroid drugs, with or without a β-
blocker, may be used to control symptoms during
this time.
There is a theoretical risk of malignant change in the irradiated gland, although it is very uncommon. There is no convincing evidence of an increased risk of developing an unrelated cancer in the long term with the dose of radioactive iodine administered. Nevertheless, it is current practice not to use radioio­dine in young women who may become pregnant during treatment, as there is a very real danger of affecting the infant’s thyroid. It is also not used when there is thyroid eye disease or there are concerns about tracheal compression. Another disadvantage of this treatment is the high incidence of late hypo­thyroidism, which requires replacement therapy with T4.
Complications ofthyroidectomy
In addition to the hazards of any surgical operation, there are special complications to consider following thyroidectomy. These can be divided into hormonal disturbances (the thyroid itself and the adjacent parathyroid glands) and injury to closely related ana­tomical structures.
Hormonal:
1
a
Paraesthesiae, owing to coincidental parathy-
roid removal or bruising.
b Tetany (parathyroid removal or bruising). c Thyroid crisis. d Hypothyroidism, owing to extensive removal of
thyroid tissue.
e Late recurrence of hyperthyroidism owing to
inadequate excision of the hyperthyroid gland.
2 Damage to related anatomical structures:
a Recurrent laryngeal nerve injury. b Injury to trachea. c Pneumothorax.
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3 The complications of any operation, especially:
Haemorrhage.
a b
Sepsis.
c
Postoperative chest infection. Hypertrophic scarring (keloid).
d
Some of these complications require further con-
sideration here.
Hypoparathyroidism
This may result from inadvertent removal of the para­thyroids or their injury during operation. The patient may develop paraesthesiae or tetany (see Chapter40) a few days postoperatively with typical carpopedal spasms, which may be induced by tourniquet around the arm (Trousseau’s sign, see Chapter40), and a posi­tive Chvostek’s sign (see Chapter40); this is elicited by tapping lightly over the zygoma, when the facial mus­cles will be seen to contract.
Treatment
Treatment consists of giving oral calcium together with vitamin D derivatives (ergocalciferol or alfacal­cidol) or 10 mL of 10% calcium gluconate intrave­nously if symptoms are severe. Often, the tetany is transient and the injured parathyroids recover; in other cases, permanent treatment with alfacalcidol is required. Parathormone is not used.
In addition to frank tetany, which occurs in about 1% of cases, milder degrees of hypoparathyroidism may occur and may present with mental changes
(depression or anxiety neurosis), skin rashes and bilateral cataracts. Low postoperative calcium is treated by the administration of oral calcium and/or vitamin D daily by mouth.
Thyroid crisis
An acute exacerbation of hyperthyroidism seen imme­diately postoperatively is now extremely rare because of the careful preoperative preparation of these patients. It is a frightening phenomenon, with mania, hyperpy­rexia and marked tachycardia, which may lead to death from heart failure. The cause is not fully understood, but it may be due to a massive release of thyroxine from the hyperactive gland during the operation.
Treatment
Treatment comprises heavy sedation, propranolol, antithyroid medication, iodine and cooling by means of ice packs.
Recurrent laryngeal nerve injury
The recurrent laryngeal nerve lies in the groove between the oesophagus and trachea in close rela­tionship to the inferior thyroid artery (Figure 39.2). Here it is at risk of division, injury from stretching or compression by oedema or blood clot.
If one nerve alone is damaged, the patient may have little in the way of symptoms apart from slight hoarseness because the opposite vocal cord compen­sates by passing across the midline during phonation.
(a) (b) (c)
Figure39.2 The relationship of the recurrent laryngeal nerve to the thyroid gland and the inferior thyroid artery.
However, if both recurrent nerves are damaged there
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is almost complete loss of voice and serious narrowing of the airway; a temporary tracheostomy may be required, although an incomplete injury may recover in time. It is estimated that the nerve is injured in about 2–3% of thyroidectomies.
Vocal cord assessment by flexible nasendoscopy should be performed prior to thyroid surgery, and is essential for patients with known malignancy, previ­ous neck surgery and for patients with hoarseness or stridor.
It is also possible to injure the external branch of the superior laryngeal nerve resulting in a lower, less powerful voice.
Haemorrhage
If this occurs shortly after thyroidectomy, it can be life- threatening, as bleeding into the thyroid bed and haematoma formation cause respiratory distress by causing venous congestion and laryngopharyngeal oedema. Symptoms and signs include dysphagia, odynophagia, respiratory distress, neck swelling, ooz­ing from the wound and pain.
Treatment
This may be an extreme emergency and must be dealt with at once by decompressing the neck in the ward. The skin and the subcutaneous sutures are removed, the wound is opened and the blood clot expressed. The patient can then be transferred to theatre, anaes­thetized, bleeding points secured and the wound resutured.
Thyroid tumours
Classication
Benign
• Follicular adenoma.
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d
Medullary carcinoma.
e
Lymphoma (rare).
Secondary:
2
a
Direct invasion from adjacent structures, for
example, oesophagus.
Rare site for blood- borne deposits e.g. from
b
renal carcinoma.
