ECE2016 Eposter Presentations Clinical case reports - Pituitary/Adrenal (81 abstracts)
1Department of Internal Medicine, Keimyung University Dongsan Medical Center, Daegu, Republic of Korea; 2Department of Internal Medicine, University College of Medicine, Busan, Republic of Korea.
Background: Pregnancy with Cushing syndrome (CS) is rare because infertility is associated with hypogonadotrophic hypogonadism by cortisol and androgens excess. Here we reported the cases of CS that presented signs and symptoms of CS after delivery.
Case reports: The first case is a 30-year-old woman who presented 8 months after second baby delivery amenorrhea even though she stopped breastfeeding. For 3 months before her visit, she gained weight and had easy bruisability. She had a history of gestational diabetes. On physical examination, she had moon face, buffalo hump and abdominal striae with purple colored pigmentation. Urine hCG was negative. Plasma adrenocorticotropic hormone (ACTH) was high and low dose dexamethasone test was not suppressed. The brain magnetic resonance image showed a 6 mm sized adenoma in the left side of pituitary gland. A transsphenoidal adenomectomy was performed. Shortly after operation, she had adrenal insufficiency. However, 5 months later, clinical symptoms improved and her pituitary-adrenal function was normalized.
The second case is a 33-year-old woman who presented 5 months after delivery 14 kg weight gain. She was diagnosed with hypertension 3 years ago. On physical examination, she had moon face, acne, hirsutism, central obesity and abdominal striae; 75 g oral glucose tolerance test showed diabetes. Plasma ACTH was normal and low dose dexamethasone test. Other hormone related adrenal gland was normal. The abdominal computed tomography showed 35 mm sized enhancing mass in the right adrenal gland. Laparascopic adrenalectomy was performed and she took hydrocortisone for adrenal insufficiency, anti-hypertensive drug for hypertension and metformin for diabetes. One year after operation, clinical symptoms and metabolic parameters were normalized and she stopped all medications.
Conclusion: CS with pregnancy is rare. We reported cases that manifested CS after delivery and resolved after operation.