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THYROID CANCERS
Learning objectives
• Epidemiology
• Causes and Risk Factors
• Classification
• Clinical Presentation
• Diagnosis
• Management
Epidemiology
• Commonest endocrine malignancy
• 1% of all malignancies
• 0.6 per million
• Good prognosis
• Extent of surgery is debated
• Annual Incidence is 3.7 per 100,000
• Sex Ratio is 3:1 (Female:Male)
• Can occur in any age group
Causes and Risk Factors
• Genetics:
• Abnormal RET oncogene may cause MTC.
• MEN 2A, 2B Syndrome.
• Family History:
• Hx of goiters increase risk for Follicular Ca.
• Radiation Exposure:
• Radiation therapy to Head / Neck (<15 y).
• Exposure to Radioactive Iodine during childhood, or other radioactive
substances (Chernobyl) ↑ risk - Papillary carcinoma.
Causes and Risk Factors
• Chronic Iodine deficiency ↑ risk for Follicular carcinoma.
• Gender:
• Female > Males.
Thyroid Neoplasm
Benign Malignant
Secondary
Primary
Follicular
Cells
Parafollicular
Cells
Lymphoid
Cells
Lymphoma
Medullary
Differentiated Undifferentiated
Anaplastic
Follicular
Papillary
Hurthle Cell
Presentation
• Solitary or Multiple thyroid nodules
• Neck Nodes
• Hoarse voice of recent onset
• Mediastinal adenopathy
• Bone or lung metastasis
Important History
• Radiation to neck / chest
• MEN syndrome
• Family history
• Diarrhoea
• Adrenal tumour
• Recent change in a pre-existing goitre
• Size change/nodularity
• Vocal cord palsy
Evaluation
• Thyroid profile
• Serum Thyroglobulin
• Serum Calcitonin
• Thyroid scan
• Hot/warm/cold nodule 20% malignant
• Serum Ca++
Diagnosis
• Laboratory:
• TSH
• T3, T4
• Serum Thyroglobulin
• Serum Thyroid Antibodies
• FNA
• Imaging
• U/S
• C.T
• MRI
• Scintigraphy
Laboratory
• Most patients are Euthyroid.
• Hyperfunctioning nodule  1% chance of malignancy.
• Serum Tg cannot differentiate between benign and
Malignant nodules
• Tg is used for:
• F/U after total thyroidectomy
• Serial F/U for non-operative treatment
• Serum Calcitonin  patients with MTC, or with family hx of
MTC (MEN2)
FNA Cytology
• Single most important test.
• U/S guidance improve the sensitivity.
• Accuracy ranges from 70 – 95%.
• Nodules
• FNAC cannot differentiate between Benign and
Malignant Follicular Neoplasia
Imaging
• U/S is the investigation of choice.
• C.T  Regional and distant metastases
• MRI  Limited role in the diagnosis
Useful in detecting cervical LN
metastases
• Scintigraphy (I-123)
• Characterizing funtioning nodules
• Staging of follicular and papillary Ca
US features malignancy
• Hypoechoic
• Tall>wide
• Irregular margins
• Microcalcifications
• LN involvement
• Extrathyroidal spread
Prognosis
Tumor Prognosis
Papillary Ca.
74-93% long-term survival
rate
Follicular Ca.
43-94% long-term survival
rate
Hurthle Cell Ca.
20% mortality rate at 10
years
Medullary Ca.
80% 10-year survival rate
45% with LN involvement
Anaplastic Tumor
Median survival of 4 to 5
months at time of diagnosis
Papillary Carcinoma
MC Thyroid ca (80%)
Related to radiation exposure in I-sufficient areas.
F:M - 2:1
Mean age 30 - 40 y
Slow growing painless mass. Euthyroid-status.
LN metastases is common, may be the presenting symptom
(LAT?).
Distant metastases is uncommon at initial presentation.
Develop in 20% of cases. (Lungs, liver, bones,brain)
Papillary Carcinoma
• FNA biopsy is diagnostic.
• Treatment
• Ipsilateral Lobectomy + Isthmusectomy (No LN metastasis)
• Near-total or Total Thyroidectomy + Modified-radical or Functional neck
dissection (+ve LN metastasis).
