Hypophysectomy: Difference between revisions
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Latest revision as of 17:16, 22 March 2025
Hypophysectomy is a surgical procedure that involves the removal of the pituitary gland. This procedure is typically performed to treat tumors of the pituitary gland. The pituitary gland is a small, pea-sized organ located at the base of the brain, and it is responsible for producing various hormones that regulate critical body functions.
Indications[edit]
Hypophysectomy is primarily indicated for the treatment of pituitary tumors. These tumors can cause various symptoms, including headaches, vision problems, and hormonal imbalances. In some cases, pituitary tumors can be life-threatening. Other conditions that may necessitate a hypophysectomy include Cushing's disease, prolactinoma, and acromegaly.
Procedure[edit]
A hypophysectomy can be performed using different surgical approaches, depending on the size and location of the tumor. The most common approach is the transsphenoidal approach, where the surgeon accesses the pituitary gland through the nose and the sphenoid sinus. Another approach is the transcranial approach, where the surgeon accesses the pituitary gland through an incision in the scalp and a hole in the skull.
Risks and Complications[edit]
Like any surgical procedure, a hypophysectomy carries certain risks and potential complications. These may include infection, bleeding, cerebrospinal fluid leakage, and damage to surrounding structures. There is also a risk of hormonal imbalances following the procedure, which may require lifelong hormone replacement therapy.
Postoperative Care[edit]
After a hypophysectomy, patients are typically monitored in the hospital for several days. They may need to take hormone replacement medications to compensate for the loss of the pituitary gland. Regular follow-up appointments are necessary to monitor the patient's hormone levels and to check for any signs of tumor recurrence.


