Results 131 to 140 of about 8,531 (170)
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CRYSTALLOID STRUCTURE IN ADRENOCORTICAL ADENOMA
Acta Pathologica Japonica, 1985The presence of crystalloid structures was demonstrated in the cytoplasm of a huge adrenocortical adenoma ultrastructurally. The crystalloids were classified into four types, and they differed from those of spironolactone bodies or intramitochondrial bodies in their size and shape. The structures of the crystalloids resembled the crystalloids of Reinke
M, Kitazawa +6 more
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The functional spectrum of adrenocortical adenomas
Medical Hypotheses, 1993Adrenocortical adenomas (ACA) are frequently discovered at autopsy. Nowadays, modern radiologic techniques incidentally uncover the usually silent ACA during lifetime. On the basis of various reports and the results of endocrine tests, i.e. dexamethasone suppression (DST) and CRH response, we characterize 3 major types of functioning ACA.
J, Hensen, M, Buhl, W, Oelkers
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Symptomatic Intraspinal Oncocytic Adrenocortical Adenoma
Endocrine Pathology, 2008Most intraspinal neoplasms of epithelial origin are metastases from primary carcinomas. Benign epithelial tumors are rarely found at this site. We here present the case of a 44-year-old woman with a lesion in the cauda equina that fulfilled the radiologic criteria of schwannoma and caused clinical symptoms for 3 years. The excised tumor was composed of
Jens, Schittenhelm +3 more
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ADRENOCORTICAL ADENOMA WITH PRIMARY ALDOSTERONISM IN CULTURE
Acta Pathologica Japonica, 1986Four adrenocortical adenomata with primary aldosteronism (Conn's adenomata) were examined by light and electron microscopy employing cell culture methods. Unstimulated cells existed as a unit of the clusters, but Conn's ademona cells reacted to ACTH. The cultured cells produced mostly cortisol under ACTH‐stimulation as time passed.
K, Matsuo, H, Tsuchiyama
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VIRILIZING ADRENOCORTICAL ADENOMA RESPONSIVE TO GONADOTROPHIN
Acta Endocrinologica, 1975ABSTRACT A virilizing adrenocortical adenoma was demonstrated in a young female. Urinary 17-ketosteroid excretion and subfractions, plasma testosterone level and urinary 17-ketogenic steroid excretion were markedly increased. Dehydroepiandrosterone was the main constituent of the androgen excess.
M, Blichert-Toft +3 more
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Fine Structure of a Virilizing Adrenocortical Adenoma
Beiträge zur Pathologie, 1976An adrenocortical adenoma associated with adrenogenital syndrome in a two-year-old boy was investigated light and electron microscopically. Urinary 17-ketosteroid excretion was considerably elevated and unresponsive to dexamethasone administration. The level returned to normal after surgical removal of the tumour.
K, Gorgas, P, Böck, S, Wuketich
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ADRENOCORTICAL ADENOMA WITH CUSHING'S SYNDROME IN CULTURE
Acta Pathologica Japonica, 1986Two adrenocortical adenomata with Cushing's syndrome were examined employing cell culture methods. The results revealed that the clear‐type cells changed into compact‐type cells, and that the compact cells played a role in the production and secretion of steroid hormones. Furthermore, it is likely that they underwent fragmentation and produced collagen
K, Matsuo, H, Tsuchiyama
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Calcified aldosterone-producing adrenocortical adenoma
Clinical Imaging, 1996We report the first case of benign aldosteronoma of an ordinary size with calcifications. We review the clinical, clinical imaging, histopathological, and laboratory features of aldosterone-producing adrenal adenoma versus carcinoma. We conclude that no single feature is diagnostic, and the full range of data must be considered.
T M, Jelic +11 more
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Mutational landscape of non-functional adrenocortical adenomas
Endocrine-Related Cancer, 2022Adrenal incidentalomas are the most frequent human neoplasms. Recent genomic investigations on functional adrenocortical tumors have demonstrated that somatic mutations in PRKACA and KCNJ5 responsible for the development of adrenocortical adenomas (ACAs)
Luming Wu +10 more
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Ultrastructural Study of Virilizing Adrenocortical Adenoma
American Journal of Clinical Pathology, 1973Electron microscopic study of an adrenocortical adenoma from a 32-year-old woman with biochemical and clinical manifestations of virilization disclosed its component cells to exhibit mitochondrial and other features of reticularis cells. This identification allows for its ultrastructural distinction from lesions encountered in Cushing’s syndrome and ...
E R, Fisher, T S, Danowski
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