Acute Crit Care.  2022 Aug;37(3):269-275. 10.4266/acc.2022.00864.

Transient splenial lesions of the corpus callosum and infectious diseases

Affiliations
  • 1Department of Neurology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea

Abstract

comTransient splenial lesion of the corpus callosum can be observed in various diseases such as cancer, drug use, metabolic disorders, and cerebrovascular disorders, as well as in patients with infectious diseases. During the coronavirus disease 2019 (COVID-19) pandemic, there were increasing reports of these lesions being detected on brain imaging tests performed in patients with neurological symptoms. On brain magnetic resonance imaging, findings suggestive of cytotoxic edema are observed in the splenium; these are known to disappear with improvement of clinical symptoms. Cytokinopathy caused by infection increases the permeability of the blood–brain barrier and activates the glial cells of the brain to induce cytotoxic edema. Most patients have a good prognosis. The causes, mechanism, diagnosis, treatment and prognosis of transient splenial lesions of the corpus callosum will be summarized in this review.

Keyword

corpus callosum; COVID-19; infections; magnetic resonance imaging

Figure

  • Figure 1. Sagittal view of the corpus callosum. G: genu; R: rostrum; B: body; S: splenium.

  • Figure 2. Two types of transient splenial lesions of the corpus callosum. Splenial lesions produce a high signal intensity on T2 diffusion-weighted imaging, a low signal intensity on T1 imaging, and decreased apparent diffusion on a coefficient map. (A) Small round lesion in the center of the splenium (arrows). (B) Boomerang sign. Lesion in the splenium extending into the adjacent cerebral white matter (arrowheads).


