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Current Opinion in Oncology, 2006
Adrenocortical carcinoma is a rare malignancy, accounting for 0.02% of all annual cancers reported. Given the generally advanced stage at diagnosis, the overall 5-year survival remains poor, varying between 20 and 45%. While older studies purported an improved outcome for functional tumors in adult patients, this has not been borne out in more recent ...
Steven E, Rodgers +3 more
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Adrenocortical carcinoma is a rare malignancy, accounting for 0.02% of all annual cancers reported. Given the generally advanced stage at diagnosis, the overall 5-year survival remains poor, varying between 20 and 45%. While older studies purported an improved outcome for functional tumors in adult patients, this has not been borne out in more recent ...
Steven E, Rodgers +3 more
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Journal of Urology, 2008
Adrenocortical carcinoma (ACC) is a rare cancer with a generally poor prognosis. In approximately 60% of cases the initial clinical manifestations are due to hypersecretion of adrenocortical hormones. Cushing's syndrome is the most frequent hormonal manifestation.
Camil J, Chouairy +2 more
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Adrenocortical carcinoma (ACC) is a rare cancer with a generally poor prognosis. In approximately 60% of cases the initial clinical manifestations are due to hypersecretion of adrenocortical hormones. Cushing's syndrome is the most frequent hormonal manifestation.
Camil J, Chouairy +2 more
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Virilising adrenocortical carcinoma
BMJ Case Reports, 2021Adrenocortical carcinoma (ACC) is a rare malignancy, with an estimated annual incidence of 0.7–2 cases per million and a median overall survival of 3–4 years. Hormone-secreting ACCs represent most cases; of these, only a small minority presents with virilisation alone. Early diagnosis is key to increase the chances of a better outcome.
Diogo Nunes, Correia +2 more
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Urologic Clinics of North America, 1989
In reviewing the experience of a number of authors and investigators, it is clear that early diagnosis of adrenocortical carcinoma is essential for cure. Of all the modalities of therapy currently available, surgical resection holds the most promise for cure or prolonged survival.
J I, Barzilay, A G, Pazianos
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In reviewing the experience of a number of authors and investigators, it is clear that early diagnosis of adrenocortical carcinoma is essential for cure. Of all the modalities of therapy currently available, surgical resection holds the most promise for cure or prolonged survival.
J I, Barzilay, A G, Pazianos
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Cancer, 2000
The clinical features and natural history of adrenocortical carcinoma are highly dependent on the type of center reporting their experience. Observations from oncology services suggest a high incidence of nonfunctioning tumors, whereas reports from endocrine clinics emphasize excessive corticoid and androgen production in the majority of tumors.
Venâncio Alves +1 more
exaly +3 more sources
The clinical features and natural history of adrenocortical carcinoma are highly dependent on the type of center reporting their experience. Observations from oncology services suggest a high incidence of nonfunctioning tumors, whereas reports from endocrine clinics emphasize excessive corticoid and androgen production in the majority of tumors.
Venâncio Alves +1 more
exaly +3 more sources
World Journal of Urology, 1999
Abstract Adrenocortical carcinoma is a rare tumor with an annual incidence of between 0.5 and 2 cases per million (Brennan 1987; National Cancer Institute 1975). This is in contrast to the incidence of adenomas of the adrenal gland yielding a relatively frequent finding of an ‘ incidentaloma’ in patients having cross- sectional imaging ...
R D, Schulick, M F, Brennan
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Abstract Adrenocortical carcinoma is a rare tumor with an annual incidence of between 0.5 and 2 cases per million (Brennan 1987; National Cancer Institute 1975). This is in contrast to the incidence of adenomas of the adrenal gland yielding a relatively frequent finding of an ‘ incidentaloma’ in patients having cross- sectional imaging ...
R D, Schulick, M F, Brennan
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Adrenocortical Carcinoma in Children
Journal of Urology, 1983Adrenocortical carcinoma in childhood is a rare yet potentially fatal disease. We present 5 cases of adrenocortical carcinoma detected and managed in childhood. Of the 5 patients 4 presented with clinical signs of excess corticosteroid production and 1 presented suddenly with abdominal pain. All patients had palpable abdominal masses.
R, Kay, O P, Schumacher, E S, Tank
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Advances in Anatomic Pathology, 2014
Adrenocortical carcinoma is a rare endocrine tumor with a poor prognosis. These tumors can be diagnostically challenging, and diagnostic algorithms and criteria continue to be suggested. Myxoid and oncocytic variants are important to recognize to not confuse with other tumors.
Lori A, Erickson +2 more
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Adrenocortical carcinoma is a rare endocrine tumor with a poor prognosis. These tumors can be diagnostically challenging, and diagnostic algorithms and criteria continue to be suggested. Myxoid and oncocytic variants are important to recognize to not confuse with other tumors.
Lori A, Erickson +2 more
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Oncocytic adrenocortical carcinoma
Urology, 2004Oncocytic adrenocortical carcinoma is rare. To our knowledge, only 6 cases have been previously reported. We describe an additional case of oncocytic adrenocortical carcinoma. A 54-year-old man presented with a right subcostal mass. Computed tomography demonstrated a massive tumor in the right abdomen.
Kazushi, Tanaka +7 more
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Management of Adrenocortical Carcinoma
Current Oncology Reports, 2019Adrenocortical carcinoma (ACC) is a rare endocrine malignancy typically with poor prognosis. This review aims to summarize the current knowledge regarding the clinical management of ACC.Surgery remains the cornerstone for localized ACC management. In more advanced cases, debulking surgery when feasible can help with hormonal control and may allow the ...
Sina, Jasim, Mouhammed Amir, Habra
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