Ossifying Fibroma of Maxilla in a Female Affected by Neurofibromatosis Type 1
Ossifying fibroma is a benign fibro-osseous lesion found exclusively in jaws. It has a predilection for premolar–molar region in the mandible. The occurrence of OF as solitary lesions with no underlying disease is common in jaws. However its co-existence in patients with neurofibromatosis type 1 (NF...
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Veröffentlicht in: | Indian journal of otolaryngology, and head, and neck surgery and head, and neck surgery, 2019-11, Vol.71 (Suppl 3), p.2087-2090 |
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container_title | Indian journal of otolaryngology, and head, and neck surgery |
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creator | Jendi, Shoeb Kasim Khatib, Shuaib Mistry, Jagruti Wagh, Ashwin Vaidya, Kedar Kokane, Gauri |
description | Ossifying fibroma is a benign fibro-osseous lesion found exclusively in jaws. It has a predilection for premolar–molar region in the mandible. The occurrence of OF as solitary lesions with no underlying disease is common in jaws. However its co-existence in patients with neurofibromatosis type 1 (NF1) has not been described in jaws. NF1, also known as von Recklinghausen’s disease or peripheral neurofibromatosis, is an autosomal dominant multisystem disorder that approximately affects 1 in 2500–3000 births. The common manifestations of this disease include Café-au-lait macules, skinfold freckling, cutaneous neurofibromas, blue-red and pseudoatrophic macules on skin, plexiform neurofibroma, scoliosis, optic glioma. So far only one case of ossifying fibroma (OF) in such patients has been reported in the skull but not in the maxillofacial region. We report a case of OF of the maxilla in a 45 year old female suffering from NF1. To the best of our knowledge this is the first case report where OF occurred in the maxilla in patient with NF1. |
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It has a predilection for premolar–molar region in the mandible. The occurrence of OF as solitary lesions with no underlying disease is common in jaws. However its co-existence in patients with neurofibromatosis type 1 (NF1) has not been described in jaws. NF1, also known as von Recklinghausen’s disease or peripheral neurofibromatosis, is an autosomal dominant multisystem disorder that approximately affects 1 in 2500–3000 births. The common manifestations of this disease include Café-au-lait macules, skinfold freckling, cutaneous neurofibromas, blue-red and pseudoatrophic macules on skin, plexiform neurofibroma, scoliosis, optic glioma. So far only one case of ossifying fibroma (OF) in such patients has been reported in the skull but not in the maxillofacial region. We report a case of OF of the maxilla in a 45 year old female suffering from NF1. To the best of our knowledge this is the first case report where OF occurred in the maxilla in patient with NF1.</description><identifier>ISSN: 2231-3796</identifier><identifier>EISSN: 0973-7707</identifier><identifier>DOI: 10.1007/s12070-018-1491-4</identifier><identifier>PMID: 31763299</identifier><language>eng</language><publisher>New Delhi: Springer India</publisher><subject>Brain cancer ; Clinical Report ; Genetic disorders ; Glioma ; Head & neck cancer ; Head and Neck Surgery ; Jaw ; Maxillofacial surgery ; Medicine ; Medicine & Public Health ; Neurological disorders ; Otolaryngology ; Otorhinolaryngology ; Tumors</subject><ispartof>Indian journal of otolaryngology, and head, and neck surgery, 2019-11, Vol.71 (Suppl 3), p.2087-2090</ispartof><rights>Association of Otolaryngologists of India 2018</rights><rights>Indian Journal of Otolaryngology and Head & Neck Surgery is a copyright of Springer, (2018). All Rights Reserved.</rights><rights>Copyright Springer Nature B.V. