tyroid cancer
TRANSCRIPT
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THYROD CANCERTHYROD CANCERProf.Dr.YUSUF BKEYProf.Dr.YUSUF BKEY
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IntoductionIntoduction Consistent techniques of thyroid surgery dateConsistent techniques of thyroid surgery date
back approximately 100 yearsback approximately 100 years Theodor Kocher of Bern, Switzerland made majorTheodor Kocher of Bern, Switzerland made major
contibutions to thyroid the understanding ofcontibutions to thyroid the understanding ofthyroid disease and thyroid surgerythyroid disease and thyroid surgery
1872 - performed his first thyroidectomy1872 - performed his first thyroidectomy 1901 - had performed 2,000 thyroid procedure1901 - had performed 2,000 thyroid procedure 1901 - overall operative mortality had decreased1901 - overall operative mortality had decreased
from 50% tofrom 50% to 4.5%4.5% 1909 - won the nobel prize for his work1909 - won the nobel prize for his work
(Cady,(Cady,1991, Soh,1996)1991, Soh,1996)
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Statistics of Thyroid CancerStatistics of Thyroid Cancer 1.0%-1.5%1.0%-1.5% of all new cancer cases in the United Statesof all new cancer cases in the United States
(Sessions, 1993, Silverberg, 1989)(Sessions, 1993, Silverberg, 1989) ten fold less than that of lung, breast, or colorectalten fold less than that of lung, breast, or colorectalcancercancer
8,000-14,0008,000-14,000 new cases diagnosed eachnew cases diagnosed eachyear (Sessions,year (Sessions,1993, Geopfert, 1998)1993, Geopfert, 1998)
3%3% of patients who die of other causes have occult thyroidof patients who die of other causes have occult thyroidcancer andcancer and 10%10% have microscopic cancers (Robbins, 1991)have microscopic cancers (Robbins, 1991)
35%35% of thyroid gland at autopsy in some studies haveof thyroid gland at autopsy in some studies havepapillary carcinomas (
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Statistics of Thyroid CancerStatistics of Thyroid Cancer(continued)(continued)
4%-7%4%-7% of adults in North America haveof adults in North America havepalpable thyroid nodulespalpable thyroid nodules (Mazzaferri, 1993,(Mazzaferri, 1993,Vander, 1968)Vander, 1968)
4:14:1 women to menwomen to men (Mazzaferri, 1993)(Mazzaferri, 1993) Overall, fewer thanOverall, fewer than 5%5% of nodules areof nodules are
malignantmalignant (Mazzaferri, 1988)(Mazzaferri, 1988)
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HistoryHistory
SymptomsSymptoms The most common presentation of a thyroidThe most common presentation of a thyroid
nodule, benign or malignant, is a painlessnodule, benign or malignant, is a painlessmass in the region of the thyroid glandmass in the region of the thyroid gland(Goldman, 1996)(Goldman, 1996)..
Symptoms consistent with malignancySymptoms consistent with malignancyPainPain
dysphagiadysphagiaStridorStridorhemoptysishemoptysisrapid enlargementrapid enlargement
hoarsenesshoarseness
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HistoryHistory (continued...)(continued...)