• Prophylactic LN dissection is unnecessary.
Follicular Carcinoma
• 10% of all thyroid cancers.
• More common in I-deficient areas.
• F:M - 3:1
• Mean age- 50 yrs.
• Solitary thyroid nodule, rapid increase in size and long-
standing goiter.
• Cervical LN metastasis is uncommon at presentation (5%),
distant metastasis may be present.
• Hyperfunctioning < 1%. (S&S of Thyrotoxicosis)
Follicular Carcinoma
• FNA biopsy cannot differentiate between benign and
malignant follicular tumors.
• Pre-operative diagnosis of malignancy is difficult unless there is distant
metastasis.
• Large follicular tumor > 4 cm in old individual  CA.
• Treatment:
• Thyroid Lobectomy (at least 80% are benign adenomas)
• Total-Thyroidectomy in older individual with tumor > 4cm (50% chance of
malignancy).
• Prophylactic nodal dissection is unnecessary.
Post-operative Management
• Thyroid hormone
• Replacement therapy
• Suppression of TSH release
• At 0.1 μU/L in Low-risk group
• < 0.1 μU/L in High-risk group
• Thyroglobulin measurement
• At 6-months interval then annually when disease-free
• < 2ng/mL in total or near-total + Hormones
• < 5ng/mL in hypothyroid patients.
• Level > 2ng/mL = Recurrence/Persistent thyroid tissue
Post-operative Management
• Radioiodine Therapy:
• ETE , LN + , Aggressive histo (Tall, Columnar)
• RAI is less sensitive than Tg in detecting metastatic disease.
• I-131 detect and treat 75% of metastatic differentiated thyroid
tumors.
Medullary Carcinoma
• 5% of all thyroid malignancies.
• Arise from Parafollicular cells, concentrated in
superolateral aspect of thyroid lobes.
• Most cases are sporadic, 25% are inherited
(Germline mutation in RET oncogene).
• F:M - 1.5:1
• Age b/w 50 - 60 yrs.
• Neck mass + palpable cervical LN (15-20%).
• Local pain or aching is common.
Medullary Carcinoma
• MTC secretes a range of compounds:
• Calcitonin, CEA, CGRP, PG A2 and F2α, Seritonin.
• May develop flushing and diarrhoea, Cushing’s
syndome (ectopic ACTH).
• Diagnosis
• Hx and P/E (Family hx of similar tumors).
• ↑ Serum Calcitonin, ↑ CEA
• FNAC
• Screen patient for:
• RET point mutation.
• Coexisting Pheochromocytoma (24-hour urinary level
of VMA, catecholamine, metanephrine).
• Hyperparathyroidism (Serum calcium).
Medullary Carcinoma
• Treatment:
• > 50% are bilateral, ↑ Multicentricity.
• Total Thyroidectomy + :
• Bilateral central node dissection as routine (No LN
involvement)
• Bilateral Modified-Radical Neck dissection (palpable LN)
• Ipsilateral Prophylactic nodal dissection in tumor size > 1.5cm.
• External Beam radiation for unresectable residual or
recurrent tumor.
Anaplastic Carcinoma
• 1% of all thyroid malignancies.
• Women > Men.
• Majority present at 7th - 8th decade of life.
• Rapidly enlarging in size.
• May be painful, with dyphonia, dyspnea, dysphagia.
• LN are usually involved at presentation.
• ± Distant metastasis.
Anaplastic Carcinoma
• FNAC is diagnostic.
• Treatment:
• Most aggressive thyroid tumor.
• Total Thyroidectomy if resectable.
• Adjuvant Chemotherapy + Radiotherapy slightly improve long-term
survival.
Prognostication
• AMES – Age, Mets , Extent , Size
• AGES – Age, Grade, Extent ,Size
• MACIS (Post op) – Mets, Age, Completeness of resection,
Invasion , Size
Thyroid Surgeries
STT, NTT
Complications of Thyroid Surgery
• Vascular (post op ?)
• Nerve injuries – RLN , Ext Br SLN
• PTH
• Thyroid deficiency
Management
• Medical
• Radioactive Iodine ablation therapy – High risk disease
Gross ETE ,M1 disease
• Chemotherapy (Adriamycin, Cisplatin).
