1. Surgical diseases of the adrenal gland Flashcards
Height of adrenals
T12
Arterial supply
- Superior suprarenal a (← inferior phrenic a.)
- Middle suprarenal a. (← abdominal aorta)
- Inferior suprarenal a. (← renal a.)
Adrenalectomy indications
Tumors less than 4 cm should be monitored clinically and radiologically.
Tumors greater than 6 cm should be surgically removed.
Types of adrenalectomies
- Retroperitoneal: small tumors, patient face down
- Transabdominal: greater tumors and pediatrics
- Laparoscopic: small tumors
Surgical treatment of Cushing syndrome
- Pituitary → transsphenoidal resection
- Ectopic ACTH → resection of the primary lesion, if possible (often not possible as it is SCLC)
- Primary adrenal causes → removal of the adrenal gland containing the tumor
perioperative and postoperative considerations for primary Cushings patients
glucocorticoid replacement is given both pre- and post-op, as the pituitary-adrenal axis is suppressed
Conn syndrome - primary hyperaldosteronism indication
Surgery only happen in case of an aldosterone-producing adrenal adenoma (APA), which account for 67% of cases
Conn syndrome surgical approaches
Posterior or laprascopic approach
Pharmacological conciderations for Conn syndrome patients that has undergone surgery
The patient should be treated with spironolactone preoperatively for 2 to 3 weeks to control blood pressure and to correct hypokalemia
pheochromocytoma surgery
use “no touch” technique and early ligation of vein during operation
Adrenocortical Carcinoma
Complete surgical removal = only cure