Adult-onset cerebello-brainstem-dominant form of X-linked adrenoleukodystrophy with auditory pathway involvement: A case report

X-linked adrenoleukodystrophy (X-ALD) is classified into several clinical subtypes. Among them, the cerebello-brainstem-dominant form is rare, and its symptoms and imaging findings can mimic spinocerebellar degeneration (SCD), making diagnosis difficult. Herein, we report a case that we initially di...

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Published inTenri Medical Bulletin Vol. 27; no. 1; pp. 33 - 39
Main Authors Yokota, Yusuke, Minami, Akihiko, Kawase, Kango, Taniguchi, Takanori, Okubo, Gosuke, Shinde, Akiyo, Kanao, Shotaro, Kubo, Takeshi, Suenaga, Toshihiko, Yasumura, Sumika, Suzuki, Mizue, Ota, Rie, Yuge, Shunsuke, Noma, Satoshi, Yamashita, Naoki, Saito, Ayako, Kim, Hyunjin, Noda, Toshiyuki, Nakamura, Yuri, Yasuo, Shunsuke, Imaeda, Masaki
Format Journal Article
LanguageEnglish
Published Tenri Foundation, Tenri Institute of Medical Research 25.12.2024
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Online AccessGet full text
ISSN1344-1817
2187-2244
2187-2244
DOI10.12936/tenrikiyo.27-009

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Abstract X-linked adrenoleukodystrophy (X-ALD) is classified into several clinical subtypes. Among them, the cerebello-brainstem-dominant form is rare, and its symptoms and imaging findings can mimic spinocerebellar degeneration (SCD), making diagnosis difficult. Herein, we report a case that we initially diagnosed as SCD but was eventually diagnosed as the cerebello-brainstem-dominant form of X-ALD. The patient presented with psychiatric symptoms in adulthood. He subsequently developed gait disturbance and was referred to the neurology department of our hospital. Initial magnetic resonance imaging (MRI) showed atrophy of the cerebellum and pons, and abnormal signals in various regions, including the middle cerebellar peduncles, the corpus callosum, infero-posterior part of the bilateral thalami, and lateral edges of the midbrain, on T2-weighted imaging. The patient was followed up as SCD; however, his symptoms and MRI findings worsened. Further examination was performed, and the diagnosis of X-ALD was made. Abnormal signals in the thalami and midbrain on MRI are considered to correspond to the medial geniculate bodies and the brachia of the inferior colliculus, respectively. They constitute the auditory pathway, which is an evaluation item in Loes score, an imaging-based scoring system for patients with X-ALD. Recognizing abnormalities in the bilateral auditory pathway may aid accurate diagnosis of X-ALD.
AbstractList X-linked adrenoleukodystrophy (X-ALD) is classified into several clinical subtypes. Among them, the cerebello-brainstem-dominant form is rare, and its symptoms and imaging findings can mimic spinocerebellar degeneration (SCD), making diagnosis difficult. Herein, we report a case that we initially diagnosed as SCD but was eventually diagnosed as the cerebello-brainstem-dominant form of X-ALD. The patient presented with psychiatric symptoms in adulthood. He subsequently developed gait disturbance and was referred to the neurology department of our hospital. Initial magnetic resonance imaging (MRI) showed atrophy of the cerebellum and pons, and abnormal signals in various regions, including the middle cerebellar peduncles, the corpus callosum, infero-posterior part of the bilateral thalami, and lateral edges of the midbrain, on T2-weighted imaging. The patient was followed up as SCD; however, his symptoms and MRI findings worsened. Further examination was performed, and the diagnosis of X-ALD was made. Abnormal signals in the thalami and midbrain on MRI are considered to correspond to the medial geniculate bodies and the brachia of the inferior colliculus, respectively. They constitute the auditory pathway, which is an evaluation item in Loes score, an imaging-based scoring system for patients with X-ALD. Recognizing abnormalities in the bilateral auditory pathway may aid accurate diagnosis of X-ALD.
