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A Rare Case of Sheehan Syndrome With Cardiac Tamponade
Sheehan syndrome, also called postpartum hypopituitarism, is primarily caused by ischemic necrosis of the pituitary resulting from a complicated pregnancy. As the clinical presentations occur years after the complication, it is difficult to diagnose this condition. In this report, we discuss the cas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123339/ https://www.ncbi.nlm.nih.gov/pubmed/35607582 http://dx.doi.org/10.7759/cureus.24329 |
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author | Zain, Ahmer Sivakumar, Ashwin Akah, Ozo Shiza, Saher T Mahadevaiah, Ashwini Khan, Aadil |
author_facet | Zain, Ahmer Sivakumar, Ashwin Akah, Ozo Shiza, Saher T Mahadevaiah, Ashwini Khan, Aadil |
author_sort | Zain, Ahmer |
collection | PubMed |
description | Sheehan syndrome, also called postpartum hypopituitarism, is primarily caused by ischemic necrosis of the pituitary resulting from a complicated pregnancy. As the clinical presentations occur years after the complication, it is difficult to diagnose this condition. In this report, we discuss the case of a 35-year-old female with altered mental status, generalized edema, and loss of appetite. The condition was complicated due to the comorbidities of multiple medical conditions such as massive pericardial effusion and untreated jaundice. Her anorexic condition perfectly masked the malnourished appearance of the patient. After multiple laboratory tests and diagnostic imaging, the empty sella turcica of the patient propounded Sheehan syndrome. Replacement of the deficient hormones improved her condition after two weeks. Patients with complicated pregnancy history should be advised for diagnostic imaging early in life to appropriately manage Sheehan syndrome. A delay in diagnosis can have significant health and financial loss. Hormone replacement therapy is the only viable option as there is no cure to treat necrosed pituitary. |
format | Online Article Text |
id | pubmed-9123339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-91233392022-05-22 A Rare Case of Sheehan Syndrome With Cardiac Tamponade Zain, Ahmer Sivakumar, Ashwin Akah, Ozo Shiza, Saher T Mahadevaiah, Ashwini Khan, Aadil Cureus Internal Medicine Sheehan syndrome, also called postpartum hypopituitarism, is primarily caused by ischemic necrosis of the pituitary resulting from a complicated pregnancy. As the clinical presentations occur years after the complication, it is difficult to diagnose this condition. In this report, we discuss the case of a 35-year-old female with altered mental status, generalized edema, and loss of appetite. The condition was complicated due to the comorbidities of multiple medical conditions such as massive pericardial effusion and untreated jaundice. Her anorexic condition perfectly masked the malnourished appearance of the patient. After multiple laboratory tests and diagnostic imaging, the empty sella turcica of the patient propounded Sheehan syndrome. Replacement of the deficient hormones improved her condition after two weeks. Patients with complicated pregnancy history should be advised for diagnostic imaging early in life to appropriately manage Sheehan syndrome. A delay in diagnosis can have significant health and financial loss. Hormone replacement therapy is the only viable option as there is no cure to treat necrosed pituitary. Cureus 2022-04-20 /pmc/articles/PMC9123339/ /pubmed/35607582 http://dx.doi.org/10.7759/cureus.24329 Text en Copyright © 2022, Zain et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Internal Medicine Zain, Ahmer Sivakumar, Ashwin Akah, Ozo Shiza, Saher T Mahadevaiah, Ashwini Khan, Aadil A Rare Case of Sheehan Syndrome With Cardiac Tamponade |
title | A Rare Case of Sheehan Syndrome With Cardiac Tamponade |
title_full | A Rare Case of Sheehan Syndrome With Cardiac Tamponade |
title_fullStr | A Rare Case of Sheehan Syndrome With Cardiac Tamponade |
title_full_unstemmed | A Rare Case of Sheehan Syndrome With Cardiac Tamponade |
title_short | A Rare Case of Sheehan Syndrome With Cardiac Tamponade |
title_sort | rare case of sheehan syndrome with cardiac tamponade |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123339/ https://www.ncbi.nlm.nih.gov/pubmed/35607582 http://dx.doi.org/10.7759/cureus.24329 |
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