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Title: Endocrinology overview
Description: Layout of all of the main endocrine conditions: Diabetes Thyroid Parathyroid Adrenals Pituitary - Growth hormone, Prolactin, ADH Laid out comparing hyper and hypo state (description, cause, presentation, diagnosis and management) Written by final year medical student, for other medical students, biology students, nurses, health science students, and anyone with an interest! Really easy to understand, and gives you everything you need to know!

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HYPER-­‐  

HYPO-­‐  

Glucose  -­‐  DIABETES  
Description  
Metabolic  disorder  of  multiple  aetiology  
characterized  by  chronic  hyperglycaemia,  
disturbances  in  other  macronutrients  resulting  
from  defects  in  insulin  secretion,  action  or  both  
 
 
TYPE  1  
TYPE  2  
Aetiology  
Autoimmune  beta  cell   Insulin  secretionê  
destruction  by  Auto  
+/-­‐  insulin  resistance  
é
Abs:  
Obesity  
-­‐Insulin  
MODY  (AD  form  of  
-­‐Islet  cell  
T2DM)
-­‐Glutamic  acid  
Metabolic  syndrome  
decarboxylase  (GAD)  
Association  with  other  
AI  conditions
...
Polyuria  
complications  
2
...
Weight-­‐loss  
DKA  
Low  C-­‐peptide  
Diagnosis  

Management  

Complications  

PITUITARY    
Description  

Clinical  +  raised  venous  
glucose
...
 
Glucose  tolerance  test  
>11
...
g
...
   
Insulin  pump  
DAFNE  

Retinopathy  
Neuropathy  
Nephropathy  
Diabetic  foot  
Infections  

 

Oral  glucose  
tolerance  test  
Incidental  finding  

1st
...
Sulphonylurea,  
Glitazone,  DPP-­‐
IV  inhibitor  
3rd
...
 
Injectable  
insulin,  GLP-­‐1  
agonists  
Retinopathy  
Nephropathy  
Erectile  dysfunction  
Macro  vascular  
disease  
Cerebrovascular  
disease  
Diabetic  foot  
Infections  

Blood  glucose  <3
...
Plasma  hypoglycaemia  
2
...
Resolution  of  symptoms  with  treatment  
 

Quick  acting  CHO  followed  by  longer  acting  CHO  
-­‐  10-­‐20g  of  oral  glucose  
-­‐  if  unresponsive  75-­‐80ml  20%  glucose  
 
repeat  capillary  BM  after  10-­‐15  
 
Glucagon  1mg  IM  or  SC  

Hypoglycaemia  unawareness  
Coma  
Cognitive  impairment  

Failure  of  anterior  pituitary
...
 Loss  of  axis  in  the  same  order:  
1
...
LH  
3
...
ACTH  
5
...
Prolactin  and  ADH  

 

HYPER-­‐  

HYPO-­‐  

Aetiology  

 

Management  

 

Tumours  
Radiotherapy  
Infarction/haemorrhage  (apoplexy)  
Trauma  
Hormone  replacement  therapy:  
ACTH  –  hydrocortisone  
TSH  –  thyroxine  
FSH/LH  –  testosterone/oestrogen  
GH  –  Growth  hormones  

Prolactin  
Aetiology  

Prolactinoma  (macro  <1cm)  
Physiological  –  lactation  and  pregnancy  
Drugs  that  inhibit  dopamine  
(Metoclopramide/Haloperidol)  
Stalk  effect  (lack  of  inhibitory  dopamine)  
Presentation  
Galactorrhoea  
Headaches  
Visual  field  defect  (mass  effect)  
Amenorrhoea/erectile  dysfunction  
Diagnosis  
Serum  prolactin  >6000  (N<500)  
Other  endocrine  function  (TFTs,  Cortisol)  
Visual  fields  and  acuity  (monitoring  of  
prolactinoma  in  pregnancy)  
MRI  pituitary  
 
Management  
Dopamine  Agonists  (cabergaline)  
Surgery  
 
Anti-­‐Diuretic  Hormone  –  DIABETES  INSIPIDUS  
Description  
 

Aetiology  

 

