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Sheehan Syndrome

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MRI of the Pituitary Gland

Abstract

Sheehan syndrome corresponds to a pituitary necrosis following severe postpartum hemorrhage and hypovolemia. It has been suggested that a small sella may be a risk factor and play a role in the pathogenesis of the necrosis. Improvement in obstetric care, blood transfusion, and embolization of uterine arteries have permitted a drastic reduction in the frequency of this complication in Western countries. Sheehan syndrome may manifest itself very early after delivery, with headache and hypopituitarism responsible for lack of milk production immediately or some weeks later. Hyponatremia can also be observed. More usually, Sheehan syndrome is diagnosed years later.

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Further Reading

  • Bakiri F, Bendib SE, Maoui R et al (1991) The sella turcica in Sheehan syndrome: computerized tomographic study in 54 patients. J Endocrinol Invest 14(3):193–196

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  • Keleştimur F (2003) Sheehan syndrome. Pituitary 6(4):181–188

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  • Sert M, Tetiker T, Kirim S et al (2003) Clinical report of 28 patients with Sheehan syndrome. Endocr J 50(3):297–301

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Bonneville, JF. (2016). Sheehan Syndrome. In: MRI of the Pituitary Gland. Springer, Cham. https://doi.org/10.1007/978-3-319-29043-0_44

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  • DOI: https://doi.org/10.1007/978-3-319-29043-0_44

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-29041-6

  • Online ISBN: 978-3-319-29043-0

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