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妊娠早期梅克尔憩室轴性扭转致急性腹膜炎:一例报告

Axial torsion of Meckel's diverticulum causing acute peritonitis in the first trimester of pregnancy: a case report.

作者信息

Nagata Hiromitsu, Nishizawa Hiroyasu, Mashima Susumu, Shimahara Yasuyuki

机构信息

Department of Surgery, Yamatokoriyama Hospital, 1-62 Asahichou, Yamatokoriyama, Nara, 639-1013, Japan.

出版信息

Surg Case Rep. 2019 Dec 5;5(1):190. doi: 10.1186/s40792-019-0754-y.

Abstract

BACKGROUND

Meckel's diverticulum is considered the most prevalent congenital anomaly of the gastrointestinal tract. Approximately 4% of patients are symptomatic with complications such as bleeding, intestinal obstruction, and inflammation, while axial torsion of Meckel's diverticulum is rare, particularly in pregnancy.

CASE PRESENTATION

A 31-year-old woman in week 15 of pregnancy complained of epigastric pain, nausea and vomiting. Clinical diagnosis was severe hyperemesis gravidarum. Because the symptoms persisted during hospitalization, CT was performed and revealed dilated small bowel loops with multiple air-fluid levels. In the right mid-abdomen, there was a large part of air containing a cavity connected to the small intestine, which was considered a dilated bowel loop. Emergency laparotomy was performed and axial torsion of a large Meckel's diverticulum measuring 11 cm was found at a few centimeters proximal to the ileocecal valve. Ileocecal resection including Meckel's diverticulum was performed. The postoperative course was uneventful. At 40 weeks gestation, she had vaginal delivery of normal baby.

CONCLUSION

The physiological and anatomical changes in pregnancy can make a straightforward clinical diagnosis difficult. Prompt diagnosis and management were needed in order to avoid significant maternal and fetal risks. The use of imaging examinations, especially CT examination, with proper timing may be helpful to prevent delay in diagnosis and surgical intervention. Here, we report the case of a patient with axial torsion of Meckel's diverticulum in pregnancy. To our knowledge, axial torsion of Meckel's diverticulum in the first trimester of pregnancy has not been reported in the English medical literature.

摘要

背景

梅克尔憩室被认为是胃肠道最常见的先天性异常。约4%的患者会出现诸如出血、肠梗阻和炎症等并发症的症状,而梅克尔憩室的轴向扭转很少见,尤其是在妊娠期。

病例介绍

一名31岁处于妊娠15周的女性主诉上腹部疼痛、恶心和呕吐。临床诊断为重度妊娠剧吐。由于住院期间症状持续存在,遂进行了CT检查,结果显示小肠袢扩张,有多个气液平面。在右中腹部,有一大片含气腔与小肠相连,被认为是扩张的肠袢。遂进行了急诊剖腹手术,发现在回盲瓣近端几厘米处有一个长11厘米的大型梅克尔憩室发生了轴向扭转。进行了包括梅克尔憩室在内的回盲部切除术。术后病程顺利。妊娠40周时,她经阴道分娩出一个正常婴儿。

结论

妊娠期的生理和解剖变化可能使临床诊断变得困难。需要及时诊断和处理,以避免对母婴造成重大风险。适时使用影像学检查,尤其是CT检查,可能有助于防止诊断和手术干预的延迟。在此,我们报告一例妊娠期梅克尔憩室轴向扭转的病例。据我们所知,英文医学文献中尚未报道过妊娠早期梅克尔憩室轴向扭转的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494b/6895344/3e986c11eebe/40792_2019_754_Fig1_HTML.jpg

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