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Thyroid Cancer

Reviewed and updated by practising UK GPs, overseen by our Clinical Advisory Officer.

🧭 When to suspect

Thyroid cancer is uncommon – roughly 1% of all cancers, with around 3,800 new UK cases a year and a rising incidence. It is about three times more common in women, with a peak in women aged 35–39 and in men aged 65–70.

The great majority present with a single, often painless thyroid lump (nodule) or a diffuse neck swelling (goitre).

The reassuring background is that most thyroid nodules are benign – only a small minority prove malignant – but the primary-care task is to make sure the sinister minority is not missed.

Refer any unexplained thyroid lump on the suspected cancer pathway (previously the two-week wait), and recognise the rare airway emergency. A rapidly enlarging, hard goitre causing stridor – think anaplastic carcinoma or a large compressive goitre – needs same-day admission, not a routine referral.

Check thyroid function in parallel, but remember that a normal thyroid-stimulating hormone (TSH) never excludes cancer – most thyroid cancers are euthyroid.

Raise suspicion particularly with:

• Rapid growth

• A hard or fixed nodule

• Cervical lymphadenopathy

• Hoarseness or compressive symptoms (dysphagia, stridor)

• Risk factors: childhood neck irradiation, a family history of thyroid cancer or a familial syndrome (multiple endocrine neoplasia type 2 [MEN2], familial adenomatous polyposis)

A new nodule at the extremes of age (a child, or an adult over 65) also warrants heightened concern. A rapidly enlarging mass on a background of Hashimoto's should also raise the possibility of primary thyroid lymphoma.

Type Key features Prognosis/notes
Papillary (~80–85%)

• Commonest

• Younger adults and women

• Spreads via cervical lymphatics

• Often multifocal

• Excellent prognosis

• Linked to childhood radiation

Follicular (~10%)

• Older patients

• Haematogenous spread (lung, bone)

• Good prognosis

• Fine-needle aspiration cytology (FNAC) cannot distinguish from adenoma – needs histology

Medullary (~5%)

• Parafollicular C cells

• Secretes calcitonin

• ~25% familial (MEN2/RET)

• Variable

• The one to genetic-test

Anaplastic (~1–2%)

• Elderly

• Rapidly enlarging, hard, fixed mass

• Airway compromise

• Aggressive, poor prognosis

• Airway emergency

Source: NICE NG12 · NICE NG230


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