Skip to main content
Top
Published in: Acta Neurologica Belgica 5/2020

01-10-2020 | Original Article

Does restricted diffusion in the splenium indicate an acute infarct?

Authors: Zeynep Ezgi Balcik, Songül Senadim, Aslı Keskek, Ayşe Ozudogru, Ayhan Koksal, Aysun Soysal, Dilek Atakli

Published in: Acta Neurologica Belgica | Issue 5/2020

Login to get access

Abstract

Objective

Although splenial lesions are rare, they are frequently associated with ischemic infarcts, antiepileptic drug toxicity or abrupt discontinuation, viral encephalitis, and metabolic disturbances. In this study, we evaluated clinical and imaging findings and aetiology in 16 patients with splenium lesions.

Methods

Between 2013 and 2017, patients with splenium lesions were examined. Magnetic resonance imaging (MRI) was performed using a 1.5-T unit with fluid attenuation inversion recovery sequences. Additionally, diffusion-weighted imaging (DWI) and apparent diffusion coefficient (ADC) maps were examined.

Results

The patients were 11 males and 5 females; the mean age was 52.3 ± 20.3 (22–87) years. The patients were admitted with the following conditions: consciousness disorder (n = 7, 43.7%), headache (n = 3, 18.7%), seizure (n = 3, 18.7%), ataxia (n = 3, 18.7%), hemiparesis (n = 4, 25%), meaningless speech (n = 2, 12.5%), fever (n = 3, 18.7%), perioral numbness (n = 1, 6.2%), and diplopia (n = 1, 6.2%). Hyperintensity in the splenium was observed in DWI sequences in all patients on MRI. Fourteen patients (87.5%) showed hypointensity in the same region on ADC. In patients with ischemic infarcts, the splenium lesions were most commonly observed in the area of the posterior cerebral artery (n = 4, 25%). MRI showed splenial signal changes in DWI sequences in all patients. Hyperintensity in the splenium was observed in DWI sequences in all patients on MRI. Fourteen patients (87.5%) showed hypointensity in the same region on ADC. The aetiologies were defined as multiple sclerosis (n = 1, 6.2%), ischemic infarction (n = 4, 25%), tuberculous meningitis (n = 3, 18.7%), viral encephalitis (n = 2, 12.5%), hypernatremia (n = 1, 6.2%), brain tumour (n = 1, 6.2%), Marchiafava-Bignami syndrome (n = 1, 6.2%), head trauma (n = 1, 6.2%), substance use (n = 1, 6.2%), and epilepsy (n = 1, 6.2%).

