MALIGNANCIES
S3 UNIT
INTRODUCTION
? Commonest endocrine malignancy
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? 1% of all malignancies? Annual incidence - 3.7 per 1,00, 000 population
? Sex ratio 3:1 (Female : Male)
TOPICS
? Anatomy -Alphy Theres Teji
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? Physiology and clinical -Ameena Muhammedevaluation
? Aetiopathogenesis & -Amruthavarshini B.V
classification
? Investigation - Anagha K Karun
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? Differentiated thyroid -Anakha MCarcinoma
? Anaplastic carcinoma, -Anamika S
Medullary carcinoma,
Thyroid lymphoma
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? Surgery & complications -Anandhu J B? Prognosis & postop follow - Andrews Paul
up
THYROID
ANATOMY
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ALPHY THERESEMBRYOLOGY OF THYROID
? Thyroid gland- endodermal cells of floor
of pharynx
? Parafollicular cel s- neural crest
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ANOMALIES OF POSITION
LINGUAL
THYROID
WEIGHT & DIMENSIONS
? Normal gland weighs : 20-25gm
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? Each lobe : 5cm in length3cm in breadth
2cm in thickness
? Isthmus : 1 . 2 c m in length & 1 . 2 c m in breadth
SITUATION AND EXTENT
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CAPSULES OF THYROID
? True capsule: Peripheral
condensation of the
connective tissue of gland
? False capsule: Pretracheal
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layer of deep cervical fasciaRELATIONS OF THE LOBES
Lobes are conical in shape
having:
? An apex
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? A base? Three surfaces:
lateral, medial and posterolateral
? Two borders: anterior
and posterior
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? Apex
Superior thyroid artery
External laryngeal nerve
? Base
Inferior thyroid artery
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Recurrent laryngeal nerveLateral surface:
? Sternohyoid
? Superior belly of omohyoid
? Sternothyroid
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? Anterior border ofleidomastoid
sternocleidomastoid
Medial
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surface2 tubes- trachea
oesophagus
2 muscles
inferior
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constrictorcricothyroid
2 nerves
ext.laryngeal
recurrent
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laryngealPosterolateral
surface: carotid sheath,
ansa cervicalis & cervical
sympathetic chain
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Anterior border:anterior branch of superior
thyroid artery
Posterior border:
? Inferior thyroid artery
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? Anastomosis between superiorand inferior thyroid arteries
? Parathyroid gland
? Thoracic duct on left side
RELATIONS OF ISTHUMUS
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? Two surfaces:Anterior and posterior
o
r
? Two borders:
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superior and inferiorBLOOD SUPPLY OF THYROID
ARTERIAL SUPPLY
? Superior thyroid artery
? Inferior thyroid artery
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? Thyroidea imaarteries
VENOUS DRAINAGE
? Superior thyroid vein
? Middle thyroid vein
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? Inferior thyroid vein? Kochers vein
LYMPHATIC DRAINAGE
JUGULAR LYMPH NODES
? periglandular ? prelaryngeal (Delphian) ? pretracheal
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? paratracheal (along RLN) ? sup mediastinum ? deep cervical ? thoracicduct
? Upper part via prelaryngeal LN to upper deep CLN
? Lower part via pretracheal and paratracheal LN to lower deep CLN
NERVE SUPPLY
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? Mainly from middle cervicalganglion
? Partly from superior and
inferior cervical ganglion
HISTOLOGY
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? Follicles- structuralunit
? Secretory cells-
follicular and
parafollicular
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PARATHYROID GLANDS
? Two pairs-superior and
inferior
? Lie on the posterior border
of thyroid
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? Secrete parathormone? blood supply from inferior
thyroid arteries
PHYSIOLOGY AND CLINICAL
EVALUATION
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AmeenaMuhammed
PHYSIOLOGY
OF THYROID
GLAND
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THYROID HORMONES
Follicular cells- Thyroxine[T4] 93%,
Triiodothyronine[T3] 7%
Parafollicular cells- Calcitonin
IODINE HEMOSTASIS
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? Iodine- essential for hormone synthesis? Daily requirement - 150 mcg
? Absorbed by intestine
Excretory routes
Urine - 80%
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Stool- 15%Rest through bile
THYROID HORMONE SYNTHESIS
1. Iodide trapping
Transport of iodide ions into colloid
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Na+- I- symporter2. OXIDATION
Iodide ion is oxidised to iodine by
peroxidase
3. BINDING
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Iodine+ tyrosine residues of thyroglobulin =MIT & DIT
4. COUPLING REACTION
MIT+DIT = T3
DIT+DIT= T4
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5. HORMONE RELEASE
? When hormones are needed, Endocytosis and
Proteolysis of iodinated thyroglobulin
? Release of T3 ,T4 into circulation
? In blood, bound to albumin, thyroxine binding
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globulin (TBG), thyroxine binding prealbumin(TBPA)
? Unbound T3 & T4 is functional
6. PERIPHERAL CONVERSION
? Major product secreted is T4
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? About 35% secreted T4 is converted intoT3 by 5'-deiodinase
? T3 is four times potent than T4 & causes
the peripheral actions.
