Department of Human Resources Development for General Practitioner, Shimane Prefectural Central Hospital, Izumo, Shimane, Japan.
Department of Emergency Medicine, Shimane Prefectural Central Hospital, Izumo, Shimane, Japan.
Am J Case Rep. 2023 Jan 25;24:e938207. doi: 10.12659/AJCR.938207.
BACKGROUND Pneumatosis cystoides intestinalis (PCI) is a rare condition in which cystic gas is found in the submucosal and serosal tissues of the intestinal wall. CASE REPORT The patient, an 84-year-old woman, was referred to us because of abdominal distention and diarrhea lasting 2 weeks. On initial physical examination, there was marked abdominal distention without tenderness. Blood tests revealed no abnormalities, but simple abdominal radiographs showed gas in the small intestine. Contrast-enhanced computed tomography showed massive emphysema in the intestinal wall with no signs of portal gas or intestinal ischemia. The patient was diagnosed with PCI, and the prognosis was good. The patient showed improvement when managed with an elimination diet and follow-up. CONCLUSIONS Herein, we present the characteristics and diagnosis of PCI because the imaging findings of PCI can appear more severe than the actual condition, causing it to be mistaken for other serious diseases, which leads to unnecessary surgical procedures.
肠气囊肿症(PCI)是一种罕见的疾病,其特征为肠壁黏膜下和浆膜下组织中有囊状气体。
患者为 84 岁女性,因腹胀和腹泻持续 2 周而就诊。初次体格检查发现腹部明显膨隆,但无压痛。血液检查未见异常,但腹部平片显示小肠内有气体。增强 CT 显示肠壁广泛气肿,无门静脉积气或肠缺血迹象。患者被诊断为 PCI,预后良好。经饮食排除和随访治疗,患者症状改善。
本文介绍了 PCI 的特征和诊断,因为 PCI 的影像学表现可能比实际情况更严重,导致其被误诊为其他严重疾病,从而导致不必要的手术。