[Downloaded free from http://www.pediatricneurosciences.com on Sunday, May 6, 2018, IP: 181.64.241.187] Letter to the Editor
3. Malone HE, Nicholl H, Coyne I. Fundamentals of estimating sample size. Nurse Res 2016;23:21‑5. 4. Panayiotopoulos CP. Neonatal Seizures and Neonatal Syndromes. The Epilepsies: Seizures, Syndromes and Management. Ch. 5. Oxfordshire (UK): Bladon Medical Publishing; 2005. Available from: https://www.ncbi.nlm.nih.gov/books/NBK2599/. [Last accessed on 2017 May 05].
This is an open access article distributed under the terms of the Creative Commons Attribution‑NonCommercial‑ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non‑commercially, as long as the author is credited and the new creations are licensed under the identical terms.
Access this article online Quick Response Code: Website: www.pediatricneurosciences.com
DOI: 10.4103/jpn.JPN_61_17
How to cite this article: Mandal A, Sahi PK. Levetiracetam as a first-line agent for neonatal seizure. J Pediatr Neurosci 2017;12:395-6. © 2018 Journal of Pediatric Neurosciences | Published by Wolters Kluwer - Medknow
Intramedullary Cysticercosis without Neurological Deficit Dear Sir, Ranjan et al. presented an interesting case with “Intramedullary Cysticercosis (ICC) without Neurological Deficit.”[1] Ranjan et al. mentioned that “to best of our knowledge, this is the first case of ICC without neurological involvement.”[1] We agree that the case is rare, but we do not agree with this conclusion, and the problem might be due to a good literature review. We would like to take the note that there are already some publications on ICC without neurological complication. At least, Parmar et al. reported two cases of ICC without neurological complication.[2] It is no doubt that the silent asymptomatic CC is possible and usually missed underdiagnosed. Financial support and sponsorship
Nil.
Address for correspondence: Dr. Beuy Joob, Sanitation 1 Medical Academic Center, Bangkok, Thailand. E‑mail:
[email protected]
References 1. 2.
Ranjan R, Tulika, Chand S, Agnihotri A. Solitary intramedullary cervical cysticercosis without neurological deficit: A Rare case report. J Pediatr Neurosci 2017;12:99‑101. Parmar H, Shah J, Patwardhan V, Patankar T, Patkar D, Muzumdar D, et al. MR imaging in intramedullary cysticercosis. Neuroradiology 2001;43:961‑7.
This is an open access article distributed under the terms of the Creative Commons Attribution‑NonCommercial‑ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non‑commercially, as long as the author is credited and the new creations are licensed under the identical terms. Access this article online Quick Response Code: Website: www.pediatricneurosciences.com
Conflicts of interest
There are no conflicts of interest.
DOI: 10.4103/jpn.JPN_83_17
Beuy Joob, Viroj Wiwanitkit
1
Sanitation 1 Medical Academic Center, Bangkok, Thailand, 1Department of Tropical Medicine, Hainan Medical University, Hainan Sheng, China
How to cite this article: Joob B, Wiwanitkit V. Intramedullary cysticercosis without neurological deficit. J Pediatr Neurosci 2017;12:396. © 2018 Journal of Pediatric Neurosciences | Published by Wolters Kluwer - Medknow
Primary Intracranial Extraosseous CNS Ewing's Sarcoma: A Distinct Entity Dear Sir, Ewing’s sarcoma (EWS)/peripheral primitive neuroectodermal tumor (pPNET) is an aggressive malignant small round blue cell neoplasm that frequently manifests in the second decade of life, 396
accounting for 4% of childhood and adolescent malignancies.[1] Primary extraosseous EWS of the central nervous system (CNS‑EES) is an extremely uncommon entity with only a handful of cases reported till date. CNS‑EES is histologically similar to central PNET
Journal of Pediatric Neurosciences ¦ Volume 12 ¦ Issue 4 ¦ October-December 2017