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Thyroiditis

From Surgopaedia

Inflammation of the thyroid gland

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Hashimoto's thyroiditis (chronic lymphocytic or autoimmune thyroiditis)

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    • Chronic, progressive autoimmune disorder characterised by diffuse lymphocytic infiltration with formation of germinal centres, follicular cell atrophy, Hurthle cell metaplasia, Hurthle cell nodules, and fibrosis
    • Risk factors
      • Familial (RR of 9 with first-degree relatives)
      • Autoimmune conditions
      • Female (10:1 ratio)
    • Pathophysiology
      • Presence of circulating autoantibodies to thyroid antigens
      • Results in a chronic autoimmune destructive process involving the formation of immune complexes and complement in the basement membrane of follicular cells
      • Leads to infiltration of lymphocytes into the thyroid follicles and eventual fibrosis
      • Decreases the effective number of follicles available to produce thyroid hormones
      • Associated with an increased risk of papillary thyroid cancer
    • Presentation
      • Can be thyrotoxic or hypothyroid
      • Usual goitre symptoms
      • Nontender, diffusely firm, bumpy or bosselated thyroid gland
      • Rapidly enlarging goitre should raise concerns for thyroid lymphoma - needs FNA + flow cytometry
    • Workup
      • Antimicrosomal and antithyroglobulin antibody titres
        • TPOAb and TgAb
        • See 'thyroid physiology/biomarkers' for details
      • TSH +/- free T4/T3
      • USS neck not technically necessary, but can be done if neck pain or globus sensation
        • Coarse, heterogenous and hypoechoic parenchymal echotexture with increase vascularity, often with the presence of fine echogenic septae producing a pseudonodular appearance
        • Size can range from diffusely or focally enlarged to small and atrophic
        • May be enlarged lymph nodes around it
        • Any suspicious thyroid nodules or lymph nodes should be worked up with FNA
      • Diagnosis can also be made by FNA
    • Treatment
      • Thyroid replacement if hypothyroid, which results in a decrease in goitre size
      • Otherwise no treatment
    • Indications for thyroidectomy
      • Large goitre and compressive symptoms
      • Associated nodular disease if suspicion of cancer

Post-partum thyroiditis

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    • Typically short-lived - resolution in 2-4 months
    • Short course of exogenous replacement may be necessary

Subacute granulomatous (de Quervain's) thyroiditis

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    • Self-limited inflammation of thyroid occurring after a viral URTI and lasting 1-3 months
    • Acute onset pain, swelling, thyrotoxicosis, low-grade fevers, elevated ESR
    • Multi-nucleated giant cell granulomas, with granulomatous changes in the thyroid follicles
    • NSAIDs may be useful, or failing that, prednisolone 40mg daily
    • No surgical indications
    • Vast majority of patients return to a euthyroid state spontaneously

Painless or silent or postpartum thyroiditis (lymphocytic thyroiditis)

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    • Autoimmune-mediated, self-limited disease
    • Thyrotoxic phase then euthyroid phase then hypothyroid then recovery
    • Recurrences common
    • Surgery not indicated

