Dr. Saleh M. Aldaqal MBBS, FRCSI,SBGS Assistant Professor and Consultant General And laparoscopic...

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Endocrine surgery Dr. Saleh M. Aldaqal MBBS, FRCSI,SBGS Assistant Professor and Consultant General And laparoscopic Surgery(france), Department of Surgery, Faculty of Medicine, King Abdulaziz University.

Transcript of Dr. Saleh M. Aldaqal MBBS, FRCSI,SBGS Assistant Professor and Consultant General And laparoscopic...

Endocrine surgery

Dr. Saleh M. Aldaqal MBBS, FRCSI,SBGS

Assistant Professor and Consultant General And laparoscopic

Surgery(france), Department of Surgery, Faculty of

Medicine, King Abdulaziz University.www.dr-aldaqal.com

Endocrine surgeryParathyroid - hyper and hypo parathyroidismAdrenal tumors - cushing syndrome - conn`s disease - pheochromocytomas - adrenocortical carcinoma - incidentilenomaPancreatic endocrine tumorsCarcinoid tumors

ParathyroidSuperior parathy. 4 th branchial pouchInferior parathy. 3 rd branchial pouch (

50% ectopic)90% 4 glands, 10% 5-6 glands.Both receive blood supply from inferior

thyroid artery.Direct feedback by Ca level, no pituitaty

control.PTH has direct effect on bone ( osteoclast)

and kidneys ( tubular reabsorption) and indirect effect on the GIT ( renal vitam. D ).

Hyper parathyrodismPrimary : due to disease in the gland as adenoma

(80%), hyperplasia ( 15%), carcinoma (5%) ( high ca. and PTH ) treatment : surgery

Secondary : compensatory response to hypoca. - CRF ( hyperphosphatemia, reduction in vitam. D ) - intestinal malabsorption syndrom ( ca. level at lower normal, high PTH ) treatment : calcium, vitam. D, phosphate binder Indication of surgery : sever renal osteodystrophy

Hyper parathyroidismTertiary : - long standing secondary

hyperparathyroidism lead to autonomous hyperfuncion of the gland.

- high PTH, high normal to elevated ca. level. - 10% required surgery. - indication of surgery : - persistant hyperca. And elevated PTH

with normal renal function -extensive soft tissue calcification with tumoral calcinosis -calciphylaxis

Hypo parathyroidism Secondary to thyroidictomy90% dut to ischemia to the gland10% accidental removal of the glandSigns and symptomsTreatment asymptomatic, mild symptoms, sever

symptoms

Adrenal gland80% cortex - zona glomerulosa…..aldosteron

(mineralocorticoid) - zona fasciculata, reticularis ….cortison,

androgen (glucocorticoid) under ACTH control

20% medulla - adrenalin, noradrenalin

Normal Anatomy, Abdominal-pelvic CT

Liver Spleen

Inferior vena cava

aorta

Stomach

Vertebra

Ribs

Vertebra

Left kidney

Right kidney

Left portal vein

Left adrenal

Cushing syndromeDefenition Causes : - 90% iatroginc exogenous - 10% endogenous ( 70% pituitary adenoma, 29% adrenal

causes, 1% ectopic production due to carcinoma as ca. lung)

Adrenal causes : most commonly due to adenoma, followed by

carcinoma and rarly due to hyperpasia.

Cushing syndromeDiagnosis : - 24 h urinary free cortisol - to confirm the diagnosis , low dose

dexamethasone suppression test. - then ACTH level, if low, adrenal causes - if ACTH level high, then high dose

dexamethasone suppression test ( pituitary or ectopic ).

Conn`s disease ( primary hyperaldosteronism)

Aldosteron secretion is under control of renin-angiotensin system, serum potassium.

Sustained hypertension , Hypokalemia.

95% adrenal adenoma ( surgical)

5% adrenal hyperplasia (medical )

Pheochromocytomas Adrenal medulla10% tumor - 10% bilateral - 10% malignant - 10% extra adrenal ( paraganglia cells in

abdomen, carotid body, urinary bladder) - younger than 20 years of age - 10% MEN II

Pheochromocytomas Symptoms : headache, paroxysmal hypertensive

episode, palpitations, sweating..)Diagnosis - 24 h urinary catecholamines and metabolites ( metanephrines, VMA ) - CT- scan - MIBG isotop scan ( monoiodobenzylguanidine )Treatment : surgical - pre operative preparation with alph-

blocker as phenoxybenzamine , fluid…

Carcinoid tumorArise from neural crest cells.Site : - GIT : any site, most common is appendix,

ileum, rectum. - extraintestinal : bronchus and ovary.Prognosis depend on the size ; < 1 cm 20-

30% L.N metastasis. > 2 cm 80% L.N metastasis.

Lead to extensive fibrosis, fixation and kinking of the bowel.

Carcinoid tumorCan lead to carcinoid syndrome. - flushing, diarrhea, asthma, valvular heart

disease. - secret serotonin. - diagnosis : 24h urinary 5-HIAA - developed when there is extensive liver

metastasis, or extra intestinal tumor. - treatment : surgery, somatostatin

Pancreatic endocrine tumorInsulinomaWhipple`s triad - symtoms of fasting hypoglcemia. - fasting hypoglycemia < 50 mg/dl. - relieved by glucose administration.Single, benign tumor.Treatment : surgical

Gastrinoma Zollinger-Ellison syndrom.

Increase secretion of gastrin.

recuurant peptic ulcer and diarrhea.

Could associated with MEN I.

Glucagon-secreting tumor

DiabetsAnemiaWeight lossDVTCutaneous lesion ( necrolytic migratory

erythema)

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