Cushing Syndrome due to Adrenocortical Carcinoma During Pregnancy

Author:

Morris Jack Andrew1ORCID,Campbell Peter2,Xu Lily3,O’Sullivan Anthony John34

Affiliation:

1. Endocrinologist, Shoalhaven Hospital , Nowra, NSW, 2541 , Australia

2. Breast Endocrine Surgeon, St. George Hospital , Kogarah, NSW, 2217 , Australia

3. Department of Endocrinology , St. George Hospital, Kogarah, NSW, 2217 , Australia

4. Professor of Medicine, St George and Sutherland Campus, School of Clinical Medicine, UNSW Sydney , Kogarah, NSW, 2217 , Australia

Abstract

Abstract Cushing syndrome resulting from adrenocortical carcinoma in pregnancy is exceedingly rare. There are no validated guidelines to establish a diagnosis or guide management in pregnancy. We provide a case of a 31-year-old woman presenting for management of diabetes in pregnancy who appeared cushingoid. She was subsequently diagnosed with ACTH-independent Cushing syndrome and experienced preterm labor at 33 weeks’ gestation, delivering a healthy infant. Four weeks postpartum, the patient underwent a left adrenalectomy and was subsequently diagnosed with adrenocortical carcinoma.

Publisher

The Endocrine Society

Reference10 articles.

1. Clinical features of adrenocortical carcinoma, prognostic factors and the effect of mitotane therapy;Luton;N Engl J Med,1990

2. Adrenal disorders in pregnancy;Abdelmannan;Endocrinol Metab Clin North Am,2011

3. Special Aspects of Cushing’s Syndrome: Pregnancy

4. Adrenal disease in pregnancy;Lekarev;Best Pract Res Clin Endocrinol Metab,2011

5. ADIPS consensus guidelines for the testing and diagnosis of gestational diabetes mellitus in Australia;Nankervis

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