Assessment of neck lump and thyroid cancer Flashcards

1
Q

What should you ask in a hx of a patient presenting with a neck lump?

A
How long has the lump been present?
Is it painful?
Has it changed? If so, over what time frame?
Are there symptoms of recent infection of nearby structures (cough, cold, sore throat, earache, toothache, skin problems, head lice, bites)?
Has there been a fever?
Does eating affect the lump?
Is there pain on swallowing?
Is there any effect on voice?
Does the person smoke?
Is there a history of travel?
Is there a past history of cancer?
Are there red flag symptoms of systemic illness such as:
-Night sweats.
-Weight loss.
-Unexplained bruising or bleeding.
-Persistent fatigue.
-Breathlessness.
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2
Q

How do you examine a neck lump?

A

Location of the lump.
Examine the:
-Anterior triangle (bordered by the midline, the body of the mandible and the anterior border of sternocleidomastoid).
-Posterior triangle (bordered by the posterior border of sternocleidomastoid, the clavicle and the trapezius).
-Midline.
Whether it is tender, hot, red, inflamed.
Consistency, size, mobility.
How deep the lump is: whether it is intradermal (suggesting sebaceous cyst with a central punctum, or a lipoma), subcutaneous or within deeper tissue.
Whether it is pulsatile.
Whether it is a solitary lump or if there is more than one.
Whether it moves on swallowing (thyroid, thyroglossal cysts).
Whether it moves when the person sticks out their tongue (thyroglossal cysts).

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3
Q

Which further examination can you do to establish the cause of a neck lump?

A

Examination of the skin of the head and neck for rashes, lesions or infection.

Examination of the ears, nose and throat.

Examination of the mouth - for malignancy, dental issues. If parotid disease is suspected, identify the orifice of parotid duct and palpate with the patient’s head tilted backwards.

Examination of the chest.

Examination for lymphadenopathy or organomegaly elsewhere.

Checking for compression of the airway or vasculature.

Taking note of general clues of systemic illness, such as jaundice, pallor, petechiae, bruising, excoriation.

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4
Q

What are the differentials of a neck lump?

A

Reactive lymph nodes
Bacterial causes such as s.aureus, TB and secondary syphilis.
Viral causes such as EBV, CMV, HIV and HSV.
Parasitic causes such as head lice, fungal infections and toxoplasmosis
Non-infective causes such as sarcoidosis
In children, consider cat scratch disease and Kawasaki disease
Malignant lymph nodes: leukaemia, lymphoma and mets.
Lipomas and other benign tumours such as fibromas, neuromas and vascular tumours.
Thyroid swellings including nodules and cancers
Thyroglossal cysts, cystic hygroma and dermoid cyst.
Branchial cyst, laryngocele and pharyngeal pouch.
Sarcoma and skin malignancy.

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5
Q

How does thyroid swellings present?

A

May be hypo-, eu- or hyperthyroid symptomatically

Moves upwards on swallowing

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6
Q

How do thyroglossal cysts form?

A

The thyroid develops from the floor of the pharynx and descends into the neck during its development.

It is connected to the tongue by the thyroglossal duct. The foramen cecum is the point of attachment of the thyroglossal duct to the tongue. The thyroglossal duct normally atrophies but in some people may persist and give rise to a thyroglossal duct cyst.

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7
Q

How does thyroglossal cyst present?

A

Thyroglossal cyst is more common in patients < 20 years old

  • Usually midline, between the isthmus of the thyroid and the hyoid bone
  • Moves upwards with protrusion of the tongue
  • Non-tender and mobile
  • May be painful if infected
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8
Q

What is cystic hygroma?

A

Cystic hygroma is a congenital lymphatic lesion (lymphangioma) typically found in the neck, classically on the left side

Most are evident at birth, around 90% present before 2 years of age

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9
Q

What are dermoid cysts?

