{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T12:12:57Z","timestamp":1789560777588,"version":"build-2803163510"},"reference-count":9,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"Suppl 2","license":[{"start":{"date-parts":[[2026,4,9]],"date-time":"2026-04-09T00:00:00Z","timestamp":1775692800000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2026,9]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Rhabdomyosarcoma (RMS) is an uncommon malignant soft-tissue tumor, with diaphragmatic spindle cell RMS being extremely rare in adults. A 41-year-old male patient had progressive breathlessness and right-sided pleuritic chest pain. Imaging and biopsy that includes X-ray, computed tomography, magnetic resonance imaging, histopathology, and immunohistochemistry established a large thoracoabdominal spindle cell RMS. Early diagnosis, careful imaging, and combined treatment were important, and they helped increase knowledge of this unusual entity.<\/jats:p>","DOI":"10.4103\/aam.aam_833_25","type":"journal-article","created":{"date-parts":[[2026,4,10]],"date-time":"2026-04-10T04:00:17Z","timestamp":1775793617000},"page":"S388-S391","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["A Rare Case of Spindle Cell Rhabdomyosarcoma of the Diaphragm in Adult with Thoracoabdominal Extension"],"prefix":"10.4103","volume":"25","author":[{"given":"Sharvari Shashikant","family":"Gulve","sequence":"first","affiliation":[{"name":"Department of Radiodiagnosis, Dr. D. Y. 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