Thiamine Deficiency in a Child with Short Bowel Syndrome and Review
10.5223/pghn.2019.22.5.493
- Author:
Ioannis ROILIDES
1
;
Konstantina VASILAKI
;
Ioannis XINIAS
;
Elias IOSIFIDIS
;
Charalampos ANTACHOPOULOS
;
Emmanuel ROILIDES
Author Information
1. 3rd Department of Pediatrics, Hippokration General Hospital, Thessaloniki, Greece. roilides@med.auth.gr
- Publication Type:Case Report
- Keywords:
Wernicke encephalopathy;
Total parenteral nutrition;
Thiamine deficiency;
Short bowel syndrome
- MeSH:
Child;
Enterocolitis, Necrotizing;
Gait Disorders, Neurologic;
Humans;
Intestine, Small;
Male;
Parenteral Nutrition, Total;
Paresis;
Parturition;
Short Bowel Syndrome;
Strabismus;
Thiamine Deficiency;
Thiamine;
Vitamins;
Wernicke Encephalopathy
- From:Pediatric Gastroenterology, Hepatology & Nutrition
2019;22(5):493-499
- CountryRepublic of Korea
- Language:English
-
Abstract:
Thiamine (vitamin B₁) is a water-soluble vitamin that is not endogenously synthesized in humans. It is absorbed by the small intestine, where it is activated. Its active form acts as a coenzyme in many energy pathways. We report a rare case of thiamine deficiency in a 3.5-year old boy with short bowel syndrome secondary to extensive bowel resection due to necrotizing enterocolitis during his neonatal age. The patient was parenteral nutrition-dependent since birth and had suffered from recurrent central catheter-related bloodstream infections. He developed confusion with disorientation and unsteady gait as well as profound strabismus due to bilateral paresis of the abductor muscle. Based on these and a very low thiamine level he was diagnosed and treated for Wernicke encephalopathy due to incomplete thiamine acquisition despite adequate administration. He fully recovered after thiamine administration. After 1999 eight more cases have been reported in the PubMed mostly of iatrogenic origin.
