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dc.contributor.authorTanacan, Atakan
dc.contributor.authorYalcin, Abdullah
dc.contributor.authorUnal, Canan
dc.contributor.authorAkinci, Seda Banu
dc.contributor.authorBeksac, Mehmet Sinan
dc.date.accessioned2019-12-12T06:41:21Z
dc.date.available2019-12-12T06:41:21Z
dc.date.issued2018
dc.identifier.issn2090-6684
dc.identifier.urihttps://doi.org/10.1155/2018/9719374
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046142/
dc.identifier.urihttp://hdl.handle.net/11655/16661
dc.description.abstractBackground 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.
dc.relation.isversionof10.1155/2018/9719374
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleFatal Postpartum Hemorrhage In A Patient With Niemann-Pick Disease Type B
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalCase Reports in Obstetrics and Gynecology
dc.contributor.departmentKadın Hastalıkları ve Doğum
dc.identifier.volume2018
dc.description.indexPubMed


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