Drug-induced thyroiditis

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    • Significant adverse effect
      • Interferon alpha
      • Amiodarone
        • Type I - pre-existing goitre - iodine-induced increase in thyroid hormone synthesis
          • Analogous to thyroiditis with normal/high RAI uptake - in this instance, there is excess thyroid hormone synthesis due to iodine load in amiodarone.
        • Type II - more common - no pre-existing thyroid disease - destruction of follicular cells resulting in increased release of stored thyroid hormones - can be very slow to resolve due to stored amiodarone in fat. Analogous to thyroiditis with destruction of gland and release of pre-formed thyroid hormone.
          • High-dose pred will be needed - often for a good 4-week course of high-dose (50mg daily)
          • Radioactive iodine is ineffective
          • Persistent amiodarone induced thyrotoxicosis despite medical therapy needs a total thyroidectomy
Type 1 Type 2
Underlying thyroid disease Yes (Multinodular goiter, Grave’s) No
Time after starting amiodarone Short (median 3 months) Long (median 30 months)
24-hour iodine uptake Low-Normal (may rarely be high in iodine deficient regions) Low to Suppressed
Thyroid Ultrasound Diffuse or Nodular Goiter may be present Normal or small gland
Vascularity on Echo-color Doppler ultrasound Increased Absent
T4/T3 ratio Usually <4 Usually >4
TgAb / TPOAb/ TSI May be present Usually absent
Circulating interleukin-6 Normal to high Sometimes markedly elevated but usually doesn’t differentiate from AIT1
  • Note
    • Amiodarone directly inhibits conversion of T4 to T3, so T3 is typically normal
    • Usually sestamibi study is necessary to exclude AIT1
    • Look for features of pre-existing disease e.g. thyroiditis on USS to differentiate between AIT1 and AIT2
    • Treat with prednisolone and carbimazole and cease amiodarone
    • If worsening thyrotoxicosis on good medical therapy, consider thyroidectomy (I have seen a three-week trial of medical therapy in practice)
    • Sestamibi can differentiate between AIT1 and AIT2 - there will be uptake present in AIT1, but not AIT2
    • Pertechnetate study is not useful because need to be off amiodarone for two months prior for it to be diagnostic
  • Tyrosine kinase inhibitors

Radioiodine-induced thyroiditis

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    • Transient, resolves within a week with simple analgaesia and anti-inflammatories

Riedel's thyroiditis

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    • Extremely rare chronic idiopathic inflammatory disease - inflammation followed by fibrosis of thyroid and adjacent structures
    • Associations
      • 1/3 of patients have fibrosis elsewhere
      • PSC
      • Orbital pseudotumour
      • Autoimmune diseases including Addison's/diabetes
    • Presentation
      • Enlarging, tender goitre
      • Patients often suspected of having anaplastic carcinoma
      • Rock hard fixed neck mass
      • Often have clinically significant airway obstruction, dysphagia and dysphonia
    • Workup
      • TSH - generally high
      • Serum calcium
      • USS. FNA is often impossible due to hardness of mass!
      • CT CAP to look for fibrosis elsewhere and evaluate the rock-hard neck mass
      • Definitive diagnosis requires open biopsy - distinguished from thyroid cancer with immunohistochemistry
      • Isthmusectomy can relieve obstruction
    • Management
      • Often end up requiring surgery to exclude anaplastic cancer, or to treat obstructive symptoms
      • Surgery very challenging due to obliteration of planes and landmarks
      • Resect only the necessary segments to achieve the operative goal
    • Prognosis
      • May stabilise, resolve spontaneously, or progress over time
      • Treat with high-dose corticosteroids
      • Tamoxifen reduces goitre size
      • Will need levothyroxine
      • Rituximab may help
      • May need to treat hypoparathyroidism
      • No increased risk of thyroid cancer

Acute suppurative thyroiditis

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    • Rare and potentially life-threatening infection
    • Pathophysiology
      • Often occurs in immunocompromised patients
      • Generally haematogenous spread
      • Possible underlying congenital pyriform sinus fistula
      • Most commonly Staph or strep
    • Presentation
      • Neck pain
      • Dysphagia
      • Odynophagia
      • Tender goitre (unilateral)
      • Sepsis
      • Usually euthyroid
    • Treatment
      • Abx - staph/strep most common
      • USS to confirm diagnosis with thyroid aspirate MCS
      • CT to assess for anatomical reason for infection ?fistula/abscess
      • Abscess drainage - try USS guided first, then open

Presentation

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  • Neck pain/tenderness
  • Enlargement of thyroid
  • Thyroid dysfunction
  • Fever
  • Can be euthyroid, thyrotoxic, or hypothyroid

Workup

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  • TSH, T3, T4
  • Antimicrosomal Ab titre
  • ESR/CRP - will be elevated in de Quervain's
  • Thyroid scintigraphy
  • USS
  • CT - primarily to determine extent of substernal extension and mass effect