在进行正常、顺利的结肠镜检查后出现急性呼吸困难。

IF 2.6 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinics and research in hepatology and gastroenterology Pub Date : 2024-06-19 DOI:10.1016/j.clinre.2024.102405
Claire Ginestet , Julie Deyrat , Xavier Dray , Thibault Voron
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引用次数: 0

摘要

一名 62 岁的男性因急性呼吸窘迫被转到急诊室,他既往有睡眠呼吸暂停综合征、脐疝和左腹股沟疝修补术病史。12 小时前,他因有结肠腺瘤家族史而接受了结肠镜筛查。这次结肠镜检查完整、正常、顺利。胸部 X 光平片显示结肠胀大,一直延伸到右胸的上三分之一处(图 1)。进一步询问病史后,患者回忆起多年前通过 CT 扫描发现的右侧膈疝。之前在接受结肠筛查评估时,他并没有提到过这一情况。患者被送入外科重症监护室。CT 扫描证实患者患有右侧膈疝,回肠末端和升结肠有内容物,没有肠系膜缺血的迹象,肺部大面积塌陷。使用鼻胃吸引器的保守治疗很快改善了患者的病情。他于第 6 天出院。膈疝修补术安排在 10 周后进行。腹腔镜检查显示右侧膈肌穹隆完全缺失(图 2;图 3),因此改为开腹手术进行完全修复。术后情况无异常。患者于第 6 天出院。随访 1 个月,一切正常。先天性膈疝非常罕见,通常在产前或新生儿呼吸窘迫时被诊断出来,需要进行新生儿紧急修补术[1,2]。在诊断不足或被忽视的成人中,这种情况可能会危及生命,就像我们的病人一样[3,4]。因此,即使是无症状的患者,也强烈建议进行手术修复[5]。复发是例外情况。
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Acute respiratory distress following an otherwise normal, uneventful, screening colonoscopy

A 62-year-old man with a past history of sleep apnea syndrome, umbilical and left inguinal hernia repairs, was referred to the emergency room for acute respiratory distress. He had underwent a screening colonoscopy 12 h earlier for a family history of colonic adenoma. This colonoscopy was complete, normal, and uneventful.

A plain chest X-ray showed a distended colon extending to the upper third of the right side of the chest (Fig. 1). Further anamnesis helped the patient to remember a right diaphragmatic hernia, well-documented by CT-scan years ago. He had not previously mentioned this condition, when evaluated for colon screening.

The patient was admitted to the surgical intensive care unit. A CT-scan confirmed a right diaphragmatic hernia with terminal ileum and ascending colon content, no sign of mesenteric ischemia, and massive pulmonary collapse. Conservative treatment with nasogastric suction quickly improved the patient's condition. He was discharged at day-6. Diaphragmatic hernia repair was scheduled 10 weeks later. Laparoscopy showed a complete agenesis of the right diaphragmatic dome (Fig. 2; Fig. 3), and was therefore converted into laparotomy for complete surgical repair. Postoperative course was unremarkable. Patient was discharged on day-6. Follow-up at 1 month was uneventful.

Congenital diaphragmatic hernias are rare and usually diagnosed in the pre- natal period or in neonates with respiratory distress, calling for emergency neonatal repair [1,2]. In underdiagnosed or neglecting adults, the condition can be life-threatening, as seen in our patient [3,4]. Surgical repair is therefore strongly recommended, even in asymptomatic patients [5]. Recurrences are exceptional.

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来源期刊
CiteScore
4.30
自引率
3.70%
发文量
198
审稿时长
42 days
期刊介绍: Clinics and Research in Hepatology and Gastroenterology publishes high-quality original research papers in the field of hepatology and gastroenterology. The editors put the accent on rapid communication of new research and clinical developments and so called "hot topic" issues. Following a clear Editorial line, besides original articles and case reports, each issue features editorials, commentaries and reviews. The journal encourages research and discussion between all those involved in the specialty on an international level. All articles are peer reviewed by international experts, the articles in press are online and indexed in the international databases (Current Contents, Pubmed, Scopus, Science Direct). Clinics and Research in Hepatology and Gastroenterology is a subscription journal (with optional open access), which allows you to publish your research without any cost to you (unless you proactively chose the open access option). Your article will be available to all researchers around the globe whose institution has a subscription to the journal.
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