51 Tumours of the Thyroid and Parathyroid Glands • Usually present as solitary nodule or dominant nodule in MNG • Middle-aged women • Not premalignant • Rarely become toxic • Encapsulated • Microscopic patterns: Follicular Microfollicular Hürthle cell Embryonal • Malignancy excluded by ruling out capsular or vascular invasion on histology • Family history of thyroid cancer • Exposure to ionizing radiation • 80% of thyroid malignancy • “Only” thyroid cancer in children • 5th decade • Presents as thyroid nodule • Microcarcinoma <1 cm diameter • Histological subtypes: Pure papillary Mixed papillary–follicular (most common) Follicular • Psammoma bodies in fibrous stalk • Ground-glass “orphan Annie” nuclei • High incidence of LNs in levels III to VII (60%) • Primary tumour may be impalpable—therefore often presents with LNs • 20% have pulmonary mets at presentation • Bony mets less common • More aggressive in older age groups—may invade larynx/trachea • 10-year survival >90% • 6th decade • 20% of all thyroid malignancies • Decreasing incidence in endemic goitre areas • Commonly presents as solitary thyroid nodule • May present with mets—bone/lung in 20 to 30% • Non-vesicular nuclei • Histology required following surgical resection to determine diagnosis • Aka eosinophilic/oncocytic/oxyphilic cell • More aggressive variant of follicular ca (2% total) • Is possibly a degenerative/metaplastic phenomenon • Found in: Nodular goitres Chronic lymphocytic thyroiditis Diffuse toxic goitre Post-radiation Post-chemotherapy Aging thyroids • Malignant tumours display capsular and vascular invasion • May invade surrounding tissue and extrathyroid structures • LN mets common • 5% of all thyroid malignancies • May occur as part of MEN syndrome: MEN IIA MEN IIB Familial non-MEN Sporadic • Bilateral in 90% of cases with MEN • LN mets in 25 to 30% • Arise from parafollicular/C cells • Calcitonin = tumour marker • Uniform spindle-shaped cells with variable fibrous stroma on histology • Account for <5% of all lymphoma • Classically rapidly increasing swelling in neck of an elderly woman • Immunocytochemistry needed to distinguish from anaplastic carcinoma • Usually arises on background of chronic autoimmune thyroiditis • Most are high-grade B-cell NHL • Mostly stage I or II • Occasionally thyroid involved in widespread systemic lymphoma • Elderly women • Often long-standing enlargement of thyroid • Rapid increase in size associated with pain referred to ear and hoarseness ± airway obstruction • Aggressively malignant with high metastatic potential • Commonly invade surrounding structures • Most patients dead within 1 year of presentation • Kidney and breast • CXR Tracheal deviation Mediastinal extension/LNs Pulmonary mets Co-morbidity • USS Tumour size Diagnosing MNGs Excludes contralateral disease Evaluate complex cysts Fine calcification 85 to 95% specific for papillary thyroid ca Combined with FNA for initial diagnosis Evaluate metastatic neck disease if suspected combined with FNA and thyroglobulin washout • CT scan Avoid the use of iodinated contrast media when performing CT scans. This may reduce the subsequent radioiodine uptake by thyroid tissue and therefore delay its use Assess extent of larger tumours including larynx/trachea/oesophagus/major vessels Demonstrates nodal deposits in neck/mediastinum Direct retrosternal extension Pulmonary mets • MRI scan Assess possible vessel involvement (MR angiography) No contrast required • Scintigraphy Poorly specific and sensitive Technetium-99m mostly used due to cost and availability 90% of nodules are cold 20% risk of malignancy in a cold nodule (50% if cyst excluded on USS) Hot nodules unlikely to be malignant 123I-MIBG used for suspected MEN 131I radioiodine used for post-operative ablation and to search for mets • TFTs—mandatory • Thyroid autoantibodies May assist diagnosis of chronic lymphocytic thyroiditis Predict post-operative hypothyroidism Helps interpretation of thyroid function and thyroglobulin Preop thyroglobulin not helpful Serum calcium and calcitonin—if medullary ca suspected • The British Thyroid Association (Guidelines 2007) recommend either use of TNM staging or MACIS systems to determine when a patient is low risk or high risk for recurrence. • TNM: Tumour size, node metastases, and distant metastases • MACIS: Metastases, age at presentation, completeness of surgical resection, invasion (extra thyroidal), size • Age > 45 years • Male
51.1 Benign Tumours
51.2 Malignancy Risk Factors
51.3 Malignant Tumours
51.3.1 Papillary Adenocarcinoma
51.3.2 Follicular Adenocarcinoma
51.3.3 Hürthle Cell Tumours
51.3.4 Medullary Thyroid Carcinoma
51.3.5 Lymphoma
51.3.6 Anaplastic Cancers
51.3.7 Metastatic Deposits
51.4 Radiology
51.5 Laboratory Investigations
51.5.1 Prognostic Factors
51.6 Poor Prognostic Factors for DTC
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Tumours of the Thyroid and Parathyroid Glands
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