• Immunotherapy (Kinase inhibitors) – Sorafenib,
Levatinib
• Post-operative Thyroid hormone.
• Replacement therapy.
• Suppression of TSH release. (↓ recurrence)
Thank you

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Ca thyroid

  • 2. Learning objectives • Epidemiology • Causes and Risk Factors • Classification • Clinical Presentation • Diagnosis • Management
  • 3. Epidemiology • Commonest endocrine malignancy • 1% of all malignancies • 0.6 per million • Good prognosis • Extent of surgery is debated • Annual Incidence is 3.7 per 100,000 • Sex Ratio is 3:1 (Female:Male) • Can occur in any age group
  • 4. Causes and Risk Factors • Genetics: • Abnormal RET oncogene may cause MTC. • MEN 2A, 2B Syndrome. • Family History: • Hx of goiters increase risk for Follicular Ca. • Radiation Exposure: • Radiation therapy to Head / Neck (<15 y). • Exposure to Radioactive Iodine during childhood, or other radioactive substances (Chernobyl) ↑ risk - Papillary carcinoma.
  • 5. Causes and Risk Factors • Chronic Iodine deficiency ↑ risk for Follicular carcinoma. • Gender: • Female > Males.
  • 7. Presentation • Solitary or Multiple thyroid nodules • Neck Nodes • Hoarse voice of recent onset • Mediastinal adenopathy • Bone or lung metastasis
  • 8. Important History • Radiation to neck / chest • MEN syndrome • Family history • Diarrhoea • Adrenal tumour • Recent change in a pre-existing goitre • Size change/nodularity • Vocal cord palsy
  • 9. Evaluation • Thyroid profile • Serum Thyroglobulin • Serum Calcitonin • Thyroid scan • Hot/warm/cold nodule 20% malignant • Serum Ca++
  • 10. Diagnosis • Laboratory: • TSH • T3, T4 • Serum Thyroglobulin • Serum Thyroid Antibodies • FNA • Imaging • U/S • C.T • MRI • Scintigraphy
  • 11. Laboratory • Most patients are Euthyroid. • Hyperfunctioning nodule  1% chance of malignancy. • Serum Tg cannot differentiate between benign and Malignant nodules • Tg is used for: • F/U after total thyroidectomy • Serial F/U for non-operative treatment • Serum Calcitonin  patients with MTC, or with family hx of MTC (MEN2)
  • 12. FNA Cytology • Single most important test. • U/S guidance improve the sensitivity. • Accuracy ranges from 70 – 95%. • Nodules • FNAC cannot differentiate between Benign and Malignant Follicular Neoplasia
  • 13.
  • 14.
  • 15. Imaging • U/S is the investigation of choice. • C.T  Regional and distant metastases • MRI  Limited role in the diagnosis Useful in detecting cervical LN metastases • Scintigraphy (I-123) • Characterizing funtioning nodules • Staging of follicular and papillary Ca
  • 16. US features malignancy • Hypoechoic • Tall>wide • Irregular margins • Microcalcifications • LN involvement • Extrathyroidal spread
  • 17. Prognosis Tumor Prognosis Papillary Ca. 74-93% long-term survival rate Follicular Ca. 43-94% long-term survival rate Hurthle Cell Ca. 20% mortality rate at 10 years Medullary Ca. 80% 10-year survival rate 45% with LN involvement Anaplastic Tumor Median survival of 4 to 5 months at time of diagnosis
  • 18. Papillary Carcinoma MC Thyroid ca (80%) Related to radiation exposure in I-sufficient areas. F:M - 2:1 Mean age 30 - 40 y Slow growing painless mass. Euthyroid-status. LN metastases is common, may be the presenting symptom (LAT?). Distant metastases is uncommon at initial presentation. Develop in 20% of cases. (Lungs, liver, bones,brain)
  • 19. Papillary Carcinoma • FNA biopsy is diagnostic. • Treatment • Ipsilateral Lobectomy + Isthmusectomy (No LN metastasis) • Near-total or Total Thyroidectomy + Modified-radical or Functional neck dissection (+ve LN metastasis). • Prophylactic LN dissection is unnecessary.
