1990
DOI: 10.1136/pgmj.66.773.221
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Successful treatment with ketoconazole of Cushing's syndrome in pregnancy

Abstract: Patients with Cushing's syndrome rarely become pregnant. This is a high risk situation both for the fetus and the mother, if untreated. We report a patient with Cushing's syndrome due to adrenocortical adenoma who became pregnant and was successfully treated with ketoconazole during the last period of pregnancy.

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Cited by 71 publications
(27 citation statements)
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“…In this case, it was very difficult to control the congestive heart failure. [7,[14][15][16], whereas a number of reports recommended surgical treatment [9,17,18]. In the second trimester of pregnancy, surgical treatment has been recommended for patients with severe hypercortisolism, but conservative treatment was recommended for patients with mild hypercortisolism [9].…”
Section: Discussionmentioning
confidence: 99%
“…In this case, it was very difficult to control the congestive heart failure. [7,[14][15][16], whereas a number of reports recommended surgical treatment [9,17,18]. In the second trimester of pregnancy, surgical treatment has been recommended for patients with severe hypercortisolism, but conservative treatment was recommended for patients with mild hypercortisolism [9].…”
Section: Discussionmentioning
confidence: 99%
“…In two of the four cases ketoconazole was used during the first trimester of pregnancy. [7][8][9][10] In the rat, ketoconazole crosses the placenta and is teratogenic, and in humans it is classified as FDA category C. A recent population-based case-control study did not find a higher rate of congenital abnormalities in infants born to mothers who had received oral ketoconazole treatment during pregnancy; however, the number of exposed cases and controls was too small to allow for solid conclusions. 11 Moreover, ketoconazole has antiandrogenic effects through inhibition of aromatase activity.…”
Section: Discussionmentioning
confidence: 90%
“…Theo btained products feature common structural motifs of biologically and pharmaceutically active compounds. [50] This method was applicable to primary alkylamines with ahydroxy or amino group in the b-o rg-position, providing five-and six-membered heterocyclic compounds.T he reaction scope included aromatic products generated from polycyclic arenes (naphthalene,p henanthrene,9 ,9-dimethylfluorene) as well as functionalized anisole derivatives containing iodo,e ster,a mide, nitrile,ortert-butyl moieties.…”
Section: Electrochemical Càha Minationmentioning
confidence: 99%