先天性膈疝的心包内疝

Mohamed H Koura, Hamid Qoura, M. Nayar, Mohammed J Al Sajwani
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摘要

心包内膈疝是一种罕见的疾病,英文文献中只报道了少数病例。1在2010-2011年的八个月时间里,我们在阿曼苏丹国皇家医院治疗了两例先天性心包内膈膜疝。第一例在出生前未被诊断为膈疝。出生后,新生儿被诊断为心包积液,CT可以做出正确诊断。第二例经产前扫描诊断为膈疝,产后胸部X光检查证实为左侧先天性膈疝,但术中发现为前膈疝,伴有肝和部分肠进入心包囊的心包内疝。两名新生儿出生后均因呼吸窘迫而插管。第一例使用聚四氟乙烯(PTFE)补片修复缺损,第二例不使用补片修复。在这两种情况下,除了缺陷外,隔膜两侧的其余部分都完好无损;囊缺失,出现心包缺损。两名新生儿出院时情况良好。
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Intra pericardial herniation in congenital diaphragmatic hernia
Intrapericardial diaphragmatic hernia is a rare condition with only few cases reported in the English language literature.1 During a span of eight months in 2010-2011 we treated two cases of congenital intra pericardial diaphragmatic hernia in Royal Hospital in the Sultanate of Oman. The first case was not diagnosed antenatally as diaphragmatic hernia. Post-natally the neonate was diagnosed as having pericardial effusion and correct diagnosis arrived at by CTs can. The second case was diagnosed by antenatal scan as diaphragmatic hernia and confirmed in postnatal period by chest X-Ray as left congenital diaphragmatic hernia but intra-operative finding was an anterior diaphragmatic hernia with intra pericardial herniation of the liver and part of the bowel into the pericardial sac. Both neonates were intubated after birth due to respiratory distress. A polytetrafluoroethylene (PTFE) patch was used for repair of the defect in first case and the second case was repaired without a patch. In both cases, apart from the defect, the rest of the diaphragm, on either side, was intact; sac was absent and a pericardial defect was present. Both neonates were discharged in good condition.
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