TSH enhances the hormone production by
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increasing:?Iodination of tyrosine
?Proteolysis of thyroglobulin
?Number, size & secretory activity of cells
REGULATION OF SYNTHESIS
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ACTIONS OF THYROID HORMONES
1. EFFECT ON BASAL METABOLISM
Increases the basal rate of metabolism
Increases heat production (Calorigenic action)
BMR increased to about 80% in
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hyperthyroidism2. CARDIOVASCULAR SYSTEM
Increase heart rate
Increases myocardial contraction
Increases systolic blood pressure
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Decreases diastolic blood pressureEnhances erythropoesis.
3. EFFECT ON GROWTH & DEVELOPMENT
Facilitate the effect of GH on tissues
Promote linear growth of bones
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Enhance the activity of chondrocyte in CartilageIncreases the osteoid activity and Bone remodelling
Eruption and development of Teeth
4. EFFECT ON NERVOUS TISSUE
Differentiation and maturation of brain cells
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Growth of cerebral and cerebellar cortices andbasal ganglia
Development of synaptic connection
5. GI TRACT
Enhance motility
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Increases production of digestive juices.Increases appetite and food intake
6. EFFECTS ON REPRODUCTIVE SYSTEM
Follicular maturation and ovulation
Promote spermatogenesis
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7. EFFECT ON KIDNEYIncreases renal outflow and GFR
CLINICAL EVALUATION
HISTORY TAKING
EXAMINATION
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HISTORY TAKING
AGE
Papillary ca: young
Follicular ca: middle aged
Anaplastic ca, Lymphoma : old age
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SEXFemales: male= 3:1
SWELLING
Papillary & follicular - slow growth
Anaplastic - fast growth
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PAIN
Painless to start
PRESSURE EFFECT
Hoarseness, dysphagia, dyspnoea
PAST HISTORY
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Radiation exposureFAMILY HISTORY
MEN 2A, 2B
Cowden syndrome
Gardner syndrome
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EXAMINATION
SIGNS OF MALIGNANCY
Stony hard swelling
Restriction of lateral mobility
infiltration of surrounding tissues.
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Lymphadenopathy in neckBerry's Sign
Horner Syndrome
Features of infiltration
Laryngotracheal complex- stridor & hemoptysis
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Recurrent laryngeal nerve - hoarsenessEsophagus - dysphagia/ odynophagia
Carotid sheath - Berry's sign
Cervical sympathetic chain - Horner's syndrome
Evidence of Metastasis -
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Pulsatile bony swelling in scalp or any pathologicalfracture.
