Professional Documents
Culture Documents
• LYMPHATIC DRAINAGE:
• FROM PRELARYNGEAL &
PRETRACHEAL NODES TO THE
UPPER, MID & DEEP CERVICAL
NODES.
HISTOLOGY OF THYROID GLAND
• FOLLICULAR CELLS:
LINE THE FOLLICLES &
SECRETE T3 & T4. DURING
ACTIVE PHASE LINING IS
COLUMNAR & IN RESTING
PHASE CUBOIDAL.
• PARAFOLLICULAR
CELLS (C CELLS): LIGHT
CELLS LIE IN BETWEEN
FOLLICLES. SECRETE
THYROCALCITONIN WHICH
PROMOTES DEPOSITION OF
CALCIUM IN SKELETAL &
OTHER TISSUES PRODUCING
HYPOCALCAEMIA.
DEVELOPMENT OF THYROID GLAND
FATE OF THE THYROGLOSSAL DUCT
• ECTOPIC THYROID
ESP-LINGUAL
THYROID
• PYRAMIDAL LOBE
• LEVATOR GLANDULAE
THYROIDAE
• THYROGLOSSAL CYST
PHYSIOLOGY OF THE THYROID GLAND
• IODINE– IODIDE (98%
TAKEN UP BY THYROID BY
IODIDE TRAPPING
MECHANISM)– MIN 20μg
OF IODINE REQD PER
DAY– IN THE GLAND
PEROXIDASE ENZYME
CONVERTS IT BACK TO
IODINE– BINDS WITH
TYROSINE TO FORM
TRIIODO AND
TETRAIODO TYROSINE.
• TRH (HYPOTHALAMUS)–
TSH (PITUTARY)–
THYROID GLAND
FUNCTIONS OF THE THYROID GLAND
IMPORTANCE OF HISTORY TAKING
• Useful to:
• Differentiate benign nodules from
malignant ones
• To know the type of malignancy.
• Diagnose thyroiditis which can mimic
malignancy.
• Pitfalls:-
• Cant differentiate betw follicular
adenoma and malignancy
• Not very useful in cyst.
WHAT IS GOITRE &
HOW DO YOU CLASSIFY IT?
• ENLARGEMENT OF THE THYROID GLAND
IRRESPECTIVE OF IT’S CAUSE IS CALLED
‘GOITRE’
• CLASSIFICATION:-
• SIMPLE- 1-DIFFUSE 2-NODULAR 3-
COLLOID
• TOXIC- DIFFUSE OR NODULAR
(SOLITORY OR MULTI)
• NEOPLASTIC- A- BENIGN B-
MALIGNANGT
• THYROIDITIS:- A- ACUTE SUPPURATIVE
THYROIDITIS B- AUTOIMMUNE OR
HASHIMOTO’S C- SUBACUTE OR DE
QUERVAIN’S D- RIEDEL’S
SIMPLE GOITRE
• FAMILIAL- ENZYME DEFICIENCY
• ENDEMIC- HILLY
REGIONS(IODINE DEFN)
• GOITROGENS- CABBAGE,
CAULIFLOWER, TURNIPS AND
CALCIUM.
• PHYSIOLOGICAL
• IDIOPATHIC OR SPORADIC
• SPECIAL GOITRES:-
• JODBASEDOW DISEASE:-
EXCESSIVE IODINE CONSUMPTION
WITH THYROTOXICOSIS
• PENRED’S SYNDROME:- A DEAF
PATIENT WITH GOITRE SINCE
BIRTH.
THYROTOXICOSIS
• GRAVE’S DISEASE:- DUE TO
L.A.T.S.
• YOUNG FEMALE F:M=6:1
• SECONDARY THYROTOXICOSIS
IS MORE COMMON IN OLDER PTS
WITH MULTINODULAR GOITRE
• TACHYCARDIA, PALPITATION,
ATRIAL FIBRILLATION, HIGH
SYSTOLIC AND LOW DIATOLIC BP,
LASTLY C.C.F.
• JODBASEDOW DZ
• EARLY STAGE OF DEQUERVAIN’S
THYROIDITIS
• THYROTOXICOSIS FACTITIA
• NEONATAL THYROTOXICOSIS
INVESTIGATIONS
• SUBTOTAL THYROIDECTOMY- 4-
5gms TISSUE IS KEPT ON BOTH
SIDES.
• CHRONIC:-
• HASHIMOTO’S DISEASE OR
AUTOIMMUNE
• SUBACUTE OR DE QUERVAIN’S DISEASE
• RIEDEL’S THYROIDITIS
HASHIMOTO’S THYROIDITIS
• MOST COMMON
• ALSO CALLED CHRONIC LYMPHOCYTIC THYROIDITIS
• AUTOIMMUNE DISEASE
• FAMILIAL- AUTOIMMUNE GASTRITIS & PERNICIOUS ANAEMIA
ASSOCIATED.
