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Thyroid Neoplasms
Thyroid Neoplasms
MALIGNANCIES
• BENIGN
• MALIGNANT
• BENIGN
• Follicular adenoma can be –
1. Colloid (commonest type);
2. Fetal (microfollicular – has potential for
microinvasion);
3. Embryonal (atypical – has potential for
microinvasion);
4. Hurthle cell/oxyphil or oncocytic (has
potential for microinvasion);
5. hyalinising trabecular adenoma.
PES Institute of Medical Sciences & Research
THYROID NEOPLASMS
• MALIGNANT
• Primary thyroid malignancies can also be
classified according to aggressiveness:
• 1. Well-differentiated (e.g. papillary carcinoma,
follicular carcinoma)
• 2. Intermediate (e.g. medullary carcinoma,
Hürthle cell carcinoma)
• 3. undifferentiated (e.g. anaplastic carcinoma)
• DTC
• . Papillary carcinoma (80%).
• Follicular carcinoma (10%).
• Hurthle cell carcinoma behaves like follicular
carcinoma.
• PTC- 80%
• FTC – 10%
• MTC- 6%
• ATC – 1%
• LYMPHOMA
• HURTHLE CELL CANCER
MOST COMMON’S
• M.C OVERALL-PAPILLARY CA >
FOLLICULAR CA
• M.C IN ENDEMIC AREAS- FOLLICULAR CA
• M.C IN CYSTIC LESION- PAPLILLARY CA
ETIOLOGY
• Radiation either external or radioiodine can cause papillary
carcinoma thyroid.
• Earlier irradiation was practised to head and neck region to
treat benign conditions like tonsillitis, adenoids, thymus
enlargement, acne vulgaris, haemangiomas during first two
decades of life
• Pre-existing multinodular goitre. It turns into follicular
carcinoma of thyroid.
• Medullary carcinoma thyroid is often familial.
• Hashimoto’s thyroiditis may predispose to NHL/papillary
carcinoma of thyroid.
FAMILIAL
• COWDEN SYNDROME
• CARNEY’S COMPLEX ( NOT CARNEY’S
TRIAD)
• FAP
• HERIDITAY PAPILLARY THYROID AND
RENAL NEOPLAS SYNDROME
• GENETICS
PTC
BRAF V600E – INITIATING MUTATION
FOUND IN 50% CASES
RET/PTC REARRANGEMENT
RET/PTC-1 – MORE COMMON
LESS AGGRESSIVE
RET/PTC-3 – LESS COMMON
AGGRESSIVE
PES Institute of Medical Sciences & Research
THYROID NEOPLASMS
FTC
N- RAS MUTATION
HURTHLE CELL CANCER
MITOCHONDRIAL DNA ALTERATIONS
ANAPLASTIC CANCER
P 53 GENE MUTATION
MEDULLARY CANCER
RET PROTO-ONCOGENE
• GENETICS
FOLLICULAR ADENOMAS
• RAS MUTATION IS SEEN IN 40% CASES.
FOLLICULAR ADENOMAS
• Most common benign thyroid neoplasm.
• This neoplasm is derived from follicular
epithelium The TSH receptor signalling
pathway plays an important role in the
pathogenesis of adenoma.
• A typical thyroid adenoma is a solitary,
spherical lesion that compresses adjacent
normal tissue
FOLLICULAR ADENOMAS
FOLLICULAR ADENOMAS
SPREAD
PTC – L.N
FTC – BLOOD( PULSATILE SECONDRIES )
MEDULLARY- L.N
ANAPLASTIC- LOCAL INVASION
PTC
• Most common type of thyroid cancer 70–90%
of well-differentiated thyroid malignancies.
• Predominant thyroid cancer in individuals
exposed to external radiation in neck during
childhood.
• More common in females (2:1), mean age at
presentation is 30–40 years.
• Slow growing malignant tumor, tends to be
multifocal.
FTC
• Account for about 10% of thyroid cancers and
more commonly in iodine-deficient areas.
• Most of the follicular pattern thyroid
malignancies represent the follicular variant of
papillary carcinoma and share the natural
history and many features of papillary
carcinoma.
• Older population (50 years or more) are
commonly affected.
• More common in females (3 : 1)
PES Institute of Medical Sciences & Research
THYROID NEOPLASMS -FTC
FOLLOW UP
• Proper clinical examination in the neck for
residual/nodal disease and for distant spread
• Whole body radioisotope scan after one week of
surgery to see residual tumour in the neck or
metastases .
• Estimation of thyroglobulin at regular intervals is very
important—once in 6 months
• Follow up whole body radioisotope scan at 3–6 months
intervals. Thyroxine should be stopped for 6 weeks.
But it is commonly done if thyroglobulin level in the
blood is significantly high.
Prognosis
• Prognosis is good and it is one of the curable
malignancies.
• 99% SURVIVAL RATE.
HTC
• A subtype of follicular carcinoma closely resembles
follicular thyroid carcinoma on gross and
microscopic appearance.
• The tumor contains abundance of oxyphilic cells or
oncocytes and characterized by vascular or
capsular invasion.
• More often multifocal, bilateral and more likely
metastasize to regional nodes and distant sites.
• Work up and management are similar to follicular
carcinoma
PES Institute of Medical Sciences & Research
THYROID NEOPLASMS -HTC
MTC
• It arises from the parafollicular ‘C’ cells which is
derived from the ultimobranchial body (neural
crest).
• C cells are more in upper pole of the thyroid
gland or at junction of upper 1/3rd and lower
2/3rd.
• It contains characteristic ‘amyloid stroma’
wherein malignant cells are dispersed.
Immunohistochemistry reveals calcitonin in
amyloid.
PES Institute of Medical Sciences & Research
THYROID NEOPLASMS - MTC
• MALIGNANT LYMPHOMA
• It is NHL type. Occurs in a pre-existing
Hashimoto’s thyroiditis.
• FNAC is useful to diagnose the condition
(Often trucut biopsy).
• Chemotherapy and radiotherapy is the main
treatment.
• Rarely total thyroidectomy is done to enhance
the results.