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婴幼儿期先天性食管旁疝

Congenital paraesophageal hernia in infancy and childhood.

作者信息

Al-Salem A H

机构信息

Division of Pediatric Surgery, Department of Surgery, Qatif Central Hospital, PO Box 18432, Qatif 31911, Kingdom of Saudi Arabia.

出版信息

Saudi Med J. 2000 Feb;21(2):164-7.

Abstract

OBJECTIVES

Congenital paraesophageal hernia is a rare condition in the pediatric age group. The symptomatology of these patients is usually non-specific in the form of repeated attacks of chest infection and/or recurrent attacks of vomiting but can be associated with serious complications such as intrathoracic gastric volvulus.

METHODS

Between 1989 and 1997, 6 children with paraesophageal hernia were treated at our hospital.

RESULTS

Six children (4 males and 2 females) were treated for congenital paraesophageal hernia. Their age at presentation ranged from 2 days to 21/2 years (mean 1.3 years). Two presented with recurrent chest infection, while 3 others had recurrent attacks of vomiting with fullness and pain in the epigastrium in one of them. One of our patients presented acutely immediately after birth with respiratory distress while another was found to have intrathoracic gastric volvulus. Chest x-ray was suggestive of paraesophageal hernia in all of them but the diagnosis was confirmed by Barium swallow and meal. Intraoperatively there was a hernial sac in all of them. The surgical treatment consisted of excision of the hernial sac after reducing the stomach and tightening of the crura of the esophageal hiatus. Nissen's fundoplication was added in 3 patients, but in one of them this was dismantled because of tight repair. Anterior and fundal gastropexy was added in one patient, while 2 had tightening of the crura only.

CONCLUSION

Congenital paraesophageal hernia, although rare in the pediatric age group, can present acutely with respiratory distress or intrathoracic gastric volvulus. Physicians caring for these patients should be aware of such a presentation and complication and paraesophageal hernia should be included in the differential diagnosis of children with repeated attacks of chest infection and/or vomiting. The rarity of this condition in children makes it difficult to evaluate the true necessity of adding an antireflux procedure in these patients. We feel some form of gastropexy may be a more appropriate procedure to be added to the repair.

摘要

目的

先天性食管旁疝在儿童年龄组中是一种罕见疾病。这些患者的症状通常不具特异性,表现为反复的胸部感染发作和/或反复的呕吐发作,但可能与严重并发症如胸腔内胃扭转相关。

方法

1989年至1997年间,我院治疗了6例食管旁疝患儿。

结果

6例患儿(4男2女)接受了先天性食管旁疝治疗。他们就诊时的年龄范围为2天至2.5岁(平均1.3岁)。2例表现为反复的胸部感染,另外3例有反复的呕吐发作,其中1例伴有上腹部饱胀和疼痛。我们的1例患者出生后立即急性出现呼吸窘迫,另1例被发现有胸腔内胃扭转。所有患儿胸部X线均提示食管旁疝,但通过吞钡造影和餐检查确诊。术中所有患儿均有疝囊。手术治疗包括在将胃复位后切除疝囊并收紧食管裂孔的脚。3例患者加做了Nissen胃底折叠术,但其中1例因修复过紧而拆除。1例患者加做了前壁和胃底胃固定术,2例仅收紧了食管裂孔的脚。

结论

先天性食管旁疝虽然在儿童年龄组中罕见,但可急性表现为呼吸窘迫或胸腔内胃扭转。诊治这些患者的医生应意识到这种表现和并发症,食管旁疝应纳入反复出现胸部感染和/或呕吐发作儿童的鉴别诊断中。这种疾病在儿童中的罕见性使得难以评估在这些患者中加做抗反流手术的真正必要性。我们认为某种形式的胃固定术可能是修复术中更合适加做的手术。

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