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Clinical Surgery
OVERVIEW
• Thyroiditis
• Anaplastic Ca
o Pain is referred to the ear if it infiltrates surrounding structures
• Bleeding into a cyst1:809 or a necrotic nodule in a multinodular goitre1:807
Clinical Surgery
A 30 year old female labourer presents with a painless lump at the lower neck anteriorly for the past 1 and ½ years. It moves up with swallowing. It has
slowly progressively increased in size. She is clinically hyperthyroid, but there is no evidence of compressive symptoms or malignant features.
What is the most likely diagnosis?
Thyrotoxicosis/ Hyperthyroid
Introduction6:722 Graves’ Vs. Plummer’s
• Thyrotoxicosis
o Symptoms and signs of increased metabolic rate and
Graves' Disease6:726,727 Plummer’s Disease6:728
sympathetic activity due to increased amount of thyroid
hormones • Immunological disorder • In long standing multinodular
• Hyperthyroidism • TSI: Thyroid stimulating goiter
o Syndrome resulting from hyperactivity of thyroid gland Immunoglobulin (IgG) • One or more of the nodules
which produce excess hormones o Previously known as become toxic
• Any age Long Acting Thyroid • Middle aged female
• Female: Male = 8:1 Stimulants (LATS)5 • Late onset
o All types of simple goitre are common in the females owing • Diffuse hyperplasia of the gland • Eye signs are rare
to the presence of oestrogen receptors in thyroid tissue1:806 • Young women: Age 20 – 40 • No dermopathy
years • Dominant symptoms
Causes6:722 • Strong family history o Cardiovascular
Associated With Hyperthyroidism • Gradual or abrupt onset
• Primary • Dominant symptoms
o Graves: Diffuse goiter o Eye signs (Infiltrative
§ Thyroid stimulating antibodies (IgG) ophthalmopathy)
o Plummer’s disease: Toxic MNG o Hypermetabolic
o Toxic adenoma: Solitary nodule symptoms
• Secondary • Thyroid dermopathy seen in a
o TSH-secreting pituitary adenoma (rare) minority
• Minimal cardiovascular problems
Not Associated With Hyperthyroidism
• Transient thyrotoxicosis
o Thyroiditis: Large amount of preformed hormones is
released after the destruction of follicles
• Struma ovari
o Struma ovarii is a rare ovarian teratoma defined by the
presence of thyroid tissue comprising more than 50% of the
overall mass
• Factitious thyrotoxicosis: Exogenous intake of thyroid hormones
Clinical Surgery
Thyroid Status
Clinical Surgery
How will you treat this patient?
Treatment1:812
Clinical Surgery
What are the differences of each drug?
Drugs
Clinical Surgery
Radiodioactive Iodine
• I-131 administered orally as sodium iodide in solution or a capsule.5
Clinical Surgery
Surgery
As the house officer in the ward, how will you prepare this patient for surgery?
Clinical Surgery
The patient returns to the ward following total thyroidectomy. You are the
receiving house officer. What will you do?
• Receive the patient
• Monitor: BP. PR, RR, UOP
• Keep propped up (Reduce oedema/ swelling of the site) and give steam
inhalation
• Observe for difficulty in breathing, stridor and post-operative complications
• Adequate pain relief
• IV fluids followed by oral feeding once patient regained consciousness
• Early mobilization
Clinical Surgery
6 hours after the patient was brought to the ward, the nurse calls and informs you that the patient is dyspnoic with noisy in breathing.
What is the most likely diagnosis? What is the cause?
Causes
How do you treat stridor? You are the house officer at a surgical clinic, how would you assess and
Treatment1:815 manage a patient coming to the clinic after thyroidectomy?
