The Medical and Surgical Management of Thyroid, Pituitary and Adrenal disorders Flashcards

1
Q

Endocrine glands

A

Ductless

Release a product into bloodstream for transport to target organs

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2
Q

Hormones

A

Chemical signals produced by endocrine glands

Affect target organs a distance from release site

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3
Q

Targets

Mechanism of interaction

A

Organs, tissues and cells capable of responding to hormone

Presence of receptor which binds to hormone

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4
Q

Thyroid gland
Physiology
Biochem
Why is it unique

A

Largest of all endocrine glands
Produces
- T4 and T3 which regulate basal metabolic rate
- calcitonin which regulates blood Ca2+ levels
Stores large amount of inactive hormone within extracellular follicles

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5
Q

Thyroid gland - surface anatomy

Where are parathyroids located

Which major vessels surround it

A

Shields anterior and lateral surfaces of lower respiratory tract
Between posterior border of thyroid gland and its sheath (2 on each side)
Internal jugular vein and common carotid lie postero-lateral

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6
Q

Measurement of thyroid hormone

Which types are important

A

Thyroxine - T4
Free triodothyronine - T3
Thyroid stimulating hormone - TSH

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7
Q

Autoimmune Hypothyroidism
3 causes and hormone concs
Do they produce goitre?

A

Primary failure of thyroid gland - less T3 and T4 but TSH up
Secondary failure to hypothalamic or pituitary failure - less T3, T4, less TSH (and or TRH)
Dietary iodine deficiency - less T3 and T4 but TSH XS

Goitre - Yes, No, Yes

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8
Q

Clinical features of hypothyroidism

A
Weight gain 
Lethargy 
Increased fatigue
Cold intolerance
Hair loss
Dry skin 
Deafness 
Muscle weakness
Facial puffiness
Goitre 
Bradycardia
Delayed reflexes
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9
Q

Causes of hypothyroidism

Primary

Secondary and tertiary

A
Dyshormonogenesis 
Iodine deficiency
Autoimmunity 
Post radioactive iodine
Post thyroidectomy 
Iodine excess
Pituitary tumours
Pituitary granulomas 
Empty sella 
Isolated TRH deficiency 
Hypothalamic disorders
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10
Q

Indications for hypothyroidism screening

Methods of investigation

A
Congenital hypothyroidism 
Tx for hyperthyroidism 
Neck irradiation 
Pituitary surgery/irradiation 
Lithium or amidoarone tx 

Thyroid fx test
thyroid antibodies
levothyroxine

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11
Q

Dental complications in hypothyroidism

A
Delayed eruption
Enamel hypoplasia 
macroglossia
Micrognathia
thick lips
Dysgeusia
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12
Q

Hyperthyroidism - causes
3 causes
Hormone concs
Goitre?

A

Abnormal thyroid stimulating immunoglobulin e.g Grave’s disease - XS T3 and T4 but less TSH

Secondary to XS hypothalamic or pituitary secretion - Increased T3 and T4, increased TSH and/or TRH

Hypersecreting thyroid tumour - increased T3 and T4, less TSH

No, yes, no (not in traditional sense)

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13
Q

Causes of hyperthyroidism

Common and rare

A
Autoimmune thyroid disease 
- graves
- postpartum thyroiditis 
Toxic nodular goitre 
Toxic adenoma - one nodule producing XS thyroid hormone 

Amiodarone induced
De Quervain’s thyroiditis
Thyrotroph adenoma
hCG hyperthyroidism

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14
Q

Clinical features of hyperthyroidism

A
Weight loss
Heat intolerance 
Anxiety 
Increased sweating and appetite 
Palpitations 
Loose bowels 
Goitre
Tremor 
Warm moist skin 
Tachycardia
Eye signs 
Thyroid murmur
Muscle weakness
Atrial fibrillation
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15
Q

Grave’s disease
Clinical features
Investigations

A
Diffuse goitre
Eye signs - diplopia, exophthalmos 
Myxoedema (swelling of skin) 
Vitiligo 
Family history of thyroid disease 

