Pelizzo Gloria, Codrich Daniela, Zennaro Floriana, Dell'oste Clara, Maso Gianpaolo, D'Ottavio Giuseppina, Schleef Juergen
Department of Pediatric Surgery, Children's Hospital of Trieste, IRCCS Burlo Garofolo, Via dell'Istria 65/1, 34137 Trieste, Italy.
Pediatr Surg Int. 2008 Sep;24(9):1061-5. doi: 10.1007/s00383-008-2194-9. Epub 2008 Jul 31.
Prenatal ultrasound (US) diagnosis and postnatal outcome are reviewed in three babies with the complex form of meconium peritonitis (MP), the cystic type. Perinatal management is discussed. Large intra-abdominal cysts with signs of calcifications were detected during the second mid-trimester. Meconium ascites and polyhydramnios appeared between 32 and 35 weeks of gestation. Signs of anaemia were assessed on median cerebral artery peak systolic velocity. Sudden appearance of hydrops and anaemia required preterm delivery, neonatal resuscitation and urgent abdominal drainage. Postnatal US imaging confirmed prenatal sonographic evidence. Abdominal X-ray showed calcifications and no free abdominal air. Intestinal diversion was performed in two patients on their first day of life and evolution was uneventful. Hospital death occurred in one baby, who was submitted to delayed surgery due to unstable hemodynamic conditions. Distal ileal perforation walled off by pseudocysts was detected in all cases. One baby was found to be affected by cystic fibrosis. Ileal intussusception was described in the non-surviving infant. The cystic type of MP may have a potentially rapid lethal course and the onset of foetal anaemia and polyhydramnios is a bad prognostic factor. Severe evolution in hydrops and foetal distress may occur at any moment suggesting the persistence of a leakage or re-rupture of the cysts with new meconium spillage into the abdomen. Prenatal detection of ascites, polyhydramnios and pseudocysts requires a strict follow-up, and timing of delivery has to be planned in a tertiary centre. Postnatal radiological imaging does not offer further information over prenatal imaging and surgical decision should not be influenced by the absence of abdominal free air. Urgent abdominal drainage at birth, followed by intestinal diversion of persistent intestinal perforation on the first day of life, may prevent bacterial colonisation and improve prognosis.
对3例患有复杂型胎粪性腹膜炎(MP)囊性型的婴儿进行了产前超声(US)诊断及产后转归回顾,并讨论了围产期管理。孕中期发现巨大腹腔囊肿伴钙化迹象。孕32至35周出现胎粪性腹水和羊水过多。通过大脑中动脉收缩期峰值流速评估贫血迹象。水肿和贫血的突然出现需要早产、新生儿复苏及紧急腹腔引流。产后超声成像证实了产前超声检查结果。腹部X线显示有钙化且无游离腹腔气体。2例患者在出生第一天进行了肠造口术,病情进展平稳。1例婴儿因血流动力学不稳定接受延迟手术,最终死亡。所有病例均检测到由假囊肿包裹的回肠远端穿孔。1例婴儿被发现患有囊性纤维化。死亡婴儿存在回肠套叠。MP囊性型可能有潜在的快速致死病程,胎儿贫血和羊水过多的出现是不良预后因素。水肿和胎儿窘迫的严重进展可能随时发生,提示囊肿持续渗漏或再次破裂,有新的胎粪溢入腹腔。产前检测到腹水、羊水过多和假囊肿需要严格随访,分娩时机必须在三级中心进行规划。产后放射学成像并未提供比产前成像更多的信息,手术决策不应受无腹腔游离气体的影响。出生时紧急腹腔引流,随后在出生第一天对持续性肠穿孔进行肠造口术,可预防细菌定植并改善预后。