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Acute Sheehan's syndrome manifesting initially with diabetes insipidus postpartum: a case report and systematic literature review.
Olmes, Gregor Leonhard; Solomayer, Erich-Franz; Radosa, Julia Caroline; Sklavounos, Panagiotis; Agne, Philipp; Schunk, Stefan J; Haj Hamoud, Bashar.
Afiliação
  • Olmes GL; Department of Gynecology, Obstetrics and Reproductive Medicine, Saarland University Hospital, Homburg, Germany. gregor.olmes@uks.eu.
  • Solomayer EF; Department of Gynecology, Obstetrics and Reproductive Medicine, Saarland University Hospital, Homburg, Germany.
  • Radosa JC; Department of Gynecology, Obstetrics and Reproductive Medicine, Saarland University Hospital, Homburg, Germany.
  • Sklavounos P; Department of Gynecology, Obstetrics and Reproductive Medicine, Saarland University Hospital, Homburg, Germany.
  • Agne P; Department of Internal Medicine IV - Nephrology, Saarland University Hospital, Homburg, Germany.
  • Schunk SJ; Department of Internal Medicine IV - Nephrology, Saarland University Hospital, Homburg, Germany.
  • Haj Hamoud B; Department of Gynecology, Obstetrics and Reproductive Medicine, Saarland University Hospital, Homburg, Germany.
Arch Gynecol Obstet ; 306(3): 699-706, 2022 09.
Article em En | MEDLINE | ID: mdl-34779875
ABSTRACT

PURPOSE:

Acute Sheehan's syndrome is a rare, but potentially life-threatening, obstetric event that can be complicated by diabetes insipidus. Little information on the diagnosis and treatment of Sheehan's syndrome with diabetes insipidus is available. We report on a 28-year-old patient who developed acute Sheehan's syndrome with diabetes insipidus after giving birth, and on a systematic review of similar cases.

METHODS:

We performed a systematic review of the literature cataloged in PubMed and Google Scholar using the keywords "Sheehan syndrome" OR "Sheehan's syndrome" AND "diabetes insipidus" to identify relevant case reports published between 1990 and 2021. Eight Reports met the inclusion criteria (English-language abstracts available, onset in the puerperium, information about the day of the onset).

RESULTS:

In the present case, postpartum curettage was necessary to remove the residual placenta. The total amount of blood loss was severe (2500 ml). On the second day postpartal, the patient developed polyuria. Laboratory analysis revealed hypernatremia with increased serum osmolality and decreased urinary osmolality. Hormone analysis showed partial hypopituitarism involving the thyroid, corticotropic, and gonadotropic axes. The prolactin level was elevated. Brain magnetic resonance imaging showed pituitary gland infarction. Desmopressin therapy was initiated and resolved the polyuria. Hormone replacement therapy was administered. Four months later, the patient was well, with partial diabetes insipidus. The literature review indicated that this case was typical in terms of symptoms and disease onset. Most reported cases involve hypotension and peripartum hemorrhage, but some patients without hemorrhage also develop Sheehan's syndrome. Elevated prolactin levels are uncommon and associated with poor prognosis in patients with Sheehan's syndrome.

CONCLUSION:

Acute Sheehan's syndrome with diabetes insipidus involves nearly all pituitary hormone axes, indicating severe disease. Prolactin elevation could suggest that a case of Sheehan's syndrome is severe.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus / Hemorragia Pós-Parto / Hipopituitarismo Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Systematic_reviews Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus / Hemorragia Pós-Parto / Hipopituitarismo Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Systematic_reviews Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article