  • 20. Follicular Carcinoma • 10% of all thyroid cancers. • More common in I-deficient areas. • F:M - 3:1 • Mean age- 50 yrs. • Solitary thyroid nodule, rapid increase in size and long- standing goiter. • Cervical LN metastasis is uncommon at presentation (5%), distant metastasis may be present. • Hyperfunctioning < 1%. (S&S of Thyrotoxicosis)
  • 21. Follicular Carcinoma • FNA biopsy cannot differentiate between benign and malignant follicular tumors. • Pre-operative diagnosis of malignancy is difficult unless there is distant metastasis. • Large follicular tumor > 4 cm in old individual  CA. • Treatment: • Thyroid Lobectomy (at least 80% are benign adenomas) • Total-Thyroidectomy in older individual with tumor > 4cm (50% chance of malignancy). • Prophylactic nodal dissection is unnecessary.
  • 22. Post-operative Management • Thyroid hormone • Replacement therapy • Suppression of TSH release • At 0.1 μU/L in Low-risk group • < 0.1 μU/L in High-risk group • Thyroglobulin measurement • At 6-months interval then annually when disease-free • < 2ng/mL in total or near-total + Hormones • < 5ng/mL in hypothyroid patients. • Level > 2ng/mL = Recurrence/Persistent thyroid tissue
  • 23. Post-operative Management • Radioiodine Therapy: • ETE , LN + , Aggressive histo (Tall, Columnar) • RAI is less sensitive than Tg in detecting metastatic disease. • I-131 detect and treat 75% of metastatic differentiated thyroid tumors.
  • 24. Medullary Carcinoma • 5% of all thyroid malignancies. • Arise from Parafollicular cells, concentrated in superolateral aspect of thyroid lobes. • Most cases are sporadic, 25% are inherited (Germline mutation in RET oncogene). • F:M - 1.5:1 • Age b/w 50 - 60 yrs. • Neck mass + palpable cervical LN (15-20%). • Local pain or aching is common.
  • 25. Medullary Carcinoma • MTC secretes a range of compounds: • Calcitonin, CEA, CGRP, PG A2 and F2α, Seritonin. • May develop flushing and diarrhoea, Cushing’s syndome (ectopic ACTH). • Diagnosis • Hx and P/E (Family hx of similar tumors). • ↑ Serum Calcitonin, ↑ CEA • FNAC • Screen patient for: • RET point mutation. • Coexisting Pheochromocytoma (24-hour urinary level of VMA, catecholamine, metanephrine). • Hyperparathyroidism (Serum calcium).
  • 26. Medullary Carcinoma • Treatment: • > 50% are bilateral, ↑ Multicentricity. • Total Thyroidectomy + : • Bilateral central node dissection as routine (No LN involvement) • Bilateral Modified-Radical Neck dissection (palpable LN) • Ipsilateral Prophylactic nodal dissection in tumor size > 1.5cm. • External Beam radiation for unresectable residual or recurrent tumor.
  • 27. Anaplastic Carcinoma • 1% of all thyroid malignancies. • Women > Men. • Majority present at 7th - 8th decade of life. • Rapidly enlarging in size. • May be painful, with dyphonia, dyspnea, dysphagia. • LN are usually involved at presentation. • ± Distant metastasis.
  • 28. Anaplastic Carcinoma • FNAC is diagnostic. • Treatment: • Most aggressive thyroid tumor. • Total Thyroidectomy if resectable. • Adjuvant Chemotherapy + Radiotherapy slightly improve long-term survival.
  • 29. Prognostication • AMES – Age, Mets , Extent , Size • AGES – Age, Grade, Extent ,Size • MACIS (Post op) – Mets, Age, Completeness of resection, Invasion , Size
  • 31. Complications of Thyroid Surgery • Vascular (post op ?) • Nerve injuries – RLN , Ext Br SLN • PTH • Thyroid deficiency
  • 32. Management • Medical • Radioactive Iodine ablation therapy – High risk disease Gross ETE ,M1 disease • Chemotherapy (Adriamycin, Cisplatin). • Immunotherapy (Kinase inhibitors) – Sorafenib, Levatinib • Post-operative Thyroid hormone. • Replacement therapy. • Suppression of TSH release. (↓ recurrence)