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Artículos de revistas sobre el tema "Cerebellitis"

Autor: Grafiati
Publicado: 7 de junio de 2025
Última modificación: 2 de agosto de 2025

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1

Riverol, Mario, Pablo Irimia, and Eduardo Martínez-Vila. "Cerebellitis." Lancet 362, no. 9394 (2003): 1449. http://dx.doi.org/10.1016/s0140-6736(03)14688-0.

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2

Gökçe, Şule, Zafer Kurugol, and Aslı Aslan. "A Rare Cause of Childhood Cerebellitis-Influenza Infection: A Case Report and Systematic Review of Literature." Case Reports in Pediatrics 2017 (2017): 1–5. http://dx.doi.org/10.1155/2017/4039358.

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Acute cerebellitis is a benign neurologic condition generally caused by viral or bacterial infections. Influenza associated cerebellitis is extremely rare; a 6-year-old boy with acute cerebellitis, who presented with fever, vomiting, weakness, febrile seizure, and acute cerebellar features, is discussed in this article.
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3

Majda-Stanislawska, Ewa. "Mumps Cerebellitis." European Neurology 43, no. 2 (2000): 117. http://dx.doi.org/10.1159/000008147.

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4

Nigrovic, L. E., C. Lumeng, C. Landrigan, and V. W. Chiang. "Rotavirus Cerebellitis?" Clinical Infectious Diseases 34, no. 1 (2002): 130. http://dx.doi.org/10.1086/323560.

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5

Sawaishi, Yukio, and Goro Takada. "Acute cerebellitis." Cerebellum 1, no. 3 (2002): 223–28. http://dx.doi.org/10.1080/14734220260418457.

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6

Condé, Ibrahima1 4. Barry Mamadou ciré4 5. Diallo Fatoumata Binta3 4. Kourouma Hamidou3 Hyjazi Marie Elisabeth1 Kaba Ibrahima1 Diaby Macka1 4. Diallo Abdoul Salam1. "Childhood Cerebellitis about a case in the paediatric department of Kamsar Hospital, Guinea." ISRG Journal of Arts Humanities & Social Sciences (ISRGJAHSS) III, no. I (2025): 190–93. https://doi.org/10.5281/zenodo.14697847.

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<strong>Abstract</strong> <em>Cerebellitis is a rare inflammation of cerebellar structures. We report the case of an 8-year-old girl, a student, presenting with acute post-infectious cerebellitis complicated by marked cerebellar atrophy. </em> <em>The evolution under solumedrol and physiotherapy sessions was favorable; the child walks with a few falls.</em> <strong>Keywords:</strong> <em>cerebellitis, child, pediatrics, kamsar.</em>
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7

Asmi, Ravouf, Zarka Amin Masoodi, Imran Rangreze, Mushtaq Ahmad Wani, and Sheikh Nawaz. "Acute Post Infectious Cerebellitis Presenting as Hydrocephalus: A Rare Presentation." JMS SKIMS 13, no. 2 (2010): 67–69. http://dx.doi.org/10.33883/jms.v13i2.55.

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Acute post infectious cerebellitis, also known as acute cerebellar ataxia, is a rare inflammatory syndrome often characterized by cerebellar dysfunction of rapid onset. Although usually benign and self-limiting, acute cerebellitis may manifest a fulminant course. We describe a patient referred to our center with acute cerebellitis, complicated by hydrocephalus. An 32-year-old female presented with headache, nausea, vomiting, and gait and limbs ataxia 2 weeks after following a respiratory tract infection. CT showed obstructive hydrocephalus. MRI showed bilateral cerebellar swelling with hyperin
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8

Schneider, L. B., and V. D. Salanga. "Benign acute cerebellitis." Cleveland Clinic Journal of Medicine 54, no. 2 (1987): 91–94. http://dx.doi.org/10.3949/ccjm.54.2.91.

