endocrine system

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ADRENAL AND OTHER ENDOCRINE SYSTEM A OVERVIEW Dr Saravanakumar

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Page 1: Endocrine system

ADRENAL AND OTHER ENDOCRINE SYSTEM

A OVERVIEW

Dr Saravanakumar

Page 2: Endocrine system

Major endocrine systems in the body

Thyroid gland Parathyroid , calcitonin Pancreas Adrenal gland Pituitary gland The gonads Others Kidney , heart , pineal gland

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Adrenal gland - Anatomy

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Function

Adrenal medulla - secretes adrenalin , nor adrenalin , dopamine

Adrenal cortex - steroid hormones 1. mineralocorticoids- aldosterone 2. glucocorticoids –cortisol , corticosterone3. sex hormones – DHEA ,androstenedione

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Incidentaloma Definition Incidentaloma is an adrenal mass,

detected incidentally by imaging studies conducted for other reasons.

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Prevalence -incidentalomas

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Imaging study – CT and MRI

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TREATMENT

Hypertension , hypokalemia , suppressed reninactivity , female predominanceLAB tests and imaging aid the diagnosis

TREATMENT Spironolatone,Anti Hypertensive'ssurgery

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Cushing's syndrome ACTH Dependent

1) Pituitary adenoma – Cushing's disease 2) ACTH Secreting tumours – small cell lung

Ca,foregut carcinoid ,pancreatic Neuroendocrine tumours , medullary Ca thyroid

ACTH independent – adrenal tumours

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Treatment Medical therapy

with metyrapone or ketoconazole

trans-sphenoidal resection or radiotherapy

Adrenalectomy- unilateral or bilateral

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Adrenal carcinoma Primary – very rare Bimodal age

distribution, female predominance

Poor prognosis Difficulty in diagnosis 60 % Cushing's synd. Surgery followed by

chemo and radiotherapy

Secondary breast, lung, renal,

gastric, pancreatic, ovarian and colorectal cancer

Treat the primary

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Disorders of adrenal medulla

Pheochromocytoma Paraganglioma

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Pheochromocytoma Pheochromocytoma is known as the ’10 per

cent tumour’ as 10 per cent of tumours are inherited, 10 per cent are extra-adrenal, 10 per cent are malignant, 10 per cent are bilateral and 10 per cent occur in children

Hereditary Pheochromocytoma -Multiple endocrine neoplasia type 2 (MEN 2),Familial paraganglioma (PG) syndrome, von Hippel–Lindau (VHL) syndrome, Neurofibromatosis (NF) type 1

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SWISS CHEESE CONFIGURATION

IN CT123I-MIBG

(metaiodobenzylguanidine)

single-photon emission computed tomography

(SPECT)

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MANAGEMENT

To start with α-blocker (phenoxy benzamine)

Add β blocker if necessary Plan for surgery Yearly lifelong follow up

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Other tumours 1) Neuroblastoma 2) Ganglioneuroma