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先天性腹壁发育不全合并结肠闭锁

Gastroschisis Complicated by Colonic Atresia.

机构信息

Department of General Surgery, UTHSC COM Chattanooga, Chattanooga, TN, USA.

出版信息

Am Surg. 2023 Jun;89(6):2762-2763. doi: 10.1177/00031348211048848. Epub 2021 Nov 3.

DOI:10.1177/00031348211048848
PMID:34730464
Abstract

INTRODUCTION

Gastroschisis with colonic atresia is a rare association. Due to its rarity and variation in presentation, no standardized surgical treatment option exists. Complicated gastroschisis is associated with a higher morbidity and mortality than intestinal atresia or gastroschisis alone.

METHODS

This is a case report of a neonate with congenital gastroschisis. On day of life 1, a silo was placed. On day of life 4, the upper portion of silo contents appeared more congested with dusky discoloration and the patient was oliguric. She was taken to the operating room for exploration.

RESULTS

The patient required resection of the terminal ileum and an atretic portion of the cecum due to necrosis. Four days later, primary closure of the gastroschisis defect was performed with creation of an end ileostomy. Elective ileostomy takedown was performed 5 months later. She returned to the operating room for anastomotic revision and gastrostomy tube placement for intestinal dysmotility and prolonged ileus. Tube feedings were discontinued 3 months post-operatively.

CONCLUSIONS

Gastroschisis with intestinal atresia is associated with increased hospital length of stay, longer duration of parenteral nutrition, more severe intestinal dysfunction, increased surgical complications, and higher mortality than gastroschisis or intestinal atresia alone. With associated colonic atresia, loss of a significant length of bowel due to necrosis, including the ileocecal region, is almost unavoidable. An already compromised blood supply to the atretic bowel is further impaired by a tight abdominal wall defect and postnatal increases in gravitational force. Complicated gastroschisis remains a complex surgical challenge requiring further discussion.

摘要

引言

先天性腹裂合并结肠闭锁较为罕见。由于其罕见性和表现多样性,目前尚无标准化的手术治疗方案。复杂型先天性腹裂的发病率和死亡率高于单纯肠闭锁或先天性腹裂。

方法

这是一例新生儿先天性腹裂的病例报告。在出生后第 1 天,患儿接受了造口袋治疗。在出生后第 4 天,造口袋内容物的上半部分出现充血和暗紫色变色,患儿出现少尿。遂将患儿转至手术室进行探查。

结果

患儿因坏死而切除了回肠末端和盲肠的闭锁部分。4 天后,对先天性腹裂缺损进行了一期缝合,并建立了末端回肠造口术。5 个月后,择期行回肠造口还纳术。患儿因肠动力障碍和长时间肠梗阻返回手术室进行吻合口修复和胃造口管放置。术后 3 个月停止肠内喂养。

结论

先天性腹裂合并肠闭锁与住院时间延长、肠外营养时间延长、更严重的肠道功能障碍、手术并发症增加和死亡率增加有关,高于单纯先天性腹裂或肠闭锁。合并结肠闭锁时,由于坏死,包括回盲部在内的大量肠段几乎不可避免地丢失。原本就受到损害的闭锁肠段的血液供应,会因腹壁缺损和出生后重力增加而进一步受损。复杂型先天性腹裂仍然是一个复杂的手术挑战,需要进一步讨论。

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