11.03.2017 Views

DR Medhat MRCP

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

DIABETES INSIPIDUS (DI)<br />

- Polyuria ( > 50ml/kg/day [> 3L urine /day in 60 kg patient) ) due to either deficient or<br />

inefficient ADH.<br />

Aetiology of polyuria :<br />

Deficient ADH Inefficient ADH inappropriate water intake<br />

Cranial (hypothalamic)<br />

DI<br />

Nephrogenic DI<br />

Dyspogenic DI<br />

- Primary:<br />

1. Idiopathic (+++). 1. Idiopathic. 1. 1ry (psychogenic)<br />

2. Genetic : 2. Genetic : polydepsia.<br />

- DIDMOAD - X-linked recessive<br />

- Autosomal dominant. - Autosomal dom.<br />

- Autosomal recessive - Autosomal recessive<br />

- Secondary :<br />

1. Trauma (head injury) 1. Tubulo-interstitial dis.<br />

2. Tumour (craniopharyngioma) - Obstructive uropathy.<br />

3. Pituitary surgery. - Pyelonephritis.<br />

4. Histiocytosis X, TB, Sarcoid. - Sickle cell disease.<br />

2. Hypercalcaemia.<br />

3. Hypokalaemia<br />

4. Drugs (lithium)<br />

(Dmeclocycline)<br />

DIDMOAD syndrome = DI + DM +Optic atrophy + Deafness<br />

Also known as (Wolfarm`s syndrome)<br />

Clinical picture :<br />

1) Polyuria (> 3L /day) / polydipsia by day & night :<br />

- If the patient can sleep deeply for continuous 8 hrs , diagnosis of cranial<br />

& nephrogenic DI is unlikely.<br />

2) Dehydration .<br />

3) C/P of the cause e.g visual disturbance + headache if pituitary tumour<br />

compressing the optic chiasma.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!