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Case Reports International journal of surgery case reports. 2025 Jun 11:132:111500. doi: 10.1016/j.ijscr.2025.111500 N/A0.62025

Double ileo-ileal intussusception secondary to inflammatory pseudotumor in an adult: A rare case report

成人炎症性假瘤继发双重回肠套叠:一例罕见病例报告 翻译改进

Sarthak Satpathy  1, Sibaprashad Pattanayak  2, Jitendra Kumar Sahoo  3, Satyaswarup Patnaik  4, Umesh Chandra Behera  5, Chinmay Samantaray  6

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作者单位

  • 1 Department of General Surgery, MKCG Medical College and Hospital, Berhampur, Odisha, India. Electronic address: sarthak.satpathy108@gmail.com.
  • 2 Department of General Surgery, MKCG Medical College and Hospital, Berhampur, Odisha, India. Electronic address: sibaprashad234@gmail.com.
  • 3 Department of General Surgery, MKCG Medical College and Hospital, Berhampur, Odisha, India. Electronic address: drjitendraksahoo@gmail.com.
  • 4 Department of General Surgery, MKCG Medical College and Hospital, Berhampur, Odisha, India.
  • 5 Department of General Surgery, MKCG Medical College and Hospital, Berhampur, Odisha, India. Electronic address: umeshchandraat66@gmail.com.
  • 6 Department of General Surgery, MKCG Medical College and Hospital, Berhampur, Odisha, India. Electronic address: chinmay.samantaray@gmail.com.
  • DOI: 10.1016/j.ijscr.2025.111500 PMID: 40516510

    摘要 中英对照阅读

    Introduction: Adult intussusception is rare and typically associated with an underlying lead point. Inflammatory pseudotumor, a rare benign lesion of uncertain etiology, can serve as such a lead point in the small bowel. The occurrence of double intussusception in this context is exceptionally uncommon.

    Presentation of case: A 55-year-old woman presented with signs of small bowel obstruction. Imaging(Fig. 1-11) revealed ileo-ileal intussusception. Intraoperatively(Fig. 16-18), a Double intussusception configuration was observed where one intussuscepted segment acted as the lead point for a second. A firm lesion at the apex was resected. Histopathology confirmed Inflammatory Pseudotumor(Fig. 12-15). The patient recovered uneventfully and remained asymptomatic at 6-month follow-up.

    Discussion: Double intussusception is extremely rare in adults. In this case, an inflammatory pseudotumor triggered an initial ileo-ileal intussusception, which subsequently served as the lead point for a second. The unusual etiology and configuration can pose diagnostic challenges, as radiological imaging may not fully reveal the complexity. Surgical intervention was required for definitive management.

    Conclusion: Double ileo-ileal intussusception caused by an inflammatory pseudotumor represents an exceedingly rare etiology of acute intestinal obstruction in adults. Prompt surgical treatment is critical. This case highlights the importance of considering rare benign tumors as potential lead points in adult intussusception.

    Keywords: Adult intussusception; Case report; Ileum; Inflammatory pseudotumor; Intussusception; Small bowel obstruction.

    Keywords:ileo-ileal intussusception; inflammatory pseudotumor

    介绍: 成人肠套叠罕见,通常与潜在的病灶点有关。炎性假瘤是一种病因不明的罕见良性病变,在小肠中可以作为这种病灶点。在这种情况下发生双层肠套叠极为罕见。

    病例呈现: 一位55岁女性因小肠梗阻症状就诊。影像学检查(图1-11)显示回肠回肠肠套叠。术中观察到(图16-18),一个双层肠套叠结构,其中一个肠套叠段作为第二个肠套叠的病灶点。切除并切除了顶端的一个硬结病变。病理结果确认为炎性假瘤(图12-15)。患者恢复顺利,在六个月随访中无症状。

    讨论: 成人双层肠套叠极为罕见。在本例中,一个炎性假瘤触发了初始的回肠回肠肠套叠,后者随后作为第二个肠套叠的病灶点。这种不寻常的原因和结构可能给诊断带来挑战,因为放射学影像可能无法完全揭示其复杂性。手术干预对于明确管理是必需的。

    结论: 由炎性假瘤引起的双层回肠回肠肠套叠在成人急性肠道梗阻中代表一种极为罕见的原因。及时进行外科治疗至关重要。此案例强调了考虑罕见良性肿瘤作为成年肠套叠病灶点的重要性。

    关键词: 成人肠套叠;病例报告;回肠;炎性假瘤;肠套叠;小肠梗阻。

    关键词:回肠回肠套叠; 炎性假瘤

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