• Prop up • I would assess his general well-being, complications of surgery and plan
o Makes breathing easier future management
• 100 % O2 via face mask • General
• Monitor o Relief of symptoms
o RR, PR, BP, SaO2 • Surgical complications
o Level of consciousness o Pain
• Look out for cyanosis o Swelling
• Inform seniors, anesthetist, theatre o Difficulty in breathing/ noisy breathing
• Find and treat the underlying cause o Features of hypocalcemia: Perioral or peripheral numbness,
• Find and treat the underlying cause tingling, spasm
o Tracheomalcia/Bilateral, partial RLN damage: Re-intubate o Features of hypothyroidism: Lethargy, loss of appetitite,
o Haematoma: Remove sutures in the ward to release some constipation
pressure and evacuate the haematoma in the theatre1:815 • Further management
o Laryngeal odema: IV dexamethasone and re-intubate o Trace and review histology report
o Hypocalcaemia: IV 10% Calcium Gluconate 10ml, monitor o Do thyroid function tests and serum calcium as necessary and
calcium levels decide on replacement therapy
o Give pain relief as necessary
Clinical Surgery
A 45 year old housewife, with a family history thyroid malignancy, presented with a painless thyroid enlargement for the past 6 months. It has rapidly increased in
size, with hoarseness of voice noticed since 2 weeks back.
What is the most likely diagnosis?
THYROID TUMOURS
Introduction 1:816
Benign
• Follicular adenoma
Malignant
• Primary malignancies
o Follicular epithelial cells
§ Differentiated
• Follicular carcinoma
• Papillary carcinoma
§ Undifferentiated
• Anaplastic carcinoma
o Para-follicular ‘C’ cells
§ Medullary carcinoma
o Lymphoid cells
§ Lymphoma
• Secondary malignancies
o Metastatic
§ Kidney
§ Breast3:183
§ Lung3:183
§ Prostate3:183
o Local infiltration
§ Upper aero-digestive tract squamous cancer
Clinical Surgery
Clinical Features
2:416-418, 421, 422
Complications/ Metastasis4:240
• Cervical lymphadenopathy: Papillary Ca2:431
• Bone: Highly vascular
o Warm, pulsatile scalp lump: Follicular Ca1:818
Clinical Surgery
Investigations Staging 1:819
American Joint Committee on Cancer
o USS neck
o Solitary nodule or dominant nodule of MNG Tumour
o Look for USS features of malignancy • Tx: Primary cannot be assessed
• T0: No evidence of primary
• T1: Intrathyroidal tumour ≤2cm
• FNAC (if nodules are not classified as fully benign in USS) 1:808
o T1a: ≤1 cm
o T1b: >1 cm ≤2 cm
• Thyroid function tests • T2: Intrathyroidal tumour >2cm but ≤4 cm
• T3: Intrathyroidal tumour >4 cm or any tumour with minimal extrathyroid
extension
• CECT of neck and thorax • T4: Any size with extensive extra thyroidal extension
o LN involvement
o To assess extent of airway invasion1:803 Nodes
• Nx: Cannot be assessed
• MRI: Superior at determining the presence of prevertebral fascia • N0: No regional node metastases
invasion1:803 • N1: Regional node metastases
Metastases
• PET-CT scan: May be considered in recurrent thyroid cancer1:803
• Mx: Cannot be assessed
• M0: No metastases
• Radio isotope scan: I-131 • M1: Metastases present
o Cold nodule: 80% are benign1:804
• Thyroglobulin1:803
o As a baseline level
• Medullary cancer3:184
o Check serum calcium
o Exclude pheaochromocytoma
Clinical Surgery
Your patient has a malignant solitary nodule. What are the principals of treating this patient?
Thy2 • Thy2: Benign colloid nodule • 2 benign results 3-6months apart are needed for
confirmation of benign disease.
