Endocrinology
Pituitary Tumours
Endocrine vs local effects
Local effects: CNS + visual fields (optic chiasm compressionbitemporal hemianopia)+ headache
Prolactinoma
Most common pituitary tumour. Usually a microadenoma i.e. <1cm. Most are sporadic; also MEN1. Of lactotroph cells. P
PC: oligo/amenorrhea, galactorrhoea, decreased libido and fertility, erectile dysfunction
Ix: prolactin serum level. MRI pituitary
Mx: Mainstay is medical. Ergot dopamine agonists e.g. cabergoline (need an echocardiogram with this as it leads to valve disease)
Differential Dx: metaclopramide, domperidone, haloperidol, pregnancy/lactation, hypothyroidism, PCOS, CRF
Non-functioning pituitary adenoma
Second commonest pituitary tumour
PC: mass effects and/or hypopituitarism; rarely, pituitary apoplexy (bleed into pituitary gland, differential diagnosis of SAH)
Mx: monitor with annual MRI. Replace hormones. Transphenoidal pituitary resection, radiotherapy.
Hypopituitarism
PC: Weight loss/gain; lethargy; hypotension; oligo/amenorrhoea; decreased libido and fertility; thirst, polyuria, polydipsia
Biochem: Often done in 1 blood test:
IGF1
Prolactin
LF, FSH
TSH, T4, T3
9am testosterone/oestradiol
9am cortisol
Urine and plasma osmolalities
U & Es (hyponatraemia in SIADH)
Mx: Replace hormones in this order: Hydrocortisone; levothyroxine; sex hormones; GH replacement. If there is posterior hypopituitarism, treat diabetes insipidus with desmopressin.
Acromegaly
Anterior pituitary somatotroph cells, majority spontaneous, macroadenomas, in MEN1 or FIPA syndromes.
PC:
Musculoskeletal: increased interdental space, frontal bossing, prognathism, carpal tunnel syndrome, osteoarthritis, soft tissue swelling, macroglossia
Respiratory: sleep apnoea
Metabolic: diabetes mellitus/impaired glucose tolerance
Cardio: hypertension, LVH
Nervous: pituitary tumour effects, carpal tunnel syndrome, diabetic polyneuropathy, nerve compression elsewhere e.g. facial nerve through temporal petrous bone
Gastrointestinal: colonic polypsmalignancy
Dx: random IGF1 level high. Random GH levels are not useful. Oral glucose tolerance test shows no suppression of GH.
Mx: transphenoidal pituitary resection. If large, give somatostatin analogue or radiotherapy.
Cushing’s Syndrome
Microadenoma of corticotroph cells of anterior pituitary true Cushing’s Disease
PC:
Skin: acne, hirsutism, striae, thin skinbruising
Metabolic: centripetal obesity, interscapular and supraclavicular fat pads, ‘buffalo hump’, ‘moon face’, impaired glucose tolerance
Cardio: hypertension
Musculoskeletal: proximal myopathy, osteoporosis
Dx: May not see microadenoma on MRI pituitary. No suppression of cortisol on low dose dexamethasone test. Then do a high dose dexamethasone test to if CRH is inappropriately high too (for hypothalamic CRH production). Can do inferior petrosal sinus sampling to lateralise the tumour prior to surgery.
Mx: Surgery. Fails: more surgery. Bilateral adrenalectomy if severe (Nelson’s Syndrome: accelerated growth of ACTH-cells due to no negative feedback from circulating cortisol)
Adrenal Cushing’s
An adrenal adenoma or carcinoma produces corticosteroid. ACTH is low.
Dx: Failure to suppress on low dose dexamethasone and ACTH is low.
Mx: Adrenalectomy and medical cortisol-producing blockers.
Risks: Increased risk of PE, DVT, and overwhelming infection.
PCOS
To diagnose, need two out of three of: oligo/amenorrhoea; hyperandrogenism; polycystic ovaries on USS. Exclude Cushing’s, CAH, pituitary adenoma, testosterone-producing tumours.
Mx: lose weight, metformin, Dianette, androgen receptor blocker (spironolactone) or androgen production blocker (finasteride).