TSH receptor antibody checks
Thyroglobulin antibodies
Thyroid radioisotope

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16
Q

Mechanism of action of TSH receptors

A

TSH binds to receptor and regulatory protein is stimulated

Cascade reaction intracellularly

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17
Q

Treatment of hyperthyroidism

Side effects of medical tx

A

Medical - nausea, vomiting, leukopenia –> agranulocytosis, aplastic anaemia, drug fever and cholestatic jaundice

Surgical

Radioactive iodine

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18
Q

Dental complications of hyperthyroidism

A

Accelerated dental eruption
Mx or md osteoporosis due to increased turnover of bone
Increased caries risk
Periodontal disease
Increased sensitivity to epinephrine –> arrhythmias or palpitations
Surgery, oral infection + stress may trigger crises

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19
Q

Referral criteria for thyroid nodules

A
New onset
Increase in size 
Pain onset
Associated speech disturbance
Lymphadenopathy 
Patient/doctor concern
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20
Q

Pituitary disorders - causes

Investigations

A

Empty sella
Hormone XS
Hormone deficiency
Tumour mass effects - can affect optic chiasm and reduce periphery vision

Hormonal tests
If abnormal –> MRI of pituitary

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21
Q

Local effects of pituitary mass

A

Headaches
Visual field defects
CSF rhinorrhoea - can get fluid leakage via nasal cavity
Cranial nerve palsy and temporal lobe epilepsy

