PubMed · 1988 · 10 citations · 0 references
MedicineEndocrinologyObstetricsEndocrine SurgeryMaternal-fetal MedicineReproductive EndocrinologyAdrenal DisordersAdrenal EndocrinologyAdrenal TumorsEndocrine DiseaseEndocrine DisordersEndocrine TumorsAdrenal PathophysiologyAdrenocortical SecretionAdrenocorticotropic Hormone-secreting AdenomasCushing Syndrome PathophysiologyFetal MortalityMaintenance Hormonal TherapySerum Cortisol MeasurementUrinary Cortisol
Pregnancy rarely occurs in women with Cushing's syndrome, and when it does, fetal mortality and morbidity are very high. We describe a 30-year-old woman who was found to have severe Cushing's syndrome in the 22nd week of her first pregnancy, after a year of unsuccessful attempts to conceive. The patient had the majority of the symptoms and signs characteristic of the syndrome. Laboratory examinations revealed hypokalemia of 2.7 mEq/l, serum cortisol 39.5 micrograms/dl without diurnal variation, free urinary cortisol 1,850 to 3,500 micrograms/24 h, 17-hydroxycorticosteroids (OHCS) 52.5 mg/24 h, 17-ketosteroids (KS) 12 mg/24 h, and ACTH 29 pg/ml. No suppression was observed upon dexamethasone administration (2 and 8 mg). Ultrasound examination of the adrenal glands revealed a left adrenal tumor with a diameter of 4.2 cm. An adrenocortical adenoma was successfully excised in the 24th week of pregnancy. During the 37th week of pregnancy, she delivered a normal baby girl. Postoperatively, the patient was put on maintenance therapy. One year after delivery, mother and child are in perfect health.