An Extremely Rare Cause of Isolated Congenital Anosmia.

IF 0.4 Q4 OTORHINOLARYNGOLOGY Case Reports in Otolaryngology Pub Date : 2022-07-07 eCollection Date: 2022-01-01 DOI:10.1155/2022/9692716
Chia Saw, Noel David Friesen, Anthony Bartley
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Abstract

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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孤立性先天性嗅觉缺失的一种极为罕见的病因。
在西澳大利亚,一名14岁的青少年被她的家庭医生转介到一家地区儿科门诊,患有嗅觉缺失症。病人不记得她以前的嗅觉能力,提示可能是先天性嗅觉缺失。她在儿科门诊接受了评估。“非对比高分辨率mri脑扫描与缺失协议”被要求作为一线调查的选择由治疗儿科医生。MRI报告为“嗅束缺失,嗅球体积保留”。我们报告一例极其罕见的“孤立性嗅道发育不全且嗅球完整”的病例,并讨论孤立性先天性嗅觉缺失(ICA)床边评估的临床方法。先天性嗅觉缺失可能是嗅球发育不全的表现;然而,人们对孤立性嗅道发育不全及其治疗方案知之甚少。向患者提供诊断和安全建议。
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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
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发文量
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审稿时长
13 weeks
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