Primary epiploic appendagitis: 3 case reports

4Citations
Citations of this article
22Readers
Mendeley users who have this article in their library.

Abstract

Acute Epiploic Appendagitis is a rare self limiting disease that represents ischaemic infarction of an epiploic appendix. It is usually discovered incidentally on imaging of abdomen done for other causes of acute abdominal pain. It is difficult to diagnose clinically due to the lack of pathognomonic clinical features, since it is characterized by a sudden onset of sharp localized pain either in the left or right iliac fossa with minimal gastrointestinal symptoms, which can simulate a surgical clinical picture. Awareness of imaging findings of this entity is important to arrive at a correct diagnosis and to avoid unnecessary hospitalization and surgery. We report cases of three male patients presenting with acute flank pain who were diagnosed as case of Primary epiploic appendagitis. All 3 patients were treated conservatively.

Cite

CITATION STYLE

APA

Ahmad, S., Khan, Z. A., Sheikh, M. Y., Khan, S., Rehman, A. U., & Uddin, B. (2011). Primary epiploic appendagitis: 3 case reports. Journal of the Pakistan Medical Association, 61(1), 83–85. https://doi.org/10.64203/nemj/kzrp6618

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free