Chiam Keng Hoong, Sannasey Sumithra, Rajaintharan Sandhya, Muthukaruppan Raman
Gastroenterology Unit, Queen Elizabeth Hospital, Kota Kinabalu, Sabah, Malaysia.
Radiology Department, Queen Elizabeth Hospital, Kota Kinabalu, Sabah, Malaysia.
Ann Transl Med. 2022 Dec;10(23):1290. doi: 10.21037/atm-2022-61.
Adult-onset colonic intussusception is a rarely encountered condition that leads to large intestinal obstruction with time. Patients often present with a variety of symptoms that are non-specific making it challenging to arrive at a definitive diagnosis. This is worrying as diagnostic delay could lead to a significant increase in morbidity and mortality. We wish to present and describe a case of an atypical endoscopic finding of colocolic intussusception secondary to ascending colon cancer.
Sixty-seven-year-old lady was referred for 1 month's duration of passing melenic stools with mucus followed by a week's complain of hematochezia. Clinical examination and other relevant blood results were unremarkable except for iron deficiency anemia. Initial colonoscopy revealed a large mass within the splenic flexure with inconclusive biopsies. A more detailed colonoscopy repeated the following day revealed a massive, black-to-yellowish lesion within the splenic flexure with no viable mucosa seen. Colonic bezoar was initially suspected, however various endoscopic retrieval methods proved futile. Switching to a slimmer diagnostic gastroscope, the colon was carefully negotiated until a large ulcer was found within the ascending colon, adjacent to the mass' origin. An emergency CT abdomen and subsequently extended right hemicolectomy performed revealed a colocolic intussusception with sealed perforation secondary to an ascending colonic mass acting as an intussusceptum. Histopathology evaluation confirmed an ascending colon adenocarcinoma (pT2N0M0) amidst a background of extensive ischemic changes.
Endoscopic descriptions of colonic intussusception are unusual given their rarity. Furthermore, these lesions can mimic a colonic bezoar as a result of fecal accretion and this can ultimately lead to false diagnostic and therapeutic decisions. In such instances, clarification with a CT scan before management decision can potentially avert unnecessary endoscopic intervention and complications.
成人起病的结肠套叠是一种罕见的疾病,随着时间的推移会导致大肠梗阻。患者常表现出各种非特异性症状,这使得做出明确诊断具有挑战性。这令人担忧,因为诊断延迟可能导致发病率和死亡率显著增加。我们希望希望呈现示并描述一例因升结肠癌继发的结肠结肠套叠的非典型内镜表现病例。
一名67岁女性因持续1个月排柏油样便伴黏液,随后一周出现便血而就诊。除缺铁性贫血外,临床检查和其他相关血液检查结果均无异常。初次结肠镜检查发现脾曲有一个大肿块,活检结果不明确。次日重复进行更详细的结肠镜检查,发现脾曲有一个巨大的、从黑色到淡黄色的病变,未见存活的黏膜。最初怀疑是结肠粪石,然而各种内镜取出方法均无效。改用更细的诊断性胃镜,小心地通过结肠,直到在升结肠内靠近肿块起源处发现一个大溃疡。急诊腹部CT检查,随后进行扩大右半结肠切除术,结果显示为结肠结肠套叠,继发于作为套入部的升结肠肿块的封闭穿孔。组织病理学评估证实为升结肠腺癌(pT2N0M0),伴有广泛的缺血性改变背景。
鉴于结肠套叠罕见,其内镜描述并不常见。此外,这些病变可能因粪便堆积而类似结肠粪石,最终可能导致错误的诊断和治疗决策。在这种情况下,在做出管理决策前进行CT扫描明确情况可能避免不必要的内镜干预和并发症。