A

Dermoid cysts are derived from pluripotent stem cells and are located in the midline

  • Most commonly in a suprahyoid location
  • They have heterogeneous appearances on imaging and contain variable amounts of calcium and fat
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10
Q

What is a pharyngeal pouch?

A

The pharyngeal pouch is more common in older men

  • Represents a posteromedial herniation between thyropharyngeus and cricopharyngeus muscles
  • Usually not seen but if large then a midline lump in the neck that gurgles on palpation
  • Typical symptoms are dysphagia, regurgitation, aspiration and chronic cough
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11
Q

What is a brachial cyst?

A

A brachial cyst is an oval, mobile cystic mass that develops between the sternocleidomastoid muscle and the pharynx

  • Develop due to failure of obliteration of the second branchial cleft in embryonic development
  • Usually present in early adulthood (late teens)
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12
Q

What are the differentials for a neck lump in children?

A

Congenital: branchial cyst, thyroglossal cyst, dermoid cyst, vascular malformation

Inflammatory: reactive lymphadenopathy, lymphadenitis.

Neoplastic: lymphoma, thyroid tumour, salivary gland tumour

Neck lumps are more likely to be inflammatory than malignant in children and young people.

Congenital and developmental lumps are also more likely in children and young people.

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13
Q

When do neck lumps develop acutely?

A

Inflammatory lumps usually arise suddenly and resolve within 2-6 weeks. Progressive enlargement over a short time is more likely to be malignant.

A transient nature to the swelling and an association with eating suggest salivary gland blockage. Associated symptoms often give the clue to the cause of reactive lymph nodes or indeed malignant nodes.

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14
Q

Which neck lumps are hard?

A

A hard mass is more likely to be malignant.

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15
Q

Which neck lumps are mobile?

A

Congenital masses are usually smooth and mobile.

Reactive lymph nodes are mobile.

Thyroid gland swellings and thyroglossal cysts move on swallowing, and a thyroglossal cyst moves when the tongue is moved outwards.

A fluctuant mass suggests a cystic nature. Tenderness suggests infection. A laryngocele enlarges with blowing or the Valsalva manoeuvre.

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16
Q

Which neck lumps present in the midline?

A

Midline lumps are likely to be thyroid in origin or thyroglossal/dermoid cysts.

Submandibular swellings may be related to the submandibular gland.

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17
Q

Which neck lumps present in the posterior triangle?

A

Posterior triangle lumps are most commonly lymph nodes, although lymph nodes are a common cause of swellings in all areas of the neck.

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18
Q

Which neck lumps are likely to be bilateral?

A

Bilateral swellings (tender) crossing the mandibular angle are likely to be parotid infection (mumps).

19
Q

Which neck lump is likely to present in the supraclavicular fossa?

A

A lump in the left supraclavicular fossa (a Virchow’s node) may indicate an infraclavicular metastatic malignancy such as lung or upper gastrointestinal tumours.

20
Q

What are the investigations done to assess neck lumps?

A

Investigations will be guided by clinical assessment but may include:

  • FBC and ESR (within 48 hours if generalised lymphadenopathy to exclude leukaemia).
  • TFTs.
  • Viral serology - eg, EBV, cytomegalovirus, toxoplasmosis.
  • Throat swab.
  • CXR (within two weeks for supraclavicular lymph node swelling or persistent cervical node in a person over 40 years old)
  • Ultrasound scan - for thyroid swellings and as a first-line imaging option where diagnosis is unclear, with or without a view to ultrasound-guided fine-needle aspiration biopsy.
  • Radionucleotide scanning (if masses of parathyroid or thyroid glands).
  • CT or MRI scan.
21
Q

When should you refer a patient with a neck lump?

A

Referral is usually to an ear, nose and throat (ENT) specialist but findings may dictate referral to a dermatologist, oral surgeon, dermatologist, or chest physician.

Any new neck mass persisting beyond six weeks should be referred. Referral more immediately may be appropriate in some cases.