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22
Q

Hormone deficiency of GH

and Tx

A

Growth hormone

  • short stature
  • abnormal proportions
  • reduced muscle mass
  • poor QoL

Tx - growth hormone

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23
Q

Hormone deficiency of LH/FSH

Tx

LH and FSh usually feed back to GnRH to inhibit production

A

Luteinising hormone/follicle stimulating

  • hypogonadism
  • reduced sperm count
  • infertility
  • menstruation problems

Testosterone for males

Progesterone for females

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24
Q

Hormone deficiency of TSH

Tx

A

Thyrotropin stimulating hormone

Hypothyroidism

Levothyroxine

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25
Hormone deficiency of ACTH Tx
Adrenocorticotropic hormone - adrenal failure - decreased pigment hydrocortisone
26
Hormone deficiency of ADH Tx
Anti-diuretic hormone - diabetes insipidus - decreased water absorption therefore polyuria and polydipsia DDAVP
27
Hypopituitarism causes
``` Tumours Radiotherapy Trauma Infarction Infiltration of pituitary Infection of pituitary e.g syphilis Sheehan's syndrome (post partum pituitary necrosis) ```
28
Acromegaly
Pituitary disorder XS GH secretion 4/million per year equal sex incidence
29
Clinical features of acromegaly Head Other areas
``` Coarse facial features Enlarged supraorbital ridges Separation of teeth Prognathism Macroglossia ``` ``` Headaches Spade-like hands Joint pain XS sweating Hypertension Impaired glucose tolerance ```
30
Treatment of acromegaly
Investigations: IGF1, dynamic tests, MRI pituitary Surgical resection – Transphenoidal surgery, Transfacial Surgery - biochemical control 80% microadenomas 50% macro*more than 10mm* adenomas  Somatostatin analogues – 40% complete responders - inhibits GH production  Pegvisomant reduces IGF-1 to levels > 90% - growth hormone receptor antagonist - inhibitor  Radiotherapy in unsuccessful surgery
31
Dental complications of acromegaly
```  Jaw Malocclusion  Difficulty in speech due to macroglossia  Teeth mobility  Missing teeth  Teeth separation  Thickening of alveolar processes  Enlarged posterior roots  In 50% upper airways obstruction caused by pharyngeal hypertrophy and macroglossia with obstructive sleep apnoea. ```
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Adrenal disorders CAUSES OF CUSHING SYNDROME Adrenal tumour = XS Cortisol decreased ACTH Pituitary tumour = XS ACTH and XS cortisol
Cushing's syndrome XS glucocorticoids corticotropin releasing hormone released from hypothalamus --. ACTH release from pituitary ``` CORTISOL RELEASED ON A RHYTHM Pit tumour Adrenal tumour Ectopic ACTH tumour Iatrogenic ```
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Clinical features of Cushing's
``` Weight gain Menses problems Moon face Acne Bruising Glucose intolerance Hyper pigmentation Muscle weakness Plethora Hirsutism Oedema Can result from long term steroid use ```
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Management of Cushing's syndrome Investigations Treatment
Hormonal tests Radiological tests - MRI, CT chest and adrenal Surgery, drugs, radiotherapy
35
Disease involving adrenal insufficiency
Addison's disease
36
Causes of adrenal insufficiency Primary Secondary
``` Autoimmune Tuberculosis Fungal infections Adrenal haemorrhage Congenital adrenal hypoplasia Sarcoidosis Amyloidosis Metastatic neoplasia ``` After exogenous glucocorticoids After treatment for Cushing's (EXCESS ACTH) Hypothalamic or pituitary tumours
37
Clinical features of adrenal insufficiency
``` Weakness Skin and mucous membrane pigmentation Loss of weight, emaciation, anorexia, vomiting, diarrhoea Hypotension Salt craving - loss of salt in urine Hypoglycaemic episodes ```
38
Management of adrenal insufficiency Investigations Tx
Hormonal tests - measuring cortisol, ACTH and adrenal antibodies Radiological - MRI pituitary CT or MRI adrenals Tx - hydrocortisone replacement treatment
39
Primary adrenal insufficiency
Adrenal gland is insufficient and not producing enough cortisol ACTH will increase Pigmentation due to ACTH secreted with melanin stimulating hormone which binds to skin
40
Secondary adrenocortical insufficiency
Low ACTH therefore cortisol not stimulated
41
Glucocorticoid cover for dental procedures Need to prevent patient from undergoing steroid crisis
On treatment therapy e.g asthma, rheumatoid arthritis ◦ Prednisolone > 7.5mg ◦ Hydrocortisone > 30mg ◦ Dexamethasone > 0.75mg  On replacement therapy ◦ Addison’s e.g. Hydrocortisone 20/10mg - own production is not sufficient ◦ ACTH deficiency 10/5/5mg Simple Procedures - when giving LA : double dose one hour before surgery, double dose oral medication for 24 hours Major Procedures/GA: hydrocortisone 100mg im at induction and double dose oral medication for 24 hours
42
Surgery and other endocrine disorders
Hyperthyroidism Pheochromocytoma Cushing's - avoid infections and pathological fractures Refer to endocrinologist
