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Intracranial hypertension and empty Sella from adrenal adenoma and excessive and prolonged steroid usage: a case report

BACKGROUND: There is only one documented case of intracranial hypertension (IH) and empty sella from cortisol-producing adrenal adenoma so far. And IH and empty sella caused by long-term exogenous hypercortisolism has never been reported before. The purpose of this case report is to alert clinicians...

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Autores principales: Zhao, Naiqian, Yang, Weixia, Li, Xiaoyan, Wang, Li, Feng, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760717/
https://www.ncbi.nlm.nih.gov/pubmed/35033053
http://dx.doi.org/10.1186/s12902-021-00931-2
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author Zhao, Naiqian
Yang, Weixia
Li, Xiaoyan
Wang, Li
Feng, Ying
author_facet Zhao, Naiqian
Yang, Weixia
Li, Xiaoyan
Wang, Li
Feng, Ying
author_sort Zhao, Naiqian
collection PubMed
description BACKGROUND: There is only one documented case of intracranial hypertension (IH) and empty sella from cortisol-producing adrenal adenoma so far. And IH and empty sella caused by long-term exogenous hypercortisolism has never been reported before. The purpose of this case report is to alert clinicians to glucocorticoid-induced IH. CASE PRESENTATION: We present retrospectively a 50-year-old woman with cortisol-secreting adrenal adenoma, who progressed to intractable intracranial hypertension and a markedly expanded empty sella due to improper treatment. In 2011, the patient presented with hypertension, lack of cortisol circadian rhythm, low ACTH, a left adrenal adenoma and a partial empty sella, but did not receive low-dose dexamethasone suppression test (LDDST) and 24-h urinary cortisol. In 2014, she exhibited truncal obesity, raised cortisol, LDDST non-suppression, high urinary free cortisol and low ACTH, proving her cortisol-producing adrenal adenoma. She was simultaneously diagnosed with unexplained IH because of papilledema and elevated intracranial pressure, and her partial empty sella changed to a complete empty sella. In 2015, she underwent adrenal adenoma resection. From 2015 to 2018, she kept taking dexamethasone at least 2 mg daily without her doctors’ consent. During this period, she developed transient cerebrospinal fluid rhinorrhea, and her empty sella further worsened. After switching to low dose hydrocortisone, her papilledema disappeared completely, but optic atrophy has become irreversible. CONCLUSIONS: The patient seems to be just an extreme case, but it may reveal and illustrate a general phenomenon: Both cortisol-producing adrenal adenoma and long-term exogenous hypercortisolism could cause varying degrees of elevated intracranial pressure and empty sella. Clinicians should remain vigilant for this phenomenon in patients with cortisol-producing adrenal adenoma or excessive and prolonged steroid usage and give them corresponding examinations to identify this complication.
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spelling pubmed-87607172022-01-18 Intracranial hypertension and empty Sella from adrenal adenoma and excessive and prolonged steroid usage: a case report Zhao, Naiqian Yang, Weixia Li, Xiaoyan Wang, Li Feng, Ying BMC Endocr Disord Case Report BACKGROUND: There is only one documented case of intracranial hypertension (IH) and empty sella from cortisol-producing adrenal adenoma so far. And IH and empty sella caused by long-term exogenous hypercortisolism has never been reported before. The purpose of this case report is to alert clinicians to glucocorticoid-induced IH. CASE PRESENTATION: We present retrospectively a 50-year-old woman with cortisol-secreting adrenal adenoma, who progressed to intractable intracranial hypertension and a markedly expanded empty sella due to improper treatment. In 2011, the patient presented with hypertension, lack of cortisol circadian rhythm, low ACTH, a left adrenal adenoma and a partial empty sella, but did not receive low-dose dexamethasone suppression test (LDDST) and 24-h urinary cortisol. In 2014, she exhibited truncal obesity, raised cortisol, LDDST non-suppression, high urinary free cortisol and low ACTH, proving her cortisol-producing adrenal adenoma. She was simultaneously diagnosed with unexplained IH because of papilledema and elevated intracranial pressure, and her partial empty sella changed to a complete empty sella. In 2015, she underwent adrenal adenoma resection. From 2015 to 2018, she kept taking dexamethasone at least 2 mg daily without her doctors’ consent. During this period, she developed transient cerebrospinal fluid rhinorrhea, and her empty sella further worsened. After switching to low dose hydrocortisone, her papilledema disappeared completely, but optic atrophy has become irreversible. CONCLUSIONS: The patient seems to be just an extreme case, but it may reveal and illustrate a general phenomenon: Both cortisol-producing adrenal adenoma and long-term exogenous hypercortisolism could cause varying degrees of elevated intracranial pressure and empty sella. Clinicians should remain vigilant for this phenomenon in patients with cortisol-producing adrenal adenoma or excessive and prolonged steroid usage and give them corresponding examinations to identify this complication. BioMed Central 2022-01-15 /pmc/articles/PMC8760717/ /pubmed/35033053 http://dx.doi.org/10.1186/s12902-021-00931-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Zhao, Naiqian
Yang, Weixia
Li, Xiaoyan
Wang, Li
Feng, Ying
Intracranial hypertension and empty Sella from adrenal adenoma and excessive and prolonged steroid usage: a case report
title Intracranial hypertension and empty Sella from adrenal adenoma and excessive and prolonged steroid usage: a case report
title_full Intracranial hypertension and empty Sella from adrenal adenoma and excessive and prolonged steroid usage: a case report
title_fullStr Intracranial hypertension and empty Sella from adrenal adenoma and excessive and prolonged steroid usage: a case report
title_full_unstemmed Intracranial hypertension and empty Sella from adrenal adenoma and excessive and prolonged steroid usage: a case report
title_short Intracranial hypertension and empty Sella from adrenal adenoma and excessive and prolonged steroid usage: a case report
title_sort intracranial hypertension and empty sella from adrenal adenoma and excessive and prolonged steroid usage: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760717/
https://www.ncbi.nlm.nih.gov/pubmed/35033053
http://dx.doi.org/10.1186/s12902-021-00931-2
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