Results 221 to 230 of about 130,771 (285)
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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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Treatment of Adrenocortical Carcinoma.
Surgical Pathology Clinics, 2019Adrenocortical carcinoma (ACC) is a rare malignancy with a poor prognosis. ACC is capable of secreting excess adrenocortical hormones, which can compound morbidity and compromise clinical outcomes.
A. Vaidya, Matthew A. Nehs, K. Kilbridge
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A Diagnostic Approach to Adrenocortical Tumors.
Surgical Pathology Clinics, 2019Adrenocortical tumors range from primary bilateral micronodular or macronodular forms of adrenocortical disease to conventional adrenocortical adenomas and carcinomas.
Anjelica Hodgson, Sara Pakbaz, O. Mete
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Human Pathology, 1992
We report a previously undescribed virilizing malignant adrenocortical tumor in an 21-month-old infant with elevated serum alphafetoprotein. The tumor consists of a peculiar mixture of immature epithelial and mesenchymal elements as well as slit-like spaces partially lined by primitive epithelial cells.
K, Molberg +3 more
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We report a previously undescribed virilizing malignant adrenocortical tumor in an 21-month-old infant with elevated serum alphafetoprotein. The tumor consists of a peculiar mixture of immature epithelial and mesenchymal elements as well as slit-like spaces partially lined by primitive epithelial cells.
K, Molberg +3 more
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American Journal of Clinical Pathology, 1995
Cytopathologic smears and/or imprints of human adrenal cortex (9 cases) and its disorders were examined, including adrenocortical nodule (3 cases), adrenocortical adenoma (23 cases), carcinoma (8 cases), and renal cell carcinoma (6 cases). Immunocytochemistry directed against 3 beta-hydroxysteroid dehydrogenase and adrenal-4-binding protein (Ad4BP), a ...
H, Sasano, S, Shizawa, H, Nagura
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Cytopathologic smears and/or imprints of human adrenal cortex (9 cases) and its disorders were examined, including adrenocortical nodule (3 cases), adrenocortical adenoma (23 cases), carcinoma (8 cases), and renal cell carcinoma (6 cases). Immunocytochemistry directed against 3 beta-hydroxysteroid dehydrogenase and adrenal-4-binding protein (Ad4BP), a ...
H, Sasano, S, Shizawa, H, Nagura
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The American Journal of Surgical Pathology, 1991
We studied three cases of adrenocortical neoplasms that were detected incidentally after radiological examination of the abdomen. These cases did not demonstrate any clinical evidence of adrenocortical abnormalities, such as virilization. Macroscopically, the tumors were light to dark tan on cut surface.
H, Sasano +5 more
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We studied three cases of adrenocortical neoplasms that were detected incidentally after radiological examination of the abdomen. These cases did not demonstrate any clinical evidence of adrenocortical abnormalities, such as virilization. Macroscopically, the tumors were light to dark tan on cut surface.
H, Sasano +5 more
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Does Adrenocortical Hyperplasia Result in Adrenocortical Carcinoma?
New England Journal of Medicine, 1957ONLY 72 cases of masculinizing tumors of the adrenal cortex were reported in a recent twenty-year survey.1 In the case reported below, symptoms of masculinization were present for thirty years before the removal of an adrenocortical carcinoma. There was responsiveness both to stimulation by ACTH and to inhibition by adrenal corticoids.
G J, Hamwi, R A, Serbin, F A, Kruger
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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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Adrenocortical oncocytic neoplasm: A systematic review☆
Surgery, 2018Background: Adrenocortical oncocytic neoplasms are rare tumors, generally regarded as benign and hormonally nonfunctional. We performed a systematic review to update the literature on adrenocortical oncocytic neoplasms by reviewing patient and tumor ...
John J. Kanitra +5 more
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Adrenocortical Cancer Treatment
Hormone Research in Paediatrics, 2009<i>Background:</i> With a reported incidence of 1 to 2 cases per million, adrenocortical cancer (ACC) is a rare disease with poor prognosis. Age distribution shows two peaks: early childhood and between age 40 and 50 years, with females more frequently affected.
PATALANO A, BRANCATO V, MANTERO, FRANCO
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