Fritsch Alessandra, Müller Ana Lúcia Letti, Sanseverino Maria Teresa Vieira, Kessler Rejane Gus, Barrios Patricia Martins Moura, Patusco Lucas Mohr, Magalhães José Antonio de Azevedo
Centro Obstétrico, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brasil.
Rev Bras Ginecol Obstet. 2012 Jul;34(7):310-5. doi: 10.1590/s0100-72032012000700004.
To identify the etiology of nonimmune hydrops fetalis cases in pregnant women diagnosed and referred for prenatal care.
Retrospective analysis of cases with nonimmune hydrops fetalis that were monitored between March 1992 and December 2011. Diagnosis was confirmed by the presence of fetal subcutaneous edema (≥ 5 mm) with effusion in at least one serous cavity using obstetric ultrasound, and etiological investigation was conducted with cytogenetic (karyotype), infectious (syphilis, parvovirus B19, toxoplasmosis, rubella, cytomegalovirus, adenovirus and herpes simplex), hematologic and metabolic (inborn errors) analysis and fetal echocardiography. Twin pregnancies were excluded. Statistical analysis was performed using the χ² test for adhesion (software R 2.11.1).
We included 116 patients with nonimmune hydrops fetalis; the etiology was elucidated in 91 cases (78.5%), while 25 cases (21.5%) were classified as idiopathic. Most cases had a chromosomal etiology, for a total of 26 cases (22.4%), followed by lymphatic etiology with 15 cases (12.9% with 11 cases of cystic hygroma), and cardiovascular and infectious etiology with 14 cases each (12.1%). In the remaining cases, the etiology was thoracic in 6.9% (eight cases), malformation syndromes in 4.3% (five cases), extrathoracic tumors in 3.4% (four cases), metabolic in 1.7% (two cases), and hematologic, gastrointestinal and genitourinary in 0.9% (one case each). During the postnatal period, 104 cases were followed up until the 40th day of life, and 12 cases had intrauterine fetal death. The survival rate of these 104 newborns was 23.1% (24 survived).
An attempt should be made to clarify the etiology of hydrops diagnosed during pregnancy since the condition is associated with a wide spectrum of diseases. It is especially important to determine whether a potentially treatable condition is present and to identify disease at risk for recurrence in future pregnancies for adequate pre-conception counseling.
确定诊断为非免疫性胎儿水肿并转诊至产前护理机构的孕妇病例的病因。
对1992年3月至2011年12月间监测的非免疫性胎儿水肿病例进行回顾性分析。通过产科超声检查发现胎儿皮下水肿(≥5mm)且至少一个浆膜腔有积液来确诊,采用细胞遗传学(核型)、感染性(梅毒、细小病毒B19、弓形虫病、风疹、巨细胞病毒、腺病毒和单纯疱疹病毒)、血液学和代谢(先天性疾病)分析以及胎儿超声心动图进行病因调查。排除双胎妊娠。使用R 2.11.1软件进行卡方检验以进行黏附性统计分析。
我们纳入了116例非免疫性胎儿水肿患者;91例(78.5%)明确了病因,25例(21.5%)被归类为特发性。大多数病例病因是染色体方面的,共26例(22.4%),其次是淋巴系统病因,有15例(12.9%,其中11例为囊状水瘤),心血管和感染性病因各有14例(12.1%)。其余病例中,病因是胸部问题的占6.9%(8例),畸形综合征占4.3%(5例),胸外肿瘤占3.4%(4例),代谢性病因占1.7%(2例),血液学、胃肠道和泌尿生殖系统病因各占0.9%(各1例)。在出生后阶段,104例随访至出生后第40天,12例发生宫内胎儿死亡。这104例新生儿的存活率为23.1%(24例存活)。
鉴于该病症与多种疾病相关,应尝试明确孕期诊断的水肿病因。确定是否存在潜在可治疗的病症以及识别未来妊娠中有复发风险的疾病对于进行充分的孕前咨询尤为重要。