Publication Name	World Journal of Clinical Cases
Manuscript ID	12294
Country

Received	2014-06-30 20:05
Peer-Review Started	2014-07-01 11:40
To Make the First Decision	2014-08-14 14:35
Return for Revision	2014-08-18 10:51
Revised	2014-09-17 18:49
Second Decision	2014-10-27 16:43
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2014-10-27 17:03
Articles in Press	2014-10-27 17:03
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2015-01-05 16:39
Publish the Manuscript Online	2015-01-14 10:56

ISSN	2307-8960 (online)
Open Access	This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
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Category	Neurosciences
Manuscript Type	Case Report
Article Title	Giant xanthogranuloma of the pelvis with S1 origin: Complete removal with only posterior approach, technical note
Manuscript Source	Unsolicited Manuscript
All Author List	Nicola Marotta, Alessandro Landi, Cristina Mancarella, Pierluigi Rocco, Andrea Pietrantonio, Gaspare Galati, Antonio Bolognese and Roberto Delfini
Funding Agency and Grant Number
Corresponding Author	Alessandro Landi, MD, PhD, Department of Neurology and Psychiatry, Division of Neurosurgery, Policlinico Umberto I, “La Sapienza” Università di Roma, Viale del policlinico 155, 00161 Rome, Italy. dott.alessandro.landi@gmail.com
Key Words	Xanthogranulomas; Non-Langerhans cell histiocytosis; Touton giant cells; Congenital xanthoma; Neurofibromatosis
Core Tip	Xanthogranulomas (XG) are benign lesions derived by histiocytes, also called histiocytosis with non-Langerhans cell. Isolated xanthogranuloma involving the sacral region are unique. We report the unique giant Juvenile XG arising from S1 with extension into the pelvic region in an adult spine. Complete surgical removal is the goal of the treatment and usually curative even if there is not a study in the literature with a long follow up able to confirm this. If total resection is not possible, the patients must be followed by strictly clinical examination or should undergo adjuvant radiotherapy.
Publish Date	2015-01-14 10:56
Citation	Marotta N, Landi A, Mancarella C, Rocco P, Pietrantonio A, Galati G, Bolognese A, Delfini R. Giant xanthogranuloma of the pelvis with S1 origin: Complete removal with only posterior approach, technical note. World J Clin Cases 2015; 3(1): 77-80
URL	http://www.wjgnet.com/2307-8960/full/v3/i1/77.htm
DOI	http://dx.doi.org/10.12998/wjcc.v3.i1.77

Full Article (PDF)	WJCC-3-77.pdf
Full Article (Word)	WJCC-3-77.doc
Manuscript File	12294-Review.doc
Answering Reviewers	12294-Answering reviewers.pdf
Copyright License Agreement	12294-Copyright assignment.pdf
Non-Native Speakers of English Editing Certificate	12294-Language certificate.pdf
Peer-review Report	12294-Peer review(s).pdf
Scientific Misconduct Check	12294-CrossCheck.jpg
Scientific Editor Work List	12294-Scientific editor work list.pdf