{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T07:01:46Z","timestamp":1777878106790,"version":"3.51.4"},"reference-count":16,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2026,2,19]],"date-time":"2026-02-19T00:00:00Z","timestamp":1771459200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2026,2,19]],"date-time":"2026-02-19T00:00:00Z","timestamp":1771459200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Rare Tumors"],"published-print":{"date-parts":[[2026,3]]},"abstract":"\n Background:<\/jats:bold>\n Inflammatory myofibroblastic tumour (IMT) of the pediatric laryngotracheal complex is exceedingly rare, with fewer than nine subglottic IMT cases reported in the literature up to 2025. We present an additional case and highlight the importance of early recognition.\n Case presentation:<\/jats:bold>\n A previously healthy 10-year-old boy presented with a 3-week history of progressive dyspnea on exertion and nocturnal biphasic stridor, initially mislabelled as refractory asthma. Contrast-enhanced CT revealed a left-sided subglottic soft-tissue mass that reduced the airway lumen to 2.7\u00a0mm, while rigid bronchoscopy confirmed an 80% occlusion caused by a 10\u00a0mm submucosal lesion spanning the cricoid and first tracheal ring. After emergent tracheostomy at the referring institution, he underwent lesion resection and simultaneous decannulation. Histopathology demonstrated spindle-cell proliferation within a myxoid inflammatory stroma; immunohistochemistry was\n ALK-1<\/jats:italic>\n \u2013positive, confirming IMT. Post-operative bronchoscopy on day seven showed a widely patent airway. Five years later the child remains asymptomatic and oxygen-independent, with no radiological or endoscopic evidence of recurrence.\n Conclusion:<\/jats:bold>\n This case reinforces that persistent pediatric stridor mandates prompt endoscopic evaluation and that complete surgical excision remains the gold-standard therapy for airway IMT. Given the tumour\u2019s intermediate malignant potential and a reported 18\u201340% recurrence rate when margins are positive, meticulous long-term surveillance is indispensable, and\n ALK<\/jats:italic>\n -directed therapy should be considered when resection is not feasible. Timely diagnosis and radical local therapy can avert prolonged tracheostomy and enrich the scant literature on pediatric subglottic IMT.\n <\/jats:p>","DOI":"10.1177\/20363613251407005","type":"journal-article","created":{"date-parts":[[2026,2,19]],"date-time":"2026-02-19T10:02:29Z","timestamp":1771495349000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Subglottic inflammatory myofibroblastic tumor: A rare case report in a pediatric patient"],"prefix":"10.1177","volume":"18","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0017-1446","authenticated-orcid":false,"given":"Shary","family":"Acosta Su\u00e1rez","sequence":"first","affiliation":[{"name":"Hospital Infantil Universitario de San Jos\u00e9"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lina Estefan\u00eda","family":"Bar\u00f3n M\u00e9ndez","sequence":"additional","affiliation":[{"name":"Fundaci\u00f3n Universitaria de Ciencias de la Salud - FUCS"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Diana Patricia","family":"Romero Lara","sequence":"additional","affiliation":[{"name":"Hospital Infantil Universitario de San Jos\u00e9"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2026,2,19]]},"reference":[{"key":"e_1_3_9_2_2","doi-asserted-by":"publisher","DOI":"10.4103\/lungindia.lungindia_405_17"},{"key":"e_1_3_9_3_2","doi-asserted-by":"publisher","DOI":"10.1001\/archoto.2011.153"},{"issue":"5","key":"e_1_3_9_4_2","first-page":"144","article-title":"Inflammatory myofibroblastic tumor of the trachea: a case report and review of the literature","volume":"4","author":"F\u0131ndik S","year":"2017","unstructured":"F\u0131ndik S. Inflammatory myofibroblastic tumor of the trachea: a case report and review of the literature. J Lung Pulm Respir Res 2017; 4(5): 144\u2013146.","journal-title":"J Lung Pulm Respir Res"},{"key":"e_1_3_9_5_2","doi-asserted-by":"publisher","DOI":"10.1155\/2020\/6923103"},{"key":"e_1_3_9_6_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.anl.2020.08.018"},{"key":"e_1_3_9_7_2","doi-asserted-by":"publisher","DOI":"10.1177\/01455613221083810"},{"key":"e_1_3_9_8_2","doi-asserted-by":"publisher","DOI":"10.21037\/jovs.2018.10.08"},{"key":"e_1_3_9_9_2","doi-asserted-by":"publisher","DOI":"10.1053\/jpsu.2001.23970"},{"key":"e_1_3_9_10_2","doi-asserted-by":"publisher","DOI":"10.3389\/fped.2021.543078"},{"key":"e_1_3_9_11_2","doi-asserted-by":"publisher","DOI":"10.1186\/s43054-024-00269-z"},{"issue":"6","key":"e_1_3_9_12_2","first-page":"1360","article-title":"Subglottic inflammatory myofibroblastic tumor in a child: a rare case report","volume":"135","author":"Alkheder A","year":"2025","unstructured":"Alkheder A, Al-Ghabra Y, Azar A. Subglottic inflammatory myofibroblastic tumor in a child: a rare case report. Laryngoscope 2025; 135(6): 1360\u20131365.","journal-title":"Laryngoscope"},{"key":"e_1_3_9_13_2","doi-asserted-by":"publisher","DOI":"10.1097\/MS9.0000000000002870"},{"issue":"98","key":"e_1_3_9_14_2","first-page":"171","article-title":"Pediatric inflammatory myofibroblastic tumors of the airway: two case reports with varying clinical presentation","volume":"30","author":"Kumar N","year":"2018","unstructured":"Kumar N, Saravanamuthu T, Srinivasan A, et al. Pediatric inflammatory myofibroblastic tumors of the airway: two case reports with varying clinical presentation. Iran J Otorhinolaryngol 2018; 30(98): 171\u2013176.","journal-title":"Iran J Otorhinolaryngol"},{"key":"e_1_3_9_15_2","first-page":"57","article-title":"A rare tumor of trachea: inflammatory myofibroblastic tumor diagnosis and endoscopic treatment","volume":"13","author":"\u00d6zg\u00fcl MA","year":"2014","unstructured":"\u00d6zg\u00fcl MA, Toru \u00dc, Acat M, et al. A rare tumor of trachea: inflammatory myofibroblastic tumor diagnosis and endoscopic treatment. Respir Med Case Rep 2014; 13: 57\u201360.","journal-title":"Respir Med Case Rep"},{"key":"e_1_3_9_16_2","doi-asserted-by":"publisher","DOI":"10.4081\/cp.2016.853"},{"key":"e_1_3_9_17_2","doi-asserted-by":"publisher","DOI":"10.2214\/AJR.11.7288"}],"container-title":["Rare Tumors"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/20363613251407005","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/full-xml\/10.1177\/20363613251407005","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/20363613251407005","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T23:11:59Z","timestamp":1777590719000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/20363613251407005"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,2,19]]},"references-count":16,"alternative-id":["10.1177\/20363613251407005"],"URL":"https:\/\/doi.org\/10.1177\/20363613251407005","relation":{},"ISSN":["2036-3613","2036-3613"],"issn-type":[{"value":"2036-3613","type":"print"},{"value":"2036-3613","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,2,19]]},"article-number":"20363613251407005"}}