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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-...

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Autores principales: Ahmed, Abdelwahab, Lohman, Shannon, Suresh, Suraj, Naji, Abdullah, Russell, Sarah, Alsheik, Eva, Mullins, Keith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
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.
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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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