{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,2]],"date-time":"2026-07-02T01:44:16Z","timestamp":1782956656320,"version":"3.54.5"},"reference-count":13,"publisher":null,"issue":"4","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2022,10]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>Rhabdomyosarcoma (RMS) is one of the common malignant soft-tissue sarcomas affecting children. It originates from the embryonic mesenchyme precursor of striated muscle and is frequently seen in the head-and-neck region, genitourinary system and extremities. Occasionally, it arises from the retroperitoneum, biliary tract and abdomen and is rarely seen in the sacrococcygeal area. A 4-month-male child presented with a nodule over the sacrum. Based on histopathology and immunohistochemical marker studies, a final diagnosis of RMS was rendered. There was no evidence of any teratomatous elements.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/ajps.ajps_69_21","type":"journal-article","created":{"date-parts":[[2024,5,29]],"date-time":"2024-05-29T08:05:37Z","timestamp":1716969937000},"page":"251-253","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["Congenital Sacrococcygeal Rhabdomyosarcoma"],"prefix":"10.67481","volume":"19","author":[{"given":"Renuka 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