Cytotoxic lesions of the corpus callosum: a systematic review

被引:9
作者
Moors, Selina [1 ]
Nakhostin, Dominik [1 ]
Ilchenko, Dariya [1 ]
Kulcsar, Zsolt [1 ]
Starkey, Jay [2 ]
Winklhofer, Sebastian [1 ]
Ineichen, Benjamin V. [1 ,3 ]
机构
[1] Univ Hosp Zurich, Clin Neurosci Ctr, Dept Neuroradiol, Zurich, Switzerland
[2] Oregon Hlth & Sci Univ, Dept Radiol, Portland, OR USA
[3] Univ Zurich, Ctr Reproducible Sci, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Corpus callosum; Systematic review; Magnetic resonance imaging; Central nervous system diseases; COVID-19; BRAIN; EDEMA; SPLENIUM; CHILDREN;
D O I
10.1007/s00330-023-10524-3
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
ObjectivesCytotoxic lesions of the corpus callosum (CLOCC) are a common magnetic resonance imaging (MRI) finding associated with various systemic diseases including COVID-19. Although an increasing number of such cases is reported in the literature, there is a lack of systematic evidence summarizing the etiology and neuroimaging findings of these lesions. Thus, the aim of this systematic review was to synthesize the applied nomenclature, neuroimaging and clinical features, and differential diagnoses as well as associated disease entities of CLOCC.Materials and methodsA comprehensive literature search in three biomedical databases identified 441 references, out of which 324 were eligible for a narrative summary including a total of 1353 patients.ResultsOur PRISMA-conform systematic review identifies a broad panel of disease entities which are associated with CLOCC, among them toxic/drug-treatment-associated, infectious (viral, bacterial), vascular, metabolic, traumatic, and neoplastic entities in both adult and pediatric individuals. On MRI, CLOCC show typical high T2 signal, low T1 signal, restricted diffusion, and lack of contrast enhancement. The majority of the lesions were reversible within the follow-up period (median follow-up 3 weeks). Interestingly, even though CLOCC were mostly associated with symptoms of the underlying disease, in exceptional cases, CLOCC were associated with callosal neurological symptoms. Of note, employed nomenclature for CLOCC was highly inconsistent.ConclusionsOur study provides high-level evidence for clinical and imaging features of CLOCC as well as associated disease entities.Clinical relevance statementOur study provides high-level evidence on MRI features of CLOCC as well as a comprehensive list of disease entities potentially associated with CLOCC. Together, this will facilitate rigorous diagnostic workup of suspected CLOCC cases.Key Points center dot Cytotoxic lesions of the corpus callosum (CLOCC) are a frequent MRI feature associated with various systemic diseases.center dot Cytotoxic lesions of the corpus callosum show a highly homogenous MRI presentation and temporal dynamics.center dot This comprehensive overview will benefit (neuro)radiologists during diagnostic workup.Key Points center dot Cytotoxic lesions of the corpus callosum (CLOCC) are a frequent MRI feature associated with various systemic diseases.center dot Cytotoxic lesions of the corpus callosum show a highly homogenous MRI presentation and temporal dynamics.center dot This comprehensive overview will benefit (neuro)radiologists during diagnostic workup.Key Points center dot Cytotoxic lesions of the corpus callosum (CLOCC) are a frequent MRI feature associated with various systemic diseases.center dot Cytotoxic lesions of the corpus callosum show a highly homogenous MRI presentation and temporal dynamics.center dot This comprehensive overview will benefit (neuro)radiologists during diagnostic workup.
引用
收藏
页码:4628 / 4637
页数:10
相关论文
共 40 条
[1]   Marked elevation of urinary β2-microglobulin in patients with reversible splenial lesions: A small case series [J].
Azuma, Junji ;
Nabatame, Shin ;
Katsura, Toshiya ;
Yamamoto, Kyoko ;
Kaneno, Hiroshi ;
Kijima, Eri ;
Mizoguchi, Yoshimi ;
Shimotsuji, Tunesuke ;
Yamamoto, Takehisa ;
Ozono, Keiichi .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2016, 368 :109-112
[2]   Mapping the myelin bilayer with short-T2 MRI: Methods validation and reference data for healthy human brain [J].
Baadsvik, Emily Louise ;
Weiger, Markus ;
Froidevaux, Romain ;
Faigle, Wolfgang ;
Ineichen, Benjamin Victor ;
Pruessmann, Klaas Paul .
MAGNETIC RESONANCE IN MEDICINE, 2023, 89 (02) :665-677
[3]   The splenium of the corpus callosum: embryology, anatomy, function and imaging with pathophysiological hypothesis [J].
Blaauw, J. ;
Meiners, L. C. .
NEURORADIOLOGY, 2020, 62 (05) :563-585
[4]   Reversible Splenial Lesion Syndrome (RESLES): What's in a Name? [J].
Carlos Garcia-Monco, Juan ;
Escalza Cortina, Ines ;
Ferreira, Eva ;
Martinez, Amaia ;
Ruiz, Lara ;
Cabrera, Alberto ;
Gomez Beldarrain, Marian .
JOURNAL OF NEUROIMAGING, 2011, 21 (02) :e1-e14
[5]   Reversible splenial lesion syndrome in children: Retrospective study and summary of case series [J].
Chen, Wen-Xiong ;
Liu, Hong-Sheng ;
Yang, Si-Da ;
Zeng, Si-Hui ;
Gao, Yuan-Yuan ;
Du, Zhi-Hong ;
Li, Xiao-Jing ;
Lin, Hai-Sheng ;
Liang, Hui-Ci ;
Mai, Jian-Ning .
BRAIN & DEVELOPMENT, 2016, 38 (10) :915-927
[6]   Mild encephalopathy with reversible lesion in the splenium of the corpus callosum and bilateral frontal white matter [J].
Cho, Jeong-Seon ;
Ha, Sang-Won ;
Han, Young-Su ;
Padi, Sang-Eun ;
Hong, Ki-Moo ;
Han, Jeong-Ho ;
Cho, Eun-Kyoung ;
Kim, Doo-Eung ;
Kim, Jea-Geun .
JOURNAL OF CLINICAL NEUROLOGY, 2007, 3 (01) :53-56
[7]   Excitotoxicity: Still Hammering the Ischemic Brain in 2020 [J].
Choi, Dennis W. .
FRONTIERS IN NEUROSCIENCE, 2020, 14
[8]   Expression of glutamate transporters in the adult bovine corpus callosum [J].
Domercq, M ;
Matute, C .
MOLECULAR BRAIN RESEARCH, 1999, 67 (02) :296-302
[9]   Cytotoxic Lesions of the Corpus Callosum Caused by Thermogenic Dietary Supplements [J].
Galnares-Olalde, J. A. ;
Vazquez-Mezquita, A. J. ;
Gomez-Garza, G. ;
Reyes-Vazquez, D. ;
Higuera-Ortiz, V. ;
Alegria-Loyola, M. A. ;
Mendez-Dominguez, A. .
AMERICAN JOURNAL OF NEURORADIOLOGY, 2019, 40 (08) :1304-1308
[10]   The corpus callosum in the diagnosis of multiple sclerosis and other CNS demyelinating and inflammatory diseases [J].
Garg, Nidhi ;
Reddel, Stephen W. ;
Miller, David H. ;
Chataway, Jeremy ;
Riminton, D. Sean ;
Barnett, Yael ;
Masters, Lynette ;
Barnett, Michael H. ;
Hardy, Todd A. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2015, 86 (12) :1374-1382