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A case report of nasopharyngeal inflammatory myofibroblastoma in infant
Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal soft tissue tumor characterized by borderline or low-grade malignancy. It is rare childhood tumor with an average age of onset of 10 years old. It is even rarer in infants and toddlers, and the etiology and pathogenesis of this tumor are...
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Published in: | Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery head, and neck surgery, 2023-12, Vol.37 (12), p.989-992 |
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container_title | Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery |
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creator | Cheng, Chao Zhong, Jianwen Wang, Shuncheng Liu, Dabo |
description | Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal soft tissue tumor characterized by borderline or low-grade malignancy. It is rare childhood tumor with an average age of onset of 10 years old. It is even rarer in infants and toddlers, and the etiology and pathogenesis of this tumor are still unclear. The clinical presentation of IMT is non-specific and are related to the location of the tumor. When the tumor compresses adjacent organs, it can cause pain and functional impairment. According to the current literature, IMT is most commonly found in the digestive and respiratory systems, but also occasionally occur in the genitourinary system, head and neck, and limbs. At present, there have been no reports of nasopharyngeal IMT involving nasal cavity of infants and toddlers at home and abroad.This article reports a case of a massive inflammatory myofibroblastic tumor involving the nasal cavity and nasopharynx in an infant. Plasma-assisted minimally invasive surgery was performed through multiple su |
doi_str_mv | 10.13201/j.issn.2096-7993.2023.12.013 |
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It is rare childhood tumor with an average age of onset of 10 years old. It is even rarer in infants and toddlers, and the etiology and pathogenesis of this tumor are still unclear. The clinical presentation of IMT is non-specific and are related to the location of the tumor. When the tumor compresses adjacent organs, it can cause pain and functional impairment. According to the current literature, IMT is most commonly found in the digestive and respiratory systems, but also occasionally occur in the genitourinary system, head and neck, and limbs. At present, there have been no reports of nasopharyngeal IMT involving nasal cavity of infants and toddlers at home and abroad.This article reports a case of a massive inflammatory myofibroblastic tumor involving the nasal cavity and nasopharynx in an infant. Plasma-assisted minimally invasive surgery was performed through multiple su</description><identifier>ISSN: 2096-7993</identifier><identifier>DOI: 10.13201/j.issn.2096-7993.2023.12.013</identifier><identifier>PMID: 38114319</identifier><language>chi</language><publisher>China</publisher><subject>Granuloma, Plasma Cell - pathology ; Humans ; Infant ; Nasopharynx - pathology ; Neoplasms, Muscle Tissue ; Soft Tissue Neoplasms</subject><ispartof>Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery, 2023-12, Vol.37 (12), p.989-992</ispartof><rights>Copyright© by the Editorial Department of Journal of Clinical Otorhinolaryngology Head and Neck Surgery.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38114319$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheng, Chao</creatorcontrib><creatorcontrib>Zhong, Jianwen</creatorcontrib><creatorcontrib>Wang, Shuncheng</creatorcontrib><creatorcontrib>Liu, Dabo</creatorcontrib><title>A case report of nasopharyngeal inflammatory myofibroblastoma in infant</title><title>Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery</title><addtitle>Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi</addtitle><description>Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal soft tissue tumor characterized by borderline or low-grade malignancy. It is rare childhood tumor with an average age of onset of 10 years old. It is even rarer in infants and toddlers, and the etiology and pathogenesis of this tumor are still unclear. The clinical presentation of IMT is non-specific and are related to the location of the tumor. When the tumor compresses adjacent organs, it can cause pain and functional impairment. According to the current literature, IMT is most commonly found in the digestive and respiratory systems, but also occasionally occur in the genitourinary system, head and neck, and limbs. At present, there have been no reports of nasopharyngeal IMT involving nasal cavity of infants and toddlers at home and abroad.This article reports a case of a massive inflammatory myofibroblastic tumor involving the nasal cavity and nasopharynx in an infant. Plasma-assisted minimally invasive surgery was performed through multiple su</description><subject>Granuloma, Plasma Cell - pathology</subject><subject>Humans</subject><subject>Infant</subject><subject>Nasopharynx - pathology</subject><subject>Neoplasms, Muscle Tissue</subject><subject>Soft Tissue Neoplasms</subject><issn>2096-7993</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNo9jz9PwzAUxD2AaFX6FVAWJJYE-z3nj8eqghapEgvM0XNiQ6o4DnY69NsTRGG6091PJx1j94JnAoGLx2PWxThkwFWRlkrh7AAzARkXeMWW__mCrWM8cs5BAYBSN2yBlRAShVqy3SZpKJokmNGHKfE2GSj68ZPCefgw1CfdYHtyjiYfzok7e9vp4HVPcfKO5vYHoGG6ZdeW-mjWF12x9-ent-0-PbzuXrabQzoKKKbUFtSAbWVlhWw0SuRYIiksyJpKVry1ShdSC2iw1Lkoywp03laU6xKhRYsr9vC7Owb_dTJxql0XG9P3NBh_ijUoLkVeyBxn9O6CnrQzbT2Gzs236r_z-A2X_F5f</recordid><startdate>202312</startdate><enddate>202312</enddate><creator>Cheng, Chao</creator><creator>Zhong, Jianwen</creator><creator>Wang, Shuncheng</creator><creator>Liu, Dabo</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>202312</creationdate><title>A case report of nasopharyngeal inflammatory myofibroblastoma in infant</title><author>Cheng, Chao ; Zhong, Jianwen ; Wang, Shuncheng ; Liu, Dabo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p126t-f6ac2fd48f14cb3430373a936afe8480df9b64b12c37b517782b5d8a5b732d3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>chi</language><creationdate>2023</creationdate><topic>Granuloma, Plasma Cell - pathology</topic><topic>Humans</topic><topic>Infant</topic><topic>Nasopharynx - pathology</topic><topic>Neoplasms, Muscle Tissue</topic><topic>Soft Tissue Neoplasms</topic><toplevel>online_resources</toplevel><creatorcontrib>Cheng, Chao</creatorcontrib><creatorcontrib>Zhong, Jianwen</creatorcontrib><creatorcontrib>Wang, Shuncheng</creatorcontrib><creatorcontrib>Liu, Dabo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheng, Chao</au><au>Zhong, Jianwen</au><au>Wang, Shuncheng</au><au>Liu, Dabo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case report of nasopharyngeal inflammatory myofibroblastoma in infant</atitle><jtitle>Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery</jtitle><addtitle>Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi</addtitle><date>2023-12</date><risdate>2023</risdate><volume>37</volume><issue>12</issue><spage>989</spage><epage>992</epage><pages>989-992</pages><issn>2096-7993</issn><abstract>Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal soft tissue tumor characterized by borderline or low-grade malignancy. 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source | PubMed Central |
subjects | Granuloma, Plasma Cell - pathology Humans Infant Nasopharynx - pathology Neoplasms, Muscle Tissue Soft Tissue Neoplasms |
title | A case report of nasopharyngeal inflammatory myofibroblastoma in infant |
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