Presentation  

 

Diagnosis  

 

 

 

 

 

Passage  of  large  volumes  
...
 Can  be:  
a) Cranial  
b) Nephrogenic  
 
Cranial  
Nephrogenic  
Idiopathic  
Inherited  
Congenital  
Metabolic  –  low  K+,  high  
Pituitary  Tumour  
Ca2+  
Trauma  
Drugs  –  lithium  
Infiltration  -­‐  Sarcoid  
Chronic  renal  disease  
Vascular  -­‐  heamorrhage   Post  obstructive  
Infection  –  
uropathy  
meningoencephalitis  
Polyuria  
Polydipsia  
Dehydration  
Hypernatremia  
8  hour  water  deprivation  test  –  assess  ability  to  
concentrate  urine  with  ADH
...
 
N  –  Urine  osmolality  >600  after  8  hours  
Cranial  DI  –  Urine  Osmolality  >600  after  
desmopressin  
Nephrogenic  DI  –  No  increase  in  Urine  Osmolality  
after  desmopressin  
 
MRI  pituitary  
Anterior  pituitary  function  

 

HYPER-­‐  

HYPO-­‐  

 

Management  

 

Cranial  
Treat  underlying  cause  
ADH  analogues  
(desmomelt  tabs)  
 

Nephrogenic  
Treat  underlying  cause  
Bendroflumethiazide  
NSAIDs  

Growth  Hormone  -­‐  ACROMEGALY  
Aetiology  
GH  secreting  pituitary  tumour  
Presentation  
Growth  of  hands,  jaw  and  feet  
Coarsening  of  face  
Change  in  facial  features  –  macroglossia,  
widening  of  teeth  
Obstructive  sleep  apnoea  
Cardiomyopathy  
Carpel  tunnel  (50%)  
Headache  
Sweating  
Complications  
Impaired  glucose  tolerance  
Hypertension  
LVH,  Cardiomyopathy,  Arrhythmias  
Increased  risk  of  colon  cancer  
Diagnosis  
Glucose  tolerance  test  
Glucose  should  suppress  GH  
IGF  -­‐1  
MRI  pituitary  
Visual  fields  and  acuity  
st
Management  
1  line  surgery  
Somatostatin  analogues  –  octeratide  
GH  receptor  agonists  –  pegvisomant  
Radiotherapy  
THYROID  
Aetiology  
Graves  disease  (AI)  
Toxic  multi-­‐nodular  goitre  
Toxic  adenoma  
Ectopic  thyroid  tissue  
Exogenous  –  iodine  excess,  levothyroxine  
excess  
TSH  secreting  adenoma  
Amiodarone  induced  (inhibits  conversion  of  t3-­‐
>t4)  
Presentation  
Weight  loss  
Graves  disease:  
Irritability  
Thyroid  eye  disease  –  
Diarrhoea  
exophthalmos,  opthalmoplegia,  
Tremor  
lid  retraction  and  lid  lag  
Anxiety  
Pretibial  myxoedema  
Heat  
Thyroid  Acropachy  
intolerance  
Enlarged  thyroid  
Tachycardia   Thyroid  bruit  
–  AF  
Goitre  
Brisk  
reflexes  
Diagnosis  
TFTs:  
1° TSHê  Free  T4  é
2° TSHé    Free  T4é
TRH  stimulation  test  
Auto  Abs:  
-­‐Anti-­‐TPO  
-­‐Anti-­‐thyroglobulin  
-­‐Anti-­‐TSH  receptor  
Thyroid  USS  
Iodine  uptake  scan  

 
 

 

 

 

Hashimoto’s  thyroiditis  (AI)  
Primary  Atrophic  Hypothyroidism  (AI)  
Iodine  deficiency  
Radioactive  iodine  treatmenet  
Cretinism  
Postpartum  
Thyroidectomy  
Medications  –  carbimazole,  amiodarone,  lithium  
Lethargy  
Decreased  mood  
Weight  gain  
Cold  intolerance  
Constipation  
Dementia  
Myalgia  
Bradycardia  
Slow  relaxing  reflexes  
Thin  hair  
 