Hypercalcaemia
Causes:
Primary hyperparathyroidism
Malignancy: myeloma, bone metastases
Vitamin D intoxication
Familial hypocalciuric hypercalcaemia (urinary calcium is inappropriately low, thus causing the hypercalcaemia; in contrast, in primary hyperparathyroidism the urine calcium will be appropriately high)
Drugs: thiazides, Lithium, hyperthyroidism
Immobilisation
Tertiary hyperparathyroidism
Addison’s Disease
Primary hyperparathyroidism
Usually a solitary parathyroid adenoma. Sometimes parathyroid hyperplasia. Very rarely, a parathyroid cancer (in MEN1/2).
Biochem: Increased PTH, increased plasma calcium, increased urinary calcium
Ix: USS neck. Sestamibi scan. DEXA for osteoporosis. Exclude myeloma and bone metastases. Renal USS (?tertiary hyperparathyroidism)
Mx: surgery if symptomatic, or if asymptomatic with bad biochemistry, or if symptomatic with osteoporosis
Hyperthyroidism
Causes:
Graves’ disease
MNG
Toxic adenoma
Exogenous iodine or thyroxine (weight loss, iatrogenic)
Early phase thyroiditis esp. Hashimoto’s
Amiodarone (can also cause hypothyroidism)
Lithium
TSHoma of the pituitary (rare)
Thyroid storm
Choriocarcinomaincreased betahCG
Symptoms & Signs of all types of hyperthyroidism:
Irritability, anxiety
Psychosis
Fatigue, weakness
Tremor
Tachycardia and atrial fibrillation
Sweating and heat intolerance
Diarrhoea with or without steatorrhoea
Weight loss despite increased appetite OR increased appetite leads to weight gain
Urticaria/pruritis
Proximal myopathy
Gynaecomastia
Oligo/amenorrhoea
Decreased libido
Dilated pupils
Ophthalmoplegia
Lid lag
Conjunctival suffusion or irritation
Brisk reflexes
Palmar erythema
Goitre
Symptoms & Signs unique to Graves’ disease:
Exophthalamos
Acropachy
Pretibial myxoedema
Onycholysis
Signs of vitiligo, pernicious anaemia, Addison’s, T1DM
Graves’ Disease
Anti-TSH-receptor antibodies. A diffuse symmetrical goitre with a bruit. Acropachy and eye disease are unique. Associated with other autoimmune conditions esp. vitiligo, Addison’s, T1DM and pernicious anaemia. Young women.
Ix: TFTs. TSH-receptor antibodies. Thyroid uptake scan (scintogram) if antibody negative.
Mx: Carbimazole (drug rash, arthropathy, *agranulocytosisneutropaenic sepsis*. Propylthiouracil if pregnant. Beta-blockers (propanolol gives AF and tachycardia control but also decreases T4). If CHADS-VASc highanticoagulate if in AF. *Avoid amiodarone*. Grave’s often burns out after ~1yr so monitor. If they have relapsed (more likely in smokers) then can occur total thyroidectomy with levothyroxine for life.
Multinodular goitre
Second most common cause of hyperthyroidism. The goitre is large, irregular and nodular, one lobe usually predominates. This may not produce T4. Rarely, it can have malignant transformation.
PC: hyperthyroidism. Dysphagia, orthopnoea, SOB. Pemberton’s sign (cruel to do).
Ix: TFTs, Ct (?retrosternal extension). thyroid scintogram shows patchy uptake or a hotspot.
Mx: Radioactive iodine-131. Tracheal compressionthyroidectomy. Thyroidectomy in younger patients are there is a risk of thyroid cyst haemorrhage, acute tracheal haemorrhage, toxic/malignant change, and also for cosmesis.
Toxic thyroid adenoma
Benign follicular adenoma, 10% are ‘hot’ (produce T4). All solitary nodules need an FNA. Cytology cannot reliably distinguish from carcinomas, so remove them. A thyroid scintogram would show ‘cold spots’. After thyroid surgery, thyroglobulin (a marker of thyroid tissue) should be low; if it rises, there is cancer/thyroid regrowth.
Thyroid Storm
T4 is released during surgery leading to a thyrotoxicosis crisis with a 10% mortality. It can also be triggered be stress/infection/ablation.
PC: Rapid deterioration with tachycardia,...