• FEMALES AROUND THE AGE OF 50 MOST COMMONLY
AFFECTED.
• GOITRE WITH PAIN & TENDERNESS.
• MILD HYPERTHYROIDISM FOLLOWED BY HYPOTHYROIDISM.
• FIRM TO RUBBERY IN CONSISTENCY USUALLY
MULTINODULAR
• OTHER AUTOIMMUNE DISORDERS ASSOCIATED.
• DIAGNOSTIC INV:- T.F.T., ANIBODY TITRES, NEEDLE
BIOPSY CONFIRMATORY.
• Rx- SUPPRESSIVE THERAPY WITH ELTROXIN
• INDICATIONS OF SURGERY:- 1- PRESSURE SYMPTOMS 2-
COSMETIC 3- SUSPECTED MALIGNANCY (PAPILLARY)
SUBACUTE OR
DE QUERVAIN’S THYROIDITIS
• GRANULOMATOUS THYROIDITIS
• VIRAL ORIGIN- UYSUALLY FOLLOWING URTI.
• AGE:- ANY AGE MOST COMMON IN 5TH DECADE.
• SWOLLEN PAINFUL THYROID FOLLOWED BY
CONSTITUTIONAL SYMPTOMS.
• FOUR STAGES:- ACUTELY ENLARGED, TENDER AND
HYPERTHYROID– EUTHYROID– HYPOTHYROID–
REMISSION.. LASTS ABOUT 6 MONTHS.
• INV:- NEEDLE BIOPSY
• Rx- CORTICOSTEROIDS (PREDNISOLONE 1mg/kg
BODY WT) GRADUALLY TAPPERED.
• SURGERY:- CONTRAINDICATED.
RIEDEL’S THYROIDITIS
• MIMICS MALIGNANCY
• INFILTRATES SURROUNDING TISSUES
• WOMEN IN THE 5TH DECADE MOST
COMMONLY AFFECTED.
• FIRM TO HARD SWELLING WITH ILL DEFINED
MARGINS. USUALLY IMMOBILE. PRESENCE OF
PRESSURE SYMPTOMS.
• INV:- T.F.T.- HYPOTHYROIDISM
• TREATMENT:- THYROXIN AS REPLACEMENT
• SURGERY:- TO RELIEVE PRESSURE
SYMPTOMS. USUALLY ISTHMUSECTOMY.
TUMORS OF THE THYROID GLAND
• BENIGN- MAINLY ADENOMAS. FOLLICULAR
ADENOMA.
• WOMEN IN THE MIDDLE AGE MOST
COMMONLY AFFECTED.
• VERY DIFFICULT TO DISTINGUISH FROM
MALIGNANT TUMORS BY ANY TESTS. ONLY
CAN BE KNOWN BY CAPSULAR OR
ANGIOINVASION.
• HURTHLE CELL ADENOMA IS A VARIETY OF
FOLLICULAR ADENOMA.
APPROACH TO A PATIENT WITH
SOLITORY NODULE OF THYROID
• MOST COMMON
PRESENTATION IN GOITRE
• A CHALLENGE AS IT CAN
BE ONE OF THE
FOLLOWING:-
• A BENIGN NON
FUNCTIONING OR NORMAL
FN NODULE OR CYST.
• A TOXIC NODULE
• A MALIGNANT NODULE.
MALIGNANT NEOPLASMS
• FOLLICULAR CELL ORIGIN
• DIFFERENTIATED
• PAPILLARY (60%)
• FOLLICULAR (15%)
• MIXED
• UNDIFFERENTIATED
• ANAPLASTIC (13%)
• PARAFOLLICULAR
• MEDULLARY CARCINOMA(6%)
• NON THYROID
• MALIGNANT LYMPHOMA
• SARCOMA
• METASTATIC CARCINOMA
PAPILLARY CARCINOMA
• MOST COMMON
• MULTICENTRICITY
• DEPOSITS OF CALCIUM CALLED PSAMMOMA BODIES
• LYMPH NODE METASTASIS EARLY
• DEPENDANT ON TSH STIMULATION
• LATERAL ABERRANT THYROD.
• AGE < 40 GOOD PROGNOSIS.
• PULMONARY METASTASES
• NEAR TOTAL THYROIDECTOMY WITH REMOVAL OF
NODES WITH SUPPRESSIVE DOSE OF THYROID
HORMONE.
FOLLICULAR CARCINOMA
• CAPSULAR INVASION AND VASCULAR
INVASION
• HAEMATOGENOUS SPREAD TO BONE, LUNG
AND LIVER COMMON
• HURTHLE CELL CA- A VARIETY OF FOLLICULAR
WITH LOCAL METASTASIS MORE
• OSTEOLYTIC BONY METS
• GOOD RESPONSE TO RADIO IODINE.(I-131)
• THYROGLOBULIN INDICATOR OF METS.
MEDULLARY CARCINOMA