Fetal meconium peritonitis after maternal hepatitis B: a case report and review of the literature.

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Li Zhang, Baorong Gao
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引用次数: 0

Abstract

Maternal hepatitis virus has rarely been implicated in fetal meconium peritonitis (FMP), and its underlying mechanism is largely unknown. We describe a case of FMP presumably caused by maternal chronic hepatitis B virus (HBV). A 29-year-old primigravid woman was referred to our hospital at 35 weeks of gestation for the disappearance of fetal movements. The maternal prenatal history included HBV for more than 10 years. Her HBV DNA level was suppressed (<20 IU/mL) and she was taking oral tenofovir disoproxil fumarate (300 mg/day). At 21+5 weeks, fetal ascites, echogenic bowel, and intra-abdominal calcifications were observed by abdominal ultrasound. These findings were confirmed by magnetic resonance imaging and were regarded as diagnostic for FMP. Cord blood and amniotic fluid were positive for hepatitis B e antigen and hepatitis B surface antigen. Ascites of the FMP was completely self-absorbed at 27+3 weeks. At 35 weeks of gestation, fetal movements had vanished and male stillbirth was induced. A histopathological examination of the placenta showed meconium uptake by macrophages in the amniochorionic membranes. Our findings suggest that maternal HBV can cross the placenta and induce FMP. Close surveillance may allow an early diagnosis of FMP and prevent fetal mortality.

母婴乙型肝炎后胎儿胎膜腹膜炎:病例报告和文献综述。
胎儿胎膜腹膜炎(FMP)很少与母体肝炎病毒有关,其基本机制也不清楚。我们描述了一例推测由母体慢性乙型肝炎病毒(HBV)引起的 FMP。一名 29 岁的初产妇在妊娠 35 周时因胎动消失而被转诊至我院。产妇的产前病史包括 10 多年的乙型肝炎病毒感染史。她的 HBV DNA 水平被抑制(+5 周),腹部超声检查发现胎儿腹水、肠道回声和腹腔内钙化。磁共振成像证实了这些结果,并被视为 FMP 的诊断结果。脐带血和羊水中乙肝 e 抗原和乙肝表面抗原呈阳性。FMP 的腹水在 27+3 周时完全自行吸收。妊娠 35 周时,胎动消失,诱发男性死胎。胎盘组织病理学检查显示,羊膜中的巨噬细胞吸收了胎粪。我们的研究结果表明,母体 HBV 可穿过胎盘诱发 FMP。密切监测可早期诊断 FMP 并防止胎儿死亡。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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