Abdominal distension & jaundice
Hemoptysis, dyspnoea & chest pain
ETIOPATHOGENESIS
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ANDCLASSIFICATION
AMRUTHAVARSHINI B V
AETIOLOGICAL FACTORS
1. IONIZING RADIATION
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? Most imp risk factorradiation - external/radioiodine - under 5 yrs
? Commonest papilary carcinoma thyroid
? To treat benign condition in the first two decade of life
( tonsilitis, adenoiditis...etc)
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? Adolescent - radiotherapy for Hodgkins lymphoma**Chernobyl nuclear disaster in Ukraine,1986
2.GENETIC MUTATION
3.FAMILIAL
MEN 2A
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MEN 2BFAMILIAL MTC
COWDEN SYNDROME
GARDNER SYNDROME
MEN 2A
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?Autosomal dominant inheritance?Mutation of RET protooncogenes
?Characterized by :
Pheochromocytoma
Hyperparathyroidism
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Medul ary carcinoma of thyroidMEN 2B
?RET mutation
?Characterized by:
Medullary carcinoma thyroid
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PheochromocytomaMucosal neuromas of
lip,tongue,inner eyelid
Marfanoid habitus
Familial Medulary Thyroid Carcinoma
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?RET proto-oncogene mutation?only Medullary thyroid cancer
?20% of total cases of MCT
COWDEN SYNDROME
?AD inheritence - Mutation of PTEN gene on
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chr 10?Characterized by;
Differentiated thyroidcarcinoma
Carcinoma breast
Multiple hamartomas of skin
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Neuroendocrine tumorEndometrial cancer
GARDNER SYNDROME
Autosomal dominant inheritance
Mutation of APC gene in chromosome 5
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Familial adenomatous polyposisMultiple polyp in colon which predisposes to colon
cancer
?Characterized by:
Papillary carcinoma of thyroid
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Colorectal cancerCancer of ampulla of vater
Hepatoblastoma
Osteomas of the jaw
CHRPE
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Primary brain tumors4. PRE EXISTING MNG
Follicular thyroid carcinoma
Dominant or rapidly growing
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nodules in long standinggoiters
5. ENDEMIC AREAS
?Low iodine areas
? Follicular carcinoma - Increased TSH
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secretion6. HASHIMOTO'S THYROIDITIS
?Also caled diffuse non goitrous thyroiditis
? Hyperplasia - fibrosis - infiltration with plasma cels and
lymphocytes
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?Non Hodgkins Lymphoma?Half of the primary thyroid LYMPHOMA
CLASSIFICATION OF
THYROID NEOPLASMS
BENIGN follicular
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adenomaMALIGNANT primary follicular cells Follicular
differentiated (10%)
Papillary
(80%)
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follicular cells Anaplasticundifferentiated (5%)
parafollicular Medullary
cells (2.5%)
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lymphoid cells Lymphoma(2.5%)
MALIGNANT secondary metastatic colon,breast
melanoma,
local kidney
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infiltrationINVESTIGATIONS OF
THYROID MALIGNACIES
ANAGHA K KARUN
INVESTIGATIONS
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THYROID FUNCTION TEST [TFT]THYROID IMAGING {USG,CT,MRI,PET scan,
X-RAY}
FINE NEEDLE ASPIRATION CYTOLOGY
[FNAC]
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RADIOISOTOPE SCANNING{Tc 99m,I 123}THYROID FUNCTION TESTS
? Immunochemiluminometric assay.
? Measures TSH, free T3 and free T4.
? Total T3 and T4 depend on TBG.
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? Free T3 and T4 are important.ULTRASONOGRAPHY
? Gold standard investigation
? Use high frequency probe in the
range 7.5-16 MHz
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? Number, size, shape, margin, vascularity,microcalcification
USES
?To differentiate cystic & solid swellings
?Non palpable , deep nodules
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?Features of malignancy?Lymph node assessment for metastasis
?USG guided FNAC
FEATURES OF MALIGNANCY
Hypo echoic
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Increased vascularityMicro calcifications
No peripheral halo
Poorly defined borders
Taler than wide
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LN involvementFNAC
? To conclude pathological diagonosis
? 95% accuracy,
83% sensitivity, 92% specificity
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? USG guided aspiration? Advantages :
- patient compliant
- simple & quick to perform
- repeated readily
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?C/I : Toxic nodulePROCEDURE
1.
10cc syringe & 23G needle inserted
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2. Multiple passes are made( Minimum 6 aspirations )3. capillary & suction technique
4. Papanicolaou stain
? Adequate smear: 6 aspiration with 6 cluster of cells
each containing 20 cells
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Disadvantages
? Not possible to dif erentiate folicular adenoma and carcinoma.
? Sampling error (False neg. rate: 1-6% ) in non guided
FNAC.
RADIO ISOTOPE SCANNING
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? I 123 or Tc 99m? INDICATION
? Solitary thyroid nodule - toxic
? HOT : 5% malignant
? COLD : 20% malignant
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X RAY
? Preoperatively, tracheal deviation or compression
? Retrosternal extension
COMPUTED
TOMOGRAPHY
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INDICATIONS? Retrosternal goitre
? Malignancy ( T&N Staging)
? Giant goitre with tracheal compression and
displacement
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? Berry sign +veIodine used with iv contrast , so not used in
malignancies.
