Cushing’s Disease due to ACTH Secreting Pituitary Microadenoma: A Single Institutional Experience of Four Cases
نویسندگان
چکیده
منابع مشابه
Cushing's syndrome due to ACTH-secreting pheochromocytoma.
Ectopic secretion of adrenocorticotropic hormone (ACTH) is an infrequent cause of Cushing's syndrome. We report a case of ectopic ACTH syndrome caused by a pheochromocytoma. A 53-year-old female with clinical features of Cushing s syndrome presented with serious recurrent hypertensive crisis. Endocrinological investigation confirmed the diagnosis of ectopic ACTH production and revealed markedly...
متن کاملPituitary Radiotherapy for Cushings Disease
Background: The treatment of choice for Cushing’s disease is pituitary surgery. Second-line treatments include repeat pituitary surgery, radiation therapy, medical therapy, and bilateral adrenalectomy. The most used modalities to irradiate patients with Cushing’s disease include fractionated radiotherapy and single-dose Gamma Knife. We aim to review the efficacy and safety of radiotherapy in pa...
متن کاملPituitary Surgery for Cushings Disease
In this article, the present status of neurosurgical operations for Cushing’s disease is briefly reviewed. Transsphenoidal surgery is considered the treatment of choice in most patients with Cushing’s disease once the diagnosis has been established. In a considerable proportion of patients, even sophisticated imaging does not directly depict the tiny micro adenoma. The search for the tumor is t...
متن کاملSphenoidal Ectopic ACTH-secreting Pituitary Adenoma
INTRODUCTION Ectopic pituitary adenoma is defined as adenoma that occurs outside the sella without any continuity with the normal pituitary gland [1]. Since its description for the first time in 1909 by Erdheim in the vomero-sphenoidal region, about 75 cases have been reported in literature [2-12]. Sphenoid sinus followed by the suprasellar region remains the most common site for these adenomas...
متن کامل[Hyperthyroidism due to a TSH-secreting pituitary tumor].
A 28-year-old female with a 12-year history of goiter is presented. She had both clinical and laboratory evidence of hyperthyroidism, and her serum TSH was persistently and markedly elevated after treatment with antithyroid drugs. A TRH stimulation test resulted in no further rise in serum TSH after cessation of medication. Menses were regular and serum prolactin levels were normal. Serum LH an...
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ژورنال
عنوان ژورنال: Indian Journal of Neurosurgery
سال: 2020
ISSN: 2277-954X,2277-9167
DOI: 10.1055/s-0040-1713333