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Anorexia and the hippocampus: A case report
Eating disorders have been shown to be associated with epilepsy, typically associated with the temporal lobe and usually of non-dominant hemisphere origin. We report the case of a 56-year-old woman with drug resistant epilepsy, localized to the dominant left hippocampus. She experienced an increasin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800335/ https://www.ncbi.nlm.nih.gov/pubmed/36590373 http://dx.doi.org/10.1016/j.ebr.2022.100577 |
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author | Farhadi, Dara S. Estofan, Leonel Privitera, Michael |
author_facet | Farhadi, Dara S. Estofan, Leonel Privitera, Michael |
author_sort | Farhadi, Dara S. |
collection | PubMed |
description | Eating disorders have been shown to be associated with epilepsy, typically associated with the temporal lobe and usually of non-dominant hemisphere origin. We report the case of a 56-year-old woman with drug resistant epilepsy, localized to the dominant left hippocampus. She experienced an increasing frequency of seizures over a two-year period associated with loss of appetite and substantial weight loss independent of antiseizure medication changes. Extensive workup eliminated gastrointestinal and paraneoplastic etiologies. There was no history of psychiatric illness, including anorexia nervosa. Pre-surgical workup showed mesial temporal sclerosis on MRI and video-EEG was consistent with ipsilateral medial temporal seizure onset. The patient underwent laser interstitial ablation of the left amygdala and hippocampus, which resulted in a cessation of seizures. Within 24 h of the laser ablation, her appetite returned to normal and, within 8 months she regained 26 lbs. To our knowledge, this is the first case report of a patient with dominant temporal lobe epilepsy with anorexia that was temporally associated with escalating seizure frequency and stopped with treatment and cessation of seizures, suggesting a causal and pathogenic relationship. |
format | Online Article Text |
id | pubmed-9800335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98003352022-12-31 Anorexia and the hippocampus: A case report Farhadi, Dara S. Estofan, Leonel Privitera, Michael Epilepsy Behav Rep Case Report Eating disorders have been shown to be associated with epilepsy, typically associated with the temporal lobe and usually of non-dominant hemisphere origin. We report the case of a 56-year-old woman with drug resistant epilepsy, localized to the dominant left hippocampus. She experienced an increasing frequency of seizures over a two-year period associated with loss of appetite and substantial weight loss independent of antiseizure medication changes. Extensive workup eliminated gastrointestinal and paraneoplastic etiologies. There was no history of psychiatric illness, including anorexia nervosa. Pre-surgical workup showed mesial temporal sclerosis on MRI and video-EEG was consistent with ipsilateral medial temporal seizure onset. The patient underwent laser interstitial ablation of the left amygdala and hippocampus, which resulted in a cessation of seizures. Within 24 h of the laser ablation, her appetite returned to normal and, within 8 months she regained 26 lbs. To our knowledge, this is the first case report of a patient with dominant temporal lobe epilepsy with anorexia that was temporally associated with escalating seizure frequency and stopped with treatment and cessation of seizures, suggesting a causal and pathogenic relationship. Elsevier 2022-12-12 /pmc/articles/PMC9800335/ /pubmed/36590373 http://dx.doi.org/10.1016/j.ebr.2022.100577 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Farhadi, Dara S. Estofan, Leonel Privitera, Michael Anorexia and the hippocampus: A case report |
title | Anorexia and the hippocampus: A case report |
title_full | Anorexia and the hippocampus: A case report |
title_fullStr | Anorexia and the hippocampus: A case report |
title_full_unstemmed | Anorexia and the hippocampus: A case report |
title_short | Anorexia and the hippocampus: A case report |
title_sort | anorexia and the hippocampus: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9800335/ https://www.ncbi.nlm.nih.gov/pubmed/36590373 http://dx.doi.org/10.1016/j.ebr.2022.100577 |
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