Risk factorsRisk factors((continued)continued)
Age and SexAge and SexBenign nodules occur most frequently inBenign nodules occur most frequently in
women 20-40 yearswomen 20-40 years (Campbell, 1989)(Campbell, 1989)5%-10% of these are malignant5%-10% of these are malignant (Campbell, 1989)(Campbell, 1989)Men have a higher risk of a nodule beingMen have a higher risk of a nodule being
malignantmalignantBelfiore and co-workers found that:Belfiore and co-workers found that:
the odds of cancer in men quadrupled by the age ofthe odds of cancer in men quadrupled by the age of6464
a thyroid nodule in a man older than 70 years hada thyroid nodule in a man older than 70 years had
a 50% chance of being malignanta 50% chance of being malignant
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HistoryHistory (continued)(continued)
Family HistoryFamily History History of family member withHistory of family member with
medullary thyroid carcinomamedullary thyroid carcinoma
History of family member with otherHistory of family member with otherendocrine abnormalities (parathyroid,endocrine abnormalities (parathyroid,adrenals)adrenals)
History of familial polyposisHistory of familial polyposis(Gardners syndrome)(Gardners syndrome)
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Evaluation of the thyroid NoduleEvaluation of the thyroid Nodule((Physical ExamPhysical Exam))
Examination of the thyroid nodule:Examination of the thyroid nodule:consistency - hardconsistency - hard vs.vs. softsoft
size -size - < 4.0 cm< 4.0 cmMultinodularMultinodular vs.vs. solitary nodulesolitary nodule multi nodular -multi nodular - 3%3% chance of malignancychance of malignancy
(Goldman, 1996)(Goldman, 1996)
solitary nodule -solitary nodule - 5%-12%5%-12% chance of malignancychance of malignancy
(Goldman, 1996)(Goldman, 1996)Mobility with swallowingMobility with swallowingMobility with respect to surrounding tissuesMobility with respect to surrounding tissuesWell circumscribedWell circumscribed vs.vs. ill defined bordersill defined borders
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Physical ExamPhysical Exam (continued)(continued) Examine for ectopic thyroid tissueExamine for ectopic thyroid tissue Indirect or fiberoptic laryngoscopyIndirect or fiberoptic laryngoscopy
vocal cord mobilityvocal cord mobilityevaluate airwayevaluate airway
preoperative documentation of any unrelatedpreoperative documentation of any unrelatedabnormalitiesabnormalities
Systematic palpation of the neckSystematic palpation of the neckMetastatic adenopathy commonly found:Metastatic adenopathy commonly found:
in the central compartment (level VI)in the central compartment (level VI) along middle and lower portion of the jugular veinalong middle and lower portion of the jugular vein
(regions III and IV) and(regions III and IV) and Attempt to elicit Chvosteks signAttempt to elicit Chvosteks sign
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Evaluation of the Thyroid NoduleEvaluation of the Thyroid Nodule(Blood Tests)(Blood Tests)
Thyroid function testsThyroid function teststhyroxine (T4)thyroxine (T4)
triiodothyronin (T3)triiodothyronin (T3)thyroid stimulating hormone (TSH)thyroid stimulating hormone (TSH)
Serum CalciumSerum Calcium
Thyroglobulin (TG)Thyroglobulin (TG)CalcitoninCalcitonin
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Solitary Thyroid NoduleSolitary Thyroid Nodule HistoryHistory
Duration, recent enlargement, voice change, H/ODuration, recent enlargement, voice change, H/Ohypo/hyperthyroidism, irradiation, F/H goitre/cancerhypo/hyperthyroidism, irradiation, F/H goitre/cancer
Physical examinationPhysical examination
Dominant nodule, movement on deglutition, cervicalDominant nodule, movement on deglutition, cervicallymph nodes, fixation, hardnesslymph nodes, fixation, hardness
Thyroid function studiesThyroid function studies
Serum TSHSerum TSH
T4 & T3 levelsT4 & T3 levels
Antibody levels; ATA, AMA 1:100Antibody levels; ATA, AMA 1:100
Thyroid imaging; Scanning (99mTc, 123I, 131I)Thyroid imaging; Scanning (99mTc, 123I, 131I)
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Solitary Thyroid NoduleSolitary Thyroid Nodule CXRCXR
UltrasoundUltrasound
Solid/cysticSolid/cystic
MulticentricMulticentric
