Basile Eric J, Ahmed Ammar, Rahman Eraad, Rafa Omar, Frankini Elisabeth L, Modica Anthony
Internal Medicine, Touro College of Osteopathic Medicine, New York City, USA.
Medicine, Global Health, McMaster University, Hamilton, CAN.
Cureus. 2022 Mar 8;14(3):e22975. doi: 10.7759/cureus.22975. eCollection 2022 Mar.
Chilaiditi sign is a rare incidental radiographic finding where bowel is interposed between the diaphragm and the liver, often seen as air under the right hemidiaphragm. A majority of patients with Chilaiditi sign are asymptomatic and remain so throughout their lifetime. Chilaiditi sign is recategorized as Chilaiditi syndrome if it becomes symptomatic and is a very rare etiology of bowel obstruction. As bowel obstruction confers a huge financial burden to the health care system, studies of even the rarer etiologies are of significant value. Particularly in the case of Chilaiditi syndrome, the free air under the right hemidiaphragm can lead physicians to prematurely conclude pneumoperitoneum, which would require an emergent surgical evaluation. It is through the incorporation of a broad differential and clinical presentation that physicians can decrease the inappropriate allocation of hospital resources and unnecessary surgical procedures; additionally, keeping Chilaiditi syndrome on the differential may prevent unnecessary surgical intervention, cost to the patient, and downstream complications. Bowel obstruction secondary to Chilaiditi syndrome is most commonly treated with conservative management including intravenous fluids, bowel rest, decompression, and laxatives. If the symptoms worsen and progress to full bowel obstruction, surgical intervention has shown great efficacy. We report a case of a 69-year-old male who presented to the emergency department for progressively worsening abdominal pain, nausea, and vomiting incidentally found to have colonic interposition with mild colonic dilatation on computed tomography (CT) imaging. The patient was diagnosed with bowel obstruction secondary to Chilaiditi syndrome and treated non-surgically with rapid recovery.
奇莱迪蒂征是一种罕见的偶然影像学发现,即肠管位于膈肌和肝脏之间,常表现为右侧膈下积气。大多数奇莱迪蒂征患者无症状,且终生如此。如果奇莱迪蒂征出现症状,则被重新归类为奇莱迪蒂综合征,它是肠梗阻的一种非常罕见的病因。由于肠梗阻给医疗系统带来巨大经济负担,因此对即使是更罕见病因的研究也具有重要价值。特别是在奇莱迪蒂综合征的情况下,右侧膈下的游离气体可能导致医生过早诊断为气腹,而气腹需要紧急进行手术评估。通过综合考虑广泛的鉴别诊断和临床表现,医生可以减少医院资源的不当分配和不必要的手术程序;此外,将奇莱迪蒂综合征纳入鉴别诊断范围可以避免不必要的手术干预、患者的费用以及下游并发症。奇莱迪蒂综合征继发的肠梗阻最常采用保守治疗,包括静脉补液、肠道休息、减压和使用泻药。如果症状恶化并发展为完全性肠梗阻,手术干预已显示出很好的疗效。我们报告一例69岁男性患者,因进行性加重的腹痛、恶心和呕吐到急诊科就诊,计算机断层扫描(CT)成像偶然发现结肠间位伴轻度结肠扩张。该患者被诊断为奇莱迪蒂综合征继发的肠梗阻,并通过快速康复进行了非手术治疗。