MRI
? MR Angiography : vessel wall
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involvement? Advantage over CT:
-no iodine contrast
-no radiation exposure
POSITRON EMISSION
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TOMOGRAPHY[PET]?Recurrence and metastasis
LARYNGOSCOPY
?Preoperatively
?Mobility of VC
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?Flexible LaryngoscopyUSES
Medico legal use
S.THYROGLOBULIN:
v No significance in initial evaluation
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v in follow-upv pre operative evaluation
Normal value 3?40ng/mL
INTRAOPERATIVE FROZEN SECTION
? Confirm nodal
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involvement in PTC.? Can avoid 2nd
procedure
DIFFERENTIATED THYROID
CARCINOMAS
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ANAKHA M? Differntiated thyroid carcinomas are;
Papillary thyroid carcinoma
Follicular thyroid carcinoma
Hurthle cell carcinoma
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PAPILLARY THYROID CARCINOMA
? Most common malignancy -80%
? Excellent prognosis
? Important risk factor- radiation exposure in
childhood
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? More common in females 2.5:1 ratio? Peak incidence less than 40 years of age
? Micropapillary carcinoma
? Diffuse sclerosing variant
? Encapsulated variant
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? Tall cell variant? Columnar cell variant
CLINICAL FEATURES
? Palpable nodule ;incidental imaging finding;
painless lateral mass
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? Lymphadenopathy is usually present? Compression features less common
? Slowly progressive and less aggressive
tumour
? Spread via lymphatics
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? Multicentricity can be anticipated in 70% ofpatients
? GROSS FEATURES
-It can be hard or of varying consistency
-It can be solitary or multinodular
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? MICROSCOPY- orphan annie eye nucleus
- papillary projections with psammomma
bodies ,cystic spaces
PSAMMOM
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PAPILLARMA
BODIES
Y
PATTERN
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ORPHAN ANNIE NUCLEI
FOLLICULAR THYROID CARCINOMA
? 10% of all thyroid malignancies
? More commonly seen in female 3:1
? 40 to 60 yrs of age
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? Either de novo or pre existing MNG? Capsular invasion and angio invasion
? More aggressive,mortality twice than
papillary carcinoma
? Lymph node involement is less common
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? Less favourable prognosis? Blood born metastases common
CLINICAL FEATURES
? Presents as painless thyroid mass
? May coexist with MNG 5-10% CASES
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? In advanced disease-hoarseness of voice
-stridor
-berry's sign
-pathologic fractures
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-pulsatile bony swelling in the scalpHURTHLE CELL CARCINOMA
? Subtype of follicular thyroid carcinoma
? Consists of oxyphilic cells
? Increased no of mitochondria ,enlarged
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granular eosinophilic cytoplasm? 60-70 years of age
? More aggressive behaviour
? Secrete thyroglobulin
? 30% multicentric
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? More chances of lymphatic spread? Cells with abundant granular eosinophilic
cytoplasm
INVESTIGATIONS
? TSH levels
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? FNAC of thyroid nodule and lymph node? Ultrasound scan neck, CT scan neck
TNM STAGING
TUMOUR
? Tx ?Primary cannot be assessed
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? T0-No evidence of primary? T1-Tumour - 2cm
T1a ? 1 cm
T1b-> 1 2cm
? T2-limited to thyroid >2cm but 4cm
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? T3 ?Limited to thyroid >4 cm or any tumour with minimalextrathyroid extension
? T4 ? Any size with extensive extra thyroid extension
T4a :moderately advanced
T4b :very advanced
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NODES
? Nx- Cannot be assessed
? N0- No regional node metastases
? N1-Regional node metastases
N1a-level 6
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N1b-any/all other levelsMETASTASES
? Mx-Cannot be assessed
? M0-No metastases
? M1-Metastases present
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AJCC STAGING OF DTC
? STAGE <45 yrs
Stage 1- any T any N M0
Stage 2 ? any T any N M1
? STAGE >45 yrs
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Stage 1 ?T1a,T1b,T2N0M0Stage 2 ?T3N0M0
- T1,T2,T3N1M0
Stage 3-T4a any N M0
Stage 4A- T4bAny N M0
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Stage 4b-Any T any N M1TREATMENT
? Papillary thyroid carcinoma
? Total thyroidectomy + CCND
? Follicular thyroid carcinoma
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- Total thyroidectomy +CCNDIf lymph node seen in USG and proven in
FNAC? lateral lymph node dissection
MEDULLARY
CARCINOMA
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THYROIDANAMIKA S
INTRODUCTION
? 2 .5% of thyroid carcinoma
? Tumours of parafolicular C cells
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FORMS1. Sporadic form (80%)
2.Familial form(10 to 20%)
Medullary Thyroid carcinoma
(MTC)
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INHERITEDSPORADIC
10-20%
80%
FAMILIAL Non
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MEN 2AMEN MTC
MEN 2B
FAMILIAL
SPORADIC
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BILATERAL ANDORIGINATE IN ONE LOBE
MULTICENTRICITY
YOUNGER AGE GROUP
ANY AGE
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ASSOCIATED WITH C CELLHYPERPLASIA
1.More aggressive
2.RET gene point mutation.
