{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,20]],"date-time":"2026-08-20T14:46:53Z","timestamp":1787237213487,"version":"build-2736575974"},"reference-count":15,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2019,6,18]],"date-time":"2019-06-18T00:00:00Z","timestamp":1560816000000},"content-version":"vor","delay-in-days":17,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pathology International"],"published-print":{"date-parts":[[2019,6]]},"abstract":"<jats:p>\n                    A 35\u2010year\u2010old Japanese man who had experienced hoarseness for 10 years presented with a vocal cord lesion. A gross examination revealed a left vocal cord polyp occupying two\u2010thirds of the vocal space. The endoscopically resected lesion contained scattered atypical fibroblastic, stellate, or ganglion\u2010like cells with mucoid stroma. Vacuolated cells were also seen. Lymphoplasmacytic infiltrate was largely undetectable. A vocal cord polyp was first suspected, but well\u2010differentiated liposarcoma and inflammatory myofibroblastic tumor (IMT) were included in the differential diagnoses. The tumor cells were positive for anaplastic lymphoma kinase (ALK), calponin, and vimentin, and negative for other smooth muscle markers by immunohistochemistry. Structures resembling myofibroblasts were not observed by electron microscopy, which confirmed abundant rough endoplasmic reticulum in the tumor cells and accumulated lipid droplets in some tumor cells.\n                    <jats:italic>ALK<\/jats:italic>\n                    gene rearrangement was detected by fluorescence in situ hybridization, and\n                    <jats:italic>TIMP3\u2013ALK<\/jats:italic>\n                    fusion was confirmed by 5\u2032 rapid ampli\ufb01cation of cDNA ends. We diagnosed the lesion as an IMT, and an\n                    <jats:italic>ALK\u2010<\/jats:italic>\n                    rearranged stellate cell tumor may be postulated. This is the first report of a fusion partner gene of\n                    <jats:italic>ALK<\/jats:italic>\n                    in a case of laryngeal IMT.\n                  <\/jats:p>","DOI":"10.1111\/pin.12796","type":"journal-article","created":{"date-parts":[[2019,6,19]],"date-time":"2019-06-19T05:45:58Z","timestamp":1560923158000},"page":"366-371","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":15,"title":["Vocal cord inflammatory myofibroblastic tumor with mucoid deposits harboring TIMP3\u2013ALK fusion: A potential diagnostic pitfall"],"prefix":"10.1111","volume":"69","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6428-0222","authenticated-orcid":false,"given":"Kenji","family":"Yorita","sequence":"first","affiliation":[{"name":"Department of Diagnostic Pathology Japanese Red Cross Kochi Hospital  Kochi 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