Abdominal Epilepsy: Report of two cases and literature review

Author:

Zhang Ying1,An Ying2,Qi Jialong2,Song Zhengji2

Affiliation:

1. Medical school, Kunming University of Science and Technology

2. Yunnan Digestive Endoscopy Clinical Medical Center, Department of Gastroenterology. The First People's Hospital of Yunnan Province.

Abstract

Abstract

Abdominal epilepsy (AE) is a rare form of epilepsy characterized by paroxysmal abdominal pain accompanied by syncope. It often presents diagnostic challenges due to its diverse clinical manifestations. Herein, we present two cases, a 28-year-old male and a 55-year-old female, with a decade-long history of intermittent abdominal pain and syncope. Despite multiple consultations, a definitive diagnosis remained elusive until electroencephalography (EEG) revealed characteristic abnormalities. Two cases underscore the importance of recognizing AE as a potential cause of unexplained abdominal pain and syncope. Therefore, we recommend that for patients with unexplained abdominal pain accompanied by altered consciousness, after ruling out common causes, consideration should be given to AE. In the meantime, we summarize the possible molecular mechanisms for AE development.

Publisher

Research Square Platform LLC

Reference13 articles.

1. Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress;Ding X;Front Cell Infect Microbiol,2022

2. Role of Gut Microbiota through Gut-Brain Axis in Epileptogenesis: A Systematic Review of Human and Veterinary Medicine. Biology (Basel);Gernone F,2022

3. Neuroprotection of cannabidiol in epileptic rats: Gut microbiome and metabolome sequencing;Gong X;Front Nutr,2022

4. Crosstalk between peripheral and the brain-resident immune components in epilepsy;Mu X;J Integr Neurosci,2022

5. Microbiota-Gut-Brain Axis and Epilepsy: A Review on Mechanisms and Potential Therapeutics;Ding M;Front Immunol,2021

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