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Posterior Quadrantic Dysplasia: MRI Diagnosis of a Lesser Known Cause of Pediatric Intractable Epilepsy.

作者信息

Reghunath Anjuna, Ghasi Rohini Gupta, Bhargava Abhimanyu, Bhambri Narinder Kumar

机构信息

Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.

出版信息

J Pediatr Neurosci. 2018 Jan-Mar;13(1):112-115. doi: 10.4103/JPN.JPN_88_17.

DOI:10.4103/JPN.JPN_88_17
PMID:29899786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5982479/
Abstract

Posterior quadrantic dysplasia (PQD) is a rare cause of pediatric intractable epilepsy. It is a sporadic cortical development malformation that involves the posterior three lobes of a single hemisphere and spares the frontal cortex. Very few cases have been reported in the literature, mostly as anecdotal reports or as a part of large series of refractory epilepsy. It is essential to know about this lesser known entity and differentiate it from other more common similar anomalies such as multilobar cortical dysplasia and hemimegalencephaly as new motor-sparing neurosurgical disconnective procedures have led to dramatically reduced mortality and morbidity rates, apart from gifting the affected children a better quality of life. Magnetic resonance imaging (MRI) is pivotal in astute diagnosis of the condition and accurate delineation of boundaries of the lesion to aid in neurosurgical management. We report one such case of PQD presenting with refractory epilepsy, which was diagnosed on MRI.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/59789da711b9/JPN-13-112-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/8ed49639cb27/JPN-13-112-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/01b36eab96cb/JPN-13-112-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/dd922d664d9a/JPN-13-112-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/59789da711b9/JPN-13-112-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/8ed49639cb27/JPN-13-112-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/01b36eab96cb/JPN-13-112-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/dd922d664d9a/JPN-13-112-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b152/5982479/59789da711b9/JPN-13-112-g004.jpg

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引用本文的文献

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Hemi-Hemimegalencephaly or Posterior Quadrantic Dysplasia, a Rare Cause of Focal Epilepsy in an Otherwise Healthy Young Woman: A Case Report.半侧巨脑畸形或后象限发育异常,一名健康年轻女性局灶性癫痫的罕见病因:病例报告
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本文引用的文献

1
Posterior quadrant disconnection for refractory epilepsy: A case series.后象限离断术治疗难治性癫痫:病例系列
Ann Indian Acad Neurol. 2014 Oct;17(4):392-7. doi: 10.4103/0972-2327.144006.
2
Surgery for posterior quadrantic cortical dysplasia. A review.后象限皮质发育异常的手术治疗。综述。
Childs Nerv Syst. 2014 Nov;30(11):1859-68. doi: 10.1007/s00381-014-2449-9. Epub 2014 Oct 9.
3
Disconnective surgery in posterior quadrantic epilepsy: experience in a consecutive series of 10 patients.后部象限性癫痫的离断性手术:10 例连续病例的经验。
Neurosurg Focus. 2013 Jun;34(6):E10. doi: 10.3171/2013.3.FOCUS1362.
4
Temporoparietooccipital disconnection in children with intractable epilepsy.难治性癫痫患儿的颞顶枕叶连接中断
J Neurosurg Pediatr. 2011 Jun;7(6):660-70. doi: 10.3171/2011.4.PEDS10454.
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Epilepsy surgery of posterior quadrant dysplasia in the first year of life: experience of a single centre with long term follow-up.婴儿期后外侧脑区发育不良致癫癎的手术治疗:单中心长期随访经验
Seizure. 2011 Jan;20(1):27-33. doi: 10.1016/j.seizure.2010.09.015. Epub 2010 Oct 15.
6
Hemimegalencephaly: a study of abnormalities occurring outside the involved hemisphere.半侧巨脑症:对受累半球以外出现的异常情况的研究。
AJNR Am J Neuroradiol. 2007 Apr;28(4):678-82.
7
Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformation.后象限发育异常或半侧巨脑症:一种典型的脑畸形。
Neurology. 2004 Jun 22;62(12):2214-20. doi: 10.1212/01.wnl.0000130459.91445.91.
8
Hemimegalencephaly: a longitudinal MR study.半侧巨脑症:一项纵向磁共振成像研究
AJNR Am J Neuroradiol. 1994 Sep;15(8):1479-82.