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Advances in translational research of the rare cancer type adrenocortical carcinoma
Nature Reviews. Cancer, 2023Chandrayee Ghosh +2 more
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Surgery, 1986
From 1962 to 1985, 47 patients with carcinoma of the adrenal cortex were treated at Memorial Sloan-Kettering Cancer Institute. There were 21 men and 26 women. Seventy-two percent of the tumors were functional and 28% were nonfunctional. Despite the advent of ultrasonography and computerized tomography, these tumors were infrequently diagnosed until ...
K, Cohn, L, Gottesman, M, Brennan
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From 1962 to 1985, 47 patients with carcinoma of the adrenal cortex were treated at Memorial Sloan-Kettering Cancer Institute. There were 21 men and 26 women. Seventy-two percent of the tumors were functional and 28% were nonfunctional. Despite the advent of ultrasonography and computerized tomography, these tumors were infrequently diagnosed until ...
K, Cohn, L, Gottesman, M, Brennan
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The American surgeon, 1991
Ten patients, seven women and three men, ages 47 to 76 years (mean 58.6 years), treated for adrenal cortical carcinoma between 1971 and 1989, were reviewed. Three (30%) of the tumors were nonfunctioning. The remaining seven (70%) were functioning, six of them occurring in women.
R A, Decker, M E, Kuehner
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Ten patients, seven women and three men, ages 47 to 76 years (mean 58.6 years), treated for adrenal cortical carcinoma between 1971 and 1989, were reviewed. Three (30%) of the tumors were nonfunctioning. The remaining seven (70%) were functioning, six of them occurring in women.
R A, Decker, M E, Kuehner
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The Netherlands journal of medicine, 2007
Adrenocortical carcinoma is a rare disease with a poor prognosis. Patients can present with a hormonal syndrome or with general symptoms from an abdominal mass. The pathogenesis is unknown. Sometimes the adrenocortical carcinoma is associated with tumour syndromes such as the Beckwith-Wiedemann and Li-Fraumeni syndrome; however, most tumours are ...
C I M, van Ditzhuijsen +2 more
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Adrenocortical carcinoma is a rare disease with a poor prognosis. Patients can present with a hormonal syndrome or with general symptoms from an abdominal mass. The pathogenesis is unknown. Sometimes the adrenocortical carcinoma is associated with tumour syndromes such as the Beckwith-Wiedemann and Li-Fraumeni syndrome; however, most tumours are ...
C I M, van Ditzhuijsen +2 more
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Bilateral Adrenocortical Carcinoma
Southern Medical Journal, 1967H, Payan, J, Lancaster
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Adrenocortical carcinoma — towards genomics guided clinical care
Nature Reviews Endocrinology, 2019J. Crona, F. Beuschlein
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Surgical Oncology Clinics of North America, 2023
Lisa Kenney, Marybeth Hughes
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Lisa Kenney, Marybeth Hughes
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Acta medica Croatica : casopis Hravatske akademije medicinskih znanosti, 2017
Adrenocortical carcinoma is a rare entity. However, it is the most common type of cancerous adrenal gland tumor with poor prognosis. Approximately 4 to 12 per 1 million people develop this type of tumor, which begins in the adrenal cortex. Adrenocortical carcinoma can occur at any age. Women tend to be diagnosed slightly more often than men.
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Adrenocortical carcinoma is a rare entity. However, it is the most common type of cancerous adrenal gland tumor with poor prognosis. Approximately 4 to 12 per 1 million people develop this type of tumor, which begins in the adrenal cortex. Adrenocortical carcinoma can occur at any age. Women tend to be diagnosed slightly more often than men.
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Next-generation therapies for adrenocortical carcinoma.
Best practice & research. Clinical endocrinology & metabolism, 2020B. Altieri +3 more
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