{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,1]],"date-time":"2022-04-01T19:25:33Z","timestamp":1648841133477},"reference-count":19,"publisher":"Spandidos Publications","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["mol clin onc"],"DOI":"10.3892\/mco.2019.1969","type":"journal-article","created":{"date-parts":[[2019,12,17]],"date-time":"2019-12-17T08:45:20Z","timestamp":1576572320000},"source":"Crossref","is-referenced-by-count":0,"title":["Malignant peripheral nerve\u2011sheath tumors in an adolescent patient with mosaic localized NF1: A case report"],"prefix":"10.3892","author":[{"given":"Hiroki","family":"Hagizawa","sequence":"first","affiliation":[{"name":"Department of Orthopedic Surgery, Osaka International Cancer Institute, Osaka 541\u20118567, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shigenori","family":"Nagata","sequence":"additional","affiliation":[{"name":"Department of Diagnostic Pathology and Cytology, Osaka International Cancer Institute, Osaka 541\u20118567, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Toru","family":"Wakamatsu","sequence":"additional","affiliation":[{"name":"Department of Orthopedic Surgery, Osaka International Cancer Institute, Osaka 541\u20118567, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoshinori","family":"Imura","sequence":"additional","affiliation":[{"name":"Department of Orthopedic Surgery, Osaka International Cancer Institute, Osaka 541\u20118567, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takaaki","family":"Tanaka","sequence":"additional","affiliation":[{"name":"Department of Orthopedic Surgery, Osaka International Cancer Institute, Osaka 541\u20118567, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hidetatsu","family":"Outani","sequence":"additional","affiliation":[{"name":"Department of Orthopedic Surgery, Osaka University Hospital, Suita, Osaka 565\u20110871, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eiichi","family":"Konishi","sequence":"additional","affiliation":[{"name":"Department of Pathology, Kyoto Prefectural University of Medicine, Kyoto 602\u20118566, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Norifumi","family":"Naka","sequence":"additional","affiliation":[{"name":"Department of Orthopedic Surgery, Osaka International Cancer Institute, Osaka 541\u20118567, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hironari","family":"Tamiya","sequence":"additional","affiliation":[{"name":"Department of Orthopedic Surgery, Osaka International Cancer Institute, Osaka 541\u20118567, Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2249","published-online":{"date-parts":[[2019,12,17]]},"reference":[{"key":"key20200713202707_b1-mco-0-0-1969","author":"Fletcher"},{"key":"key20200713202707_b2-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"2006","DOI":"10.1002\/1097-0142(19860515)57:10<2006::aid-cncr2820571022>3.0.co;2-6","article-title":"Malignant peripheral nerve sheath tumors. A clinicopathologic study of 120 cases","volume":"57","author":"Ducatman","year":"1986","journal-title":"Cancer"},{"issue":"756395","key":"key20200713202707_b3-mco-0-0-1969","doi-asserted-by":"publisher","DOI":"10.1155\/2009\/756395","article-title":"Survival in malignant peripheral nerve sheath tumours: A comparison between sporadic and neurofibromatosis type 1-associated tumours","volume":"2009","author":"Porter","year":"2009","journal-title":"Sarcoma"},{"key":"key20200713202707_b4-mco-0-0-1969","doi-asserted-by":"crossref","first-page":"837","DOI":"10.1001\/archderm.1977.01640060133020","article-title":"Segmental neurofibromatosis","volume":"113","author":"Miller","year":"1977","journal-title":"Arch Dermatol"},{"key":"key20200713202707_b5-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1016\/s0147-0272(82)80016-0","article-title":"Neurofibromatosis: Clinical heterogeneity","volume":"7","author":"Riccardi","year":"1982","journal-title":"Curr Probl Cancer"},{"key":"key20200713202707_b6-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"1433","DOI":"10.1212\/wnl.56.11.1433","article-title":"The clinical and diagnostic implications of mosaicism in the neurofibromatoses","volume":"56","author":"Ruggieri","year":"2001","journal-title":"Neurology"},{"key":"key20200713202707_b7-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"342","DOI":"10.3171\/jns.2000.92.2.0342","article-title":"Malignant peripheral