Lymph node involvementLymph node involvement Ultrasound-assisted FNAUltrasound-assisted FNA
CT/MRI of neckCT/MRI of neck
Mainly for large/recurrent cancersMainly for large/recurrent cancers
Vascular/lymphatic invasionVascular/lymphatic invasion Cervical/mediastinal metastasisCervical/mediastinal metastasis
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Solitary Thyroid NoduleSolitary Thyroid Nodule FNAC (Fine Needle Aspiration Cytology)FNAC (Fine Needle Aspiration Cytology)
Easy, safe, cost effectiveEasy, safe, cost effective
Negative predictive valueNegative predictive value 89%- 98%89%- 98%
False Negative rateFalse Negative rate 6%6%
False Positive rateFalse Positive rate 4%4%
FNAC CytodiagnosisFNAC Cytodiagnosis
BenignBenign Colloid adenoma, thyroiditis, cystColloid adenoma, thyroiditis, cyst
MalignantMalignant Papillary (70%), follicular (15%), medullary (5%-10%),Papillary (70%), follicular (15%), medullary (5%-10%),
anaplastic(3%), lymphoma (3%), metastasis (rare)anaplastic(3%), lymphoma (3%), metastasis (rare)
IndeterminateIndeterminate Microfollicular, Hurthle cell, embryonal neoplasmMicrofollicular, Hurthle cell, embryonal neoplasm
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Solitary Thyroid NoduleSolitary Thyroid Nodule
FNAC ResultFNAC Result
BenignBenign Observe and repeat FNAC 1 yearObserve and repeat FNAC 1 year
MalignantMalignant SurgerySurgery
IndeterminateIndeterminate serum TSH normalserum TSH normal SurgerySurgery
Serum TSH lowSerum TSH low ScintiscanScintiscan
InadequateInadequate Repeat FNARepeat FNA
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Thyroid CancerThyroid Cancer IncidenceIncidence 1%1%
M/F ratioM/F ratio 3:13:1 Risk factorsRisk factors
Radiation exposureRadiation exposure
ExternalExternal Medical treatment for benign conditionsMedical treatment for benign conditions
Medical treatment for malignanciesMedical treatment for malignancies
Environmental exposure- Nuclear weapons or accidentsEnvironmental exposure- Nuclear weapons or accidents
InternalInternal Medical treatment of benign condition with I131Medical treatment of benign condition with I131
Diagnostic tests with I131Diagnostic tests with I131
Environmental- fallout from nuclear weaponsEnvironmental- fallout from nuclear weapons
Other factorsOther factors Diet- Iodine deficiency, goitrogensDiet- Iodine deficiency, goitrogens
Hormonal factors- female gender predominanceHormonal factors- female gender predominance
Benign thyroid diseaseBenign thyroid disease
AlcoholAlcohol
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Classification of Malignant ThyroidClassification of Malignant ThyroidNeoplasmsNeoplasms
Papillary carcinomaPapillary carcinoma Follicular variantFollicular variant Tall cellTall cell Diffuse sclerosingDiffuse sclerosing EncapsulatedEncapsulated
Follicular carcinomaFollicular carcinoma Overtly invasiveOvertly invasiveMinimally invasiveMinimally invasive
Hurthle cellHurthle cell carcinomacarcinoma AnaplasticAnaplastic carcinomacarcinoma
Giant cellGiant cell Small cellSmall cell
Medullary CarcinomaMedullary Carcinoma MiscellaneousMiscellaneous
SarcomaSarcoma LymphomaLymphoma
Squamous cellSquamous cellcarcinomacarcinoma
MucoepidermoidMucoepidermoidcarcinomacarcinoma
Clear cell tumorsClear cell tumors Pasma cell tumorsPasma cell tumorsMetastaticMetastatic
Direct extentionDirect extention
KidneyKidney
ColonColon MelanomaMelanoma
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Thyroid CancerThyroid Cancer
PathologyPathology
Papillary carcinoma;Papillary carcinoma; 60-70% of all cases60-70% of all cases
MultifocalMultifocal
Nonencapsulated, but circumscribedNonencapsulated, but circumscribed Lymphatic spreadLymphatic spread
80% 10 year survival80% 10 year survival Follicular carcinomaFollicular carcinoma
15-20% of thyroid cancers15-20% of thyroid cancers
Usually encapsulatedUsually encapsulated 60% 10 year survival60% 10 year survival
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Well-Differentiated Thyroid CarcinomasWell-Differentiated Thyroid Carcinomas(WDTC) - Papillary, Follicular, and Hurthle(WDTC) - Papillary, Follicular, and Hurthle CCellell
Pathogenesis - unknownPathogenesis - unknown Papillary has been associated with the RETPapillary has been associated with the RET
