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膈疝

Diaphragmatic Hernia

作者信息

Spellar Kayleigh, Sharma Sanjeev, Gupta Nagendra

机构信息

Royal Devon and Exeter

Texas Health Resources

Abstract

A diaphragmatic hernia is a protrusion of abdominal contents into the thoracic cavity due to a defect within the diaphragm. Diaphragmatic hernia is commonly a congenital phenomenon; however, acquired cases also occur. The reported incidence of diaphragmatic hernia is approximately 0.8 to 5 out of 10,000 live births. Acquired diaphragmatic hernias typically occur following blunt or penetrating trauma, which results in a rupture of the diaphragm, accompanied by herniation of abdominal content; however, acquired diaphragmatic hernias can also occur spontaneously or due to iatrogenic causes. Acquired diaphragmatic hernia is rare but can be life-threatening, resulting in bowel incarceration and strangulation with an overall mortality rate of up to 31%. Congenital diaphragmatic hernia is a developmental defect of the diaphragm that results in the herniation of abdominal viscera into the chest cavity. Neonates with congenital diaphragmatic hernia usually present with respiratory distress early in the first few hours of life. The respiratory distress associated with the congenital diaphragmatic hernia may be mild. Occasionally, the accompanying respiratory distress is so severe that it can be life-threatening. With antenatal diagnosis and improved neonatal care, survival has been remarkably improved, but a notable risk of morbidity and mortality remains in infants with congenital diaphragmatic hernia. Diaphragmatic injury is rare, complicating less than 1% of all patients with trauma. However, the incidence includes up to 3% of all abdominal injuries. Isolated diaphragmatic injuries are uncommon and are usually reported in the context of complicated abdominal and thoracic injuries. Notwithstanding the probability of an obvious herniated abdominal viscera in the thoracic cavity in the chest radiographs, the subtle cases should not be underestimated. Therefore, a high index of suspicion is strongly recommended to avoid the debilitating morbidity associated with delayed and missed diagnosis.

摘要

膈疝是指由于膈肌缺损导致腹腔内容物突入胸腔。膈疝通常是一种先天性疾病;不过,也有后天性病例。据报道,膈疝的发病率约为每10000例活产中有0.8至5例。后天性膈疝通常发生在钝性或穿透性创伤之后,这会导致膈肌破裂,并伴有腹腔内容物疝出;然而,后天性膈疝也可能自发出现或由医源性原因引起。后天性膈疝很少见,但可能危及生命,可导致肠管嵌顿和绞窄,总体死亡率高达31%。先天性膈疝是膈肌的一种发育缺陷,会导致腹腔脏器疝入胸腔。患有先天性膈疝的新生儿通常在出生后的头几个小时内就会出现呼吸窘迫。先天性膈疝伴发的呼吸窘迫可能较轻。偶尔,伴发的呼吸窘迫会非常严重,甚至危及生命。随着产前诊断和新生儿护理的改善,存活率有了显著提高,但先天性膈疝患儿仍有明显的发病和死亡风险。膈肌损伤很少见,在所有创伤患者中并发症发生率不到1%。然而,在所有腹部损伤中,其发生率高达3%。孤立性膈肌损伤并不常见,通常在复杂的腹部和胸部损伤背景下报道。尽管胸部X线片可能显示胸腔内有明显的腹腔脏器疝出,但对于细微的病例也不应低估。因此,强烈建议保持高度怀疑,以避免因诊断延迟和漏诊而导致的致残性发病。

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