Hind Qajia MD , Chaimaa Jabbari MD , Salma El Kadiri MD , Saleck Choumad MD , Yassine Eddahoumi MD , Omar El Aoufir PHD , Laila Jroundi PHD
{"title":"Wernicke encephalopathy revealing occult gastric adenocarcinoma: Radiological and clinical insights","authors":"Hind Qajia MD , Chaimaa Jabbari MD , Salma El Kadiri MD , Saleck Choumad MD , Yassine Eddahoumi MD , Omar El Aoufir PHD , Laila Jroundi PHD","doi":"10.1016/j.radcr.2025.08.078","DOIUrl":null,"url":null,"abstract":"<div><div>Wernicke’s encephalopathy (WE) is an acute neuropsychiatric disorder caused by thiamine deficiency, often underdiagnosed in non-alcoholic patients. We report a rare case of Wernicke encephalopathy in a 60-year-old male presenting with diplopia, dizziness, and gait instability secondary to prolonged vomiting and malnutrition.</div><div>Contrast-enhanced thoracoabdominal CT revealed irregular wall thickening of the antropyloric region of the stomach with heterogeneous soft-tissue density and multiple hepatic hypodense lesions showing peripheral enhancement, consistent with metastatic spread. Brain MRI demonstrated symmetric FLAIR hyperintensities involving the medial thalami, mammillary bodies, and periaqueductal gray matter, without diffusion restriction, consistent with Wernicke encephalopathy. Lesions measured 3mm in the mammillary bodies. Prompt administration of thiamine led to rapid clinical improvement.</div><div>This case is notable as occult gastric cancer presented primarily through neurological symptoms of WE, highlighting the importance of considering neoplastic causes in non-alcoholic presentations.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 12","pages":"Pages 6159-6162"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1930043325008118","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Wernicke’s encephalopathy (WE) is an acute neuropsychiatric disorder caused by thiamine deficiency, often underdiagnosed in non-alcoholic patients. We report a rare case of Wernicke encephalopathy in a 60-year-old male presenting with diplopia, dizziness, and gait instability secondary to prolonged vomiting and malnutrition.
Contrast-enhanced thoracoabdominal CT revealed irregular wall thickening of the antropyloric region of the stomach with heterogeneous soft-tissue density and multiple hepatic hypodense lesions showing peripheral enhancement, consistent with metastatic spread. Brain MRI demonstrated symmetric FLAIR hyperintensities involving the medial thalami, mammillary bodies, and periaqueductal gray matter, without diffusion restriction, consistent with Wernicke encephalopathy. Lesions measured 3mm in the mammillary bodies. Prompt administration of thiamine led to rapid clinical improvement.
This case is notable as occult gastric cancer presented primarily through neurological symptoms of WE, highlighting the importance of considering neoplastic causes in non-alcoholic presentations.
期刊介绍:
The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.