TFTs:  
1° TSHé  Free  T4  ê
2° TSHê    Free  T4ê
Auto  Abs:  
-­‐Anti-­‐TPO  
-­‐Anti-­‐thyroglobulin  
-­‐Anti-­‐TSH  receptor  
 

 

HYPER-­‐  

HYPO-­‐  

Management  

B-­‐Blockers  (propranolol)  –  symptom  control  
Carbimazole  +/-­‐  levothyroxine  (block  and  
replace)  
Propylthiouracil  (in  pregnancy)  
Radioiodine  
Thyroidectomy  
Osteoporotic  fractures  
CV  disease  –  AF,  HF  
Thyrotoxic  storm  
-­‐fever  
-­‐tachycardia  
-­‐seizures    
-­‐V&D  

Lifelong  Levothyroxine  (t4)  

Primary  
Parathyroid  
adenoma  
Multi-­‐gland  
adenoma  or  
hyperplasia  
Parathyroid  
Carcinoma  
 
 

Iatrogenic  –  following  neck  surgery  
Congenital:  
-­‐DiGeorge  syndrome  
-­‐PTH  gene  defect  
-­‐AI  
Acquired:  
-­‐Neck  surgery  
-­‐Radiation  
-­‐Infiltration  (iron,  copper)  
-­‐magnesium  deficienct  

Complications  

PARATHYROID  
Aetiology  

Presentation  

Diagnosis  

Management  

Complications  

Secondary  
Hyperplasia  of  parathyroid  
gland  after  chronic  
hypocalcaemia  
Dialysis  dependant  CKD  
Vit  D  
deficiency/malabsorption  
 
PTHrP  producing  
squamous  cell  lung  CA,  
breast  CA  and  renal  cell  CA  
Secondary  
Renal  failure  
Skeletal  problems  
CV  complications  
Osteomalacia  

Primary  
Bones  –  pain,  
osteopenia  
Stones  -­‐  renal  
Groans  –  abdo  
pain,  n&v  
Thrones  –  
constipation,  
polyuria,  
haematuria  
Psychiatric  
overtones  –  
insomnia,  
cognitive  
dysfunction  
Serum  Ca2+  
Serum  Ca2+  (ê),  PTH  (é)  
(é),PTH  (é)  
 
PO42-­‐,  U+E  
X-­‐ray/CT  –  bone  
damage  
Acute  
IV  fluids  
Loop  diuretic  
Calcitonin  
Bisphosphonate  (pamidronate)  
Corticosteroids  (vit  D  intoxication)  
 
Long  term  
Surveillance  –  serum  Ca2+  and  creatinine  
Annual  DEXA  scan  
Surgery  
Cinacalcet  
Bisphonphonates  
HRT  
Hypoparathyroidism  
Recurrant  laryngeal  nerve  damage  

Pregnancy:  
-­‐Eclampsia  
-­‐Anaemia  
-­‐Low  birthweight  

Symptoms  of  hypocalcaemia  
Muscle  pain  
Bone  pain  
Abdo  pain  
Paraesthesia  of  face,  fingers  and  toes  
Facial  twitching  
Corpopedal  spasm  
Stridor  
Convulsions    
Syncope  

Serum  Ca2+,  PO42-­‐,  U+E  
PTH  
Thyroid  AutoAbs  
 
IV  calcium  
Increase  dietary  calcium  
Calcium  and  D3  supplements  
PTH  replacement  

Laryngospasm  
Neuromuscular  irritability  

QT  interval  changes  
 

HYPER-­‐  

HYPO-­‐  

ADRENALS  
Aetiology  

 

Presentation  

 

Diagnosis  

 

Management  

 

Primary  adrenal  insufficiency  
Addisons  Disease  (AI)  
Congenital  adrenal  hyperplasia  
Adrenal  TB/malignancy  
 