ArticleNumber 27-009
Author Yasumura, Sumika
Shinde, Akiyo
Kim, Hyunjin
Imaeda, Masaki
Kanao, Shotaro
Kubo, Takeshi
Yasuo, Shunsuke
Yuge, Shunsuke
Taniguchi, Takanori
Okubo, Gosuke
Ota, Rie
Noma, Satoshi
Suzuki, Mizue
Nakamura, Yuri
Yokota, Yusuke
Noda, Toshiyuki
Minami, Akihiko
Yamashita, Naoki
Saito, Ayako
Suenaga, Toshihiko
Kawase, Kango
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10.1007/s100380200090
10.2214/AJR.11.8080
10.1111/neup.12230
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2) Moser HW, Moser AB, Frayer KK, et al. Adrenoleukodystrophy: Increased plasma content of saturated very long chain fatty acids. Neurology 1981;31:1241-1249.
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9) Choi JH, Kim HS, Oh EH, et al. Cerebello-brainstem dominant form of X-linked adrenoleukodystrophy with intrafamilial phenotypic variability. Front Neurol 2022;13:999419.
23) Scarpa A, Cassandro C, Vitale C, et al. A comparison of auditory and vestibular dysfunction in Parkinson's disease and Multiple System Atrophy. Parkinsonism Relat Disord 2020;71:51-57.
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6) Loes DJ, Fatemi A, Melhem ER, et al. Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy. Neurology 2003;61:369-374.
10) Kim JH, Kim HJ. Childhood X-linked adrenoleukodystrophy: Clinical-pathologic overview and MR imaging manifestations at initial evaluation and follow-up. Radiographics 2005;25:619-631.
5) Engelen M, Kemp S, de Visser M, et al. X-linked adrenoleukodystrophy (X-ALD): Clinical presentation and guidelines for diagnosis, follow-up and management. Orphanet J Rare Dis 2012;7:51.
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3) Contreras M, Mosser J, Mandel JL, et al. The protein coded by the X-adrenoleukodystrophy gene is a peroxisomal integral membrane protein. FEBS Lett 1994;344:211-215.
11) Kumar AJ, Köhler W, Kruse B, et al. MR findings in adult-onset adrenoleukodystrophy. AJNR Am J Neuroradiol 1995;16:1227-1237.
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References_xml – reference: 21) Maillot O, Attyé A, Boyer E, et al. Post traumatic deafness: A pictorial review of CT and MRI findings. Insights Imaging 2016;7:341-350.
– reference: 12) Chen YH, Lee YC, Tsai YS, et al. Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia. PLoS One 2017;12:e0177296.
– reference: 2) Moser HW, Moser AB, Frayer KK, et al. Adrenoleukodystrophy: Increased plasma content of saturated very long chain fatty acids. Neurology 1981;31:1241-1249.
– reference: 3) Contreras M, Mosser J, Mandel JL, et al. The protein coded by the X-adrenoleukodystrophy gene is a peroxisomal integral membrane protein. FEBS Lett 1994;344:211-215.
– reference: 16) Okamoto K, Tokiguchi S, Furusawa T, et al. MR features of diseases involving bilateral middle cerebellar peduncles. AJNR Am J Neuroradiol 2003;24:1946-1954.
– reference: 7) Tan EK, Lim SH, Chan LL, et al. X-linked adrenoleukodystrophy: Spinocerebellar variant. Clin Neurol Neurosurg 1999;101:137-140.
– reference: 17) Uchino A, Sawada A, Takase Y, et al. Symmetrical lesions of the middle cerebellar peduncle: MR imaging and differential diagnosis. Magn Reson Med Sci 2004;3:133-140.
– reference: 20) Loes DJ, Hite S, Moser H, et al. Adrenoleukodystrophy: A scoring method for brain MR observations. AJNR Am J Neuroradiol 1994;15:1761-1766.
– reference: 1) Mosser J, Douar AM, Sarde CO, et al. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature 1993;361:726-730.