43
Endocrine causes of hypertension
``` Primary aldosteronism Phaechromocytoma Acromegaly Cushing's syndrome Hypothyroidism Hyperthyroidism ```
44
Calcium homeostasis
10000mg excreted in kidney | 9800mg reabsorbed into body
45
Role of calcium
Ionised - cofactor in coagulation - skeletal mineralisation - membrane stabilisation -- neuronal conduction
46
Parathyroid hormone action
Kidney - increase Ca reabsorption - reduced phosphate reabsorption - increased hydroxylation of 25-oh bit D Bone - increased bone remodelling Gut - no direct effect - increased ca absorption
47
calcium homeostasis is
an example of negative feedback
48
Abnormalities in PTH
May be appropriate - to maintain calcium balance | May be inappropriate as it can cause calcium imbalance
49
Hypocalcaemia Low serum albumin
Low total serum calcium but NOT low ionised calcium e.g serum calcium = 2.08 mol/L corrected calcium = 2.28 mmol/L
50
Causes of hypocalcaemia
vit D deficiency Hypoparathyroidism – post surgery, radiation, autoimmune disease – Hereditary (Autosomal dominant hypocalcaemia) – Syndromes (Di George, HDR [hypopara, deafness, renal dysplasia] etc) – Infiltration (Wilson’s disease, haemochromatosis) Chronic renal failure Magnesium deficiency -> linked to vitamin D deficiency Pseudohypoparathyroidism Acute pancreatitis Multiple citrated blood transfusions
51
Consequences of hypocalcaemia
``` Parasthesia Muscle spasm - hands and feet, larynx and premature labour Seizures Basal ganglia classification Cataracts Dental hypoplasia ECG abnormalities ```
52
Signs of hypocalcaemia
* History of neck surgery * Presence of other autoimmune conditions * History of congenital defects and immunodeficiency * Family history to suggest genetic cause * Drug history e.g antiepileptics * Neck scar, candidiasis, vitiligo, generalized bronzing * Growth failure, hearing loss
53
Vit D deficiency
Calcium reduced
54
Decreased PTH -->
Decreased serum calcium
55
Management of hypocalcaemia Mild and severe
Mild - oral calcium supplements - cholecalciferol (active form) if vitamin D deficiency - post-thyroidectomy --> calcium supplements - hypomagnesaemia --> magnesium supplements
56
Causes of hypercalcaemia
``` • Malignancy – bone mets, myeloma, PTHrP, lymphoma • Primaryhyperparathyroidism • Thiazides • Thyrotoxocosis • Sarcoidosis • Familial hypocalciuric / benign hypercalcaemia • Immobilisation • Milk-alkali • Adrenal insufficiency • Phaeochromocytoma 90% ```
57
Symptoms of hypercalcaemia
* Thirst, polyuria * Nausea * Constipation * Confusion coma * Pancreatitis * Gastric ulcer * Renal stones * ECG abnormalities * Short QT
58
Hypercalcaemia - signs
* Confusion, hypotonia, hyporeflexic * Dehydration * Signs of malignancy (enlarged liver, clubbing, thyroid mass, breast lump, lymph nodes) * Faecal impaction * Irregular pulse (arrhythmia,
59
Approach to hypercalcaemia Low CA --> first thing to check is PTH - if PTH normal then urine test used
• Identify any drugs that may cause hypercalcaemia (thiazides, lithium, Vitamin D) • Identify whether presence of renal failure ? Tertiary hyperparathyroidism • Check serum PTH and if high or normal perform 24-hour urine calcium excretion (Urine Calcium/Urine Creatinine x Plasma Creatinine) * If PTH high or normal and urine calcium excretion > 0.01 mmol/l – Primary Hyperparathyroidism * If PTH high or normal and urine calcium excretion < 0.01 mmol/l – FHH * If PTH low or suppressed – exclude malignancy, hyperthyroidism, Addison’s, sarcoidosis, granulomatous disorders
60
Hypercalcaemia of malignancy
reduced bone resorption calcium reabsorption and calcium absorption from gut • About 20 to 30% of patients with cancer • 80% are due to bony metastases (breast, thyroid , kidney, lung, prostate) • 20% due to PTHrP release (others secrete Vitamin D, ectopic PTH) • Osteoclastic Hypercalcaemia
61
Consequences of primary hyperparathyroidism Management
• Bones – Osteitisfibrosacystica – Osteoporosis - erosions of bone - osteitis and cysts • Kidney stones • Psychic groans – confusion • Abdominal moans – Constipation – Acute pancreatitis Indications for surgery • Serum calcium > 0.25 mmol/l from upper limit • Creatinine clearance < 60 ml/min • T-score < -2.5 at any site and/or previous fragility fracture at spine, hip, radius, femoral neck • 24 hour urine calcium >400mg/day (>10mmol/day) • Nephrocalcinosis or nephrolithiasis • < 50 years
62
Tertiary hyperparathyroidism
Renal failure --> nodular hyperplasia and autonomy
63
Management of hypercalcaemia
• Intravenous fluids Normal 0.9% saline • Loop diuretic if risk of overload ONLY • Intravenous bisphosphonates e.g pamidronate, zoledronic acid (make sure PTH sample taken) • Corticosteroids e.g Vitamin D intoxication, sarcoidosis
64
SUMMARY
PTH controls calcium balance to keep serum calcium in a narrow normal range • High or low PTH may be appropriate or inappropriate • Symptoms and causes of calcium imbalance • Think about how changes affect the feedback loop