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Ross Syndrome: A Patient with a 23-Year History

We present a 60-year-old female with a 23-year history of anhidrosis with concomitant heat intolerance. At examination, we found a right-sided tonic pupil, absent tendon reflexes, and a segmental patch of compensatory hyperhidrosis in the left lower quadrant of her trunk. To further confirm this fin...

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Autores principales: Filikci, Zuhal, Horsten, Hans-Henrik, Lindelof, Mette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184827/
https://www.ncbi.nlm.nih.gov/pubmed/32355499
http://dx.doi.org/10.1159/000507186
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author Filikci, Zuhal
Horsten, Hans-Henrik
Lindelof, Mette
author_facet Filikci, Zuhal
Horsten, Hans-Henrik
Lindelof, Mette
author_sort Filikci, Zuhal
collection PubMed
description We present a 60-year-old female with a 23-year history of anhidrosis with concomitant heat intolerance. At examination, we found a right-sided tonic pupil, absent tendon reflexes, and a segmental patch of compensatory hyperhidrosis in the left lower quadrant of her trunk. To further confirm this finding, a minor test (a starch-iodine test, which is used to evaluate the sudomotor function, sweating) was performed. Nerve conduction studies revealed evidence of a mild distal sensory polyneuropathy of the axonal type. Tilt-table testing showed signs of orthostatic hypotension with evidence of reduced sympathetic function. Skin biopsy excluded pathology in the sweat glands. Our patient met the criteria for a diagnosis of Ross syndrome. This case describes the long-term outcome of this rare entity and highlights how careful examination and bedside autonomic testing can confirm the diagnosis of autonomic neurological disorders.
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spelling pubmed-71848272020-04-30 Ross Syndrome: A Patient with a 23-Year History Filikci, Zuhal Horsten, Hans-Henrik Lindelof, Mette Case Rep Neurol Single Case − General Neurology We present a 60-year-old female with a 23-year history of anhidrosis with concomitant heat intolerance. At examination, we found a right-sided tonic pupil, absent tendon reflexes, and a segmental patch of compensatory hyperhidrosis in the left lower quadrant of her trunk. To further confirm this finding, a minor test (a starch-iodine test, which is used to evaluate the sudomotor function, sweating) was performed. Nerve conduction studies revealed evidence of a mild distal sensory polyneuropathy of the axonal type. Tilt-table testing showed signs of orthostatic hypotension with evidence of reduced sympathetic function. Skin biopsy excluded pathology in the sweat glands. Our patient met the criteria for a diagnosis of Ross syndrome. This case describes the long-term outcome of this rare entity and highlights how careful examination and bedside autonomic testing can confirm the diagnosis of autonomic neurological disorders. S. Karger AG 2020-04-08 /pmc/articles/PMC7184827/ /pubmed/32355499 http://dx.doi.org/10.1159/000507186 Text en Copyright © 2020 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Single Case − General Neurology
Filikci, Zuhal
Horsten, Hans-Henrik
Lindelof, Mette
Ross Syndrome: A Patient with a 23-Year History
title Ross Syndrome: A Patient with a 23-Year History
title_full Ross Syndrome: A Patient with a 23-Year History
title_fullStr Ross Syndrome: A Patient with a 23-Year History
title_full_unstemmed Ross Syndrome: A Patient with a 23-Year History
title_short Ross Syndrome: A Patient with a 23-Year History
title_sort ross syndrome: a patient with a 23-year history
topic Single Case − General Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184827/
https://www.ncbi.nlm.nih.gov/pubmed/32355499
http://dx.doi.org/10.1159/000507186
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