<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dashti NK</submitter><funding>NCI NIH HHS</funding><pagination>e70015</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11977784</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>63(11)</volume><pubmed_abstract>Conventional high-grade osteosarcomas are characterized by aggressive radiologic features, cytologic pleomorphism, and complex genomics. However, rare examples of osteosarcomas remain challenging due to unusual histology, such as sclerosing or osteoblastoma-like features, which may require molecular confirmation of their complex genetic alterations. We have encountered such a case in a 17-year-old man, who presented with a third metatarsal sclerotic bone lesion, found incidentally in the work-up of a foot trauma. The initial imaging revealed a lesion with sclerotic/blastic features proximally and lucent/lytic portion distally, findings interpreted consistent with osteoblastoma. The lesion was managed intra-lesionally with curettings and cryoablation; however, the microscopic findings were </pubmed_abstract><journal>Genes, chromosomes &amp; cancer</journal><pubmed_title>Malignant Bone-Forming Neoplasm With NIPBL::BEND2 Fusion.</pubmed_title><pmcid>PMC11977784</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>P50 CA217694</funding_grant_id><pubmed_authors>Dashti NK</pubmed_authors><pubmed_authors>Matcuk G</pubmed_authors><pubmed_authors>Agaimy A</pubmed_authors><pubmed_authors>Antonescu CR</pubmed_authors><pubmed_authors>Saoud C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Malignant Bone-Forming Neoplasm With NIPBL::BEND2 Fusion.</name><description>Conventional high-grade osteosarcomas are characterized by aggressive radiologic features, cytologic pleomorphism, and complex genomics. However, rare examples of osteosarcomas remain challenging due to unusual histology, such as sclerosing or osteoblastoma-like features, which may require molecular confirmation of their complex genetic alterations. We have encountered such a case in a 17-year-old man, who presented with a third metatarsal sclerotic bone lesion, found incidentally in the work-up of a foot trauma. The initial imaging revealed a lesion with sclerotic/blastic features proximally and lucent/lytic portion distally, findings interpreted consistent with osteoblastoma. The lesion was managed intra-lesionally with curettings and cryoablation; however, the microscopic findings were </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-05-15T03:17:23.801Z</modification><creation>2026-05-15T03:12:17.337Z</creation></dates><accession>S-EPMC11977784</accession><cross_references><pubmed>39604143</pubmed><doi>10.1002/gcc.70015</doi></cross_references></HashMap>