A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome
This case report describes a 46-year-old female with a history of multiple endocrine neoplasia type 1 syndrome status post-parathyroidectomy, thymectomy via robotic video-assisted thoracoscopic surgery, and pituitary adenoma resection presenting with parasympathetic hyperactivity and Parry–Romberg s...
Main Authors: | , |
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Format: | Article |
Language: | English |
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SAGE Publishing
2021-07-01
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Series: | SAGE Open Medical Case Reports |
Online Access: | https://doi.org/10.1177/2050313X211034351 |
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author | Andrea N Clapp Anna DePold Hohler |
author_facet | Andrea N Clapp Anna DePold Hohler |
author_sort | Andrea N Clapp |
collection | DOAJ |
description | This case report describes a 46-year-old female with a history of multiple endocrine neoplasia type 1 syndrome status post-parathyroidectomy, thymectomy via robotic video-assisted thoracoscopic surgery, and pituitary adenoma resection presenting with parasympathetic hyperactivity and Parry–Romberg syndrome. Parry–Romberg syndrome is a rare disorder that manifests as facial hemiatrophy. Reported symptoms include cognitive dysfunction, olfactory hallucinations, and parasympathetic hyperactivity: miosis of the right eye, anhidrosis, diarrhea, urinary incontinence, bowel incontinence, and orthostatic hypotension. Previous reports have noted associations between Parry–Romberg syndrome and sympathetic hyperactivity and dysregulation. This case report focuses on an association between Parry–Romberg syndrome and unopposed parasympathetic activity. |
first_indexed | 2024-12-22T11:32:00Z |
format | Article |
id | doaj.art-fb06602059a9404b8bacad428c39cb8a |
institution | Directory Open Access Journal |
issn | 2050-313X |
language | English |
last_indexed | 2024-12-22T11:32:00Z |
publishDate | 2021-07-01 |
publisher | SAGE Publishing |
record_format | Article |
series | SAGE Open Medical Case Reports |
spelling | doaj.art-fb06602059a9404b8bacad428c39cb8a2022-12-21T18:27:36ZengSAGE PublishingSAGE Open Medical Case Reports2050-313X2021-07-01910.1177/2050313X211034351A case of parasympathetic hyperactivity and associated Parry–Romberg syndromeAndrea N Clapp0Anna DePold Hohler1Tufts University School of Medicine, Boston, MA, USADepartment of Neurology, St. Elizabeth’s Medical Center, Brighton, MA, USAThis case report describes a 46-year-old female with a history of multiple endocrine neoplasia type 1 syndrome status post-parathyroidectomy, thymectomy via robotic video-assisted thoracoscopic surgery, and pituitary adenoma resection presenting with parasympathetic hyperactivity and Parry–Romberg syndrome. Parry–Romberg syndrome is a rare disorder that manifests as facial hemiatrophy. Reported symptoms include cognitive dysfunction, olfactory hallucinations, and parasympathetic hyperactivity: miosis of the right eye, anhidrosis, diarrhea, urinary incontinence, bowel incontinence, and orthostatic hypotension. Previous reports have noted associations between Parry–Romberg syndrome and sympathetic hyperactivity and dysregulation. This case report focuses on an association between Parry–Romberg syndrome and unopposed parasympathetic activity.https://doi.org/10.1177/2050313X211034351 |
spellingShingle | Andrea N Clapp Anna DePold Hohler A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome SAGE Open Medical Case Reports |
title | A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome |
title_full | A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome |
title_fullStr | A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome |
title_full_unstemmed | A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome |
title_short | A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome |
title_sort | case of parasympathetic hyperactivity and associated parry romberg syndrome |
url | https://doi.org/10.1177/2050313X211034351 |
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