proto-oncogene but no definitive link hasproto-oncogene but no definitive link hasbeen provenbeen proven (Geopfert, 1998)(Geopfert, 1998)
Certain clinical factors increase theCertain clinical factors increase thelikelihood of developing thyroid cancerlikelihood of developing thyroid cancer
Irradiation -Irradiation - papillary carcinomapapillary carcinoma
Prolonged elevation of TSH (iodine deficiency) -Prolonged elevation of TSH (iodine deficiency) -follicular carcinomafollicular carcinoma (Goldman, 1996)(Goldman, 1996)
relationship not seen with papillary carcinomarelationship not seen with papillary carcinoma
mechanism is not knownmechanism is not known
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WDTC - Papillary CarcinomaWDTC - Papillary Carcinoma
60%-80% of all thyroid cancers60%-80% of all thyroid cancers(Geopfert, 1998, Merino, 1991)(Geopfert, 1998, Merino, 1991)Histologic subtypesHistologic subtypes
Follicular variantFollicular variant
Tall cellTall cellColumnar cellColumnar cellDiffuse sclerosingDiffuse sclerosingEncapsulatedEncapsulated
Prognosis is 80% survival at 10 yearsPrognosis is 80% survival at 10 years(Goldman, 1996)(Goldman, 1996)
Females > MalesFemales > MalesMean age of 35 yearsMean age of 35 years (Mazzaferri, 1994)(Mazzaferri, 1994)
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WDTC - Papillary CarcinomaWDTC - Papillary Carcinoma(continued)(continued)
Lymph node involvement is commonLymph node involvement is commonMajor route ofMajor route ofmetastasis is lymphaticmetastasis is lymphatic46%-90% of patients have lymph node46%-90% of patients have lymph nodeinvolvementinvolvement
(Goepfert, 1998, Scheumann, 1984, De Jong, 1993)(Goepfert, 1998, Scheumann, 1984, De Jong, 1993)
Clinically undetectable lymph nodeClinically undetectable lymph nodeinvolvement does not worsen prognosisinvolvement does not worsen prognosis(Harwood, 1978)(Harwood, 1978)
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WDTC - Papillary CarcinomaWDTC - Papillary Carcinoma(Continued)(Continued)
Microcarcinomas - a manifestation ofMicrocarcinomas - a manifestation ofpapillarypapillary carcinomacarcinoma
Definition - papillary carcinoms smaller than 1.0 cmDefinition - papillary carcinoms smaller than 1.0 cm
Most are found incidentally at autopsyMost are found incidentally at autopsyAutopsy reports indicate that these may be presentAutopsy reports indicate that these may be present
in up to 35% of the population (Mazzaferri, 1993)in up to 35% of the population (Mazzaferri, 1993)Usually clinically silentUsually clinically silent
Most agree that the morbidity and mortality fromMost agree that the morbidity and mortality frommicrocarcinoma is minimal and near that of themicrocarcinoma is minimal and near that of thenormal populationnormal population
One study showed a 1.3% mortality rate (Hay, 1990)One study showed a 1.3% mortality rate (Hay, 1990)
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WDTC - Papillary CarcinomaWDTC - Papillary Carcinoma(continued)(continued)
PathologyPathologyGross - vary considerably in sizeGross - vary considerably in size
-- oftenoften multi-focalmulti-focal-- unencapsulated but often have a pseudocapsuleunencapsulated but often have a pseudocapsuleHistology - closely packed papillae with littleHistology - closely packed papillae with little
colloidcolloid
--psammoma bodiespsammoma bodies- nuclei are oval or elongated, pale staining withnuclei are oval or elongated, pale staining with
ground glass appearancground glass appearancee
-- Orphan Annie cellsOrphan Annie cells
WDTC F lli l C i
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WDTC - Follicular CarcinomaWDTC - Follicular Carcinoma
20% of all thyroid malignancies20% of all thyroid malignanciesWomen > Men (2:1 - 4:1)Women > Men (2:1 - 4:1) (Davis, 1992, De(Davis, 1992, DeSouza, 1993)Souza, 1993)
Mean age of 39 yearsMean age of 39 years (Mazzaferri, 1994)(Mazzaferri, 1994) Prognosis - 60% survive to 10 yearsPrognosis - 60% survive to 10 years
(Geopfert, 1994)(Geopfert, 1994)
Metastasis - angioinvasion andMetastasis - angioinvasion and
hematogenoushematogenous spreadspread15% present with distant metastases to bone15% present with distant metastases to bone
and lungand lung
