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病例报告:急性阑尾炎与嵌顿性脐疝:一种罕见的关联。

Case Report: The acute appendicitis and incarcerated umbilical hernia: a rare association.

作者信息

Corbi Letizia, Frediani Simone, Aloi Ivan Pietro, Bertocchini Arianna, Accinni Antonella, Pardi Valerio, Inserra Alessandro

机构信息

General and Thoracic Pediatric Surgery Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

出版信息

Front Pediatr. 2024 Feb 6;12:1334562. doi: 10.3389/fped.2024.1334562. eCollection 2024.

Abstract

INTRODUCTION

One of the most prevalent congenital wall abnormalities in children, umbilical hernias are often linked to premature or small-for-gestational-age babies. In cases of intestinal malrotation or if the cecum is very movable, generalized peritonitis may facilitate the imprisonment of these hernias.

CASE REPORT

We described a case of a 4-month-old baby who had a prior reducible umbilical hernia with a history of fever, vomiting, poor appetite, and constipation for around 48 h. The patient experienced significant intestinal bloating, vomiting, irreducibility of the umbilical hernia, skin pigmentation, and erythema at the umbilical site within 2 days after hospitalization. When there was no free abdominal air, a direct abdominal x-ray revealed evidence of hydro-gas stasis and various hydro-aerial levels that were pertinent to the ileum. In order to reduce the hernia, the patient had an emergency surgical treatment where the hernia sac was isolated and released from the ileal loop, which was securely attached to a fibrin plate. When the herniary sac was opened, a gangrenous and perforated appendix was found inside. On the seventh postoperative day, the patient was released from the hospital after an uncomplicated postoperative stay.

CONCLUSION

Our patient's clinical presentation is similar to that of only one other case report involving a 25-day-old male patient. Our case presented with a variant of the clinical symptoms of the previously described umbilical hernia, which became unfixable and strangulated as a result of appendix inflammation. The appendix was discovered inside the hernia sac during surgery.

摘要

引言

脐疝是儿童中最常见的先天性腹壁异常之一,常与早产儿或小于胎龄儿有关。在肠旋转不良的情况下,或者盲肠活动度很大时,全身性腹膜炎可能促使这些疝发生嵌顿。

病例报告

我们描述了一例4个月大的婴儿,该婴儿之前有可复性脐疝,伴有约48小时的发热、呕吐、食欲减退和便秘病史。患者在住院后2天内出现明显的肠胀气、呕吐、脐疝不可复、脐部皮肤色素沉着和红斑。在没有游离腹腔气体的情况下,腹部直接X线检查显示有气液瘀滞的迹象以及与回肠相关的各种气液平面。为了还纳疝内容物,患者接受了急诊手术治疗,术中将疝囊从回肠袢分离并松解,回肠袢牢固地附着在纤维蛋白板上。打开疝囊后,发现里面有一个坏疽穿孔的阑尾。术后第七天,患者在术后恢复顺利后出院。

结论

我们患者的临床表现仅与另一例涉及一名25日龄男性患者的病例报告相似。我们的病例呈现出先前描述的脐疝临床症状的一种变体,由于阑尾炎症导致疝变得无法回纳并发生绞窄。手术中在疝囊内发现了阑尾。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae06/10880186/6d189abdc660/fped-12-1334562-g001.jpg

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