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3.High levels of CEA and serum CALCITONIN.4.Not TSH dependent
5.Do not take up radioactive IODINE.
6.Diarrhoea is a feature of 30% of cases.
MEDULLARY CARCINOMA
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Cell balls and Amyloidstroma
METASTASES
Liver ,Mediastinal
nodes,
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bone(osteoblastic)lung,trachea,
Blood borne metastases common
MOSTLY TO
LIVER
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Cervical Lymphnodes 50-60%
CLINICAL FEATURES
1.Thyroid swelling-neck lymph nodes
2.HTN , Pheochromocytoma ,mucosal neuroma-MEN 2
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3.Paraneoplastic symptoms like cushings and carcinoidsINVESTIGATIONS
1.FNAC
2.SE.RUM CALCITONIN AND CEA
3.GENETIC TESTING FOR GERMLINE RET
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MUTATION4.THYROID AND NECK USG
? All patients should be screened for RET gene
point mutation ,pheochromocytoma and
hyperparathyroidism.
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? Pheochromocytoma-to prevent hypertensivecrisis
1. Serum Ca-to rule out hyperparathyroidism.
2. 24 hr urine VMA and serum metanephrin,USG
abdomen- to rule out pheochromocytoma
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3. If it is + ve ? CECT of abdomen4. CECT or MRI chest and mediastinum ? if N1disease or
calcitonin greater than 400pg/ml
4. PET scan ? recurrence, Metastasis as they do not take
up radioiodine
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TREATMENT
1.Surgery is the treatment of choice.
2.Tumour size more than 1cm,chance of
spread to regional nodes is 75%
3.Total thyroidectomy with elective central
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neck dissection.4.When central node (level 6) involved ?
Ipsilateral modified radical neck dissection.
? Hypercalcemia and PTH at time of
surgery-Only obviously enlarged
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parathyroid removed? If vascular pedicle of parathyroid is unable to
maintain ?auto transplantation of ? the gland
in sternocleidomastoid or brachioradialis of
non-dominant forearm.
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? Somatostatin analogue (octreotide ,lanreotide)for cushings syndrome , flushing
EXTERNAL BEAM RADIOTHERAPY
1.Resected T4 disease.
2.Unresected residual or recurrent tumour
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3.Symptomatic bony metastasis.POST OPERATIVELY
? Stimulated calcitonin assay to assess the
adequacy of resection
? L evothyroxine is indicated in all
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patients .? TSH-normal range
GENETIC SCREENING
MEN 2A
MEN 2 B
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FAMILIAL MCTTOTAL
TOTAL
THYROIDECTOMY
THYROIDECTOMY
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-5YEARS1 YEAR
? Prognosis is variable and depends on the stage at
diagnosis
? FMTC (best) > MEN-2A > Sporadic > MEN-2B
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(worst)? Chance of recurrence 50% & also high mortality
FOLLOW-UP
? Basal calcitonin-Fall after resection
Rise in recurrence, residual tumour and
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metastasis.? PET scan
? CEA
? USG (central and lateral neck compartments)
ANAPLASTIC
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THYROID CARCINOMAINTRODUCTION
? Undifferentiated carcinoma
? 5% of al thyroid malignancy
? Most aggressive
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? Disease specific mortality 100%? Occurs mainly in elderly women
TYPICAL MANIFESTATION
Older patient with
1. Dysphagia
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2. Cervical tenderness3. Painful, rapidly enlarging neck mass
4. Frequently have history of DTC and upto 50%
goitre
? May also Include superior venacava syndrome
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? Deteroirates into tracheal obstruction? Rapid local invasion of surrounding structures
SPREAD
? Rapid local invasion
? Blood as well as lymph spread present.
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? Sites of Mets : lung , brain, bone, liver, kidney, skin, pancreas,adrenal.