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9

Omeis, Ibrahim A., Sami Khoshyomn, Steven P. Braff, and Todd A. Maugans. "Idiopathic Lymphocytic Cerebellitis." Pediatric Neurosurgery 36, no. 1 (2002): 52–53. http://dx.doi.org/10.1159/000048351.

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10

Schijman, Edgardo. "Surgically treated cerebellitis." Child's Nervous System 18, no. 1-2 (2002): 6. http://dx.doi.org/10.1007/s00381-001-0538-z.

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11

Brito, Teresa, Inês Oliveira, Laurinda Silva, and Susana Parente. "Transient mutism, pathological laughter and cerebellar ataxia after primary varicella-zoster virus infection." BMJ Case Reports 12, no. 11 (2019): e230683. http://dx.doi.org/10.1136/bcr-2019-230683.

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Acute postinfectious cerebellitis is characterised by inflammatory involvement of the cerebellum and consequent cerebellar dysfunction, usually presenting a benign and self-limited course. Common symptoms described in the literature include ataxia, peripheral facial paralysis, aphasia, spinal dysfunction and eventually hydrocephalus. We describe a rare presentation of acute cerebellitis after varicella, in a 6-year-old child, who presented with ataxia, dysmetria, mutism and pathological laughter.
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12

Martins, William Alves, Rafael do Amaral Cristovam, and André Palmini. "Acute post-infectious cerebellitis." Arquivos de Neuro-Psiquiatria 73, no. 11 (2015): 977. http://dx.doi.org/10.1590/0004-282x20150143.

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13

Millichap, J. Gordon. "Cerebellitis and Acute Hydrocephalus." Pediatric Neurology Briefs 12, no. 5 (1998): 39. http://dx.doi.org/10.15844/pedneurbriefs-12-5-11.

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14

Millichap, J. Gordon. "Coxiella Burnetii Acute Cerebellitis." Pediatric Neurology Briefs 13, no. 1 (1999): 8. http://dx.doi.org/10.15844/pedneurbriefs-13-1-11.

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15

Millichap, J. Gordon. "Acute Cerebellitis and Hydrocephalus." Pediatric Neurology Briefs 23, no. 9 (2009): 71. http://dx.doi.org/10.15844/pedneurbriefs-23-9-9.

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16

Kornreich, Liora, Vered Shkalim-Zemer, Yoel Levinsky, Wafa Abdallah, Esther Ganelin-Cohen, and Rachel Straussberg. "Acute Cerebellitis in Children." Journal of Child Neurology 31, no. 8 (2016): 991–97. http://dx.doi.org/10.1177/0883073816634860.

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17

Dogulu, F., A. Onk, M. Kaymaz, O. Kardes, and M. K. Baykaner. "Acute cerebellitis with hydrocephalus." Neurology 60, no. 10 (2003): 1717. http://dx.doi.org/10.1212/01.wnl.0000064168.64413.ff.

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18

Montenegro, Maria Augusta, S��rgio L. M. Santos, Li Min Li, and Fernando Cendes. "Neuroimaging of Acute Cerebellitis." Journal of Neuroimaging 12, no. 1 (2002): 72–74. http://dx.doi.org/10.1111/j.1552-6569.2002.tb00095.x.

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19

Gill, D., J. P. Lin, T. Cox, and K. Pohl. "097 Acute streptococcal cerebellitis." European Journal of Paediatric Neurology 3, no. 6 (1999): A76. http://dx.doi.org/10.1016/s1090-3798(99)91188-1.

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20

HAYASE, Yukiharu, and Kiyotake TOBITA. "Probable Post-Influenza Cerebellitis." Internal Medicine 36, no. 10 (1997): 747–49. http://dx.doi.org/10.2169/internalmedicine.36.747.