• ‘High-risk’ patients need a lobectomy
Thy4 • Thy4: Probably thyroid cancer/ suspicious • Surgery to be decided at MDT meeting
• Biopsy for a suspected lymphoma
Clinical Surgery
Treatment
1:819-821
Follow Up
• Serum thyroglobulin every 6 months
• Diagnostic radioiodine scan in 6 months
o If negative, in 1 year
• If these become positive, whole body radioiodine scan, CT, MRI, PET-
CT
Clinical Surgery
Thyroid Tumours 1:818-820, 4:254, 3:183
Papillary Carcinoma Follicular Carcinoma Anaplastic Cancer Medullary Ca
Introduction • Multifocal3:183 • Unifocal • Extremely aggressive • Sporadic: 80% Vs. Familial:20%
• Non-encapsulated • Encapsulated • 50% are inoperable at diagnosis • Associated with MEN syndrome
• Causes • Can occur in pre-existing MNG • Compressive symptoms + • Also secretes
o Radiation2:431 • High in endemic goitrous areas6:733 o 5HT (Serotonin), PG,
• Compressive symptoms are rare • Compressive symptoms + ACTH, VIP, Calcitonin,
• If < 1cm size, termed as • Hurthle cell cancers CEA
microcarcinoma o Variant of follicular • Can present with diarrhea (due
o Poorer prognosis to PG or 5HT
Cell of Origin • Follicular epithelial cells • Follicular epithelial cells • Follicular epithelial cells • Parafollicular ‘C’ cells
Frequency • 80% • 10% • 5% • 2.5%
Age • 20 – 40 years • 40 – 60 years • > 60 years • 30 – 60 years Familial form in
children and young adults
Sex • Female > Male • Female > Male • Female > Male • Female = Male
Local Spread • Local infiltration + • May infiltrate • Massively infiltrates • Slow growing
Lymphatic • Yes +++ • Less • Yes +++ • Yes +
Spread • Cervical LN
Blood Spread • Less • Yes +++ Skull, ribs, long bones, • Yes +++ • Yes +
lung
• Warm and pulsatile: Vascular
Prognosis • Excellent • Good • Poor: Almost all dead within 6 • Prognosis similar to follicular
• 5 year survival is 90% • 5 year survival is 65% months1:820 5:274
Clinical Surgery
A 70 year old retired teacher, with a family history of goiter, has presented with a painless thyroid enlargement which has been present for 20 years duration. It
has progressively increased in size and is associated with compressive features but no evidence of malignancy or altered thyroid status.
What is the most likely diagnosis?
Clinical Surgery
PRIMARY HYPERPARATHYROIDISM
Introduction1:825,826 Investigations1:826-828
• Common endocrine disease • Serum parathyroid hormone (PTH) level
• Postmenopausal women: 1:500 • Serum calcium and phosphate level
• F:M = 3:1
• Incidental finding of raised serum calcium Primary Secondary1:833 Tertiary1:835
• The only known risk factor is a history of prior neck irradiation
• Pathological features PTH High High High
o 85% have a single parathyroid adenoma
o Small tumours Ca2+ High Low or Normal High
o 15% have multigland hyperplasia
• More associated with PO43- Low High High
o Familial disease (e.g. MEN syndromes type 1 and 2A)
o Chronic ingestion of lithium Diagnosis (CKD, GI
• Parathyroid cancer as a cause of primary hyperparathyroidism is rare: <1% malabsorption,
Liver disease, Vit
D deficiency)
Clinical Features1:825
• High-resolution neck ultrasound may identify tumours.
Features of hypercalcaemia
“Stones, Bones, Moans, Groans and Thrones” • Sestamibi (radioisotope) scan: Accumulates in mitochondria which are
"Bones, stones, abdominal groans and psychiatric overtones" abundant in parathyroid cells
o Localize adenomas (accurate in 50%)
• Stones
o Allows a focused approach
o Calcium based renal stones, hypercalcuria
§ Minimally invasive parathyroidectomy
• Bones
o Aches/pains localized in large joints
Treatment
o Osteopenia/osteoporosis
• Hypercalcaemic crisis is defined as serum total calcium exceeding 3.5
• Moans: Psychological/psychiatric symptoms
mmol/L
o Lethargy/ Depressed mood
• Patient typically presents with acute confusion, abdominal pain, vomiting,
o Mild memory impairment
dehydration and anuria1:826
• Groans: Non-specific gastrointestinal symptoms
o Abdominal pain
Medical: Hypercalcaemic crisis1:826 Surgical1:829
o Constipation
o Peptic ulcers • Aggressive rehydration • Bilateral neck exploration
o Acute pancreatitis • Establish large calibre IV access • Minimally invasive
• Thrones • Monitor urine output parathyroidectomy
o Polyuria • Monitor central venous pressure
o Polydypsia • IV furosemide
o Nocturia
o Constipation
Clinical Surgery
Clinical Surgery