![]() ![]() This information is not a substitute for professional medical advice. Edits to original content made by Rector and Visitors of the University of Virginia. Anna Burban, Agnieszka Koodziska, Magorzata Kobylecka, Joanna Mczewska, Piotr Sciso, Marcin Grabowski. Buszman, Jacek Piegza, Wojciech Wojakowski, Pawe Gasior. Positron emission tomography (PET)/CT scanĪ doctor will determine the best treatment plan for you dependent upon on the stage of the tumor and your overall health.Ĭontent was created using EBSCO’s Health Library. Marta Bujak, Aneta Desperak, Marek Gierlotka, Krzysztof Milewski, Krystian Wita, Zbigniew Kalarus, Joanna Fluder-Wodarczyk, Pawe Pawlus, Pawe E.Historically, about 30 of these malignancies are confined to the adrenal gland at diagnosis. 1 Although it mainly occurs in adults, children can be affected too. Images may be needed of your bodily structures. Adrenocortical carcinoma (ACC) is a rare tumor with an annual incidence of 2 cases per 1 million population. Excess hormones may produce symptoms such as: Adrenocortical carcinoma is discovered as part of a physical examination for abdominal pain. These people do not have any specific symptoms. Addisons disease, toxic psychosis, prostate hypertrophy, adrenocortical insufficiency, alcoholism, delirium tremens, diseases of the biliary tract. SymptomsĪpproximately 40% of people with adrenocortical carcinoma do not secrete any hormone. Adrenocortical Carcinoma Risk FactorsĪ genetic defect may cause adrenocortical cancer in some children, but the majority of cases are nonhereditary. ![]() The cause of adrenocortical carcinoma is unknown. ![]()
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