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21

Yildirim, Mirac, Rahsan Gocmen, Bahadir Konuskan, Safak Parlak, Dilek Yalnizoglu, and Banu Anlar. "Acute Cerebellitis or Postinfectious Cerebellar Ataxia? Clinical and Imaging Features in Acute Cerebellitis." Journal of Child Neurology 35, no. 6 (2020): 380–88. http://dx.doi.org/10.1177/0883073820901407.

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Acute cerebellitis is a rare condition often considered within the group of acute postinfectious cerebellar ataxia despite its distinctive clinical and imaging features. We retrieved clinical, laboratory, and follow-up data of 15 children diagnosed with acute cerebellitis in our department between 2011 and 2019. There were 10 boys and 5 girls aged 3-15 years, median 9.5 years. The most common first symptoms were ataxia, vomiting, and headache. Magnetic resonance imaging (MRI) generally showed bilateral symmetrical T2 hyperintense changes with moderate swelling in the cerebellar cortex. Tonsill
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22

Boussaid, Imane, Imane Chahid, Fatima Harim, Abdelhak Abkari, Daoud Bentaleb, and Wilhem Gilius. "Infectious Cerebellitis Rare Entity About Two Cases." American Journal of Pediatrics 10, no. 3 (2024): 112–16. http://dx.doi.org/10.11648/j.ajp.20241003.11.

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Introduction: Cerebellitis is an inflammatory pathology of cerebellar structures more common in children, frequently of post-infectious origin or following vaccination, seldom during a viral or bacterial infection. Ataxia is most frequently caused by dysfunction of the complex circuitry connecting the cerebellum, basal ganglia and cerebral cortex. Results: We report the case of 2 patients aged 3 and 10 years presenting acute cerebellitis of infectious origin: Ataxic syndrome associated with balance disorders and speech disorders and fever. The evolution was quickly favorable with corticosteroi
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23

Desai, Jay, and Wendy G. Mitchell. "Acute Cerebellar Ataxia, Acute Cerebellitis, and Opsoclonus-Myoclonus Syndrome." Journal of Child Neurology 27, no. 11 (2012): 1482–88. http://dx.doi.org/10.1177/0883073812450318.

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Acute cerebellar ataxia and acute cerebellitis represent a process characterized by parainfectious, postinfectious, or postvaccination cerebellar inflammation. There is considerable overlap between these entities. The mildest cases of acute cerebellar ataxia represent a benign condition that is characterized by acute truncal and gait ataxia, variably with appendicular ataxia, nystagmus, dysarthria, and hypotonia. It occurs mostly in young children, presents abruptly, and recovers over weeks. Neuroimaging is normal. Severe cases of cerebellitis represent the other end of the spectrum, presentin
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24

Sarvepalli, Tanushree, S. P. Alagappan, Krishna S. Nair, Clement Jenil Dhas, Shamitha Partheeban, and A. Murali. "Isoniazid-Induced Cerebellitis in a Chronic Kidney Disease Patient." Infectious Diseases in Clinical Practice 32, no. 4 (2024): e1361. http://dx.doi.org/10.1097/ipc.0000000000001361.

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Abstract The bacterial disease tuberculosis (TB), when it affects organs of the body other than the lungs, is called extrapulmonary TB. The treatment regimen includes the drugs isoniazid, rifampicin, pyrazinamide, and ethambutol, of which isoniazid is known to be the most active drug. Adverse drug reactions commonly include immunological as well as drug toxicity effects, with the latter being particularly important in renally impaired patients because of high risk of drug accumulation. Cerebellitis, which is an inflammatory condition that results in cerebellar dysfunction, is a rare complicati
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25

Summa, A., A. Squarcia, F. Ormitti, et al. "Pseudotumoural Hemicerebellitis: Conventional MR Imaging and MR Spectroscopy Evolution." Neuroradiology Journal 22, no. 4 (2009): 397–401. http://dx.doi.org/10.1177/197140090902200406.