Secondary  adrenal  insufficiency  
Iatrogenic  –  long  term  suppression  from  exogenous  
steroid  use  
Anorexia  
Skin  pigmentation  (buccal/palmar  creases)  
Fatigue/lethargy  
Emotional  
Dizzy  
Diarrhoea  and  vomiting  
Postural  hypotension  
Addisonian  crisis  -­‐  shock  
Bloods:  NA+ê  K+  é low  BM,  uraemia,  Ca2+é  
Short  SynACTHen  test  
-­‐cortisol  should  remain  <550  
ACTH  levels  ééé
Renin  éé aldosterone  levels  
Adrenal  Auto  Abs:  
-­‐21  hydroxylase  adrenal  auto  Abs  
Acute  
100mg  IV  hydrocortisone  
IV  fluids  
Monitor  BM  
Blood,  urine,  sputum  C+S  
 
Long  term  
5-­‐10mg  oral  hydrocortisone  
Education:  
-­‐sick  days  
-­‐IM  hydrocortisone  if  vomiting  
-­‐steroid  warning  card  

Cortisol  –  CUSHINGS  SYNDROME  
Aetiology  
ACTH  Dependant  
Cushings  Disease  –  ACTH  producing  pituitary  
adenoma  
Ectopic  ACTH  production  –  SCLC,  carcinoid  
tumours  
Ectopic  CRF  production  –  medullary  thyroid  and  
prostate  CA  
 
ACTH  Independent  
Adrenal  adenoma  
Adrenal  nodular  hyperplasia  
Iatrogenic  –  exogenous  steroids  
Presentation  
Easy  bruising  
Facial  plethora  
Striae  
Proximal  myopathy  
 
Buffalo  hump  
Euphoria  
Hypertension  
Osteoporosis  
Poor  wound  healing  
Obesity  

 

 

Thin  skin  
 

HYPER-­‐  

HYPO-­‐  

Diagnosis  

1
...
 Establish  source  of  cortisol  excess  
Plasma  ACTH  
CRH  suppression  test  
CT  pituitary  
Petrosal  sinus  sampling  (gradient  >3  =  pituitary  
driven)  
Treat  underlying  cause  
Surgery  
Radiotherapy  
CV  mortality  
Osteoporosis  
Hypertension  

 

Management  

Complications  

Aldosterone  
Description  

Production  od  aldosterone  independent  of  
RAAS,  causing  increased  Na+  and  water  
retention  
Aetiology  
Aldosterone  producing  adenoma  (Conns  
 
syndrome)  
Bilateral  adrenocortical  hyperplasia  
Adrenal  Carcinoma  
Presentation  
Hypokalaemia  
Weakness  
Cramps  
Paraesthesia  
Polyuria  
Polydipsia  
Hypertension    
Diagnosis  
Bloods:  U+E  
Renin/aldosterone  ratio  
CT/MRI  adrenals  
Management  
Laproscopic  adrenalectomy  
-­‐4  weeks  pre-­‐op  spironolactone  (BP  and  K+  
control)  
Spironalactone  
Catecholamine  -­‐  PHAEOCHROMOCYTOMA  
Aetiology  
Catecholamine  producing  tumour  of  chromaffin  
cells  in  adrenal  medulla
...
Episodic  headache  
2
...
Tachycardia  
Hypertension  
Diagnosis  
Bloods:  FBC  
Plasma  catecholamines  
24hr  free  urinary  catecholamines  
Clonidine  suppression  test  

 

 

 

 

 

 

 

 

 

 

CT/MRI  adrenals  
 

HYPER-­‐  

HYPO-­‐  

Management  

Surgery  
-­‐alpha  and  beta  blockade  to  avoid  crisis  from  
unopposed  alpha  stimulation  
Long  term  BP  control  on  follow  up  

 

 


Title: Endocrinology overview
Description: Layout of all of the main endocrine conditions: Diabetes Thyroid Parathyroid Adrenals Pituitary - Growth hormone, Prolactin, ADH Laid out comparing hyper and hypo state (description, cause, presentation, diagnosis and management) Written by final year medical student, for other medical students, biology students, nurses, health science students, and anyone with an interest! Really easy to understand, and gives you everything you need to know!