Introduction: Diabetes Insipidus (DI) is a common complication following pituitary surgery. It has been traditionally reported in the range of 5 to 15% after transsphenoidal resection of pituitary adenomas. Here we report our experience with Diabetes Insipidus following Endoscopic resection of pituitary adenomas. Methods: We retrospectively reviewed the Stanford University Pituitary Adenoma database. Between the years 2007 and 2012 we identified 183 patients who underwent endoscopic resection of pituitary adenomas by the senior author (G.R.H). In the early postoperative inpatient period DI was diagnosed on the basis of symptomatology, urine output, osmolality, and serum sodium levels. In the outpatient setting, DI was followed by symptomatology and serum sodium levels. …show more content…
The median age was 50 years (range: 18–89years). All had pathological confirmation of the diagnosis. The male to female ratio was 1:1.2. Nonfunctional pituitary adenomas represented 60% (109/183) of the tumors. Median follow-up was 36 months (range: 1week - 78 months). Three charts were missing DI follow-up data. The incidence of DI was 26% (47/180) in the early postoperative inpatient period (less than one week) and 9% (17/180) in long term follow-up. For Microadenomas, 21% (9/42) had DI in the early postop period and 9.5% (4/42) in long term follow-up. For Macroadenomas, 27% (38/138) had DI in the early postop period and 9.4% (13/138) in long term follow-up. Functional tumors and old age (>50 years) were associated with higher incidence of DI
After a few years, there was a tumor in her pituitary region. The tumor was secreting excessive amounts of growth hormone, casing symptoms to appear. She had enlarged hands and feet, coarsened, enlarged facial features, coarse, oily, thickened skin, and
your doctor may recommend surgery to completely remove the tumor. If tumor is present on pituitary gland the surgery will be performed by a neurosurgeon, procedure may be done through your nose canal. If tumor is found on adrenal gland, pancreas or lungs the surgeon will be able to remove it through standard surgery. After operation you may need to take a cortisol replacement medication to provide your body with the correct amount of cortisol you need. In most cases the replacement medication works out just fine and they can live a normal
Patient 4: Meredith B., Female age 38. She’s a lawyer/rep. With an annual income of $102,000. She has type one diabetes and is expected to live eight months without the procedure. Patient 5: Hiram Y., Male age 44.
This allows for more effective communication during teaching. The second intervention for this diagnosis is to supply education and instructions in Afghan language. This can be done with special software on the computer to translate for the patient. My evaluation will be done by having the interpreter determine if the patient understands the education by return demonstration of the glucose monitor and reciting the portions of one diabetic meal. Further evaluation will be done with ultrasound to check the growth of the
Cushing’s Syndrome is a disease that involves an excess of the Adrenocorticotropic hormone (ACTH) from the pituitary gland, most likely because of cancerous cells (Helm). This causes an excess of cortisol to be made in the adrenal gland which creates the symptoms known as Cushing’s Syndrome. This can also be caused by a tumor on the adrenal gland which causes an overproduction of cortisol (Helm). Cortisol is a steroid hormone which helps regulate blood sugar as well as aid in the metabolism of protein, fat, and carbohydrates.
This could cause dysplasia of the anterior pituitary leading to the growth of a tumor (Greco, 2013, Lecture). Because he is not growing facial hair the doctors know that he is not at risk for producing too much hormone and developing a
Thyroid hormone medication can be used to replace the thyroid hormone but only those hormones which thyroid has made before the inflammation. There are two thyroid hormones T3 and T4, replacing one or both can alleviate the symptoms caused by the lack of hormones as the result of the Hashimoto’s
5. If the pituitary is so important, and Eric is not getting replacements of hormones the pituitary makes (except for the one from question 4 above), why isn’t he dead? To answer this question think through the cascade of events from the hypothalamus to effect. You will need to think about homeostatic feedback loops and the regulations of hormones. Before we can discuss why Eric is alive without a functioning pituitary gland we must first understand how the pituitary gland functions within the endocrine system.
Recently, doctors have found a treatment for hypoparathyroidism. But, the treatment results in regular injections of calcium into the body. It is like receiving another IV, except the fact that this is pure calcium. Studies show that this helps cure the disorder little by little, but there are serious side effects that occur as the patient gradually gets older. The side effects of the calcium injection include “cancer, loss of hair, thyroid getting destroyed, and diabetes” (Timmons M. 234).
The following morning, I attended the tumor board meeting with Dr. Brat, several neurosurgeons, and oncologists. During this meeting, the teams of
The likelihood recovering adrenal function after a tumor resection in Cushing’s syndrome is dependent
Molecular genetics have shown nearly all to be monoclonal, suggesting that an intrinsic pituitary defect is likely to be responsible for pituitary tumorigenesis. Occasionally, prolactinoma may be part of a multiple endocrine neoplasia syndrome (MEN-1), but this occurs too infrequently to justify MEN-1 screening in every patient with a prolactinoma. • GH- and PRL-secreting adenomas (or mammosomatotroph adenomas) Mixed growth hormone (GH)- and PRL-secreting tumors are well recognized and give rise to acromegaly in association with hyperprolactinemia.
Diagnosis: 1 - Raised T4 & T3 - Low TSH - Increased I131 uptake. - Thyroid stimulating immunoglobulin positive Histology: 1 - Macroscopic: o fleshy appearance o Absence of normal glossy look o Less colloid - Microscopic: o diffuse hyperplasia with cylindrical epithelial cells o Smaller follicles o Papillary outgrowths. Natural course1 - Most persist without treatment leading to further thyroid damage and a high mortality rate. - Rarely patients may go into spontaneous remission, these patients usually lose their abnormal immunoglobulins.
TITLE DELAYED ONSET HUGE REFRACTORY MULTILOCULATED CERVICAL PSEDOMENINGOCELE AFTER RETROMASTOID CRANIECTOMY –CASE REPORT AND REVIEW OF LITERATURE ABSTRACT Pseudomeningoceles after posterior fossa surgery pose a technical challenge to operating neurosurgeons. Cervical pseudomeningocele is unique in that herniation of neural tissue into pseudomeningocele sac produces catastrophic complications. Patient usually presents with postural headache. Treatment includes extrinsic compression, csf diversion followed by primary operative dural repair if refractory. In our case report we present a rare complication of delayed onset huge refractory multiloculated cervical psedomeningocele after retromastoid craniectomy which was surgically repaired.
In one analysis which was conducted, an additional review of the recurrence rate according to the technique used for the treatment of DC, concluded that needle fasciotomy had a recurrence rate of 60%, fasciectomies 30% and CCH infiltration only 15%