STAGING
MANAGEMENT
? Treatment of ATC is usually palliative
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? Treatment of choice -RADIOTHERAPY? Tracheal obstruction - ISTHMUSECTOMY
THYROID
LYMPHOMA
INTRODUCTION
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Uncommon lymphoma2 .5 %of al thyroid malignancies
Involve thyroid as a part of systemic
lymphoma or may arise primarily in thyroid.
PREDISPOSING FACTORS
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Autoimmune diseases (Lymphocyticthyroiditis)
Advanced age(>70 yr)
More frequent in women (four times)
SIGNS AND SYMPTOMS
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? Rapid enlarging neck mass? Hoarseness
? Dysphagia
? Fever
? Diffuse pain
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PHYSICAL EXAMINATION? Firm , slightly tender , fixed mass
INVESTIGATIONS
? Ultrasound
? MRI
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? Trucut biopsy? PET imaging
TREATMENT OF LYMPHOMA
RADI ?ATION+CHEMO= treatment of choice
Tracheal obstruction : urgent chemotherapy
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CHOP/CVDP regimen:Cyclophosphamide
Doxorubicin Vincristine
Role of surgery only in:
Biopsy
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Pressure symptomsNo response to chemo .
sURGical manaGEmEnt
and
complications
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Anandhu JBRol No : 16
q For a preoperatively proven case of
? Dif erentiated carcinoma
? Medullary Carcinoma
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TOTAL THYROIDECTOMYCentral neck dissection
Modified Radical Neck Dissection
RATIONALE FOR
TOTAL THYROIDECTOMY
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? Facilitates radioiodine ablation later.? As there is chance for multifocal d/s.
? Facilitates use of thyroglobulin as tumor
marker in fol owup.
STEPS OF SURGERY
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General anaesthesia withendotracheal intubation.
Supine position - sand bag placed transversely under the
shoulders
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A head ring ? to stabilize headTable tilted up - 15 at the head end.
ROSE'S POSITION
? Horizontal curved - Midway between the notch of
the thyroid cartilage and suprasternal notch.
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? One sternocleidomastoid to other.? Skin, superficial fascia cut upto investing layer of
deep fascia
? Flaps are raised
o Upper upto laryngeal prominence
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o Lower upto suprasternal notch? Investing layer of deep fascia is incised vertically.
? Retract strap muscles laterally
? Identify the pedicles
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1. Superior pedicle? (sup. thyroid A & V)
2. Middle pedicle
? (middle thyroid V only)
3. Inferior pedicle
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? (inferior thyroid A only)? Ligate middle thyroid vein first.
? Ligate superior thyroid A & V separately &
close to capsule (CAPSULAR LIGATION)
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? Ligate inferior thyroid A close to the glandafter safe guarding recurrent laryngeal nerve.
? ? Identification of parathyroid
? :Yellowish pink
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? :Position ? in relation to ITA-RLN junction? Sup. parathyroid ? above & behind
? Inf. Parathyroid ? below & anterior
? Identification of RLN
? 1.RIDDLE'S TRIANGLE
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o Inferior thyroid artery- aboveo Common Carotid artery- laterally (base)
o Trachea - medialy
? 2.Nerve traced upwards to point of its entry into the
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larynx at the cricothyroid junction.? 3.Tubercle of Zuckerkandl
RLN damage points.
1.At crossing with inferior
thyroid artery.
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2. In the vicinity of ligament ofBerry
3.In Riddle's Triangle
4.Tubercle Of Zuckerkandl
? Ligament of Berry is divided.
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? The thyroid gland is separated from theunderlying trachea.
? Complete hemostasis maintained
? Draining and Wound closure:
--Reapproximate strap muscles and
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platysma--Skin closure
Central compartment dissection
Thyroid and thymus
removed en bloc with
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level VI nodes-paratracheal,
pretracheal and
prelaryngeal.
? Based on lateral node status lateral neck
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dissection is done.COMPLICATIONS
OF
THYROIDECTOMY
? Intraoperative
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? Early post operative? Late post operative
INTRAOPERATIVE
COMPLICATIONS
? Haemorrhage
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? Nerve injuryEARLY POSTOPERATIVE
? Haematoma
? Laryngeal edema
? Respiratory obstruction
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? Hypoparathyroidism? RLN injury & problems
? Thyrotoxic crisis
LATE POSTOPERATIVE
? Hypothyroidism
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? Recurrent nodule? Recurrent toxicity
? Wound infection
? Granuloma / keloid
HEMORRHAGE
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PrimaryReactionary
Secondary
Treatment
?
