妊娠期回肠乙状结肠结,剖宫产时偶然发现。罕见病例报告。

IF 0.7 Q4 SURGERY
Yahouza Boka Tounga , Hamidou Soumana Diaouga , Issifou Hama Sidi Mansour , Kadi Ide , Madi Nayama , Rachid Sani
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引用次数: 0

摘要

简介及重要性:妊娠期发生肠梗阻是一种罕见的情况。回肠乙状结肠结更为罕见,但预后较差。病例介绍:我们报告一例22岁的回肠乙状结肠结患者,她在怀孕36周时因妊娠晚期出血而入院。回肠乙状结肠结是偶然发现在剖宫产指胎盘后血肿。术中发现回肠和乙状结肠坏死。在取出一名健康的男婴后,我们切除了30厘米的受病小肠和坏死的乙状结肠。我们做了回肠吻合术和哈特曼结肠造口术。患者出院后30天完成结肠造口术,按照我科的治疗方案。结果是平淡无奇的,恢复日常活动和良好的产妇和围产期预后。讨论:通过对本病例的分析,对妊娠回肠乙状体结的发病、诊断、治疗及预后等方面进行探讨。结论:妊娠回肠乙状结肠结是一种危及生命的疾病,需要多学科治疗。它可能与其他产科急诊有关,如胎盘后血肿,这是一个诊断缺陷。诊断通常是偶然发现,正如本病例报告所证明的那样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ileosigmoid knot in pregnancy, incidentally discovered during caesarean section. A rare case report

Introduction and importance

The occurrence of intestinal obstruction during pregnancy is an unusual condition. Ileosigmoid knot is even rarer but it is associated with a poor prognosis.

Case presentation

We report a case of ileosigmoid knot in a 22-year-old patient who admitted to our department with third-trimester metrorrhagia in 36-week pregnancy. Ileosigmoid knot was incidentally discovered during a caesarean section indicated for retroplacental hematoma. Intraoperatively, necrosis of the ileum and the sigmoid colon was noted. After extraction of a healthy living male newborn, we performed resection of 30 cm of involved small bowel as well as resection of the necrotic sigmoid colon. We proceeded to do primary ileal anastomosis and a Hartmann's colostomy. The patient had a closure of colostomy after 30 days from the day of discharge, according to our department's protocol. The outcome was uneventful, with return to daily activities and a good maternal and perinatal prognosis.

Discussion

Through the analysis of this case report, we discuss the etiopathogenic, diagnostic, therapeutic and prognosis aspects of ileosigmoid knot in pregnancy.

Conclusion

Ileosigmoid knot in pregnancy is a life threatening condition needing multidisciplinary management. It may be associated with other obstetric emergencies such as retroplacental hematoma, which is a diagnostic pitfall. The diagnosis is often an incidentally discovery as evidenced by this case report.
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CiteScore
1.10
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