Results 11 to 20 of about 22,616 (177)

Adrenocortical Carcinoma [PDF]

Cancers, 2021
Adrenocortical carcinoma (ACC) is an extremely rare disease, the incidence of which is 0 [...]
Berruti A., Tiberio G. A. M., Sigala S.
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Adrenocortical Carcinoma [PDF]

Endocrine Reviews, 2013
AbstractAdrenocortical carcinoma (ACC) is a rare endocrine malignancy, often with an unfavorable prognosis. Here we summarize the knowledge about diagnosis, epidemiology, pathophysiology, and therapy of ACC. Over recent years, multidisciplinary clinics have formed and the first international treatment trials have been conducted.
Tobias, Else, Alex C, Kim, Aaron, Sabolch, Victoria M, Raymond, Asha, Kandathil, Elaine M, Caoili, Shruti, Jolly, Barbra S, Miller, Thomas J, Giordano, Gary D, Hammer   +9 more
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Adrenocortical Carcinoma with Hypercortisolism [PDF]

Endocrinology and Metabolism Clinics of North America, 2018
Adrenocortical carcinoma (ACC) is a rare and aggressive tumor. ACC may be associated with different syndromes of hormone excess, most frequently Cushing's syndrome with or without hypersecretion of androgens. Recent data suggest that cortisol excess is a negative prognostic factor in advanced and localized ACC.
Puglisi S, Perotti P, Pia A, Reimondo G, Terzolo M.   +4 more
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Update in Adrenocortical Carcinoma [PDF]

The Journal of Clinical Endocrinology & Metabolism, 2013
Adrenocortical carcinoma (ACC) is an orphan malignancy that has attracted increasing attention during the last decade. Here we provide an update on advances in the field since our last review published in this journal in 2006.The Wnt/β-catenin pathway and IGF-2 signaling have been confirmed as frequently altered signaling pathways in ACC, but recent ...
Fassnacht, Martin, Kroiss, Matthias, Allolio, Bruno   +2 more
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Case Report: Surgery to remove adrenocortical oncocytic carcinoma from an Asian male

Frontiers in Surgery, 2023
Adrenocortical oncocytic carcinoma is a rare type of adrenocortical tumor. Its clinical characteristics and biological behavior need to be further evaluated after the accumulation of cases.
Hongtao Liu, Kai Huang, Dan Liu, Yehua Wang   +3 more
doaj   +1 more source

Pediatric adrenocortical carcinoma revealed by isolated Cushing syndrome: A case report

Journal of Pediatric Surgery Case Reports, 2023
Background: Adrenocortical carcinoma accounts for less than 0.2% of all pediatric malignancies. Virilization is the most common revealing sign, whereas hyperaldosteronism and Cushing syndrome are less common.We report a case of adrenocortical carcinoma ...
Hakima Chafaaoui, Assan Beaudelaire Romulus, Saad Andaloussi, Omar Dalero, Aziz Elmadi   +4 more
doaj   +1 more source

Prominent 18F-FDG Uptake in the Adrenal Gland after Contralateral Adrenalectomy in a Known Case of Adrenocortical Oncocytic Carcinoma [PDF]

Asia Oceania Journal of Nuclear Medicine and Biology, 2023
Adrenocortical carcinoma (ACC) is a rare type of cancer that is associated with a high rate of recurrence and poor prognosis. The main diagnostic approaches to adrenocortical cancer include CT scan, MRI and the promising role of 18F-FDG PET/CT.
Rakan Al-Rashdan, Mohammed Aljaberi, Ali Mohamedkhair, Akram Al-Ibraheem   +3 more
doaj   +1 more source

Giant nonfunctioning adrenal tumors: two case reports and review of the literature

Journal of Medical Case Reports, 2018
Background There are an estimated 1–2 cases per million per year of adrenocortical carcinoma in the USA. It represents a rare and aggressive malignancy; it is the second most aggressive endocrine malignant disease after anaplastic thyroid carcinoma.
George Chatzoulis, Ioannis Passos, Dimitra-Rafailia Bakaloudi, Dimitrios Giannakidis, Alexandros Koumpoulas, Konstantinos Ioannidis, Ioannis Tsifountoudis, Dimitrios Pappas, Panagiotis Spyridopoulos   +8 more
doaj   +1 more source

Pediatric adrenocortical carcinoma

Frontiers in Endocrinology, 2022
Adrenocortical carcinoma (ACC) is a rare endocrine malignancy of the adrenal gland with an unfavorable prognosis. It is rare in the pediatric population, with an incidence of 0.2-0.3 patients per million in patients under 20 years old. It is primarily associated with Li-Fraumeni and Beckwith-Wiedemann tumor predisposition syndromes in children.
Maran Ilanchezhian, Diana Grace Varghese, John W. Glod, Karlyne M. Reilly, Brigitte C. Widemann, Yves Pommier, Rosandra N. Kaplan, Jaydira Del Rivero   +7 more
openaire   +3 more sources

Quercetin-Rich Extracts from Onions (Allium cepa) Play Potent Cytotoxicity on Adrenocortical Carcinoma Cell Lines, and Quercetin Induces Important Anticancer Properties

Pharmaceuticals, 2022
Adrenocortical carcinoma (ACC) is a rare subtype of cancer, with a poor prognosis in children and adults. Mitotane is the only approved adrenolytic drug for the treatment of ACC, which has controversies regarding its efficacy and side effects on patients.
Alan A. Veiga, Ana Carolina Irioda, Bassam F. Mogharbel, Sandro J. R. Bonatto, Lauro M. Souza   +4 more
doaj   +1 more source