Lymphatic involvement is seen in 13%Lymphatic involvement is seen in 13%(Goldman, 1996)(Goldman, 1996)
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WDTC - Follicular CarcinomaWDTC - Follicular Carcinoma(Continued)(Continued)
PathologyPathologyGross - encapsulated, solitaryGross - encapsulated, solitary
Histology - very well-differentiated (distinctionHistology - very well-differentiated (distinctionbetweenbetween follicularfollicularadenoma and carcinomaidadenoma and carcinomaiddifficult)difficult)
- Definitive diagnosis - evidence- Definitive diagnosis - evidence
ofofvascularvascular and capsularand capsularinvasioninvasion
FNA and frozen section cannot accuratelyFNA and frozen section cannot accuratelydistinquishdistinquish between benign andbetween benign andmalignant lesionsmalignant lesions
WDTC H thl C ll C i
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WDTC - Hurthle Cell CarcinomaWDTC - Hurthle Cell Carcinoma
Variant of follicular carcinomaVariant of follicular carcinoma First described by AskanazyFirst described by AskanazyLarge, polygonal, eosinophilic thyroid follicularLarge, polygonal, eosinophilic thyroid follicular
cells with abundant granular cytoplasm andcells with abundant granular cytoplasm and
numerous mitochondrianumerous mitochondria(Goldman, 1996)(Goldman, 1996) Definition (Hurthle cell neoplasm) - anDefinition (Hurthle cell neoplasm) - an
encapsulated group of follicular cells with atencapsulated group of follicular cells with atleast a 75% Hurthle cell componentleast a 75% Hurthle cell component
Carcinoma requires evidence of vascular andCarcinoma requires evidence of vascular andcapsular invasioncapsular invasion
4%-10% of all thyroid malignancies4%-10% of all thyroid malignancies(Sessions,(Sessions,1993)1993)
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WDTC - Hurthle Cell CarcinomaWDTC - Hurthle Cell Carcinoma(Continued)(Continued)
Women > MenWomen > Men Lymphatic spread seen in 30% ofLymphatic spread seen in 30% of
patientspatients (Goldman, 1996)(Goldman, 1996)Distant metastases to bone and lungDistant metastases to bone and lung
is seen in 15% at the time ofis seen in 15% at the time of
presentationpresentation
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WDTC - PrognosisWDTC - PrognosisBased on age, sex, and findings at theBased on age, sex, and findings at the
time of surgerytime of surgery (Geopfert, 1998)(Geopfert, 1998)Several prognostic schemesSeveral prognostic schemes
represented by acronyms have beenrepresented by acronyms have beendeveloped by different groups:developed by different groups:
AMESAMES (Lahey Clinic, Burlington, MA)(Lahey Clinic, Burlington, MA)
GAMESGAMES (Memorial Sloan-Kettering Cancer(Memorial Sloan-Kettering CancerCenter, New York, NT)Center, New York, NT)
AGESAGES (Mayo Clinic, Rochester, MN)(Mayo Clinic, Rochester, MN)
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WDTC - PrognosisWDTC - Prognosis (Continued)(Continued)
Depending on variables, patients areDepending on variables, patients arecategorized in to one of the followingcategorized in to one of the followingthree groups:three groups:
1)1) Low risk groupLowrisk group - men younger than 40- men younger than 40yearsyears andand women younger than 50 yearswomen younger than 50 yearsregardless of histologic typeregardless of histologic type
-- recurrence raterecurrence rate -11%-11%
-- death ratedeath rate - 4%- 4%
(Cady and Rossi, 1988)(Cady and Rossi, 1988)
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WDTC - PrognosisWDTC - Prognosis (Continued)(Continued)
1)1)Intermediate risk groupIntermediate risk group
- Men older than 40 years and women older than- Men older than 40 years and women older than
50 years50 years who have papillary carcinomawho have papillary carcinoma
-- recurrence raterecurrence rate - 29%- 29%-- death ratedeath rate - 21%- 21%2)2) High risk groupHigh risk group- Men older than 40 years and women older thanMen older than 40 years and women older than
50 years who have follicular carcinoma50 years who have follicular carcinoma-- recurrence raterecurrence rate - 40%- 40%
-- death ratedeath rate - 36%- 36%
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Medullary Thyroid CarcinomaMedullary Thyroid Carcinoma
