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Atypical Presentation of Acquired Hypoganglionosis in a Patient Taking Clozapine
Acquired hypoganglionosis (HG) is a rare enteric gastrointestinal neuromuscular disorder previously associated with chronic inflammation that can lead to constipation, ileus, and even death. There is little known about the pathophysiology of acquired hypoganglionosis, and it is unclear if medication...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333039/ https://www.ncbi.nlm.nih.gov/pubmed/32670642 http://dx.doi.org/10.1155/2020/1272567 |
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author | Gisi, Catherine Munteanu, Anamaria Ku, Lawrence French, Samuel Fleischman, Michael Eysselein, Viktor |
author_facet | Gisi, Catherine Munteanu, Anamaria Ku, Lawrence French, Samuel Fleischman, Michael Eysselein, Viktor |
author_sort | Gisi, Catherine |
collection | PubMed |
description | Acquired hypoganglionosis (HG) is a rare enteric gastrointestinal neuromuscular disorder previously associated with chronic inflammation that can lead to constipation, ileus, and even death. There is little known about the pathophysiology of acquired hypoganglionosis, and it is unclear if medications are related to the development of the disease. Clozapine is an atypical antipsychotic used to treat refractory schizophrenia that is well known for its side effects including agranulocytosis and gastrointestinal dysmotility. This is an unusual case of acquired hypoganglionosis in a patient with anticholinergic toxicity on clozapine therapy. |
format | Online Article Text |
id | pubmed-7333039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-73330392020-07-14 Atypical Presentation of Acquired Hypoganglionosis in a Patient Taking Clozapine Gisi, Catherine Munteanu, Anamaria Ku, Lawrence French, Samuel Fleischman, Michael Eysselein, Viktor Case Rep Gastrointest Med Case Report Acquired hypoganglionosis (HG) is a rare enteric gastrointestinal neuromuscular disorder previously associated with chronic inflammation that can lead to constipation, ileus, and even death. There is little known about the pathophysiology of acquired hypoganglionosis, and it is unclear if medications are related to the development of the disease. Clozapine is an atypical antipsychotic used to treat refractory schizophrenia that is well known for its side effects including agranulocytosis and gastrointestinal dysmotility. This is an unusual case of acquired hypoganglionosis in a patient with anticholinergic toxicity on clozapine therapy. Hindawi 2020-06-24 /pmc/articles/PMC7333039/ /pubmed/32670642 http://dx.doi.org/10.1155/2020/1272567 Text en Copyright © 2020 Catherine Gisi et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Gisi, Catherine Munteanu, Anamaria Ku, Lawrence French, Samuel Fleischman, Michael Eysselein, Viktor Atypical Presentation of Acquired Hypoganglionosis in a Patient Taking Clozapine |
title | Atypical Presentation of Acquired Hypoganglionosis in a Patient Taking Clozapine |
title_full | Atypical Presentation of Acquired Hypoganglionosis in a Patient Taking Clozapine |
title_fullStr | Atypical Presentation of Acquired Hypoganglionosis in a Patient Taking Clozapine |
title_full_unstemmed | Atypical Presentation of Acquired Hypoganglionosis in a Patient Taking Clozapine |
title_short | Atypical Presentation of Acquired Hypoganglionosis in a Patient Taking Clozapine |
title_sort | atypical presentation of acquired hypoganglionosis in a patient taking clozapine |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333039/ https://www.ncbi.nlm.nih.gov/pubmed/32670642 http://dx.doi.org/10.1155/2020/1272567 |
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