Reference

1. Knyazeva MG. Splenium of corpus callosum: patterns of interhemispheric interaction in children and adults. Neural Plast. 2013; 2013:639430.
2. Raybaud C. The corpus callosum, the other great forebrain commissures, and the septum pellucidum: anatomy, development, and malformation. Neuroradiology. 2010; 52:447–77.
Article
3. Takanashi J, Hirasawa K, Tada H. Reversible restricted diffusion of entire corpus callosum. J Neurol Sci. 2006; 247:101–4.
Article
4. Starkey J, Kobayashi N, Numaguchi Y, Moritani T. Cytotoxic lesions of the corpus callosum that show restricted diffusion: mechanisms, causes, and manifestations. Radiographics. 2017; 37:562–76.
Article
5. Garcia-Monco JC, Cortina IE, Ferreira E, Martínez A, Ruiz L, Cabrera A, et al. Reversible splenial lesion syndrome (RESLES): what's in a name? J Neuroimaging. 2011; 21:e1–14.
Article
6. Takanashi J, Barkovich AJ, Shiihara T, Tada H, Kawatani M, Tsukahara H, et al. Widening spectrum of a reversible splenial lesion with transiently reduced diffusion. AJNR Am J Neuroradiol. 2006; 27:836–8.
7. Bulakbasi N, Kocaoglu M, Tayfun C, Ucoz T. Transient splenial lesion of the corpus callosum in clinically mild influenza-associated encephalitis/encephalopathy. AJNR Am J Neuroradiol. 2006; 27:1983–6.
8. Singh P, Gogoi D, Vyas S, Khandelwal N. Transient splenial lesion: further experience with two cases. Indian J Radiol Imaging. 2010; 20:254–7.
Article
9. Malhotra HS, Garg RK, Vidhate MR, Sharma PK. Boomerang sign: clinical significance of transient lesion in splenium of corpus callosum. Ann Indian Acad Neurol. 2012; 15:151–7.
Article
10. Cho JS, Ha SW, Han YS, Park SE, Hong KM, Han JH, et al. Mild encephalopathy with reversible lesion in the splenium of the corpus callosum and bilateral frontal white matter. J Clin Neurol. 2007; 3:53–6.
Article
11. Kakadia B, Ahmed J, Siegal T, Jovin TG, Thon JM. Mild encephalopathy with reversible splenium lesion (MERS) in a patient with COVID-19. J Clin Neurosci. 2020; 79:272–4.
Article
12. Kahilogullari G, Comert A, Ozdemir M, Brohi RA, Ozgural O, Esmer AF, et al. Arterial vascularization patterns of the splenium: an anatomical study. Clin Anat. 2013; 26:675–81.
Article
13. Mathews MS, Linskey ME, Binder DK, William P. Van Wagenen and the first corpus callosotomies for epilepsy. J Neurosurg. 2008; 108:608–13.
14. Lin D, Rheinboldt M. Reversible splenial lesions presenting in conjunction with febrile illness: a case series and literature review. Emerg Radiol. 2017; 24:599–604.
Article
15. Talukder NT, Feezel A, Lankford JE. Mild encephalitis/encephalopathy with a reversible splenial lesion associated with systemic Mycoplasma pneumoniae infection in North America: a case report. J Med Case Rep. 2022; 16:74.
Article
16. Mawatari M, Kobayashi T, Yamamoto S, Takeshita N, Hayakawa K, Kutsuna S, et al. Mild encephalitis/encephalopathy with a reversible splenial lesion due to Plasmodium falciparum malaria: a case report. Trop Med Health. 2018; 46:37.
Article
17. Sathananthasarma P, Weeratunga PN, Chang T. Reversible splenial lesion syndrome associated with dengue fever: a case report. BMC Res Notes. 2018; 11:412.
Article
18. Varol F, Ergul N, Sahin EG, Can YY, Ergul U, Guven S, et al. Can plasma exchange therapy be an option for the treatment of SARS-CoV-2 related splenial lesion syndrome: two cases from the pediatric intensive care unit. Transfus Apher Sci. 2022; 103491.
Article
19. Arıkan FA, Akdağ G, Çetiner M, Uysal N, Kabay SC. Isolated corpus callosum lesion associated with cytokine storm in COVID-19. Proc (Bayl Univ Med Cent). 2022; 35:337–8.
Article
20. DE Oliveira FA, DE Melo TF, Rocha-Filho PA. Transient lesion in the splenium of the corpus callosum associated with COVID-19. Arq Neuropsiquiatr. 2020; 78:738.
Article
21. Sawlani V, Scotton S, Nader K, Jen JP, Patel M, Gokani K, et al. COVID-19-related intracranial imaging findings: a large single-centre experience. Clin Radiol. 2021; 76:108–16.
Article
22. McLeod NA, Williams JP, Machen B, Lum GB. Normal and abnormal morphology of the corpus callosum. Neurology. 1987; 37:1240–2.
Article
23. Park MK, Hwang SH, Jung S, Hong SS, Kwon SB. Lesions in the splenium of the corpus callosum: clinical and radiological implications. Neurol Asia. 2014; 19:79–88.
24. Chen WX, Liu HS, Yang SD, Zeng SH, Gao YY, Du ZH, et al. Reversible splenial lesion syndrome in children: retrospective study and summary of case series. Brain Dev. 2016; 38:915–27.
Article
25. Baek SH, Shin DI, Lee HS, Lee SH, Kim HY, Shin KS, et al. Reversible splenium lesion of the corpus callosum in hemorrhagic fever with renal failure syndrome. J Korean Med Sci. 2010; 25:1244–6.
Article
26. Tada H, Takanashi J, Barkovich AJ, Oba H, Maeda M, Tsukahara H, et al. Clinically mild encephalitis/encephalopathy with a reversible splenial lesion. Neurology. 2004; 63:1854–8.
Article
27. Doherty MJ, Jayadev S, Watson NF, Konchada RS, Hallam DK. Clinical implications of splenium magnetic resonance imaging signal changes. Arch Neurol. 2005; 62:433–7.
Article
28. Takanashi J, Tada H, Maeda M, Suzuki M, Terada H, Barkovich AJ. Encephalopathy with a reversible splenial lesion is associated with hyponatremia. Brain Dev. 2009; 31:217–20.
Article
29. Miyata R, Tanuma N, Hayashi M, Imamura T, Takanashi J, Nagata R, et al. Oxidative stress in patients with clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS). Brain Dev. 2012; 34:124–7.
Article
30. Motobayashi M, Fukuyama T, Okuno-Yuguchi J, Tsukahara K, Nagaharu S, Hagimoto R, et al. Subclinical neuroaxonal damage in patients with clinically mild encephalitis/encephalopathy with a reversible splenial lesion. Pediatr Neurol. 2017; 74:e3–4.
Article
31. Moritani T, Smoker WR, Sato Y, Numaguchi Y, Westesson PL. Diffusion-weighted imaging of acute excitotoxic brain injury. AJNR Am J Neuroradiol. 2005; 26:216–28.
32. Conklin J, Frosch MP, Mukerji SS, Rapalino O, Maher MD, Schaefer PW, et al. Susceptibility-weighted imaging reveals cerebral microvascular injury in severe COVID-19. J Neurol Sci. 2021; 421:117308.
Article
33. Sparr SA, Bieri PL. Infarction of the splenium of the corpus callosum in the age of COVID-19: a snapshot in time. Stroke. 2020; 51:e223–6.
34. Chougar L, Shor N, Weiss N, Galanaud D, Leclercq D, Mathon B, et al. Retrospective observational study of brain MRI findings in patients with acute SARS-CoV-2 infection and neurologic manifestations. Radiology. 2020; 297:E313–23.
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