Postpartum pheochromocytoma crisis associated with cardiogenic shock and Sheehan’s syndrome

We report a case of a woman in her mid-30s who developed severe cardiac shock hours after giving birth to her second child with the need for extracorporeal haemodynamic support. Initially, postpartum cardiomyopathy was suspected, and high-urgency heart transplantation was considered. However, the endocrine work-up and imaging revealed pheochromocytoma as the cause for acute heart failure that was completely reversible. Notably, the patient also developed Sheehan's syndrome with pituitary necrosis and sustained hypopituitarism, most likely as a consequence of the haemodynamic failure during pheochromocytoma crisis. While pheochromocytoma crisis is already an extremely rare peripartum complication, the current case is-to the best of our knowledge-the first report of pheochromocytoma associated with Sheehan's syndrome. This case also highlights the clinical conundrum that pheochromocytomas can be easily overlooked in pregnancy due to non-specific symptoms and confusion with pregnancy-related hypertension or hypertension-associated other diseases. Appropriate case detection is important, especially in pregnant women with early onset of hypertension.

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Publication Details

Journal
BMJ Case Reports
Published
2025-03-01
DOI
https://doi.org/10.1136/bcr-2024-261704
Primary Topic
Adrenal and Paraganglionic Tumors
Type
article
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article

Postpartum pheochromocytoma crisis associated with cardiogenic shock and Sheehan’s syndrome

Alexander Haug, Florian W. Kiefer, David K. Wall, Christian Scheuba et al.
BMJ Case Reports
Adrenal and Paraganglionic Tumors
article

Postpartum pheochromocytoma crisis associated with cardiogenic shock and Sheehan’s syndrome

Alexander Haug, Florian W. Kiefer, David K. Wall, Christian Scheuba, Maria T. Schmook, Kristina Nieding
article en

Abstract

We report a case of a woman in her mid-30s who developed severe cardiac shock hours after giving birth to her second child with the need for extracorporeal haemodynamic support. Initially, postpartum cardiomyopathy was suspected, and high-urgency heart transplantation was considered. However, the endocrine work-up and imaging revealed pheochromocytoma as the cause for acute heart failure that was completely reversible. Notably, the patient also developed Sheehan's syndrome with pituitary necrosis and sustained hypopituitarism, most likely as a consequence of the haemodynamic failure during pheochromocytoma crisis. While pheochromocytoma crisis is already an extremely rare peripartum complication, the current case is-to the best of our knowledge-the first report of pheochromocytoma associated with Sheehan's syndrome. This case also highlights the clinical conundrum that pheochromocytomas can be easily overlooked in pregnancy due to non-specific symptoms and confusion with pregnancy-related hypertension or hypertension-associated other diseases. Appropriate case detection is important, especially in pregnant women with early onset of hypertension.

BMJ Case ReportsVol. 18(3)
European Neuroendocrine Tumor Society (DE), Medical University of Vienna (AT)
Good health and well-being
Openalex Percentile: Top 91%
Adrenal and Paraganglionic Tumors
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