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A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia
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 perf...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381905/ https://www.ncbi.nlm.nih.gov/pubmed/25870516 http://dx.doi.org/10.2147/IMCRJ.S63778 |
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author | Harano, Yumi Kitano, Atsuko Akiyama, Yurika Kotajima, Lisa Honda, Kazufumi Arioka, Hiroko |
author_facet | Harano, Yumi Kitano, Atsuko Akiyama, Yurika Kotajima, Lisa Honda, Kazufumi Arioka, Hiroko |
author_sort | Harano, Yumi |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4381905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43819052015-04-13 A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia Harano, Yumi Kitano, Atsuko Akiyama, Yurika Kotajima, Lisa Honda, Kazufumi Arioka, Hiroko Int Med Case Rep J Case Report 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. Dove Medical Press 2015-03-27 /pmc/articles/PMC4381905/ /pubmed/25870516 http://dx.doi.org/10.2147/IMCRJ.S63778 Text en © 2015 Harano et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Report Harano, Yumi Kitano, Atsuko Akiyama, Yurika Kotajima, Lisa Honda, Kazufumi Arioka, Hiroko A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia |
title | A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia |
title_full | A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia |
title_fullStr | A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia |
title_full_unstemmed | A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia |
title_short | A case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia |
title_sort | case of isolated adrenocorticotropic hormone deficiency: a rare but possible cause of hypercalcemia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381905/ https://www.ncbi.nlm.nih.gov/pubmed/25870516 http://dx.doi.org/10.2147/IMCRJ.S63778 |
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