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由孤立性黑斑息肉综合征型错构瘤性息肉引起的大量肠套叠。

Massive intussusception caused by a solitary Peutz-Jeghers type hamartomatous polyp.

作者信息

Kalliakmanis V, Perysinakis I, Koutsouvas K, Karras P, Margaris E, Angelakis C

机构信息

Surgical Department, General Hospital of Agrinio , Agrinio, Aitoloakarnania , Greece.

Third Surgical Department, Hygeia Hospital , Athens , Greece.

出版信息

Ann R Coll Surg Engl. 2018 Apr;100(4):e91-e93. doi: 10.1308/rcsann.2018.0019. Epub 2018 Feb 27.

Abstract

Intussusception is a rare cause of intestinal obstruction in adults and represents a diagnostic challenge for the surgeon. In the majority of cases, presenting symptoms are not specific, making preoperative diagnosis difficult. Several medical conditions may cause intestinal intussusception. We present the case of a 16-year-old female patient with intussusception due to a hamartomatous Peutz-Jeghers type polyp. This is an extremely rare case in which the first manifestation of the intestinal polyp was jejunojejunal intussusception very close to the duodenojejunal junction, with a necrotic intussusceptum about 50 cm long. The patient was treated successfully with enterectomy and end-to-end anastomosis. Postoperative course was uneventful and the patient is currently under gastroenterological and genetic investigation to exclude the diagnosis of Peutz-Jeghers syndrome.

摘要

肠套叠是成人肠梗阻的罕见病因,对外科医生来说是一项诊断挑战。在大多数病例中,呈现的症状并不特异,使得术前诊断困难。几种医学状况可能导致肠套叠。我们报告一例16岁女性患者,因错构瘤性黑斑息肉病型息肉导致肠套叠。这是一例极其罕见的病例,其中肠息肉的首发表现是非常靠近十二指肠空肠交界处的空肠空肠套叠,套入部坏死约50厘米长。患者接受肠切除及端端吻合术治疗成功。术后病程平稳,患者目前正在接受胃肠病学和遗传学检查以排除黑斑息肉病综合征的诊断。

相似文献

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Peutz-Jeghers syndrome. A case report.佩-吉二氏综合征。病例报告。
Acta Dermatovenerol Alp Pannonica Adriat. 2005 Mar;14(1):26-9.

引用本文的文献

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Intestinal intussusception in Peutz Jeghers syndrome: A case report.黑斑息肉综合征合并肠套叠:一例报告。
Ann Med Surg (Lond). 2020 May 4;54:106-108. doi: 10.1016/j.amsu.2020.04.013. eCollection 2020 Jun.

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