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Autoimmune Autonomic Ganglionopathy Presenting as Constipation
Autoimmune autonomic ganglionopathy (AAG) is a rare post-ganglionic disorder that causes a range of symptoms, often including gastrointestinal disorders. Patients may be seropositive or seronegative for antibodies against the nicotinic acetylcholine receptor. Here, we describe the case of a 56-year-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918276/ https://www.ncbi.nlm.nih.gov/pubmed/35308659 http://dx.doi.org/10.7759/cureus.22108 |
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author | Ahmed, Abdelwahab Lohman, Shannon Suresh, Suraj Naji, Abdullah Russell, Sarah Alsheik, Eva Mullins, Keith |
author_facet | Ahmed, Abdelwahab Lohman, Shannon Suresh, Suraj Naji, Abdullah Russell, Sarah Alsheik, Eva Mullins, Keith |
author_sort | Ahmed, Abdelwahab |
collection | PubMed |
description | Autoimmune autonomic ganglionopathy (AAG) is a rare post-ganglionic disorder that causes a range of symptoms, often including gastrointestinal disorders. Patients may be seropositive or seronegative for antibodies against the nicotinic acetylcholine receptor. Here, we describe the case of a 56-year-old woman with a previous diagnosis of sensorimotor peripheral neuropathy who presented with severe constipation that was not responsive to laxative therapy. The evaluation showed diffuse colonic hypomotility, rectal hypersensitivity, and type IV pelvic floor dysfunction. The patient was diagnosed 10 months after the presentation as having seronegative AAG, and she responded well to treatment with intravenous methylprednisolone and apheresis. |
format | Online Article Text |
id | pubmed-8918276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-89182762022-03-17 Autoimmune Autonomic Ganglionopathy Presenting as Constipation Ahmed, Abdelwahab Lohman, Shannon Suresh, Suraj Naji, Abdullah Russell, Sarah Alsheik, Eva Mullins, Keith Cureus Neurology Autoimmune autonomic ganglionopathy (AAG) is a rare post-ganglionic disorder that causes a range of symptoms, often including gastrointestinal disorders. Patients may be seropositive or seronegative for antibodies against the nicotinic acetylcholine receptor. Here, we describe the case of a 56-year-old woman with a previous diagnosis of sensorimotor peripheral neuropathy who presented with severe constipation that was not responsive to laxative therapy. The evaluation showed diffuse colonic hypomotility, rectal hypersensitivity, and type IV pelvic floor dysfunction. The patient was diagnosed 10 months after the presentation as having seronegative AAG, and she responded well to treatment with intravenous methylprednisolone and apheresis. Cureus 2022-02-10 /pmc/articles/PMC8918276/ /pubmed/35308659 http://dx.doi.org/10.7759/cureus.22108 Text en Copyright © 2022, Ahmed et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Neurology Ahmed, Abdelwahab Lohman, Shannon Suresh, Suraj Naji, Abdullah Russell, Sarah Alsheik, Eva Mullins, Keith Autoimmune Autonomic Ganglionopathy Presenting as Constipation |
title | Autoimmune Autonomic Ganglionopathy Presenting as Constipation |
title_full | Autoimmune Autonomic Ganglionopathy Presenting as Constipation |
title_fullStr | Autoimmune Autonomic Ganglionopathy Presenting as Constipation |
title_full_unstemmed | Autoimmune Autonomic Ganglionopathy Presenting as Constipation |
title_short | Autoimmune Autonomic Ganglionopathy Presenting as Constipation |
title_sort | autoimmune autonomic ganglionopathy presenting as constipation |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918276/ https://www.ncbi.nlm.nih.gov/pubmed/35308659 http://dx.doi.org/10.7759/cureus.22108 |
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