Machado Luiz E, Osborne Newton G, Bonilla-Musoles Fernando
Centro de Treinamento Per La Imagem, Bahia, Brazil.
J Perinat Med. 2002;30(1):105-10. doi: 10.1515/JPM.2002.013.
Fetal edema was recognized in the past as a complication of alloimmune disease. More recently, fetal edema is frequently seen in conditions that cause non-immune fetal hydrops with increased soft tissue thickness. Classically there is a halo pattern around fetal head, neck, thorax, and abdomen. Fetal edema is associated with karyotype abnormalities, with multiple congenital anomalies, and with certain fetal infections like parvovirus B19 that cause severe fetal anemia. In the present case there was no evidence of infection or karyotype abnormality, but there was hypoplasia of umbilical cord vessels, pulmonary hypoplasia, and pericardial effusion. The etiology of fetal hydrops may remain unknown in up to 30% of cases.
胎儿水肿在过去被认为是同种免疫疾病的一种并发症。最近,胎儿水肿在导致非免疫性胎儿水肿且软组织厚度增加的情况下经常出现。典型地,胎儿头部、颈部、胸部和腹部周围会出现晕圈样表现。胎儿水肿与染色体核型异常、多种先天性畸形以及某些导致严重胎儿贫血的胎儿感染(如细小病毒B19)有关。在本病例中,没有感染或染色体核型异常的证据,但存在脐带血管发育不全、肺发育不全和心包积液。高达30%的胎儿水肿病例病因可能仍不明。