Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zain, Ahmer, Sivakumar, Ashwin, Akah, Ozo, Shiza, Saher T, Mahadevaiah, Ashwini, Khan, Aadil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
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
_version_ 1784711533518913536
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
work_keys_str_mv AT zainahmer ararecaseofsheehansyndromewithcardiactamponade
AT sivakumarashwin ararecaseofsheehansyndromewithcardiactamponade
AT akahozo ararecaseofsheehansyndromewithcardiactamponade
AT shizasahert ararecaseofsheehansyndromewithcardiactamponade
AT mahadevaiahashwini ararecaseofsheehansyndromewithcardiactamponade
AT khanaadil ararecaseofsheehansyndromewithcardiactamponade
AT zainahmer rarecaseofsheehansyndromewithcardiactamponade
AT sivakumarashwin rarecaseofsheehansyndromewithcardiactamponade
AT akahozo rarecaseofsheehansyndromewithcardiactamponade
AT shizasahert rarecaseofsheehansyndromewithcardiactamponade
AT mahadevaiahashwini rarecaseofsheehansyndromewithcardiactamponade
AT khanaadil rarecaseofsheehansyndromewithcardiactamponade