nerve sheath tumors in the setting of segmental neurofibromatosis. Case report","volume":"92","author":"Schwarz","year":"2000","journal-title":"J Neurosurg"},{"key":"key20200713202707_b8-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"540","DOI":"10.1080\/00015550510040022","article-title":"A superficial form of malignant peripheral nerve sheath tumour associated with segmental neurofibromatosis","volume":"85","author":"Li","year":"2005","journal-title":"Acta Derm Venereol"},{"key":"key20200713202707_b9-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"959","DOI":"10.1001\/archderm.131.8.959","article-title":"Segmental neurofibromatosis: Is it uncommon or underdiagnosed?","volume":"131","author":"Ingordo","year":"1995","journal-title":"Arch Dermatol"},{"key":"key20200713202707_b10-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"71","DOI":"10.1001\/archderm.141.1.71","article-title":"Prevalence of neurofibromatosis 1 in German children at elementary school enrollment","volume":"141","author":"Lammert","year":"2005","journal-title":"Arch Dermatol"},{"key":"key20200713202707_b11-mco-0-0-1969","first-page":"20","article-title":"Precise localization of NF1 to 17q11.2 by balanced translocation","volume":"44","author":"Ledbetter","year":"1989","journal-title":"Am J Hum Genet"},{"key":"key20200713202707_b12-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"455","DOI":"10.1038\/sj.ejhg.5200493","article-title":"Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type 1 (NF1) gene","volume":"8","author":"Tinschert","year":"2000","journal-title":"Eur J Hum Genet"},{"key":"key20200713202707_b13-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"917","DOI":"10.1001\/archderm.1987.01660310085020","article-title":"Segmental neurofibromatosis","volume":"123","author":"Roth","year":"1987","journal-title":"Arch Dermatol"},{"key":"key20200713202707_b14-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"51","DOI":"10.1001\/jama.1997.03550010065042","article-title":"The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2","volume":"278","author":"Gutmann","year":"1997","journal-title":"JAMA"},{"key":"key20200713202707_b15-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"717","DOI":"10.4143\/crt.2016.271","article-title":"Outcomes of treatment for malignant peripheral nerve sheath tumors: Different clinical features associated with neurofibromatosis type 1","volume":"49","author":"Hwang","year":"2017","journal-title":"Cancer Res Treat"},{"key":"key20200713202707_b16-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"1878","DOI":"10.1043\/1543-2165(2006)130[1878:MPNSTW]2.0.CO;2","article-title":"Malignant peripheral nerve sheath tumor with rhabdomyosarcomatous differentiation (malignant triton tumor)","volume":"130","author":"Stasik","year":"2006","journal-title":"Arch Pathol Lab Med"},{"key":"key20200713202707_b17-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"57","DOI":"10.1016\/S0002-9440(10)61673-2","article-title":"NF1 deletions in S-100 protein-positive and negative cells of sporadic and neurofibromatosis 1 (NF1)-associated plexiform neurofibromas and malignant peripheral nerve sheath tumors","volume":"159","author":"Perry","year":"2001","journal-title":"Am J Pathol"},{"key":"key20200713202707_b18-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"213","DOI":"10.1002\/humu.21418","article-title":"Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)","volume":"32","author":"Messiaen","year":"2011","journal-title":"Hum Mutat"},{"key":"key20200713202707_b19-mco-0-0-1969","doi-asserted-by":"publisher","first-page":"1617","DOI":"10.1056\/NEJM198112313052704","article-title":"Von Recklinghausen neurofibromatosis","volume":"305","author":"Riccardi","year":"1981","journal-title":"N Engl J Med"}],"container-title":["Molecular and Clinical Oncology"],"original-title":[],"deposited":{"date-parts":[[2020,7,13]],"date-time":"2020-07-13T19:27:16Z","timestamp":1594668436000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.spandidos-publications.com\/10.3892\/mco.2019.1969"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,12,17]]},"references-count":19,"URL":"https:\/\/doi.org\/10.3892\/mco.2019.1969","relation":{},"ISSN":["2049-9450","2049-9469"],"issn-type":[{"value":"2049-9450","type":"print"},{"value":"2049-9469","type":"electronic"}],"subject":[],"published":{"date-parts":[[2019,12,17]]}}}