Thyroiditis
Appearance
Inflammation of the thyroid gland
[edit | edit source]Hashimoto's thyroiditis (chronic lymphocytic or autoimmune thyroiditis)
[edit | edit source]- 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
- Antimicrosomal and antithyroglobulin antibody titres
- 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
[edit | edit source]- Typically short-lived - resolution in 2-4 months
- Short course of exogenous replacement may be necessary
Subacute granulomatous (de Quervain's) thyroiditis
[edit | edit source]- 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)
[edit | edit source]- Autoimmune-mediated, self-limited disease
- Thyrotoxic phase then euthyroid phase then hypothyroid then recovery
- Recurrences common
- Surgery not indicated
Drug-induced thyroiditis
[edit | edit source]- 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 I - pre-existing goitre - iodine-induced increase in thyroid hormone synthesis
- Significant adverse effect
| 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
[edit | edit source]- Transient, resolves within a week with simple analgaesia and anti-inflammatories
Riedel's thyroiditis
[edit | edit source]- 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
[edit | edit source]- 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
[edit | edit source]- Neck pain/tenderness
- Enlargement of thyroid
- Thyroid dysfunction
- Fever
- Can be euthyroid, thyrotoxic, or hypothyroid
Workup
[edit | edit source]- 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