Benign adenoma
Although benign encapsulated nodules in the thyroid gland are common, the majority are part of a nodular colloid goitre. A small percentage represent true benign adenomas, of which 10% are ‘hot nodules’, that is, they produce excess thyroxine. Thyroid adenomas are four times more common in women.
Thyroid carcinoma
Thyroid carcinoma affects women three times as often as men and the incidence is rising. Risk fac­tors include endemic goitre, radiation exposure in childhood, familial, Hashimoto’s thyroiditis (lym­phoma), familial adenomatous polyposis and Cowden syndrome 6 per 100000 and long- term survival rates follow­ing treatment are excellent. Ten- year survival rates for papillary and follicular cancer are over 90% and 80%, respectively. Papillary and follicular cancer, together referred to as ‘differentiated thyroid can­cer’, account for approximately 90% of all thyroid cancers.
Differentiated thyroid cancer is usually curable when detected at an early stage. The high cure rate can be attributed to a multidisciplinary approach, including specialist surgery, radioiodine ablation, TSH suppression and, finally, the use of thyroglobulin as a thyroid- specific tumour marker (see later in this chapter). Despite this management strategy, a small number of patients will develop recurrence. Half of all thyroid cancer deaths are due to respiratory failure secondary to either pulmonary metastasis or airway obstruction.
9
. It has an incidence of around
Malignant
1 Primary (five main types):
a Papillary adenocarcinoma. b Follicular adenocarcinoma. c Anaplastic.
9
Cowden syndrome: Autosomal dominant condition caused by mutation in PTEN tumour suppressor gene characterised by the development of multiple hamartomas in skin and mucous membranes, but also cancers of the thyroid, breast and uterus, among others. Named after the Cowden family in whom it was rst described.
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Pathology
Papillary carcinoma
This is the most common type of thyroid cancer, con­stituting 80% of thyroid cancers. It occurs in young adults, adolescents or even children. It is a slow­growing tumour and lymphatic spread occurs late. Deposits in the regional lymph nodes may be solitary and in the past have been mistakenly regarded as lat­eral aberrant thyroid tissue. However, a careful search of the thyroid gland will reveal a well­tumour in the ipsilateral lobe.
differentiated
Follicular carcinoma
This occurs in young and middle- aged adults, the incidence peaking in the fifth decade, and accounts for 10% of thyroid cancers. It is more common in areas where endemic goitres are common. It has a tendency to spread via the bloodstream particularly to bones and lungs; lymph node spread is uncommon.
Medullary carcinoma
This arises from the parafollicular C cells and secrete calcitonin. other thyroid tumours, has a roughly equal sex dis­tribution; it accounts for 5% of thyroid cancers. It may be familial (in 25% of cases) and may be associ­ated with other cancers in the multiple endocrine neoplasia syndrome (type II, associated with phaeo­chromocytoma and either parathyroid tumours or neurofibromas; see Chapter40). The characteristic finding is deposits of amyloid between the nests of tumour cells.
The disease is usually multicentric and bilateral in all familial forms, and is associated with C cell hyperplasia. In contrast, the sporadic form is usu­ally unifocal with no associated hyperplasia. The tumour cells produce calcitonin, which acts as a tumour marker and can be used as a screening test in syndromic families or to detect recurrence in fol­low­tion cytology of medullary thyroid carcinoma may be diagnostic.
10
Calcitonin acts to lower serum calcium, stimulating osteoblast and inhibiting osteoclastic activity in bones, among other actions.
10
It may occur at any age and, unlike
up of patients after surgery. Fine- needle aspira-
Anaplastic carcinoma
This occurs in the elderly, thus reversing the usual state of affairs, in that the more malignant tumours of the thyroid occur in the older age group. Rapid local spread takes place with compression and invasion of the trachea. There is early dissemination to the regional lymphatics and bloodstream spread to the lungs, bone and brain. It accounts for around 2% of thyroid cancers.
Lymphoma
Rarely a thyroid tumour may be a non- Hodgkin’s lymphoma.
Clinical features
Tumours may present like other goitres as a lump in the neck, often more rapidly growing. Dysphagia is uncommon, and suggestive of an anaplastic tumour; more common is the complaint that swallowing is uncomfortable. Pain may occur with local infiltration, and hoarseness is suggestive of infiltration of the recurrent laryngeal nerve. Lateral cervical lymph nodes may be palpably enlarged. The patients are usually euthyroid. Ultrasound- guided core needle biopsy or fine- needle aspiration cytology is used to confirm the diagnosis.
Treatment ofdifferentiated thyroidcancer
Surgery
The management of a patient with thyroid cancer should be the responsibility of a multidisciplinary team. Well­a combination of surgery, thyroid suppression by levothyroxine and radioiodine.
Total thyroidectomy is recommended for patients with tumours greater than 4cm in diameter (pT3), or tumours of any size in association with any of the following characteristics: multifocal disease, bilateral disease, extra- thyroidal spread (pT4a), familial disease, and those with clinically or radio­logically involved nodes and/or distant metastases. Furthermore, radioiodine ablation is facilitated by total thyroidectomy.
Thyroid lobectomy is, therefore, appropriate sur­gery for unifocal, papillary tumours less than 4cm in
differentiated tumours can be treated by
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