Pituitary Necrosis Revealed by Central Diabetes Insipidus Secondary to Postpartum Hemorrhagic Shock: A Case Report

Postpartum pituitary necrosis results in Sheehan's syndrome, giving a clinical picture of complete or dissociated panhypopitiutarism. It classically involves the anterior pituitary gland and is rarely associated with central diabetes insipidus. We report the case of a 26 year old primiparous woman admitted to intensive care for haemorrhagic shock secondary to post partum haemorrhage due to cervical tear. After resuscitation and haemodynamic stabilisation, she presented with retro-orbital headaches, an absence of milk production and primary hypotonic polyuria with a negative fluid balance. Fluid restriction without improvement and a positive desmopressin test led to the diagnosis of central diabetes insipidus. As part of the aetiological investigation, magnetic resonance imaging (MRI) showed pituitary necrosis. The presence of central diabetes insipidus in the context of post-partum haemorrhage should raise the possibility of pituitary necrosis, although this association is rare. MRI is a key element in the diagnosis, particularly in the acute phase, as the clinical picture of panhypopuitarism occurs much later.

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Publication Details

Journal
EAS Journal of Anaesthesiology and Critical Care
Published
2024-10-19
DOI
https://doi.org/10.36349/easjacc.2024.v06i05.009
Primary Topic
Pituitary Gland Disorders and Treatments
Type
article
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article

Pituitary Necrosis Revealed by Central Diabetes Insipidus Secondary to Postpartum Hemorrhagic Shock: A Case Report

Arame Ndiaye, Maïmouna Touré, I Gaye, P.A. Leye et al.
EAS Journal of Anaesthesiology and Critical Care
Pituitary Gland Disorders and Treatments
article

Pituitary Necrosis Revealed by Central Diabetes Insipidus Secondary to Postpartum Hemorrhagic Shock: A Case Report

Arame Ndiaye, Maïmouna Touré, I Gaye, P.A. Leye, Fatoumata Bah, Mamadou Beye
article en

Abstract

Postpartum pituitary necrosis results in Sheehan's syndrome, giving a clinical picture of complete or dissociated panhypopitiutarism. It classically involves the anterior pituitary gland and is rarely associated with central diabetes insipidus. We report the case of a 26 year old primiparous woman admitted to intensive care for haemorrhagic shock secondary to post partum haemorrhage due to cervical tear. After resuscitation and haemodynamic stabilisation, she presented with retro-orbital headaches, an absence of milk production and primary hypotonic polyuria with a negative fluid balance. Fluid restriction without improvement and a positive desmopressin test led to the diagnosis of central diabetes insipidus. As part of the aetiological investigation, magnetic resonance imaging (MRI) showed pituitary necrosis. The presence of central diabetes insipidus in the context of post-partum haemorrhage should raise the possibility of pituitary necrosis, although this association is rare. MRI is a key element in the diagnosis, particularly in the acute phase, as the clinical picture of panhypopuitarism occurs much later.

EAS Journal of Anaesthesiology and Critical CareVol. 6(05)
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Pituitary Gland Disorders and Treatments
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