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Acute cerebellitis is an inflammatory process commonly involving both cerebellar hemispheres. Bilateral cerebellar hemispheres involvement is the most common finding. It typically occurs as a primary infectious, post-infectious or post-vaccination disorder, but is also a disease entity with heterogeneous pathogenesis including paraneoplasia. Acute cerebellitis is usually a benign, self-limiting and rarely fatal disease. Typically, cerebellar atrophy is a late consequence of the syndrome. We describe the radiological features of a case of pseudotumoural hemicerebellitis with emphasis on MRI and
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26

Kupaeva, Alina V., Evgenia A. Skornyakova, and Leonid G. Zaslavskii. "ACUTE HEMICEREBELLITIS IN ADULTS: LITERATURE REVIEW AND PERSONAL OBSERVATION." Scientific Notes of the Pavlov University 26, no. 1 (2019): 68–73. http://dx.doi.org/10.24884/1607-4181-2019-26-1-68-73.

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Acute cerebellitis is a common inflammatory syndrome typically occurring in children and only on very rare occasions in adults. Thus, there was no description of acute cerebellitis, associated with Crohn’s disease, found in Russian sources of literature. We reported a case of acute cerebellitis in 45-year-old woman with a long history of Crohn’s disease treated with Mesalazine as a basic therapy and a resection of ileotransversoanastomosis together with small intestine two months before the onset of neurological symptoms. She first presented with severe headache and left-sided cerebellar dysfu
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27

Amador, Nelly, Bernd W. Scheithauer, Caterina Giannini, and Corey Raffel. "Acute cerebellitis presenting as tumor." Journal of Neurosurgery: Pediatrics 107, no. 1 (2007): 57–61. http://dx.doi.org/10.3171/ped-07/07/057.

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28

Millichap, J. Gordon. "Acute Cerebellitis with Parvovirus Infection." Pediatric Neurology Briefs 26, no. 5 (2012): 36. http://dx.doi.org/10.15844/pedneurbriefs-26-5-4.

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29

Akçay, Nihal, Mustafa Oğur, Mehmet Emin Menentoğlu, et al. "Acute Cerebellitis in MIS-C." Pediatric Infectious Disease Journal 41, no. 1 (2021): e16-e18. http://dx.doi.org/10.1097/inf.0000000000003358.

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30

Xu, Fang, Shi Qing Ren, and Jun Yan Liu. "Acute Cerebellitis in Identical Twins." Pediatric Neurology 39, no. 6 (2008): 432–34. http://dx.doi.org/10.1016/j.pediatrneurol.2008.08.009.

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31

Mario-Ubaldo, Manto. "Cerebellitis associated with Lyme disease." Lancet 345, no. 8956 (1995): 1060. http://dx.doi.org/10.1016/s0140-6736(95)90806-4.

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32

Guerrini, Laura, Giacomo Belli, Martino Cellerini, Patrizia Nencini, and Mario Mascalchi. "Proton MR spectroscopy of cerebellitis." Magnetic Resonance Imaging 20, no. 8 (2002): 619–22. http://dx.doi.org/10.1016/s0730-725x(02)00600-8.

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33

Mills, Fionnghuala, Suzanna C. MacLennan, Catherine J. Devile, and Dawn E. Saunders. "Severe cerebellitis following methadone poisoning." Pediatric Radiology 38, no. 2 (2007): 227–29. http://dx.doi.org/10.1007/s00247-007-0635-6.

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34

Bhat, Maya Dattatraya, K. N. Vykuntaraju, Ullas V. Acharya, Premlatha Ramaswamy, and Chandrajit Prasad. "Isolated Cerebellitis in Scrub Typhus." Indian Journal of Pediatrics 82, no. 11 (2015): 1067–68. http://dx.doi.org/10.1007/s12098-015-1784-5.