Conclusion

Not every diffuse restriction observed on MRI indicates an ischemic stroke. Although radiologic images of the splenium may suggest acute ischemic infarction, the actual cause may be another pathology. Therefore, the symptoms and aetiologies of patients with splenium lesions should be considered and investigated from a wide range of perspectives.
Literature
1.
go back to reference Georgy BA, Hesselink JR, Jernigan TL (1993) MR imaging of the corpus callosum. AJR 160:949–955CrossRef Georgy BA, Hesselink JR, Jernigan TL (1993) MR imaging of the corpus callosum. AJR 160:949–955CrossRef
2.
go back to reference Oquist M, Farooq MU, Gorelick PB (2014) Restricted diffusion of the splenium of the corpus callosum in viral meningitis. Neurohospitalist 4(2):109–110CrossRef Oquist M, Farooq MU, Gorelick PB (2014) Restricted diffusion of the splenium of the corpus callosum in viral meningitis. Neurohospitalist 4(2):109–110CrossRef
3.
go back to reference Park MK, Hwang SH, Jung S, Hong SS, Kwon SB (2014) Lesions in the splenium of the corpus callosum: clinical and radiological implications. Neurol Asia 19(1):79–88 Park MK, Hwang SH, Jung S, Hong SS, Kwon SB (2014) Lesions in the splenium of the corpus callosum: clinical and radiological implications. Neurol Asia 19(1):79–88
4.
go back to reference De Lacoste MC, Kirkpatrick JB, Ross ED (1985) Topography of the human corpus callosum. J Neuropathol Exp Neurol 44(6):578–579CrossRef De Lacoste MC, Kirkpatrick JB, Ross ED (1985) Topography of the human corpus callosum. J Neuropathol Exp Neurol 44(6):578–579CrossRef
5.
go back to reference Kasow DL, Destian S, Braun C, Quintas JC, Kagetsu NJ, Johnson CE (2000) Corpus callosum infarcts with atypical clinical and radiologic presentations. Am J Neuroradiol 21:1876–1880PubMed Kasow DL, Destian S, Braun C, Quintas JC, Kagetsu NJ, Johnson CE (2000) Corpus callosum infarcts with atypical clinical and radiologic presentations. Am J Neuroradiol 21:1876–1880PubMed
6.
go back to reference Kumar S, Challam R, Naveen J, Sıngh WJ (2014) Marchiafava–Bignami disease: a case report. J Clin Diagn Res 8(8):01–02 Kumar S, Challam R, Naveen J, Sıngh WJ (2014) Marchiafava–Bignami disease: a case report. J Clin Diagn Res 8(8):01–02
7.
go back to reference Chrysikopoulos H, Andreou J, Roussakis A, Pappas J (1997) Infarction of the corpus callosum: computed tomography and magnetic resonance imaging. Eur J Radiol 25(1):2–8CrossRef Chrysikopoulos H, Andreou J, Roussakis A, Pappas J (1997) Infarction of the corpus callosum: computed tomography and magnetic resonance imaging. Eur J Radiol 25(1):2–8CrossRef
8.
go back to reference Zeal AA, Rhoton AL (1978) Microsurgical anatomy of the posterior cerebral artery. J Neurosurg 48(4):534–559CrossRef Zeal AA, Rhoton AL (1978) Microsurgical anatomy of the posterior cerebral artery. J Neurosurg 48(4):534–559CrossRef
9.
go back to reference Doherty MJ, Jayadev S, Watson NF, Konchada RS, Hallam DK (2005) Clinical implications of splenium magnetic resonance imaging signal changes. Arch Neurol 62:433–437CrossRef Doherty MJ, Jayadev S, Watson NF, Konchada RS, Hallam DK (2005) Clinical implications of splenium magnetic resonance imaging signal changes. Arch Neurol 62:433–437CrossRef
10.
go back to reference Takanashi J, Barkovich AJ, Yamaguchi K, Kohno Y (2004) Influenza-associated encephalitis/encephalopathy with a reversible lesion in the splenium of the corpus callosum: a case report and literature review. Am J Neuroradiol 25:798–802PubMed Takanashi J, Barkovich AJ, Yamaguchi K, Kohno Y (2004) Influenza-associated encephalitis/encephalopathy with a reversible lesion in the splenium of the corpus callosum: a case report and literature review. Am J Neuroradiol 25:798–802PubMed
11.
go back to reference Gallucci M, Limbucci N, Paonessa A, Caranci F (2007) Reversible focal splenial lesions. Neuroradiology 49:541–544CrossRef Gallucci M, Limbucci N, Paonessa A, Caranci F (2007) Reversible focal splenial lesions. Neuroradiology 49:541–544CrossRef
12.
go back to reference Nagpal K, Agarwal P, Kumar A, Reddi R (2017) Chikungunya infection presenting as mild encephalitis with a reversible lesion in the splenium: a case report. J Neurovirol 23(3):501–503CrossRef Nagpal K, Agarwal P, Kumar A, Reddi R (2017) Chikungunya infection presenting as mild encephalitis with a reversible lesion in the splenium: a case report. J Neurovirol 23(3):501–503CrossRef
13.
go back to reference Maeda M, Tsukahara H, Terada H, Nakaji S, Nakamura H, Oba H, Igarashi O, Arasaki K, Machida T, Takeda K, Takanashi JI (2006) Reversible splenial lesion with restricted diffusion in a wide spectrum of diseases and conditions report of eight additional cases and literature review. J Neuroradiol 33:229–236CrossRef Maeda M, Tsukahara H, Terada H, Nakaji S, Nakamura H, Oba H, Igarashi O, Arasaki K, Machida T, Takeda K, Takanashi JI (2006) Reversible splenial lesion with restricted diffusion in a wide spectrum of diseases and conditions report of eight additional cases and literature review. J Neuroradiol 33:229–236CrossRef
14.
go back to reference Garcia-Monco JC, Cortina IE, Ferreira E, Martınez A, Ruiz L, Cabrera A, Beldarrain MG (2011) Reversible Splenial Lesion Syndrome (RESLES): what’s in a name? J Neuroimaging 21:1–14CrossRef Garcia-Monco JC, Cortina IE, Ferreira E, Martınez A, Ruiz L, Cabrera A, Beldarrain MG (2011) Reversible Splenial Lesion Syndrome (RESLES): what’s in a name? J Neuroimaging 21:1–14CrossRef
15.
go back to reference Bilgic B, Bilgin Arslan A, Buluth H, Bayram A, Gokben Hizli F (2011) Marchiafava–Bignami patient with mild symptoms and the role of diffusion-weighted magnetic resonance imaging in the diagnosis. Arch Neuropsychiatry 48:277–280CrossRef Bilgic B, Bilgin Arslan A, Buluth H, Bayram A, Gokben Hizli F (2011) Marchiafava–Bignami patient with mild symptoms and the role of diffusion-weighted magnetic resonance imaging in the diagnosis. Arch Neuropsychiatry 48:277–280CrossRef
16.
go back to reference Oster J, Doherty C, Grant PE (2003) Diffusion-weighted imaging abnormalities in the splenium after seizures. Epilepsia 44:852–854CrossRef Oster J, Doherty C, Grant PE (2003) Diffusion-weighted imaging abnormalities in the splenium after seizures. Epilepsia 44:852–854CrossRef
17.
go back to reference Gambini A, Falini A, Moiola L, Comi G, Scotti G (2003) Marchiafava–Bignami disease: longitudinal MR imaging and MR spectroscopy study. Am J Neuroradiol 24:249–253PubMed Gambini A, Falini A, Moiola L, Comi G, Scotti G (2003) Marchiafava–Bignami disease: longitudinal MR imaging and MR spectroscopy study. Am J Neuroradiol 24:249–253PubMed
Metadata
Title
Does restricted diffusion in the splenium indicate an acute infarct?
Authors
Zeynep Ezgi Balcik
Songül Senadim
Aslı Keskek
Ayşe Ozudogru
Ayhan Koksal
Aysun Soysal
Dilek Atakli
Publication date
01-10-2020
Publisher
Springer International Publishing
Published in
Acta Neurologica Belgica / Issue 5/2020
Print ISSN: 0300-9009
Electronic ISSN: 2240-2993
DOI
https://doi.org/10.1007/s13760-017-0876-6

Other articles of this Issue 5/2020

Acta Neurologica Belgica 5/2020 Go to the issue