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An Extremely Rare Cause of Isolated Congenital Anosmia

A 14-year-old adolescent was referred to a regional paediatric outpatient clinic with anosmia by her family doctor in Western Australia. The patient has no recollection of her previous ability to smell, suggesting the possibility of congenital anosmia. She was assessed in the paediatric outpatient c...

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Detalles Bibliográficos
Autores principales: Saw, Chia, Friesen, Noel David, Bartley, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283015/
https://www.ncbi.nlm.nih.gov/pubmed/35847159
http://dx.doi.org/10.1155/2022/9692716
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author Saw, Chia
Friesen, Noel David
Bartley, Anthony
author_facet Saw, Chia
Friesen, Noel David
Bartley, Anthony
author_sort Saw, Chia
collection PubMed
description A 14-year-old adolescent was referred to a regional paediatric outpatient clinic with anosmia by her family doctor in Western Australia. The patient has no recollection of her previous ability to smell, suggesting the possibility of congenital anosmia. She was assessed in the paediatric outpatient clinic. A “noncontrast high-resolution MRI-brain scan with Anosmia-Protocol” was requested as the first-line investigation of choice by the treating paediatrician. The MRI was reported as “absence of olfactory tracts with preserved olfactory bulb volume.” We report an extremely rare case of “isolated agenesis of the olfactory tract with intact olfactory bulbs” and discuss the clinical approach in bedside assessment of isolated congenital anosmia (ICA). Congenital anosmia can be a presentation of olfactory bulb aplasia; however, little is known about isolated olfactory tract agenesis and its treatment options. The patient was counselled on the diagnosis and safety advice provided.
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spelling pubmed-92830152022-07-15 An Extremely Rare Cause of Isolated Congenital Anosmia Saw, Chia Friesen, Noel David Bartley, Anthony Case Rep Otolaryngol Case Report A 14-year-old adolescent was referred to a regional paediatric outpatient clinic with anosmia by her family doctor in Western Australia. The patient has no recollection of her previous ability to smell, suggesting the possibility of congenital anosmia. She was assessed in the paediatric outpatient clinic. A “noncontrast high-resolution MRI-brain scan with Anosmia-Protocol” was requested as the first-line investigation of choice by the treating paediatrician. The MRI was reported as “absence of olfactory tracts with preserved olfactory bulb volume.” We report an extremely rare case of “isolated agenesis of the olfactory tract with intact olfactory bulbs” and discuss the clinical approach in bedside assessment of isolated congenital anosmia (ICA). Congenital anosmia can be a presentation of olfactory bulb aplasia; however, little is known about isolated olfactory tract agenesis and its treatment options. The patient was counselled on the diagnosis and safety advice provided. Hindawi 2022-07-07 /pmc/articles/PMC9283015/ /pubmed/35847159 http://dx.doi.org/10.1155/2022/9692716 Text en Copyright © 2022 Chia Saw et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Saw, Chia
Friesen, Noel David
Bartley, Anthony
An Extremely Rare Cause of Isolated Congenital Anosmia
title An Extremely Rare Cause of Isolated Congenital Anosmia
title_full An Extremely Rare Cause of Isolated Congenital Anosmia
title_fullStr An Extremely Rare Cause of Isolated Congenital Anosmia
title_full_unstemmed An Extremely Rare Cause of Isolated Congenital Anosmia
title_short An Extremely Rare Cause of Isolated Congenital Anosmia
title_sort extremely rare cause of isolated congenital anosmia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283015/
https://www.ncbi.nlm.nih.gov/pubmed/35847159
http://dx.doi.org/10.1155/2022/9692716
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