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Gluten encephalopathy with psychiatric onset: case report
Many cases of coeliac disease, a gastrointestinal autoimmune disorder caused by sensitivity to gluten, can remain in a subclinical stage or undiagnosed. In a significant proportion of cases (10–15%) gluten intolerance can be associated with central or peripheral nervous system and psychiatric disord...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Bentham Science Publishers
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711951/ https://www.ncbi.nlm.nih.gov/pubmed/19558661 http://dx.doi.org/10.1186/1745-0179-5-16 |
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author | Poloni, Nicola Vender, Simone Bolla, Emilio Bortolaso, Paola Costantini, Chiara Callegari, Camilla |
author_facet | Poloni, Nicola Vender, Simone Bolla, Emilio Bortolaso, Paola Costantini, Chiara Callegari, Camilla |
author_sort | Poloni, Nicola |
collection | PubMed |
description | Many cases of coeliac disease, a gastrointestinal autoimmune disorder caused by sensitivity to gluten, can remain in a subclinical stage or undiagnosed. In a significant proportion of cases (10–15%) gluten intolerance can be associated with central or peripheral nervous system and psychiatric disorders. A 38-year-old man was admitted as to our department an inpatient for worsening anxiety symptoms and behavioural alterations. After the addition of second generation antipsychotic to the therapeutic regimen, the patient presented neuromotor impairment with high fever, sopor, leukocytosis, raised rhabdomyolysis-related indicators. Neuroleptic malignant syndrome was strongly suspected. After worsening of his neuropsychiatric conditions, with the onset of a frontal cognitive deficit, bradykinesia and difficulty walking, dysphagia, anorexia and hypoferraemic anaemia, SPET revealed a reduction of cerebral perfusion and ENeG results were compatible with a mainly motor polyneuropathy. Extensive laboratory investigations gave positive results for anti-gliadin antibodies, and an appropriate diet led to a progressive remission of the encephalopathy. |
format | Text |
id | pubmed-2711951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-27119512009-07-17 Gluten encephalopathy with psychiatric onset: case report Poloni, Nicola Vender, Simone Bolla, Emilio Bortolaso, Paola Costantini, Chiara Callegari, Camilla Clin Pract Epidemiol Ment Health Case Report Many cases of coeliac disease, a gastrointestinal autoimmune disorder caused by sensitivity to gluten, can remain in a subclinical stage or undiagnosed. In a significant proportion of cases (10–15%) gluten intolerance can be associated with central or peripheral nervous system and psychiatric disorders. A 38-year-old man was admitted as to our department an inpatient for worsening anxiety symptoms and behavioural alterations. After the addition of second generation antipsychotic to the therapeutic regimen, the patient presented neuromotor impairment with high fever, sopor, leukocytosis, raised rhabdomyolysis-related indicators. Neuroleptic malignant syndrome was strongly suspected. After worsening of his neuropsychiatric conditions, with the onset of a frontal cognitive deficit, bradykinesia and difficulty walking, dysphagia, anorexia and hypoferraemic anaemia, SPET revealed a reduction of cerebral perfusion and ENeG results were compatible with a mainly motor polyneuropathy. Extensive laboratory investigations gave positive results for anti-gliadin antibodies, and an appropriate diet led to a progressive remission of the encephalopathy. Bentham Science Publishers 2009-06-26 /pmc/articles/PMC2711951/ /pubmed/19558661 http://dx.doi.org/10.1186/1745-0179-5-16 Text en Copyright ©2009 Poloni et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Poloni, Nicola Vender, Simone Bolla, Emilio Bortolaso, Paola Costantini, Chiara Callegari, Camilla Gluten encephalopathy with psychiatric onset: case report |
title | Gluten encephalopathy with psychiatric onset: case report |
title_full | Gluten encephalopathy with psychiatric onset: case report |
title_fullStr | Gluten encephalopathy with psychiatric onset: case report |
title_full_unstemmed | Gluten encephalopathy with psychiatric onset: case report |
title_short | Gluten encephalopathy with psychiatric onset: case report |
title_sort | gluten encephalopathy with psychiatric onset: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711951/ https://www.ncbi.nlm.nih.gov/pubmed/19558661 http://dx.doi.org/10.1186/1745-0179-5-16 |
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