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35

Práxedes González, Enrique, Marta Lázaro Sáez, Álvaro Hernández Martínez, Esteban Alessandro Vogt Sánchez, Antonio Arjona Padillo, and José Luis Vega Sáenz. "Autoimmune cerebellitis in Crohn’s disease." Gastroenterología y Hepatología (English Edition) 42, no. 10 (2019): 630–31. http://dx.doi.org/10.1016/j.gastre.2019.06.005.

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36

Aylett, S. E., K. S. O'Neill, C. De Sousa, and J. Britton. "Cerebellitis presenting as acute hydrocephalus." Child's Nervous System 14, no. 3 (1998): 139–41. http://dx.doi.org/10.1007/s003810050197.

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37

Neophytides, A., S. Khan, and E. Louie. "SUBACUTE CEREBELLITIS IN LYME DISEASE." International Journal of Clinical Practice 51, no. 8 (1997): 523–24. http://dx.doi.org/10.1111/j.1742-1241.1997.tb11541.x.

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38

Tilly, CM, and JM Mack. "The headache of diagnosing cerebellitis." American Journal of the Medical Sciences 365 (February 2023): S221. http://dx.doi.org/10.1016/s0002-9629(23)00422-6.

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39

Sawaishi, Yukio, Ikuo Takahashi, Yasuhiro Hirayama, et al. "Acute cerebellitis caused byCoxiella burnetii." Annals of Neurology 45, no. 1 (1999): 124–27. http://dx.doi.org/10.1002/1531-8249(199901)45:1<124::aid-art19>3.0.co;2-b.

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40

Hanin, Al Gethami, Al Malki Fuad, Al-Tuwaijri Waleed, Ba-Armah Duaa, and Al Zahrani Ahmed. "Unilateral Weakness and Areflexia in a Child Diagnosed with Pseudo-Tumoral Acute Hemi-Cerebellitis." Asian Journal of Research and Reports in Neurology 2, no. 1 (2019): 1–6. https://doi.org/10.5281/zenodo.3522685.

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Pseudotumoral acute hemi-cerebellitis is an inflammatory condition, a self-limited disease with good prognosis, which does not need treatment in most of the cases. It is very rare worldwide, and few cases have described it before. It has a unique presentation and a characteristic neuroimage finding. The cause is not known however, it can be the primary infection, post-infectious or post vaccination disorder. The present work described that, a child was diagnosed to have pseudo- tumoral acute hemi-cerebellitis with a typical presentation in the form of unilateral weakness and areflexia, which w
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41

CH, Balasubrahmanyam. "An Unusual Cause of Cerebellitis - Case Report." Current Research in Emergency Medicine (CREM) 2, no. 6 (2022): 1–3. http://dx.doi.org/10.54026/crem/1043.

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In countries where tuberculosis is still very common, millions of patients are placed under Anti-tuberculous treatment, of which Isoniazid is a component. The unfortunate co-occurrence TB in end-stage renal disease patient influences the metabolism and excretion of isoniazid and increases the chances of adverse effects. We wish to present one such patient of ours on ATT who returned to our care with neurological symptoms. Both the disease of tuberculosis and its treatment are fraught with occurrence of neurological involvement and complications. Diligent neurological examination pointed toward
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42

Kang, Kyusik, Sung-Soo Yoon, and Byung-Woo Yoon. "Vancomycin-resistant Enterococcus faecium-associated encephalitis and concurrent cerebellitis." Open Medicine 6, no. 4 (2011): 470–74. http://dx.doi.org/10.2478/s11536-011-0041-1.

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AbstractEnterococci are uncommon etiologic agents of central nervous system infections. We describe a case of nosocomial encephalitis and concurrent cerebellitis associated with Enterococcus faecium in a man, with extranodal natural killer/T-cell lymphoma, nasal type, who underwent high-dose chemotherapy and autologous peripheral blood stem cell transplantation. Brain magnetic resonance images showed lesions in the bihemispheral cerebellar cortex with swelling and several small lesions in both cerebral hemispheres. The blood and cerebrospinal fluid cultures were positive for vancomycin-resista
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43

Gupta, Rajesh, Pejman J. Maralani, Sanjeev Chawla, Pallavi P. Gopal, and Suyash Mohan. "Advanced neuroimaging findings of pseudotumoral hemicerebellitis in an elderly male requiring surgical decompression." Journal of Neurosurgery 120, no. 2 (2014): 522–27. http://dx.doi.org/10.3171/2013.11.jns13980.

