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Fatal Postpartum Hemorrhage in a Patient with Niemann-Pick Disease Type B

机译:尼曼-匹克病B型患者的致命产后出血

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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.
机译:背景。 Niemann-Pick疾病B型(NPD B)是一种罕见的溶酶体贮积病,由酸性鞘磷脂酶活性的遗传缺陷引起。在这里,我们报告一例因严重产后出血(PPH)死亡的脾切除型NPD B患者。案例介绍。一名23岁的未产妇因严重的产后出血,在紧急子宫切除术中被捕后接受了心肺停止手术,被送入重症监护病房。该患者在怀孕期间向家人和产科医生隐瞒了疾病,并且在她留在ICU期间寻找脾切除术和严重出血的原因时发现了NPD B诊断。不幸的是,她因缺氧性脑损伤而导致了脑死亡的病程。结论。总之,医生应牢记,有脾切除史和/或无法控制的出血史的患者必须仔细评估是否存在诸如溶酶体贮积病之类的罕见疾病,并且NPD B会因产后出血而导致死亡。成人强化医生应该熟悉罕见的代谢或遗传疾病的成人表现,因为越来越多的代谢或遗传疾病的儿童能够生存到成年,并会被接纳,甚至不幸在成人ICU中死亡。

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