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先天性 Bochdalek 膈疝早发和晚发 20 年回顾:它们是不同的临床谱吗?

A twenty-year review of early and late-presenting congenital Bochdalek diaphragmatic hernia: are they different clinical spectra?

机构信息

Department of Pediatrics, Mackay Memorial Hospital, Taitung, Taiwan.

出版信息

Pediatr Neonatol. 2010 Feb;51(1):26-30. doi: 10.1016/S1875-9572(10)60006-X.

Abstract

BACKGROUND

Congenital Bochdalek diaphragmatic hernia (CDH) is easily recognized if it is present shortly after birth. However, cases of delayed CDH presentation are more subtle and therefore less easily diagnosed.

METHODS

We retrospectively analyzed 85 patients who were under 18 and diagnosed with CDH between June 1987 and May 2007. Those diagnosed before 1 month of age were categorized as having early-presenting CDH and those diagnosed after 1 month were categorized as having late-presenting CDH.

RESULTS

Of the 85 cases, 68 (80%) were early-presenting and 17 (20%) were late-presenting CDH. Respiratory symptoms were more common in early-presenting CDH, while gastrointestinal complaints were more dominant in the late-presenting group, particularly in patients with left diaphragmatic defects. Late-presenting CDH, which was more likely to be associated with chronic gastrointestinal symptoms, was associated with a lower mortality than acute early-presenting CDH with respiratory symptoms, despite the more prompt diagnosis of the latter. The small bowel was the organ most commonly herniated into the thorax. Congenital heart disease was the most commonly associated malformation, but the presence of associated anomalies did not increase mortality.

CONCLUSION

Early-presenting CDH shows acute symptoms, is readily diagnosed, and requires prompt intervention to prevent death. In contrast, late-presenting CDH shows more subtle symptoms and is more difficult to diagnose. Although the late-presenting CHD has better prognosis, it still requires surgery intervention to alleviate the symptoms. Clinicians must maintain a high index of suspicion for CDH, regardless of its presentation.

摘要

背景

如果先天性膈疝(CDH)在出生后不久即存在,则很容易被发现。然而,迟发性 CDH 表现较为隐匿,因此诊断较为困难。

方法

我们回顾性分析了 1987 年 6 月至 2007 年 5 月期间诊断为 CDH 的 85 例年龄小于 18 岁的患者。出生后 1 个月内诊断为早发性 CDH,1 个月后诊断为迟发性 CDH。

结果

85 例中,早发性 68 例(80%),迟发性 17 例(20%)。早发性 CDH 更常见呼吸系统症状,而迟发性 CDH 更常见胃肠道症状,特别是左膈缺损患者。迟发性 CDH 更易合并慢性胃肠道症状,尽管后者更易早期诊断,但死亡率低于以呼吸系统症状为表现的急性早发性 CDH。最常疝入胸腔的器官是小肠。先天性心脏病是最常见的相关畸形,但存在相关畸形并不会增加死亡率。

结论

早发性 CDH 表现为急性症状,易于诊断,需要及时干预以防止死亡。相比之下,迟发性 CDH 表现为更为隐匿的症状,更难诊断。虽然迟发性 CDH 预后较好,但仍需要手术干预以缓解症状。无论其表现如何,临床医生都必须保持对 CDH 的高度警惕。

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