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Acute cerebellitis is an inflammatory process that usually affects bilateral cerebellar hemispheres in the pediatric population. Pseudotumoral hemicerebellitis is an extremely rare presentation in which unilateral cerebellar involvement mimics a tumor that can exert significant mass effect on the surrounding structures, which may require surgical intervention. Magnetic resonance imaging characteristics that suggest cerebellitis include cerebellar swelling, T2 hyperintensity, and pial enhancement. Advanced neuroimaging, including MR perfusion and MR spectroscopy, may be helpful in excluding oth
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44

Emelifeonwu, John Amaechi, Jay Shetty, Chandrasekaran Kaliaperumal, et al. "Acute Cerebellitis in Children: A Variable Clinical Entity." Journal of Child Neurology 33, no. 10 (2018): 675–84. http://dx.doi.org/10.1177/0883073818777673.

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Acute cerebellar ataxia is the most common cause of acute ataxia in children and it usually runs a self-limiting and ultimately benign clinical course. A small proportion of children have evidence of inflammatory swelling in the cerebellum. Many of these children suffer more severe and potentially life-threatening forms of cerebellar ataxia and may need more intensive treatments including urgent neurosurgical treatments. This more severe form of acute cerebellar ataxia is often termed acute cerebellitis. Many children with acute cerebellitis have long-term neurological sequela and evidence of
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45

Venugopal, K., Vishwanath Huggi, MY Bharathraj, Mudegoudara Lingaraja, Manjunath Ganiger, and C. Suresh. "Acute cerebellitis associated with dengue fever." Journal of Mahatma Gandhi Institute of Medical Sciences 26, no. 1 (2021): 69. http://dx.doi.org/10.4103/0971-9903.319846.

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46

Gailson, Tonyot, Viresh Vohra, Arushi Gahlot Saini, and Vikas Bhatia. "Mumps infection with meningoencephalitis and cerebellitis." BMJ Case Reports 14, no. 11 (2021): e247306. http://dx.doi.org/10.1136/bcr-2021-247306.

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47

Fulco, V., L. Biaggi, L. Bembenuto, C. Routaboul, P. Carullo, and A. Schteinschnaider. "P0021 / #1218: CEREBELLITIS, CLINICAL CASE PRESENTATION." Pediatric Critical Care Medicine 22, Supplement 1 3S (2021): 47. http://dx.doi.org/10.1097/01.pcc.0000738428.56100.07.

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48

Gaggero, Gabriele, Michela Campora, Beatrice Dose, Davide Taietti, Antonio Vena, and Emanuele Delfino. "Neuro-toxoplasmosis and fatal necrotizing cerebellitis." Autopsy Case Reports 12 (2022): e2021363. http://dx.doi.org/10.4322/acr.2021.363.

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49

Uchizono, Hiromasa, Tadashi Iwasa, Hidemi Toyoda, Yukitoshi Takahashi, and Yoshihiro Komada. "Acute Cerebellitis Following Hemolytic Streptococcal Infection." Pediatric Neurology 49, no. 6 (2013): 497–500. http://dx.doi.org/10.1016/j.pediatrneurol.2013.06.003.

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50

Tatli, Ozgur, Yunus Karaca, Mucahit Gunaydin, Selim Yurtsever, and Gamze Tuten. "Cerebellitis developing after tricyclic antidepressant poisoning." American Journal of Emergency Medicine 31, no. 9 (2013): 1419.e3–1419.e5. http://dx.doi.org/10.1016/j.ajem.2013.05.001.

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