General Practice for General Internal Medicine, Haupstrasse 5, A-8940 Liezen, Austria.
Nat Rev Gastroenterol Hepatol. 2011 Jan;8(1):45-9. doi: 10.1038/nrgastro.2010.189. Epub 2010 Nov 23.
Epiploic appendagitis is a rare cause of abdominal pain. Diagnosis of epiploic appendagitis, although infrequent, is easily made with CT or ultrasonography in experienced hands. As reported in the literature, most patients with primary epiploic appendagitis are treated conservatively without surgery, with or without anti-inflammatory drugs. A small number of patients are treated with antibiotics and some patients require surgical intervention to ensure therapeutic success. Symptoms of primary epiploic appendagitis usually resolve with or without treatment within a few days. A correct diagnosis of epiploic appendagitis with imaging procedures enables conservative and successful outpatient management of the condition and avoids unnecessary surgical intervention and associated additional health-care costs. Gastroenterologists and all medical personnel should be aware of this rare disease, which mimics many other intra-abdominal acute and subacute conditions, such as diverticulitis, cholecystitis and appendicitis. This article reviews epiploic appendagitis and includes discussion of clinical findings, pathophysiology, diagnosis and therapeutic possibilities.
盲肠脂垂炎是一种罕见的腹痛原因。在有经验的医生手中,通过 CT 或超声检查,很容易诊断出盲肠脂垂炎。正如文献报道的那样,大多数原发性盲肠脂垂炎患者无需手术即可通过保守治疗治愈,无论是否使用抗炎药物。少数患者需要使用抗生素治疗,部分患者需要手术干预以确保治疗成功。原发性盲肠脂垂炎的症状通常在数天内自行缓解,无论是否接受治疗。通过影像学检查正确诊断盲肠脂垂炎可以使病情得到保守和成功的门诊管理,并避免不必要的手术干预和相关的额外医疗费用。胃肠病学家和所有医务人员都应该了解这种罕见疾病,它类似于许多其他腹腔内急性和亚急性疾病,如憩室炎、胆囊炎和阑尾炎。本文回顾了盲肠脂垂炎,并讨论了其临床发现、病理生理学、诊断和治疗可能性。