Cargando…

Taste disorder in facial onset sensory and motor neuronopathy: a case report

BACKGROUND: Taste disorder is a common symptom in the general population. Several studies have shown that patients with neurological disorders, such as amyotrophic lateral sclerosis and Parkinson’s disease, develop taste disturbance. Facial onset sensory and motor neuronopathy (FOSMN) is a rare dise...

Descripción completa

Detalles Bibliográficos
Autores principales: Ohashi, Nobuhiko, Nonami, Jin, Kodaira, Minori, Yoshida, Kunihiro, Sekijima, Yoshiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049225/
https://www.ncbi.nlm.nih.gov/pubmed/32113480
http://dx.doi.org/10.1186/s12883-020-01639-x
_version_ 1783502397439475712
author Ohashi, Nobuhiko
Nonami, Jin
Kodaira, Minori
Yoshida, Kunihiro
Sekijima, Yoshiki
author_facet Ohashi, Nobuhiko
Nonami, Jin
Kodaira, Minori
Yoshida, Kunihiro
Sekijima, Yoshiki
author_sort Ohashi, Nobuhiko
collection PubMed
description BACKGROUND: Taste disorder is a common symptom in the general population. Several studies have shown that patients with neurological disorders, such as amyotrophic lateral sclerosis and Parkinson’s disease, develop taste disturbance. Facial onset sensory and motor neuronopathy (FOSMN) is a rare disease characterized by sensory disturbance and weakness spreading from the face to the limbs caudally. We describe a patient with FOSMN who showed taste disorder as the sole initial symptom. CASE PRESENTATION: A 49-year-old man who smoked cigarettes developed taste disturbance. Despite using zinc supplements, an herbal medication, and an ointment, his taste disorder worsened. 4 years later, a tingling feeling emerged at the tip of his tongue and gradually spread to his entire lips. At 55 years of age, he showed difficulty in swallowing, followed by facial paresthesia, muscle atrophy, and weakness in the face and upper limbs without apparent upper motor neuron sign. Cessation of smoking did not improve his taste disturbance, and he was unable to discriminate different tastes on the entire tongue. In an electrogustometric study, electrical stimulation did not induce any type of taste sensation. Blink reflex showed delayed or diminished R2 responses. Needle electromyography revealed severe chronic neurogenic changes in the tongue and masseter muscles. Mild chronic neurogenic changes were also observed in the limbs. In the thoracic paraspinal muscles, active neurogenic changes were detected. Findings of hematological and cerebrospinal fluid analyses, and magnetic resonance images of the brain and spinal cord were unremarkable. One cycle of intravenous immunoglobulin therapy did not improve his symptoms. We diagnosed him as having FOSMN with the sole initial symptom of taste disorder. Nine years after the onset of taste disorder, he developed impaired sensation of touch in the right upper limb and required tube feeding and ventilator support. CONCLUSION: Taste disorder can be the initial manifestation of FOSMN and might involve the solitary nucleus.
format Online
Article
Text
id pubmed-7049225
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-70492252020-03-05 Taste disorder in facial onset sensory and motor neuronopathy: a case report Ohashi, Nobuhiko Nonami, Jin Kodaira, Minori Yoshida, Kunihiro Sekijima, Yoshiki BMC Neurol Case Report BACKGROUND: Taste disorder is a common symptom in the general population. Several studies have shown that patients with neurological disorders, such as amyotrophic lateral sclerosis and Parkinson’s disease, develop taste disturbance. Facial onset sensory and motor neuronopathy (FOSMN) is a rare disease characterized by sensory disturbance and weakness spreading from the face to the limbs caudally. We describe a patient with FOSMN who showed taste disorder as the sole initial symptom. CASE PRESENTATION: A 49-year-old man who smoked cigarettes developed taste disturbance. Despite using zinc supplements, an herbal medication, and an ointment, his taste disorder worsened. 4 years later, a tingling feeling emerged at the tip of his tongue and gradually spread to his entire lips. At 55 years of age, he showed difficulty in swallowing, followed by facial paresthesia, muscle atrophy, and weakness in the face and upper limbs without apparent upper motor neuron sign. Cessation of smoking did not improve his taste disturbance, and he was unable to discriminate different tastes on the entire tongue. In an electrogustometric study, electrical stimulation did not induce any type of taste sensation. Blink reflex showed delayed or diminished R2 responses. Needle electromyography revealed severe chronic neurogenic changes in the tongue and masseter muscles. Mild chronic neurogenic changes were also observed in the limbs. In the thoracic paraspinal muscles, active neurogenic changes were detected. Findings of hematological and cerebrospinal fluid analyses, and magnetic resonance images of the brain and spinal cord were unremarkable. One cycle of intravenous immunoglobulin therapy did not improve his symptoms. We diagnosed him as having FOSMN with the sole initial symptom of taste disorder. Nine years after the onset of taste disorder, he developed impaired sensation of touch in the right upper limb and required tube feeding and ventilator support. CONCLUSION: Taste disorder can be the initial manifestation of FOSMN and might involve the solitary nucleus. BioMed Central 2020-02-29 /pmc/articles/PMC7049225/ /pubmed/32113480 http://dx.doi.org/10.1186/s12883-020-01639-x Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Ohashi, Nobuhiko
Nonami, Jin
Kodaira, Minori
Yoshida, Kunihiro
Sekijima, Yoshiki
Taste disorder in facial onset sensory and motor neuronopathy: a case report
title Taste disorder in facial onset sensory and motor neuronopathy: a case report
title_full Taste disorder in facial onset sensory and motor neuronopathy: a case report
title_fullStr Taste disorder in facial onset sensory and motor neuronopathy: a case report
title_full_unstemmed Taste disorder in facial onset sensory and motor neuronopathy: a case report
title_short Taste disorder in facial onset sensory and motor neuronopathy: a case report
title_sort taste disorder in facial onset sensory and motor neuronopathy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049225/
https://www.ncbi.nlm.nih.gov/pubmed/32113480
http://dx.doi.org/10.1186/s12883-020-01639-x
work_keys_str_mv AT ohashinobuhiko tastedisorderinfacialonsetsensoryandmotorneuronopathyacasereport
AT nonamijin tastedisorderinfacialonsetsensoryandmotorneuronopathyacasereport
AT kodairaminori tastedisorderinfacialonsetsensoryandmotorneuronopathyacasereport
AT yoshidakunihiro tastedisorderinfacialonsetsensoryandmotorneuronopathyacasereport
AT sekijimayoshiki tastedisorderinfacialonsetsensoryandmotorneuronopathyacasereport