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首页> 外文期刊>American Journal of Case Reports >Large benign submucosal lipoma presented with descending colonic intussusception in an adult
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Large benign submucosal lipoma presented with descending colonic intussusception in an adult

机译:成人出现良性粘膜下脂肪瘤并伴结肠套叠下降

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Background: Lipoma of the large intestine is rare, account for only 5% of all gastrointestinal tumors. Lipomas are usually asymptomatic but rarely may cause bleeding, obstruction and intussusception. We present a case of a giant colonic lipoma causing descending-colonic intussusception.Case Report: 34 yo F presented with the intermittent left lower quadrant abdominal pain for 3 weeks. The pain initially was associated with bloating and constipation and for the last several days frank blood in stool, nausea and decreased appetite. CT scan of the abdomen revealed descending colonic obstruction by a 5.3 cm colonic lipomatous mass with resultant intussusception. Patient initially underwent colonoscopy that revealed polypoid lesion at 3–40 similar to lipoma with intussusception that was reduced. Patient subsequently underwent laparoscopic segmental left colectomy for the descending colonic intussusception due to large colonic lipomatous mass. Pathology confirmed the histology of lipoma.Conclusions: Adult bowel intussusception is a rare but challenging condition to diagnose in a timely manner. Preoperative diagnosis is usually missed or delayed because of nonspecific and often subacute symptoms. Lipoma is a rare cause of the intussusception. A high index of suspicion and appropriate investigations (abdominal ultrasound, CT scan and colonoscopy) can result in prompt diagnosis. Lipoma of the large intestine is very rare. Submucosal lipomas are usually asymptomatic but may cause bleeding, obstruction, intussusception, or abdominal pain. Accurate preoperative diagnosis is difficult and lipoma is often mistaken for adenomatous polyp or carcinoma. Treatment usually requires formal resection of the involved bowel segment due to high suspicion for malignancy and subsequent complications due to obstruction.
机译:背景:大肠脂肪瘤很少见,仅占所有胃肠道肿瘤的5%。脂肪瘤通常无症状,但很少引起出血,阻塞和肠套叠。本例为大肠脂肪瘤引起结肠结肠套叠下降的病例。病例报告:34岁,伴间歇性左下腹腹痛3周。最初,疼痛与腹胀和便秘有关,在最后几天,粪便中充血,恶心和食欲下降。腹部的CT扫描显示5.3 cm结肠脂肪瘤性肿块导致结肠梗阻下降,并导致肠套叠。患者最初接受了结肠镜检查,发现在3–40处出现息肉样病变,类似于带肠套叠的脂肪瘤减少了。由于结肠结肠脂肪瘤肿块较大,患者随后因腹腔肠套叠下降而进行了腹腔镜分段左结肠切除术。病理证实了脂肪瘤的组织学。结论:成人肠套叠是一种罕见的但具有挑战性的疾病,需要及时诊断。术前诊断通常由于非特异性且常常为亚急性症状而错过或延迟。脂肪瘤是肠套叠的罕见原因。高度怀疑和适当的检查(腹部超声,CT扫描和结肠镜检查)可导致迅速诊断。大肠脂肪瘤非常罕见。粘膜下脂肪瘤通常无症状,但可能引起出血,阻塞,肠套叠或腹痛。准确的术前诊断很困难,并且脂肪瘤经常被误认为是腺瘤性息肉或癌。由于高度怀疑恶性肿瘤以及阻塞引起的并发症,通常需要对受累肠段进行正式切除治疗。

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