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家族性腺瘤性息肉病患者空肠腺瘤致肠套叠中的APC基因突变

APC gene mutations in a jejunal adenoma causing intussusception in a patient with familial adenomatous polyposis.

作者信息

Ishida Hideyuki, Iwama Takeo, Inokuma Shigehisa, Takeuchi Ikuya, Hashimoto Daijo, Miyaki Michiko

机构信息

Department of Surgery, Saitama Medical Center, Saitama Medical School, 1981 Kamoda-Tsujidocho, Kawagoe 350-8550, Japan.

出版信息

J Gastroenterol. 2002;37(12):1057-61. doi: 10.1007/s005350200178.

Abstract

Adenomatous polyps of the jejunum/ileum in patients with familial adenomatous polyposis (FAP) are usually small (<5 mm) and are considered to be of little clinical importance. Genetic alterations in these polyps have not previously been analyzed. We herein report an extremely rare case of FAP presenting with intussusception caused by jejunal adenomas. Both somatic and germline mutations of the APC gene were detected in one of the polyps. A 40-year-old man with FAP was admitted for closure of an ileostomy that had been created because of an anastomotic leak after subtotal proctocolectomy with ileo-anal-canal anastomosis. During the follow-up after that surgery, he had occasionally complained of colicky abdominal pain, but it had quickly subsided. At the second laparotomy, for closure of the ileostomy, jejuno-jejunal intussusception was incidentally found, and segmental resection of the jejunum, including the leading point of the intussusception, was performed. There were five polyps clustered in the resected jejunum. Histologically, the polyps, ranging from 5 to 26 mm in diameter, were adenomas with moderate to severe atypia. Genetic examinations of one of the largest polyps, using polymerase chain reaction single-strand conformation polymorphism (PCR-SSCP) and direct sequencing methods, revealed somatic (T insertion at codon 1557) and germline mutations (4 base-pair deletion at codons 181-182) of the APC gene. This is the first evidence that the coexistence of somatic and germline alterations in the APC gene is involved in the development of a jejunal adenoma causing small-bowel intussusception.

摘要

家族性腺瘤性息肉病(FAP)患者的空肠/回肠腺瘤性息肉通常较小(<5mm),临床意义不大。此前尚未对这些息肉的基因改变进行分析。我们在此报告一例极为罕见的FAP病例,该病例因空肠腺瘤导致肠套叠。在其中一个息肉中检测到了APC基因的体细胞和种系突变。一名40岁的FAP男性因直肠结肠次全切除术后回肠肛管吻合口漏而造口,此次入院进行回肠造口关闭术。在那次手术后的随访期间,他偶尔抱怨腹部绞痛,但疼痛很快就缓解了。在第二次剖腹手术中,为关闭回肠造口,偶然发现了空肠-空肠套叠,并对包括套叠起始点在内的空肠进行了节段性切除。切除的空肠中有五个息肉聚集。组织学检查显示,这些息肉直径为5至26mm,为中度至重度异型增生的腺瘤。使用聚合酶链反应单链构象多态性(PCR-SSCP)和直接测序方法对其中一个最大的息肉进行基因检测,发现了APC基因的体细胞突变(密码子1557处插入T)和种系突变(密码子181-182处4个碱基对缺失)。这是首次有证据表明APC基因的体细胞和种系改变共存与导致小肠套叠的空肠腺瘤的发生有关。

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