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-4163ebc8c98cfdb951fd173baaf2c86f7e374e81835ecf726dc0d410c5fe49663</citedby><cites>FETCH-LOGICAL-c442t-4163ebc8c98cfdb951fd173baaf2c86f7e374e81835ecf726dc0d410c5fe49663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848415/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848415/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41488,42557,51319,53791,53793</link.rule.ids></links><search><creatorcontrib>Jendi, Shoeb Kasim</creatorcontrib><creatorcontrib>Khatib, Shuaib</creatorcontrib><creatorcontrib>Mistry, Jagruti</creatorcontrib><creatorcontrib>Wagh, Ashwin</creatorcontrib><creatorcontrib>Vaidya, Kedar</creatorcontrib><creatorcontrib>Kokane, Gauri</creatorcontrib><title>Ossifying Fibroma of Maxilla in a Female Affected by Neurofibromatosis Type 1</title><title>Indian journal of otolaryngology, and head, and neck surgery</title><addtitle>Indian J Otolaryngol Head Neck Surg</addtitle><description>Ossifying fibroma is a benign fibro-osseous lesion found exclusively in jaws. It has a predilection for premolar–molar region in the mandible. The occurrence of OF as solitary lesions with no underlying disease is common in jaws. However its co-existence in patients with neurofibromatosis type 1 (NF1) has not been described in jaws. NF1, also known as von Recklinghausen’s disease or peripheral neurofibromatosis, is an autosomal dominant multisystem disorder that approximately affects 1 in 2500–3000 births. The common manifestations of this disease include Café-au-lait macules, skinfold freckling, cutaneous neurofibromas, blue-red and pseudoatrophic macules on skin, plexiform neurofibroma, scoliosis, optic glioma. So far only one case of ossifying fibroma (OF) in such patients has been reported in the skull but not in the maxillofacial region. We report a case of OF of the maxilla in a 45 year old female suffering from NF1. To the best of our knowledge this is the first case report where OF occurred in the maxilla in patient with NF1.</description><subject>Brain cancer</subject><subject>Clinical Report</subject><subject>Genetic disorders</subject><subject>Glioma</subject><subject>Head & neck cancer</subject><subject>Head and Neck Surgery</subject><subject>Jaw</subject><subject>Maxillofacial surgery</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neurological disorders</subject><subject>Otolaryngology</subject><subject>Otorhinolaryngology</subject><subject>Tumors</subject><issn>2231-3796</issn><issn>0973-7707</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc1L7DAUxYMoOn78Ae4Cb13NTdKk3QgizlPwY6PrkKY3Y6TTjEnn8ea_t0NFcaGru7i_czicQ8gpsDNgTJ9n4EyzgkFVgKyhkDtkxmotCq2Z3iUzzgUUQtfqgBzm_MqYKEGzfXIgQCvB63pG7h9zDn4T-gWdhybFpaXR03v7P3SdpaGnls5xaTukl96jG7ClzYY-4DpFP_FDzCHTp80KKRyTPW-7jCcf94g8z6-frm6Ku8e_t1eXd4WTkg-FBCWwcZWrK-fbpi7Bt6BFY63nrlJeo9ASK6hEic5rrlrHWgnMlR5lrZQ4IheT72rdLLF12A_JdmaVwtKmjYk2mO-fPryYRfxnVCUrCeVo8OfDIMW3NebBvMZ16sfMZuxMaCjLsa3fKGCgtNB8S8FEuRRzTug_cwAz253MtJMZdzLbnYwcNXzS5JHtF5i-nH8WvQNeGJNk</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Jendi, Shoeb Kasim</creator><creator>Khatib, Shuaib</creator><creator>Mistry, Jagruti</creator><creator>Wagh, Ashwin</creator><creator>Vaidya, Kedar</creator><creator>Kokane, Gauri</creator><general>Springer India</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>04Q</scope><scope>04T</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20191101</creationdate><title>Ossifying Fibroma of Maxilla in a Female Affected by Neurofibromatosis Type 1</title><author>Jendi, Shoeb Kasim ; 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It has a predilection for premolar–molar region in the mandible. The occurrence of OF as solitary lesions with no underlying disease is common in jaws. However its co-existence in patients with neurofibromatosis type 1 (NF1) has not been described in jaws. NF1, also known as von Recklinghausen’s disease or peripheral neurofibromatosis, is an autosomal dominant multisystem disorder that approximately affects 1 in 2500–3000 births. The common manifestations of this disease include Café-au-lait macules, skinfold freckling, cutaneous neurofibromas, blue-red and pseudoatrophic macules on skin, plexiform neurofibroma, scoliosis, optic glioma. So far only one case of ossifying fibroma (OF) in such patients has been reported in the skull but not in the maxillofacial region. We report a case of OF of the maxilla in a 45 year old female suffering from NF1. 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subjects | Brain cancer Clinical Report Genetic disorders Glioma Head & neck cancer Head and Neck Surgery Jaw Maxillofacial surgery Medicine Medicine & Public Health Neurological disorders Otolaryngology Otorhinolaryngology Tumors |
title | Ossifying Fibroma of Maxilla in a Female Affected by Neurofibromatosis Type 1 |
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