Assir Central Hospital, Abha, 61231, Kingdom of Saudi Arabia.
Department of Pediatric Surgery, King Faisal Specialist Hospital and Research Center, Riyadh, 11211, Kingdom of Saudi Arabia.
J Pediatr Surg. 2011 Apr;46(4):636-639. doi: 10.1016/j.jpedsurg.2010.10.001.
The purpose was to study the impact of Down's syndrome (DS) in the diagnosis, management, and outcomes of patients with Morgagni hernia (MH).
Twenty-two (22) patients with MH treated at a tertiary center were retrospectively studied for history, findings, associated anomalies, referral diagnoses, hospital admissions, radiological procedures for diagnosis, age at which operated on, operative procedure, complications, and recurrences. Eleven did not have DS (group 1); 11 others had associated DS (group 2). The ages at operation were compared in the 2 groups using the Mann-Whitney test. More than 3 hospital admissions for symptoms and signs relevant to MH before a diagnosis of MH were considered a "delayed diagnosis."
Twenty-two patients (7 females, 15 males) aged 3 months to 10 years were seen. They presented with respiratory distress (n = 16), with vomiting (n = 5), with intestinal obstruction (n = 1), by serendipity (n = 2), and with recurrence from another hospital (n = 1). The mean age of group 1 was 14.5 months, and that of group 2 was 29.18 months; the difference was not significant (P = .621). Nine patients of group 2 were "delayed diagnosis" compared with 2 in group 1. Both delays from group 1 had severe associated anomalies. All patients underwent operative correction (17 open and 5 laparoscopic repairs). Two had recurrences, one operated on by the open method by us and another laparoscopically by the Lima technique at another center. Both had DS. Both were reoperated on by the open method.
The diagnosis of MH may be strikingly delayed when associated with DS or other severe congenital anomalies. Morgagni hernia should be strongly considered in patients with DS admitted repeatedly for chest infections. Chest x-rays in 2 planes may avoid misdiagnosis of MH. Both open and laparoscopic methods have proven satisfactory as operative treatment of MH. Recurrences were seen in patients with DS, which may be corrected by laparotomy or laparoscopically. We feel that resecting the sac and approximating the posterior lip of the defect to the anterior abdominal wall, whether in open or laparoscopic methods, may give stronger repairs, which may avoid recurrence.
研究唐氏综合征(DS)对摩根疝(MH)患者的诊断、治疗和结局的影响。
对在一家三级中心接受治疗的 22 例 MH 患者进行回顾性研究,研究内容包括病史、检查结果、合并畸形、转诊诊断、住院情况、诊断性放射学程序、手术年龄、手术方式、并发症和复发。其中 11 例患者无 DS(第 1 组),11 例患者有合并 DS(第 2 组)。采用 Mann-Whitney 检验比较两组患者的手术年龄。将 MH 相关症状和体征 3 次以上住院诊断视为“延迟诊断”。
共纳入 22 例患者(7 例女性,15 例男性),年龄 3 个月至 10 岁。他们的主要表现为呼吸窘迫(n = 16)、呕吐(n = 5)、肠梗阻(n = 1)、偶然发现(n = 2)和来自另一家医院的复发(n = 1)。第 1 组的平均年龄为 14.5 个月,第 2 组的平均年龄为 29.18 个月;两组差异无统计学意义(P =.621)。第 2 组有 9 例患者为“延迟诊断”,第 1 组有 2 例。第 1 组的两次延迟均与严重的合并畸形有关。所有患者均接受手术治疗(17 例开放手术,5 例腹腔镜手术)。2 例复发,其中 1 例由我们采用开放手术方法治疗,另 1 例由利马技术在另一家中心采用腹腔镜手术方法治疗。这两例患者均有 DS。这两例患者均再次接受开放手术治疗。
当合并 DS 或其他严重先天性畸形时,MH 的诊断可能会明显延迟。反复因胸部感染入院的 DS 患者应强烈考虑 MH。胸部 2 个平面的 X 线片可能避免 MH 的误诊。开放手术和腹腔镜手术均已被证明是 MH 手术治疗的有效方法。DS 患者可见复发,可通过剖腹手术或腹腔镜手术进行纠正。我们认为,无论是在开放手术还是腹腔镜手术中,切除疝囊并将疝囊后缘与前腹壁前缘靠拢,可能会使修补更牢固,从而避免复发。