Acute Sheehan syndrome following massive postpartum hemorrhage due to vulvar hematoma

Acute Sheehan syndrome appearing within 6 weeks postpartum is a rare form of hypopituitarism caused by postpartum hemorrhage. A 37-year-old Japanese woman experienced a vulvar hematoma after spontaneous labor at 40 weeks gestation, leading to massive postpartum hemorrhage (estimated total blood loss of 3,000 mL). Despite successful cesarean delivery and hematoma drainage, she presented 28 days postpartum with anorexia, fatigue, and hyponatremia after initial recovery. MRI revealed a swollen pituitary gland with subacute hemorrhage, confirming the diagnosis. Hormonal replacement therapy with levothyroxine, hydrocortisone, estrogen, and progesterone was initiated. This is the first reported case of acute Sheehan syndrome following a vulvar hematoma, a condition typically not considered a risk factor for this syndrome. The case highlights the importance of considering rare complications like acute Sheehan syndrome in patients with massive postpartum hemorrhage, even when the pathogenesis is clinically common, such as vulvar hematomas.

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Publication Details

Journal
AJOG Global Reports
Published
2024-09-19
DOI
https://doi.org/10.1016/j.xagr.2024.100399
Citations
1
Primary Topic
Maternal and fetal healthcare
Type
article
Field-Weighted Citation Impact
1.11
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Acute Sheehan syndrome following massive postpartum hemorrhage due to vulvar hematoma

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AJOG Global Reports
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article

Acute Sheehan syndrome following massive postpartum hemorrhage due to vulvar hematoma

Toshifumi Takahashi, Kuniaki Ota, Mika Sugihara, Koichiro Shimoya, Wataru Saito, Yoshiaki Ota, Takehiko Matsuyama
article en
1 citations

Abstract

Acute Sheehan syndrome appearing within 6 weeks postpartum is a rare form of hypopituitarism caused by postpartum hemorrhage. A 37-year-old Japanese woman experienced a vulvar hematoma after spontaneous labor at 40 weeks gestation, leading to massive postpartum hemorrhage (estimated total blood loss of 3,000 mL). Despite successful cesarean delivery and hematoma drainage, she presented 28 days postpartum with anorexia, fatigue, and hyponatremia after initial recovery. MRI revealed a swollen pituitary gland with subacute hemorrhage, confirming the diagnosis. Hormonal replacement therapy with levothyroxine, hydrocortisone, estrogen, and progesterone was initiated. This is the first reported case of acute Sheehan syndrome following a vulvar hematoma, a condition typically not considered a risk factor for this syndrome. The case highlights the importance of considering rare complications like acute Sheehan syndrome in patients with massive postpartum hemorrhage, even when the pathogenesis is clinically common, such as vulvar hematomas.

AJOG Global ReportsVol. 4(4)
Fukushima Medical University (JP), Kawasaki Medical School (JP), Koujin Hospital (JP)
Openalex Percentile: Top 18%
Maternal and fetal healthcare
1.11
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