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Release of sutures?
Evacuation of hematoma
?
Re exploration & control
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bleedingRESPIRATORY OBSTRUCTION
? Haematoma Laryngeal edema
?
Bilateral recurrent laryngeal nerve
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? paralysisHypocalcemic tetany Tracheomalacia
?
?
MANAGEMENT
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Release the tension haematoma Ifnot relieved - - - intubate
RECURRENT LARYNGEAL NERVE INJURY
? Hoarseness
? Dysphonia
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? Paralytic aphonia? Periodic aspiration
? Inef ective cough
RLN injury may be unilateral or bilateral.
UNILATERAL RLN PALSY
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? Ipsilateral paralysis of all intrinsic musclesexcept cricothyroid
In Indirect laryngoscopy,
? Vocal cord - median or paramedian
position
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MANAGEMENT
? STEROIDS ? within 7 days of injury
(Prednisolone 15mg tid for 10 days)
? SPEECH THERAPY
? MEDIALIZATION OF THE CORD -
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by Teflon injection? LARYNGOPLASTY - if compensation does
not take place
Bilateral RLN palsy
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Inspiratory stridorDyspnea or
Minimal dysphonia.
Management
? Emergency endotracheal
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intubation? Tracheostomy
? Cordectomy or endoscopic
laser treatment
? Thyroplasty
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INJURY TO THE EXTERNAL
BRANCH OF SUPERIOR
LARYNGEAL NERVE
? Approximately in 20%
? Proximity to the superior thyroid artery.
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? Loss of tension in the vocal cord? VOICE FATIGUE - Diminished power and
range in the voice.
COMBINED PARALYSIS
UNILATERAL
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? Paralysis of al muscles of larynx on one side exceptinterarytenoid.
? Cadaveric position ( 3.5mm from midline)
Treatment
? Speech therapy
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? Injection of teflon paste? Muscle or cartilage implanted to paralysed cord
BILATERAL
? Both cords in cadaveric position
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? Total anesthesia of larynxAphonia
Aspiration
Features Inability to cough
Bronchopneumonia
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Retention of secretion in the chestRespiratory arrest
Treatment
1. Tracheostomy
2. Epiglottopexy ( epiglottis is folded
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backwards and fixed to the arytenoid)3. Plication of vocal cord to prevent aspiration
HYPOPARATHYROIDISM
? Transient in 50%
? Permanent in < 2%.
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? Usually manifests within 72 hrs after surgery? The first symptom is circumoral paresthesia.
SIGNS
CHVOSTEK SIGN TROUSSEAU'S SIGN
Management
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? Emergency : 10 ml of 10% calciumgluconate I .V over 10-15 mnts
Chronic patients :
? Calcium carbonate or Calcium
citrate
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? Vitamin D3THYROTOXIC CRISIS
(THYROID STORM)
1-2 % patients
Causes
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? Inadequately prepared thyrotoxic patient? Infection, trauma, diabetic ketoacidosis,
emergency surgery, stress
Treatment
Supportive measures
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Anti adrenergic drugs ? D O C : Propranolol i.vThionamides ? Propyl thiouracil 200 mg 4th hrly
Iodide compounds ? 10-15 drops Lugol's iodide 8th
hrly
Glucocorticoids ? hydrocortisone 5 mg/kg 6th hrly
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Bile acid suppressants ? cholestyramine 4 g 6th hrlyHYPOTHYROIDISM
? For papil ary and follicular carcinoma -
suppressive dose of thyroxine (200 ? 300
mcg per day)
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? For medullary carcinoma -supplementary dose of thyroxine (25 ?