10% of all thyroid malignancies10% of all thyroid malignancies 1000 new cases in the U.S. each year1000 new cases in the U.S. each yearArises from the parafollicular cell orArises from the parafollicular cell or
C-cells of the thyroid glandC-cells of the thyroid glandderivatives of neural crest cells of the branchialderivatives of neural crest cells of the branchial
archesarchessecrete calcitonin which plays a role in calciumsecrete calcitonin which plays a role in calcium
metabolismmetabolism
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Medullary Thyroid CarcinomaMedullary Thyroid Carcinoma(Continued)(Continued)
Developes in 4 clinical settings:Developes in 4 clinical settings:Sporadic MTC (SMTC)Sporadic MTC (SMTC)Familial MTC (FMTC)Familial MTC (FMTC)Multiple endocrine neoplasia IIaMultiple endocrine neoplasia IIa
(MEN IIa)(MEN IIa)Multiple endocrine neoplasia IIbMultiple endocrine neoplasia IIb(MEN IIb)(MEN IIb)
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Medullary Thyroid CarcinomaMedullary Thyroid Carcinoma(continued)(continued)
Sporadic MTC:Sporadic MTC:
70%-80% of all MTCs70%-80% of all MTCs(Colson, 1993, Marzano, 1995)(Colson, 1993, Marzano, 1995)Mean age of 50 years (Russell, 1983)Mean age of 50 years (Russell, 1983) 75% 15 year survival (Alexander, 1991)75% 15 year survival (Alexander, 1991) Unilateral and Unifocal (70%)Unilateral and Unifocal (70%) Slightly more aggressive than FMTC and MEN IIaSlightly more aggressive than FMTC and MEN IIa 74% have extrathyroid involvement at presentation74% have extrathyroid involvement at presentation
(Russell, 1983)(Russell, 1983)
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Medullary Thyroid CarcinomaMedullary Thyroid Carcinoma(continued)(continued)
Multiple endocrine neoplasia IIbMultiple endocrine neoplasia IIb
(Wermers Syndrome, MEN III,(Wermers Syndrome, MEN III,
mucosal syndrome):mucosal syndrome):
Pheochromocytoma, multiple mucosalPheochromocytoma, multiple mucosalneuromas, marfanoid body habitusneuromas, marfanoid body habitus
90% develop MTC by the age of 2090% develop MTC by the age of 20Most aggressive type of MTCMost aggressive type of MTC15 year survival is
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Thyroid CancerThyroid Cancer Hurthle cell neoplasmHurthle cell neoplasm
5% of thyroid cancers5% of thyroid cancers
Variant of follicular cancerVariant of follicular cancer
Lymph node spread slightly higher than follicular cancerLymph node spread slightly higher than follicular cancer
Lees avidity for 131ILees avidity for 131I Medullary cancerMedullary cancer
Parafollicular C cellsParafollicular C cells
Autosomal dominance inheritance in 20%Autosomal dominance inheritance in 20%
Unilateral involvement in sporadic, bilaterality in familialUnilateral involvement in sporadic, bilaterality in familialformsforms
Calcitonin secretionCalcitonin secretion
Metastasis both by lymphatic and blood streamMetastasis both by lymphatic and blood stream
10 year survival 90% in localised disease, 70% with10 year survival 90% in localised disease, 70% withcervical mets, 20% with distant metscervical mets, 20% with distant mets
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Anaplastic Carcinoma of the ThyroidAnaplastic Carcinoma of the Thyroid
Highly lethal form of thyroid cancerHighly lethal form of thyroid cancer Median survival 70 years) (Sou, 1996)(Sou, 1996)
Mean age of 60 yearsMean age of 60 years (Junor, 1992)(Junor, 1992) 53% have previous benign thyroid disease53% have previous benign thyroid disease(Demeter, 1991)(Demeter, 1991)
47% have previous history of WDTC47% have previous history of WDTC(Demeter, 1991)(Demeter, 1991)
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Anaplastic Carcinoma of the ThyroidAnaplastic Carcinoma of the Thyroid
PathologyPathology
Classified as large cell or small cellClassified as large cell or small cellLarge cell is more common and has a worseLarge cell is more common and has a worse
prognosisprognosis
Histology - sheets of very poorlyHistology - sheets of very poorlydifferentiated cellsdifferentiated cells little cytoplasmlittle cytoplasm numerousnumerousmitosesmitoses necrosisnecrosis extrathyroidal invasionextrathyroidal invasion
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ManagementManagement
