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Fatal Postpartum Hemorrhage in a Patient with Niemann-Pick Disease Type B.
Tanacan, Atakan; Yalcin, Abdullah; Unal, Canan; Akinci, Seda Banu; Beksac, Mehmet Sinan.
Afiliação
  • Tanacan A; Division of Perinatology, Department of Obstetrics and Gynecology, Hacettepe University Medical Faculty, Ankara, Turkey.
  • Yalcin A; Department of Anaesthesiology and Critical Care Medicine, Hacettepe University Medical Faculty, Ankara, Turkey.
  • Unal C; Division of Perinatology, Department of Obstetrics and Gynecology, Hacettepe University Medical Faculty, Ankara, Turkey.
  • Akinci SB; Department of Anaesthesiology and Critical Care Medicine, Hacettepe University Medical Faculty, Ankara, Turkey.
  • Beksac MS; Division of Perinatology, Department of Obstetrics and Gynecology, Hacettepe University Medical Faculty, Ankara, Turkey.
Case Rep Obstet Gynecol ; 2018: 9719374, 2018.
Article em En | MEDLINE | ID: mdl-30050708
ABSTRACT

BACKGROUND:

Niemann-Pick Disease Type B (NPD B) is a rare lysosomal storage disorder resulting from an inherited deficiency of acid sphingomyelinase activity. Here, we report the case of a splenectomized patient with NPD B who died because of severe postpartum hemorrhage (PPH). CASE PRESENTATION A 23-year-old nulliparous woman was admitted to intensive care unit (ICU) after cardiopulmonary arrest during urgent hysterectomy because of severe postpartum bleeding. The patient concealed her disease from her family and obstetricians during her pregnancy, and her NPD B diagnosis was revealed during her stay in ICU while searching for the cause of the splenectomy and severe bleeding. Unfortunately, she had a detrimental course with hypoxic brain injury leading to brain death.

CONCLUSIONS:

In conclusion, physicians should keep in mind that patients with a history of splenectomy and/or uncontrollable hemorrhage must be carefully evaluated for rare diseases like lysosomal storage diseases and that NPD B can cause mortality because of postpartum bleeding. Adult intensivists should be familiar with adult presentations of rare metabolic or genetic diseases as more and more children with metabolic or genetic diseases will survive to adulthood and will be admitted to and unfortunately will even die in the adult ICU.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article