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青少年因乙状结肠冗长和托尔特纤维束带导致的大肠梗阻:一例罕见病例报告。

Large bowel obstruction in an adolescent caused by dolichocolon and a fibrotic band of Toldt: A rare case report.

作者信息

Ibrahim Rana, Houmani Ali, Nasrallah Jamil, Dika Zakaria

机构信息

Research Department at Saint George Hospital-Hadath, Beirut, Lebanon.

Radiology Department at Saint George Hospital-Hadath, Beirut, Lebanon.

出版信息

Int J Surg Case Rep. 2025 Sep;134:111702. doi: 10.1016/j.ijscr.2025.111702. Epub 2025 Jul 18.

Abstract

BACKGROUND

Large bowel obstruction (LBO) is uncommon in adolescents and often presents a diagnostic challenge due to its rarity and atypical causes compared to adults. Dolichocolon, a congenital elongation of the colon, and congenital fibrotic bands such as the band of Toldt are rarely reported causes of LBO in this age group.

CASE-PRESENTATION: We report a 17-year-old female with no prior medical or surgical history who presented with diffuse abdominal pain, obstipation, and abdominal distension. Imaging revealed a large bowel obstruction with a transition zone at the splenic flexure. Exploratory laparotomy identified a fibrotic band of Toldt causing extrinsic compression of the colon in the setting of dolichocolon with severe colonic dilatation. The patient underwent subtotal colectomy with ileosigmoid anastomosis. Postoperative recovery was uneventful, and the patient was discharged in good condition.

DISCUSSION

This case highlights the importance of considering congenital anatomical variants such as dolichocolon and fibrotic peritoneal bands in adolescents presenting with LBO, especially in the absence of prior surgery or malignancy. Early recognition and timely surgical intervention are crucial to prevent morbidity.

CONCLUSION

Dolichocolon combined with a fibrotic band of Toldt is a rare but significant cause of LBO in adolescents. Awareness of such anomalies can facilitate accurate diagnosis and appropriate management, leading to favorable outcomes.

摘要

背景

大肠梗阻(LBO)在青少年中并不常见,由于其罕见性以及与成人相比病因不典型,常常带来诊断挑战。先天性结肠冗长(先天性结肠伸长)以及先天性纤维带(如Toldt氏带)是该年龄组中导致LBO的罕见报道病因。

病例介绍

我们报告一名17岁女性,既往无内科或外科病史,出现弥漫性腹痛、便秘和腹胀。影像学检查显示大肠梗阻,脾曲处有移行带。剖腹探查发现一条Toldt氏纤维带,在先天性结肠冗长伴严重结肠扩张的情况下导致结肠外部受压。患者接受了次全结肠切除术及回肠乙状结肠吻合术。术后恢复顺利,患者康复出院。

讨论

该病例强调了在患有LBO的青少年中考虑先天性解剖变异(如先天性结肠冗长和纤维化腹膜带)的重要性,尤其是在无既往手术史或恶性肿瘤的情况下。早期识别和及时手术干预对于预防并发症至关重要。

结论

先天性结肠冗长合并Toldt氏纤维带是青少年LBO的一种罕见但重要的病因。认识到此类异常有助于准确诊断和恰当处理,从而带来良好预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca9d/12305333/477ab240f596/gr1.jpg

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