Case report: Cerebrotendinous Xanthomatosis masquerading as adult ADHD in psychiatric practice.

IF 3.2 3区 医学 Q2 PSYCHIATRY Frontiers in Psychiatry Pub Date : 2025-02-04 eCollection Date: 2025-01-01 DOI:10.3389/fpsyt.2025.1528204
Jongtae Kim, Yun Jeong Hong, Si Baek Lee, Seong Hoon Kim, Myung Ah Lee, Eunbuel Ko, Jeong Wook Park
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Abstract

Introduction: This case report details the presentation of a patient who initially sought consultation at a psychiatric outpatient clinic with symptoms suggestive of Attention-Deficit/Hyperactivity Disorder (ADHD); however, further evaluation revealed a diagnosis of Cerebrotendinous Xanthomatosis (CTX). CTX, a genetic disorder impacting lipid metabolism, is often overlooked in differential diagnoses due to its rarity. This case underscores the importance of considering alternative diagnoses in adults exhibiting ADHD-like symptoms without a childhood history of the disorder, adding to the literature on diagnostic complexities in psychiatric practice.

Case presentation: A 33-year-old man visited a psychiatric outpatient clinic with symptoms such as increasing distractibility and inattention, requesting an evaluation for adult ADHD. However, the absence of an ADHD history in childhood, coupled with progressive neurological symptoms and tendon xanthomas, led to further investigation. Comprehensive neurological assessments, including neuroimaging and genetic testing, ultimately diagnosed him with CTX. Treatment with chenodeoxycholic acid (CDCA) resulted in stabilization of cognitive function, although improvement in gait disturbances and tremors remained minimal.

Conclusion: This case demonstrates that CTX can masquerade as adult ADHD, emphasizing the necessity for thorough assessments in atypical ADHD presentations. Psychiatrists should consider rare metabolic disorders like CTX in similar cases, which may enable timely intervention and improve patient outcomes.

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病例报告:脑腱黄瘤病伪装成成人多动症在精神病学实践。
简介:本病例报告详细介绍了一位患者最初在精神科门诊寻求咨询,症状提示注意缺陷/多动障碍(ADHD);然而,进一步的评估显示诊断为脑腱黄瘤病(CTX)。CTX是一种影响脂质代谢的遗传性疾病,由于其罕见,在鉴别诊断中经常被忽视。这个病例强调了在没有儿童病史的成年人中考虑替代诊断的重要性,增加了精神病学实践中诊断复杂性的文献。病例介绍:一名33岁男子因注意力分散和注意力不集中等症状就诊于精神科门诊,要求对成人多动症进行评估。然而,儿童时期没有ADHD病史,加上进行性神经症状和肌腱黄瘤,导致进一步的调查。全面的神经学评估,包括神经成像和基因检测,最终诊断出他患有CTX。用鹅去氧胆酸(CDCA)治疗导致认知功能稳定,尽管步态障碍和震颤的改善仍然很小。结论:本病例表明CTX可以伪装成成人ADHD,强调了对非典型ADHD表现进行彻底评估的必要性。精神科医生应该在类似的病例中考虑罕见的代谢紊乱,如CTX,这可能使及时干预和改善患者的预后成为可能。
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来源期刊
Frontiers in Psychiatry
Frontiers in Psychiatry Medicine-Psychiatry and Mental Health
CiteScore
6.20
自引率
8.50%
发文量
2813
审稿时长
14 weeks
期刊介绍: Frontiers in Psychiatry publishes rigorously peer-reviewed research across a wide spectrum of translational, basic and clinical research. Field Chief Editor Stefan Borgwardt at the University of Basel is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. The journal''s mission is to use translational approaches to improve therapeutic options for mental illness and consequently to improve patient treatment outcomes.
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