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A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia

Authors Harano Y, Kitano A, Akiyama Y, Kotajima L, Honda K, Arioka H

Received 8 March 2014

Accepted for publication 8 May 2014

Published 27 March 2015 Volume 2015:8 Pages 77—79

DOI https://doi.org/10.2147/IMCRJ.S63778

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 2


Yumi Harano,1 Atsuko Kitano,2 Yurika Akiyama,1 Lisa Kotajima,1 Kazufumi Honda,1 Hiroko Arioka1

1Department of General Internal Medicine, 2Department of Medical Oncology, St Luke’s International Medical Center, Tokyo, Japan

Abstract: A 52-year-old woman presented with an 8-month history of epigastric pain, nausea, and weight loss. One year before, she was diagnosed with breast cancer. During the postoperative chemotherapy, she developed epigastric pain and nausea. As a result, she gradually lost 12 kg of her body weight. We performed upper gastrointestinal endoscopy, which revealed mild erosive gastritis. After the treatment with a proton pump inhibitor, her symptoms persisted. Before the admission, mild hypercalcemia was pointed out. Fluid replacement didn't improve hypercalcemia. We assessed adrenocortical function, which showed that her serum cortisol and adrenocorticotropic hormone were decreased. Through loading tests, we established diagnosis of isolated adrenocorticotropic hormone deficiency. She was treated with hydrocortisone. Soon after the treatment, her serum calcium level returned to normal and her symptoms improved. In a case of hypercalcemia unresponsive to fluid replacement, we recommend ruling out adrenal insufficiency after excluding more common diseases which induce hypercalcemia.

Keywords: hypercalcemia, breast cancer, chemotherapy, adrenocorticotropic hormone deficiency, adrenocortical insufficiency

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