22
Q

When should a GP make an urgent referral for a neck lump?

A

Make an urgent two-week wait referral through the suspected cancer pathway if:

  • The person has lost weight.
  • There is associated hoarseness, difficulty swallowing (dysphagia), or dyspnoea for three weeks or more.
  • There has been haemoptysis.
  • There are associated symptoms suggestive of lymphoma (weight loss, night sweats, fever, breathlessness, pruritus or bleeding) - two-week wait referral for adults but a 48-hour referral for children and young people up to the age of 24.
  • An unexplained enlarged lymph node is persistent.
  • There are suspicious clinical features.
  • Diagnosis is unclear.
23
Q

What is the management of neck lumps?

A

Depends on the cause.

Benign reactive lymph nodes settle on their own within six weeks, needing no treatment.

24
Q

What is the classification of thyroid cancers?

A

Differentiated thyroid carcinoma, including papillary, follicular, and Hürthle cell cancers. These arise from follicular cells of the thyroid and account for 90-95% of all thyroid malignancies.

Medullary thyroid carcinoma arises from parafollicular cells and accounts for another 6%.

Anaplastic thyroid carcinoma accounts for less than 1% of thyroid malignancies.

25
Q

What is the most common form of thyroid cancer?

A

Papillary is the most common form and presents between 35-40 years of age. It is more common in women. Spreads locally and may compress the trachea.

Follicular is the second most common form and it occurs in areas of low iodine and is three times more common in women.

26
Q

Which gender is more likely to get Hurthle cell cancer?

A

Hurthle cell is more common in women and surgical excision is the main treatment.

27
Q

What is the marker for medullary thyroid cancer?

A

Elevated serum calcitonin

28
Q

What are the prognostic factors for medullary thyroid cancer?

A

Prognostic factors that predict adverse outcome include calcitonin doubling time, advanced age at diagnosis, extent of the primary tumour, nodal disease and distant metastases.

29
Q

What is the clinical picture of anaplastic thyroid cancer?

A

The clinical diagnosis is usually easy with a large, hard mass invading the neck and causing compression (dyspnoea, cough, vocal cord paralysis, dysphagia and hoarseness). Almost 50% of the patients present with distant metastases, mostly in the lungs but also in the bones, liver and brain.

30
Q

Which type of lymphoma is thyroid lymphoma?

A

Thyroid lymphomas are almost always non-Hodgkin’s lymphomas, representing 4-10% of thyroid malignancies. More common in women.

Patients usually present with a rapidly growing mass in the neck, which may cause symptoms of obstruction such as dyspnoea and dysphagia.

31
Q

What are the risk factors for thyroid cancer?

A

Exposure to ionising radiation. The risk, especially for papillary carcinomas, is greater when exposure has occurred at a younger age.

Other risk factors include a history of goitre, thyroid nodule or thyroiditis, family history of thyroid disease, female gender and Asian race.

Genetics: approximately 20-25% of MTC are hereditary because of mutations in the RET proto-oncogene. Mutations in the RET gene cause multiple endocrine neoplasia type 2 (MEN 2), which is an autosomal dominant disorder associated with a high lifetime risk of MTC.

Cowden’s syndrome (macrocephaly, mild learning difficulties, carpet-pile tongue, with benign or malignant breast disease).

Familial adenomatous polyposis.

Obesity.

32
Q

How does thyroid cancer present?

A

Thyroid cancer presents as a thyroid nodule. Thyroid nodules are frequent (4-50% depending on the diagnostic procedures and the patient’s age); however, thyroid cancer is rare (c. 5% of all thyroid nodules).

Solitary thyroid nodules can vary from soft to hard. Hard and fixed nodules are more suggestive of malignancy than soft mobile nodules. Thyroid carcinoma is usually non-tender to palpation.

Firm cervical masses are suggestive of regional lymph node metastases. Vocal cord paralysis implies involvement of the recurrent laryngeal nerve.