Surgery is the definitive management of thyroidSurgery is the definitive management of thyroidcancer, excluding most cases of ATC and lymphomacancer, excluding most cases of ATC and lymphoma Types of operations:Types of operations:
** lobectomy with isthmusectomylobectomy with isthmusectomy- minimal operation required for a potentiallyminimal operation required for a potentially
malignant thyroid nodulemalignant thyroid nodule** total thyroidectomytotal thyroidectomy removal of all thyroid tissueremoval of all thyroid tissue- preservation of the contralateral parathyroidpreservation of the contralateral parathyroid
glandsglands** subtotal thyroidectomysubtotal thyroidectomy-- anything less than a total thyroidectomyanything less than a total thyroidectomy
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M t (WDTC) P ill dM t (WDTC) P ill d
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Management (WDTC)- Papillary andManagement (WDTC)- Papillary and
FollicularFollicular(continued)(continued)
Rationale for total thyroidectomyRationale for total thyroidectomy1) 30%-87.5% of papillary carcinomas involve1) 30%-87.5% of papillary carcinomas involve
opposite lobeopposite lobe (Hirabayashi, 1961, Russell, 1983)(Hirabayashi, 1961, Russell, 1983)
2) 7%-10% develop recurrence in the2) 7%-10% develop recurrence in thecontralateral lobecontralateral lobe (Soh, 1996)(Soh, 1996)3) Lower recurrence rates, some studies show3) Lower recurrence rates, some studies show
increasedincreased survivalsurvival (Mazzaferri, 1991)(Mazzaferri, 1991)
4) Facilitates earlier detection and tx for4) Facilitates earlier detection and tx forrecurrent orrecurrent or metastatic carcinoma with iodinemetastatic carcinoma with iodine(Soh, 1996)(Soh, 1996)
5) Residual WDTC has the potential to5) Residual WDTC has the potential todedifferentiate to ATCdedifferentiate to ATC
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Thyroid cancerThyroid cancer
Anaplastic cancerAnaplastic cancer UndifferentiatedUndifferentiated
Rapidly growing, often inoperableRapidly growing, often inoperable
Invade locally, metastasize both locally and distantlyInvade locally, metastasize both locally and distantly
Mean survival 6 monthsMean survival 6 months
5 year survival rate 7%5 year survival rate 7% LymphomaLymphoma
Rare, rapidly enlarging tumourRare, rapidly enlarging tumour
Primary or secondaryPrimary or secondary
Seventh decade, 6:1 F/M ratioSeventh decade, 6:1 F/M ratio 5 year survival rate 75-80%, when confined to thyroid5 year survival rate 75-80%, when confined to thyroid
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Thyroid cancerThyroid cancer Staging and PrognosisStaging and Prognosis
AGES and AMES scoring systemsAGES and AMES scoring systems AA Age of patientAge of patient
GG Tumour GradeTumour Grade
MM Distant metastasisDistant metastasis
EE Extent of tumourExtent of tumour
SS Size of tumourSize of tumour Both scoring systems have identified 2 distinctBoth scoring systems have identified 2 distinct
subgroups;subgroups; Low-risk groupLow-risk group; Men 40years or younger, women 50 or; Men 40years or younger, women 50 or
younger, without distant metastasis (bone & lungs)younger, without distant metastasis (bone & lungs)
Older patients with intrathyroid follicullar/papillaryOlder patients with intrathyroid follicullar/papillarycarcinoma, with minor capsular involvement with tumourscarcinoma, with minor capsular involvement with tumours< 5cms in diameter< 5cms in diameter
High risk groupHigh risk group; All patients with distant metastasis; All patients with distant metastasis
All older patients with extrathyroid papillary/follicularAll older patients with extrathyroid papillary/follicular
carcinoma & tumours >5 cms regardless of extent ofcarcinoma & tumours >5 cms regardless of extent ofdiseasedisease
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Thyroid cancerThyroid cancer
Adjuvant therapyAdjuvant therapy
TSH suppressionTSH suppression
Post operative radioactive Iodine ablationPost operative radioactive Iodine ablation
External beam radiotherapyExternal beam radiotherapy
SurveillanceSurveillance
Serum thyroglobulin levelsSerum thyroglobulin levels
CXR or CT scanCXR or CT scan
Repeat 131I if positiveRepeat 131I if positive