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Rare fetal complications associated with placental mesenchymal dysplasia: A report of two cases

机译:胎盘间质异常增生相关的罕见胎儿并发症:两例报告

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摘要

Placental mesenchymal dysplasia (PMD) is a rare disease that may be difficult to distinguish from molar pregnancy. The disease is associated with major fetal complications, including Beckwith-Wiedemann syndrome, fetal growth restriction and intrauterine fetal death. Rarely, fetal hematological disorders and liver tumors also may occur. Two patients were referred to our hospital during their second trimesters because of suspected molar pregnancies. Fetal karyotyping and maternal serum human chorionic gonadotropin level determinations led to the PMD diagnoses. In one case, the maternal clinical course was normal, but the neonate suffered from disseminated intravascular coagulation and needed a platelet transfusion. In the second case, the PMD decreased during pregnancy, but a gradually increasing fetal liver tumor appeared. The tumor was diagnosed as mesenchymal hamartoma, based on ultrasound and magnetic resonance imaging studies. The neonate was delivered without cardiovascular compromise. Due to the difficulty of immediate surgical treatment, expectant management, with close follow-up, was chosen.
机译:胎盘间质发育不良(PMD)是一种罕见的疾病,可能难以与磨牙妊娠区别开来。该疾病与主要的胎儿并发症有关,包括Beckwith-Wiedemann综合征,胎儿生长受限和子宫内胎儿死亡。胎儿血液学疾病和肝肿瘤也很少发生。两名孕妇由于怀疑有磨牙妊娠而在其中期妊娠被转介到我们医院。胎儿核型分析和孕妇血清人绒毛膜促性腺激素水平的测定导致了PMD的诊断。在一个病例中,母亲的临床过程正常,但新生儿患有弥散性血管内凝血,需要输注血小板。在第二种情况下,孕期PMD降低,但胎儿肝肿瘤逐渐出现。根据超声和磁共振成像研究,该肿瘤被诊断为间质错构瘤。新生儿分娩没有心血管损害。由于立即手术治疗的困难,选择了预期治疗并密切随访。

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