33
Q

What are the differentials of thyroid cancer?

A
Goitre 
Lymphoma 
Lymphadenopathy 
Cat scratch disease 
HIV
34
Q

What are the investigations of thyroid cancer?

A

TFTs
Serum calcitonin
USS:
-Thyroid ultrasound is extremely sensitive for thyroid nodules and is used as a first-line diagnostic procedure.
Ultrasound should also be used to explore the neck carefully to assess the status of lymph node chains.

Fine-needle aspiration cytology (FNAC):
-The results of FNAC are very sensitive for the differential diagnosis of benign and malignant nodules, although limitations include inadequate samples and follicular neoplasia.

Radionuclide imaging: distinguishing functioning toxic nodules and thyroid metastases from follicular and papillary carcinomas is best with 123iodine uptake studies
-Normal iodine uptake is seen in ‘warm’ nodules. Lesions that take up excessive amounts of iodine are called ‘hot’ and those that do not take it up are called ‘cold’.

CT and MRI scan: CT scans and MRI scans are valuable to detect local and mediastinal spread and regional lymph nodes.

35
Q

What are the USS features of thyroid cancer?

A

Ultrasound features associated with malignancy include hypoechogenicity, microcalcifications, absence of peripheral halo, irregular borders, solid aspect, intranodular blood flow and shape (taller than wide).

36
Q

What is the management of thyroid cancer?

A

Total thyroidectomy is recommended for patients with tumours greater than 4 cm in diameter, or tumours of any size in association with multifocal disease, bilateral disease, extra-thyroidal spread, familial disease, and those with clinically or radiologically involved nodes and/or distant metastases.

Radioiodine remnant ablation and therapy for differentiated thyroid cancer:

  • Patients in the definite indications include tumour larger than 4 cm, or any tumour size with gross extra-thyroidal extension or distant metastases.
  • Patients with no indications include tumour 1 cm or smaller, classical papillary or follicular variant or follicular minimally invasive without angioinvasion and no invasion of thyroid capsule.

Adjuvant external beam radiotherapy for differentiated thyroid cancer should be considered for patients with a high risk of recurrence/progression with:

  • Gross evidence of local tumour invasion at surgery with significant macroscopic residual disease; or
  • Residual or recurrent tumour that fails to concentrate radioiodine, ie loco-regional disease where further surgery or radioiodine is ineffective or impractical.
37
Q

What are the complications of thyroid cancer?

A

In expert hands surgical complications such as laryngeal nerve palsy and hypoparathyroidism are rare (<1-2%).

The primary disease can cause nerve damage, both in benign and in malignant conditions.

38
Q

What is a branchial cyst?

A

A branchial cyst is a benign, developmental defect of the branchial arches. The cyst is filled with acellular fluid with cholesterol crystals and encapsulated by stratified squamous epithelium.

39
Q

When are brachial cysts prone to infections?

A

Branchial cysts may have a fistula and are therefore prone to infection. They may enlarge following a respiratory tract infection.

40
Q

How do branchial cysts present?

A

They typically present in late childhood or early adulthood and present as asymptomatic neck lateral neck lumps and are usually located anterior to the sternocleidomastoid muscle.

There is a slight male predisposition and account for around 20% of paediatric neck masses.

41
Q

What are the typical examination findings of branchial cysts?

A
Typical examination features:
Unilateral, typically on the left side
Lateral, anterior to the sternocleidomastoid muscle
Slowly enlarging
Smooth, soft, fluctuant
Non-tender
A fistula may be seen
No movement on swallowing
No transillumination
42
Q

How do you diagnose branchial cysts?

A

Consider and exclude other malignancy
Ultrasound
Referral to ENT
Fine-needle aspiration

43
Q

How are branchial cysts managed?

A

Branchial cysts are treated by Ear Nose and Throat (ENT) surgeons and can be treated conservatively or surgically excised. Antibiotics are required for acute infections.