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Rare empty sella syndrome found after postoperative hypotension and respiratory failure: A case report
BACKGROUND: Empty sella syndrome is a condition in which the pituitary gland shrinks or flattens. Patients with empty sella syndrome often present with headache, hypertension, obesity, visual disturbances, cerebrospinal fluid (CSF) rhinorrhoea, or endocrine dysfunction. Herein, we report a rare case...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406202/ https://www.ncbi.nlm.nih.gov/pubmed/30863767 http://dx.doi.org/10.12998/wjcc.v7.i5.663 |
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author | Guo, Peng Xu, Zeng-Jun Hu, Chang-En Zheng, Yue-Ying Xu, Dan-Feng |
author_facet | Guo, Peng Xu, Zeng-Jun Hu, Chang-En Zheng, Yue-Ying Xu, Dan-Feng |
author_sort | Guo, Peng |
collection | PubMed |
description | BACKGROUND: Empty sella syndrome is a condition in which the pituitary gland shrinks or flattens. Patients with empty sella syndrome often present with headache, hypertension, obesity, visual disturbances, cerebrospinal fluid (CSF) rhinorrhoea, or endocrine dysfunction. Herein, we report a rare case of empty sella syndrome discovered after the patient experienced postoperative hypotension and respiratory failure. CASE SUMMARY: A 60-year-old man was admitted for further workup of left shoulder pain. He was assessed by the orthopaedics team and booked for internal fixation of the left clavicle. General anaesthesia with a nerve block was administered. His blood pressure continued to decrease post-operation. Endocrine tests were performed, with the results supporting a diagnosis of hypopituitarism with hypocortisolism and hypothyroidism. Brain magnetic resonance imaging demonstrated that the sella was enlarged and filled with CSF, confirming a diagnosis of empty sella syndrome. The patient was started on endocrine replacement therapy. The patient regained consciousness and spontaneous breath finally. CONCLUSION: This case highlights the importance of considering pituitary hormone insufficiency in the context of respiratory and hemodynamic failure during the perioperative period. |
format | Online Article Text |
id | pubmed-6406202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-64062022019-03-12 Rare empty sella syndrome found after postoperative hypotension and respiratory failure: A case report Guo, Peng Xu, Zeng-Jun Hu, Chang-En Zheng, Yue-Ying Xu, Dan-Feng World J Clin Cases Case Report BACKGROUND: Empty sella syndrome is a condition in which the pituitary gland shrinks or flattens. Patients with empty sella syndrome often present with headache, hypertension, obesity, visual disturbances, cerebrospinal fluid (CSF) rhinorrhoea, or endocrine dysfunction. Herein, we report a rare case of empty sella syndrome discovered after the patient experienced postoperative hypotension and respiratory failure. CASE SUMMARY: A 60-year-old man was admitted for further workup of left shoulder pain. He was assessed by the orthopaedics team and booked for internal fixation of the left clavicle. General anaesthesia with a nerve block was administered. His blood pressure continued to decrease post-operation. Endocrine tests were performed, with the results supporting a diagnosis of hypopituitarism with hypocortisolism and hypothyroidism. Brain magnetic resonance imaging demonstrated that the sella was enlarged and filled with CSF, confirming a diagnosis of empty sella syndrome. The patient was started on endocrine replacement therapy. The patient regained consciousness and spontaneous breath finally. CONCLUSION: This case highlights the importance of considering pituitary hormone insufficiency in the context of respiratory and hemodynamic failure during the perioperative period. Baishideng Publishing Group Inc 2019-03-06 2019-03-06 /pmc/articles/PMC6406202/ /pubmed/30863767 http://dx.doi.org/10.12998/wjcc.v7.i5.663 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Guo, Peng Xu, Zeng-Jun Hu, Chang-En Zheng, Yue-Ying Xu, Dan-Feng Rare empty sella syndrome found after postoperative hypotension and respiratory failure: A case report |
title | Rare empty sella syndrome found after postoperative hypotension and respiratory failure: A case report |
title_full | Rare empty sella syndrome found after postoperative hypotension and respiratory failure: A case report |
title_fullStr | Rare empty sella syndrome found after postoperative hypotension and respiratory failure: A case report |
title_full_unstemmed | Rare empty sella syndrome found after postoperative hypotension and respiratory failure: A case report |
title_short | Rare empty sella syndrome found after postoperative hypotension and respiratory failure: A case report |
title_sort | rare empty sella syndrome found after postoperative hypotension and respiratory failure: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406202/ https://www.ncbi.nlm.nih.gov/pubmed/30863767 http://dx.doi.org/10.12998/wjcc.v7.i5.663 |
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