Pharande Pramod, Balegar Virupakshappa Kiran Kumar, Mehta Bhavesh, Badawi Nadia
Department of Neonatology, Nepean Hospital, Kingswood, New South Wales, Australia.
School of Women's and Children's Health, Sydney Medical School Nepean, University of Sydney, Kingswood, New South Wales, Australia.
AJP Rep. 2018 Oct;8(4):e301-e306. doi: 10.1055/s-0038-1675337. Epub 2018 Oct 29.
We report a preterm (35 weeks) male neonate with Down's syndrome (DS) diagnosed with isolated pericardial effusion (PE) at 20 weeks of gestation. He was born by precipitous delivery, needed no resuscitation and presented within first 24 hours of life with respiratory distress, anemia due to feto-maternal bleed, hypotension, hepatomegaly, and coagulopathy. Postnatal echocardiography confirmed a 5 mm rim of PE without tamponade, normal cardiac structure, and function. He was stabilized with ventilation, packed red cell, fresh frozen plasma, inotropes (dopamine, dobutamine, and adrenaline), and steroid (hydrocortisone). Subsequent evaluation confirmed hypothyroidism, transient myeloproliferative disorder (TMD), hepatic failure due to fibrosis/cirrhosis with portal hypertension, and steroid sensitive hypotension on two occasions possibly due to adrenal insufficiency. PE completely resolved over 2 weeks. In view of progressively worsening liver failure with ascites and portal hypertension, the family opted for palliation. Literature review has been discussed regarding perinatal onset of PE in DS.
我们报告了一名患有唐氏综合征(DS)的早产(35周)男婴,其在妊娠20周时被诊断为孤立性心包积液(PE)。他因急产出生,无需复苏,在出生后的头24小时内出现呼吸窘迫、胎儿 - 母体出血导致的贫血、低血压、肝肿大和凝血病。产后超声心动图证实有5毫米宽的心包积液边缘,无心脏压塞,心脏结构和功能正常。通过通气、浓缩红细胞、新鲜冰冻血浆、血管活性药物(多巴胺、多巴酚丁胺和肾上腺素)以及类固醇(氢化可的松)使他病情稳定。随后的评估证实患有甲状腺功能减退、短暂性骨髓增殖性疾病(TMD)、因纤维化/肝硬化伴门静脉高压导致的肝衰竭,以及两次可能因肾上腺功能不全导致的对类固醇敏感的低血压。心包积液在2周内完全消退。鉴于伴有腹水和门静脉高压的肝衰竭逐渐加重,家属选择了姑息治疗。已对唐氏综合征围产期心包积液的发病情况进行了文献综述。