– reference: 15) Mascalchi M. MRI CNS atrophy pattern and the etiologies of progressive ataxias. Tomography 2022;8:423-437.
– reference: 5) Engelen M, Kemp S, de Visser M, et al. X-linked adrenoleukodystrophy (X-ALD): Clinical presentation and guidelines for diagnosis, follow-up and management. Orphanet J Rare Dis 2012;7:51.
– reference: 10) Kim JH, Kim HJ. Childhood X-linked adrenoleukodystrophy: Clinical-pathologic overview and MR imaging manifestations at initial evaluation and follow-up. Radiographics 2005;25:619-631.
– reference: 9) Choi JH, Kim HS, Oh EH, et al. Cerebello-brainstem dominant form of X-linked adrenoleukodystrophy with intrafamilial phenotypic variability. Front Neurol 2022;13:999419.
– reference: 24) Curé JK, Cromwell LD, Case JL, et al. Auditory dysfunction caused by multiple sclerosis: Detection with MR imaging. AJNR Am J Neuroradiol 1990;11:817-820.
– reference: 8) Ogaki K, Koga S, Aoki N, et al. Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: Case report and literature review. Neuropathology 2016;36:64-76.
– reference: 4) Takemoto Y, Suzuki Y, Tamakoshi A, et al. Epidemiology of X-linked adrenoleukodystrophy in Japan. J Hum Genet 2002;47:590-593.
– reference: 11) Kumar AJ, Köhler W, Kruse B, et al. MR findings in adult-onset adrenoleukodystrophy. AJNR Am J Neuroradiol 1995;16:1227-1237.
– reference: 25) Cruz RA, Varkey T, Flavia A, et al. Hearing abnormalities in multiple sclerosis: Clinical semiology and pathophysiologic mechanisms. J Neurol 2022;269:2792-2805.
– reference: 6) Loes DJ, Fatemi A, Melhem ER, et al. Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy. Neurology 2003;61:369-374.
– reference: 18) Ho ML, Moonis G, Ginat DT, et al. Lesions of the corpus callosum. AJR Am J Roentgenol 2013;200:W1-16.
– reference: 23) Scarpa A, Cassandro C, Vitale C, et al. A comparison of auditory and vestibular dysfunction in Parkinson's disease and Multiple System Atrophy. Parkinsonism Relat Disord 2020;71:51-57.
– reference: 26) Lu Z, Zhang B, Qiu W, et al. Comparative brain stem lesions on MRI of acute disseminated encephalomyelitis, neuromyelitis optica, and multiple sclerosis. PLoS One 2011;6:e22766.
– reference: 13) Rueda-Lopes FC, Hygino da Cruz LC, Jr., Doring TM, et al. Diffusion-weighted imaging and demyelinating diseases: New aspects of an old advanced sequence. AJR Am J Roentgenol 2014;202:W34-42.
– reference: 14) Andravizou A, Dardiotis E, Artemiadis A, et al. Brain atrophy in multiple sclerosis: Mechanisms, clinical relevance and treatment options. Auto Immun Highlights 2019;10:7.
– reference: 19) Bourekas EC, Varakis K, Bruns D, et al. Lesions of the corpus callosum: MR imaging and differential considerations in adults and children. AJR Am J Roentgenol 2002;179:251-257.
– reference: 22) Hoche F, Seidel K, Brunt ER, et al. Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7). Neuropathol Appl Neurobiol 2008;34:479-491.
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  doi: 10.1186/1750-1172-7-51
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Snippet X-linked adrenoleukodystrophy (X-ALD) is classified into several clinical subtypes. Among them, the cerebello-brainstem-dominant form is rare, and its symptoms...
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SubjectTerms auditory pathway
cerebello-brainstem-dominant form
magnetic resonance imaging (MRI)
X-linked adrenoleukodystrophy (X-ALD)
Title Adult-onset cerebello-brainstem-dominant form of X-linked adrenoleukodystrophy with auditory pathway involvement: A case report
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