100 mcg per day)
KELOID
STITCH GRANULOMA
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PROGNOSIS
POSTOPERATIVE CARE
FOLLOW UP
Andrews Paul
PROGNOSIS
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Many scoring systems are available? AMES
? AGES
? MACIS
? TNM
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AGES AND AMES
PARAMETER
LOW RISK
HIGH RISK
AGE (YRS)
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<40>40
GENDER
FEMALE
MALE
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EXTENDNO LOCAL EXTENTION LOCAL AND EXTRA
THYROID EXTENSION
METASTASIS
NONE
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REGIONAL OR DISTANTSIZE
<4 CM
>4 CM
GRADE
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WELL DIFFERENTIATED POORLYDIFFERENTIATED
MACIS
FACTORS
SCORE
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DISTANT METASTASIS YES3
NO
0
AGE
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<39 years3.1
>40 years
0.08 * age
INVASION INTO
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YES1
SURROUNDING AREAS NO
0
COMPLETENESS OF
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Incomplete1
SURGICAL RESECTION Complete
0
SIZE OF TUMOUR
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0.3 * size(cm)Sum Of MACIS Score
20 year survival
<
6.0
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99%6.0 ? 6.99
89%
7.0 ? 7.99
56%
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> 8.024%
Postoperative Measures
Differentiated thyroid cancers
-Radioactive iodine scanning and
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ablation-TSH suppression
-Follow up testing
RADIOIODINE
SCAN
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Goals
To identify
- any remaining normal thyroid tissue
- residual thyroid cancer cells
- metastatic disease
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Pre requisitesTSH level > 30 mU/L
-stop thyroxine for 4-6 weeks
-Patient advised to be on low iodine diet
Low doses of radioactive I? or I? is used.
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Given orally in liquid or capsule form.? I? : half life of 13 hrs, emits rays, better for
diagnostic scanning.
? I? : half life of 8 days, emits and rays.
? If positive, Radio Remnant Ablation is done
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? If negative, follow up with thyroglobulin level.? If raised Tg level ? WBS + US neck
THYROGLOBULIN ESTIMATION
Serum tumor marker for DTC
Circulating anti thyroglobulin antibodies
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interferesUndetectable levels ? after thyroidectomy
with TSH suppression
Raised levels ? recurrence/metastasis.
Level above 2ng/l ? abnormal
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RADIO REMNANT ABLATION
(RRA)
Radioactive iodine therapy (RAIT)
Purposes
? Remnant thyroid tissue ablation
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? Adjuvant therapy with the intention of targetingoccult metastatic disease
? Primary treatment of known persistent disease
Indications
? Tumor size > 4 cm
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? Gross extra thyroidal extension? Distant metastases
? Tumor size < 4 cm with lymph node metastases
? Rising serum thyroglobulin level
? Radioactive I? is used.
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? Dose : 100-200 mCi? Post ablation WBS done after 5-8 days
? In low risk patients ? with negative Tg and negative
cervical US no need for WBS
? In intermediate and high risk patients ? WBS after 6-
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12 months of ablation + Cervical US at 6,12 monthsand then annually for 3-5 years
? Concerns with RAIT
-isolation of patients
-C/I in pregnant, nursing women and
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children-Avoid pregnancy for 6 months.
? Complications : nausea and vomiting,
sialadenitis, vocal cord paralysis, bone marrow
suppression
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TSH Suppression
- To prevent hypothyroidism
- To prevent recurrence of thyroid
cancer
? T4 or levothyroxine is given orally
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? Suppressive dose of thyroxine ? 200-300 ?g/day
? For patients with high risk DTC, TSH < 0.1 mU/L
? For intermediate risk DTC, TSH b/w 0.1 ? 0.5
mU/L
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? For low risk DTC, TSH within 0.5 ? 2 mU/L? Risks associated ? subclinical thyrotoxicosis,
cardiac irregularities, osteoporosis
Follow up
Physical examination
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Lifelong TSH suppressionThyroglobulin estimation
Anti thyroglobulin antibodies
Periodic neck ultrasound
Radioiodine imaging
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Medullary Carcinoma
? Annual measurements of calcitonin and CEA
levels
? Ultrasound, CT, MRI, PET scans - localize
recurrent diseases
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? 10 year survival rate is 80%? Prognosis also depends on disease type - worst
in patients with MEN2B
Anaplastic Carcinoma
? Most aggressive form with disease specific
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mortality approaching 100%? External beam irradiation
? Palliative support and end of life planning
SUMMARY
? Commonest malignant endocrine tumor
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? Risk factors : Radiation exposure , Genetic alterations? Divided into differentiated , undif erentiated and medullary thyroid carcinomas
? Investigations:
Clinical examination ? history , physical examination Thyroid function tests
Imaging ? USG , X ray ,MRI , PET Pathological ? FNAC
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? Treatment:Papillary carcinoma ? total thyroidectomy + CCND Follicular
carcinoma ? total thyroidectomy+CCND
Medulary carcinoma ? total thyroidectomy + CC ND
Anaplastic carcinoma ? palliative treatment
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