# Acute Sheehan Syndrome With Distinctive Arginine Vasopressin Secretion and Magnetic Resonance Imaging Findings

**Authors:** Yuki Minamoto, Yumiko Sasai, Yui Yamashita, Keiko Yamagami, Ichiro Fujisawa, Naotetsu Kanamoto

PMC · DOI: 10.1210/jcemcr/luaf134 · JCEM Case Reports · 2025-07-11

## TL;DR

This paper describes a rare case of acute Sheehan syndrome in a postpartum woman with unusual vasopressin secretion and MRI findings.

## Contribution

The paper highlights distinctive AVP secretion dynamics in acute Sheehan syndrome not explained by adrenal insufficiency alone.

## Key findings

- Hyponatremia persisted despite adequate hydrocortisone treatment, indicating non-adrenal causes.
- AVP levels fluctuated with hydration status, suggesting posterior pituitary ischemia and recovery.
- 1-desamino-8-D-arginine vasopressin was temporarily effective, implying SIADH in this context.

## Abstract

Acute Sheehan syndrome is a rare condition that occurs hours to days post partum and causes hypopituitarism. It may cause hyponatremia due to adrenal insufficiency, and most patients improve with steroid therapy. However, hyponatremia is caused not only by adrenal insufficiency but also by inappropriate secretion of arginine vasopressin (AVP). We report the case of a 30-year-old Japanese primipara with massive postpartum hemorrhage and acute Sheehan syndrome. Hyponatremia developed following hypernatremia soon after the postpartum period; however, it did not improve despite adequate hydrocortisone supplementation. AVP fluctuated based on water balance and magnetic resonance imaging findings, showing distinctive AVP secretion dynamics. Oral 1-desamino-8-D-arginine vasopressin was temporarily needed during the clinical course, after which it was not needed, suggesting that impaired blood flow to the posterior pituitary lobe and its improvement may have contributed to the distinctive AVP secretion dynamics. Therefore, when hyponatremia is not improved despite adequate hydrocortisone supplementation in patients with acute Sheehan syndrome, the syndrome of inappropriate antidiuretic hormone secretion should be considered because distinctive AVP secretion dynamics can occur after severe ischemia of the pituitary gland.

## Linked entities

- **Chemicals:** hydrocortisone (PubChem CID 5754)
- **Diseases:** Sheehan syndrome (MONDO:0019618), adrenal insufficiency (MONDO:0000004), syndrome of inappropriate antidiuretic hormone secretion (MONDO:0006802)

## Full-text entities

- **Genes:** AVP (arginine vasopressin) [NCBI Gene 551] {aka ADH, ARVP, AVP-NPII, AVRP, VP}
- **Diseases:** hypernatremia (MESH:D006955), Hyponatremia (MESH:D007010), syndrome of inappropriate antidiuretic hormone (MESH:D007177), hemorrhage (MESH:D006470), adrenal insufficiency (MESH:D000309), postpartum (MESH:D006473), Sheehan Syndrome (MESH:D007018), ischemia of the pituitary gland (MESH:D010900)
- **Chemicals:** steroid (MESH:D013256), hydrocortisone (MESH:D006854)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12246542/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12246542/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12246542/full.md

---
Source: https://tomesphere.com/paper/PMC12246542