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thyroid disease
Supervised by: Dr. Mohammad Khammash
Presented by: Nurul Aina Khalid
Embryology
The first endocrine gland to develop in embryo .
The gland originates as a proliferation of
endodermal epithelial cells on the median surface of
the developing pharyngeal floor.
Descends in the neck anterior to the level hyoid
bone . Briefly remain connected to the tongue by the
thyroglossal duct which obliterates eventually leaving
proximal pit (foramen cecum ) in the tongue base .
the parafollicular C cells (calcitonin ),differentiate
from the neural crest cells that migrate from the
pharyngeal arches to the 4th pharyngeal pouch.
Anatomy
largest endocrine organ in the body approximately 2025 g in adult .
2 lobes encircles the anterolateral portion of the
trachea overlying the 2nd to 4th tracheal rings
,connected by isthmus (<4mm ).
A pyramidal lobe was found in 55% of individuals .
Extends from the isthmus and can reach the level of
the hyoid bone.
A fibrous tract may extends from the pyramidal lobe
to the hyoid bone and may harbor a
thyroglossal cyst.
Function
Produce Thyroid hormones which are critical
determinants of brain and somatic development in
infants and of metabolic activity in adults; they
also affect the function of virtually every organ
system.
The parafollicular cells (c cells) of thyroid gland
secrete calcitonin ( Ca2+ in blood ).
Physiology
Primary function of the thyroid gland is the
secretion of thyroid hormones:
T4 is primary released hormone
T3 at least 10 times more active
T4 is converted to T3 mostly peripherally.
Approach
History.
Physical exam.
Investigations .
Treatment.
Examination
Inspection
General look
Hands
Eyes
Neck
Palpation
Percussion
Auscultation.
Investigations
Investigations
TSH level
Free T4 level
Free T3 level
Thyroid antibodies (anti-thyroglobuline
antibodies, anti-peroxidase antibodies)
Thyroid ultrasound
Radio active iodine uptake
Thyroid biopsy (FNA)
Thyroid US
Give good anatomical images
of the thyroid and surrounding
structures but unfortunately
reveals more thyroid swelling
than are clinically relevant.
Cystic vs. Solid lesions
Reveal smaller nodules not
felt on exam .
The US will show the size,
shape, consistency of the
gland and whether its nodular
or not.
Isotope scanning
Goiter
Goiter
Classification of Goiter
Simple
Toxic
Inflammatory
Neoplasti
c
Autoimmune
Diffuse
hyperplastic
goiter
Physiological
Pubertal
Pregnancy
Multinodular
goiter
Diffuse
Graves
disease
Multinodular
Toxic
adenoma
Chronic
lymphocytic
thyroiditis
Hashimotos
disease
Granulomatous
De Quervains
thyroiditis
Fibrosing
Infective
Benign
Malignant
Simple Goiter
Etiology
Simple Goiter
Because of Persistent
growth stimulation by
(TSH) due to low (TH)
leading to diffuse
hyperplasia .
1. As a result of fluctuating
stimulation a mixed pattern of
areas of active lobules and
areas of inactive lobules
develops .
Stimulation increase in
puberty and pregnancy .
May persist for a long time
but its reversible if
stimulation stops early .
Presentation
Painless Goiter (diffuse or palpable nodules)
Euthyroid.
More common in females.
Complications of Neck masses.
Acute development (size or pain )Hemorrhage
Investigations
TFT
Thyriod antibodies
to differentiate from autoimmune thyroiditis
US
FNAC
Treatment
Iodine uptake: iodised salt
Thyroxin administration
(in hyperplastic stage )
Thyroidectomy
(tracheal compression , cosmatic ,
neoplastic )
Cause : thyroid stimulating antibodies (TSHRAbs)that bind to TSH receptors site and produce a
prolonged effect .
Diagnosis
High T3, T4.
Low TSH
thyroid stimulating antibodies.
Diffuse increased uptake in Isotope scan
Treatment
Medical : carbamazole or propylthiouracil
+propranolol (agranulocytosis)
Radioiodine ablation.
Surgical resection.
Presentation
Neck masses.
Hyperthyroidism
TFT
Treatment
Thyroid carcinoma
Majority present as lump in the neck , mostly euthyroid.
Rare: Less than 1% of all malignancies ,If treated
appropriately high survival rate
Types :
Follicular epithelium
Differentiated
Papillary
Follicular
Undifferentiated
Anaplastic
Not follicular
Medullary
Lymphoma
Rare secondary
When to suspect ca ?
History:
Extreme age
Neck radiation.
Family Hx. (thyroid CA or MEN-II)
Symptoms:
Voice changes.
Neck mass
Lymph node enlargement
Dysphagia.
When to suspect ca ?
Signs:
Single Nodule.
Cold nodule.
Increase calcitonin level.
Lymphadenopathy
Hard, Immobile.
Investigations
FNA
TSH
US , CT
Calcium level
CXR
Treatment
Differentiated: (papillary &follicular):
1. Total Thyroidectomy
2. Radioactive iodine.
3. Thyroxin replacement
Undifferentiated: (Anaplastic):
total thyroidectomy
. Radiotherapy (palliation)
Pre-operative preparation
1. the patient should be euthyroid (to decrease the
risk of thyroid storm)
2. Give carbimazole or beta-blocker
(propranolol )before surgery
3. Check the vocal cords.
4. Patient should be warned for possible nerve
damage intraoperatively .
Postoperative
assessment
Thyroxin T4
Thyroglobulin
Sensitive indicator for residual or
recurrent tumor
Complication of
thyroidectomy
Hemorrhage
Laryngeal edema
wound infection
Signs of hypocalcaemia
perioral numbness (1st)
Chvostek sign: It refers to an abnormal reaction
to the stimulation of thefacial nerve
Trousseau sign (when taking blood pressure)
Carpal spasm
References
Up to date
Browses introduction
THANK YOU