Ectopic Cushing s syndrome Of Unknown Origin: A Rare Case Report
Publish Year: 1397
Type: Journal paper
Language: English
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Document National Code:
JR_INTJMI-7-3_011
Index date: 7 October 2019
Ectopic Cushing s syndrome Of Unknown Origin: A Rare Case Report abstract
Background: Cushing’s syndrome is a rare disease caused by excessive secretion of cortisol by adrenalcortex (hypercortisolism). Bilateral adrenal hyperplasia due to increased secretion of adrenocorticotropichormone (ACTH) by pituitary gland is usually known as the main cause of Cushing’s syndrome. The 5-year survival rate for patient with Cushing’s syndrome is approximately 50% unless associated withtreatment. Etiologic diagnosis therefore plays an important role in prompt treatment. The purpose of thisstudy is to inspect a Cushing’s syndrome with unknown cause.Case presentation: A 36-year-old married man with complaint of periorbital and upper trunk swelling(with no buffalo hump) and lower extremity weakness presented to doctor’s clinic. He also had a one-yearhistory of blurred vision, hypertension, facial and periorbital edema and difficulty getting up from asitting. After physical examinations and laboratory testing, diagnosis of Cushing’s disease with unknowncause was made and surgical removal of both adrenal glands was suggested. He underwent bilateraladrenalectomy in two separate operations and his symptoms gradually reduced during the next months.Conclusion: According to this study and other same case report studies conducted, surgical removal ofadrenal gland is the most effective treatment if the patient does not respond to medication. Even if thecause of Cushing’s disease is not known, like the case mentioned.
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Ectopic Cushing s syndrome Of Unknown Origin: A Rare Case Report authors
Saeid Amirkhanlou
Department of Internal Medicine, Golestan University of Medical Sciences, Golestan, Iran
Mohammad Mehdi Ebrahimi
Department of Internal Medicine, Golestan University of Medical Sciences, Golestan, Iran
Arash Rezaei Shahmirzadi
Medical student, Student Research Committee, Golestan University of Medical Sciences, Golestan, Iran