{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T02:34:27Z","timestamp":1791340467508,"version":"4.3.1"},"reference-count":126,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2019,3,1]],"date-time":"2019-03-01T00:00:00Z","timestamp":1551398400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Seminars in Diagnostic Pathology"],"published-print":{"date-parts":[[2019,3]]},"DOI":"10.1053\/j.semdp.2019.02.008","type":"journal-article","created":{"date-parts":[[2019,2,28]],"date-time":"2019-02-28T13:18:16Z","timestamp":1551359896000},"page":"129-141","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":32,"title":["A contemporary review of myxoid adipocytic tumors"],"prefix":"10.1053","volume":"36","author":[{"given":"David","family":"Creytens","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1053\/j.semdp.2019.02.008_bib0001","series-title":"Cellular Pathology: As Based Upon Physiological and Pathological Histology","first-page":"625","author":"Virchow","year":"1863"},{"key":"10.1053\/j.semdp.2019.02.008_bib0002","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1046\/j.1365-2559.1999.00835.x","article-title":"Myxoid tumours of soft tissue","volume":"35","author":"Graadt van Roggen","year":"1999","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0003","doi-asserted-by":"crossref","first-page":"465","DOI":"10.1111\/j.1365-2559.2008.02967.x","article-title":"Myxoid tumours of soft tissue: the so-called myxoid extracellular matrix is heterogeneous in composition","volume":"52","author":"Willems","year":"2008","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0004","series-title":"World Health Organization Classification of Tumours; Pathology and Genetics. Tumours of Soft Tissue and Bone","author":"Fletcher CDM","year":"2013"},{"key":"10.1053\/j.semdp.2019.02.008_bib0005","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1111\/his.12311","article-title":"Liposarcomas: diagnostic pitfalls and new insights","volume":"64","author":"Dei Tos","year":"2014","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0006","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1016\/j.anndiagpath.2016.09.003","article-title":"Myxoid liposarcoma of the foot: a study of 8 cases","volume":"25","author":"Bekers","year":"2016","journal-title":"Ann Diagn Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0007","doi-asserted-by":"crossref","first-page":"1286","DOI":"10.1097\/PAS.0000000000000657","article-title":"Primary retroperitoneal myxoid liposarcomas","volume":"40","author":"Setsu","year":"2016","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0008","doi-asserted-by":"crossref","first-page":"287","DOI":"10.1111\/j.1365-2559.2012.04348.x","article-title":"Well-differentiated and dedifferentiated liposarcomas with prominent myxoid stroma: analysis of 56 cases","volume":"62","author":"Sioletic","year":"2013","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0009","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1038\/modpathol.2008.164","article-title":"Primary retroperitoneal myxoid\/round cell liposarcoma is a nonexisting disease: an immunohistochemical and molecular biological analysis","volume":"22","author":"de Vreeze","year":"2009","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0010","doi-asserted-by":"crossref","first-page":"229","DOI":"10.1309\/AJCP90YNOKBAGCDM","article-title":"The expanded histologic spectrum of myxoid liposarcoma with an emphasis on newly described patterns: implications for diagnosis on small biopsy specimens","volume":"137","author":"Fritchie","year":"2012","journal-title":"Am J Clin Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0011","first-page":"2788","article-title":"Monoclonality of multifocal myxoid liposarcoma: confirmation by analysis of TLS-CHOP or EWS-CHOP rearrangements","volume":"6","author":"Antonescu","year":"2000","journal-title":"Clin Cancer Res"},{"key":"10.1053\/j.semdp.2019.02.008_bib0012","doi-asserted-by":"crossref","first-page":"132","DOI":"10.1016\/S1525-1578(10)60628-9","article-title":"Specificity of TLS-CHOP rearrangement for classic myxoid\/round cell liposarcoma: absence in predominantly myxoid well-differentiated liposarcomas","volume":"2","author":"Antonescu","year":"2000","journal-title":"J Mol Diagn"},{"key":"10.1053\/j.semdp.2019.02.008_bib0013","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1097\/PAS.0b013e3181578d5a","article-title":"The utility of Fluorescence In Situ Hybridization (FISH) in the diagnosis of myxoid soft tissue neoplasms","volume":"32","author":"Down-Kelly","year":"2008","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0014","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1016\/j.anndiagpath.2016.09.013","article-title":"Dermatofibrosarcoma protuberans: pathology, genetics, and potential therapeutic strategies","volume":"25","author":"Thway","year":"2016","journal-title":"Ann Diagn Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0015","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1111\/cup.13130","article-title":"An unusual clinical presentation of myxoid dermatofibrosarcoma protuberans with a prominent vasculature: a potential pitfall in the diagnosis of myxoid soft tissue tumors","volume":"45","author":"Tran","year":"2018","journal-title":"J Cutan Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0016","doi-asserted-by":"crossref","first-page":"1683","DOI":"10.1038\/s41379-018-0089-4","article-title":"Alternative PDGFD rearrangements in dermatofibrosarcoma protuberans without PDGFB fusions","volume":"31","author":"Dadone-Montaudi\u00e9","year":"2018","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0017","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1002\/gcc.22663","article-title":"Dermatofibrosarcoma protuberans with a novel COL6A3-PDGFD fusion gene and apparent predilection for breast","volume":"57","author":"Dickson","year":"2018","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0018","doi-asserted-by":"crossref","first-page":"1303","DOI":"10.1038\/modpathol.2008.114","article-title":"Fluorescence in situ hybridization is a usefull ancillary diagnostic tool for extraskeletal myxoid chondrosarcoma","volume":"21","author":"Wang","year":"2008","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0019","doi-asserted-by":"crossref","first-page":"336","DOI":"10.1016\/j.humpath.2009.04.028","article-title":"Fluorescence in situ hybridization analysis of extraskeletal myxoid chondrosarcoma using EWSR1 and NR4A3 probes","volume":"41","author":"Noguchi","year":"2010","journal-title":"Hum Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0020","first-page":"764","article-title":"NR4A3 rearrangement reliably distinguishes between the clinicopathologically overlapping entities myoepithelial carcinoma of soft tissue and cellular extraskeletal myxoid chondrosarcoma","volume":"43","author":"Flucke","year":"2012","journal-title":"Virchows Arch"},{"key":"10.1053\/j.semdp.2019.02.008_bib0021","doi-asserted-by":"crossref","first-page":"1307","DOI":"10.1038\/modpathol.2010.118","article-title":"Detection of myxoid liposarcoma-associated FUS-DDIT3 rearrangement variants including a newly identified breakpoint using an optimized RT-PCR assay","volume":"23","author":"Powers","year":"2010","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0022","doi-asserted-by":"crossref","first-page":"e2569","DOI":"10.1371\/journal.pone.0002569","article-title":"FUS-DDIT3 prevents the development of adipocytic precursors in liposarcoma by repressing PPARgamma and CIEBPalpha and activating eIF4E","volume":"3","author":"P\u00e9rez-Mancera","year":"2008","journal-title":"PLoS One"},{"key":"10.1053\/j.semdp.2019.02.008_bib0023","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1038\/modpathol.2011.148","article-title":"Involvement of PI3K\/Akt pathway in myxoid\/round cell liposarcoma","volume":"25","author":"Demicco","year":"2012","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0024","doi-asserted-by":"crossref","first-page":"453","DOI":"10.1007\/s00428-015-1721-z","article-title":"Extensive lipoma-like changes of myxoid liposarcoma: morphologic, immunohistochemical, and molecular cytogenetic analyses","volume":"466","author":"Iwasaki","year":"2015","journal-title":"Virchows Arch"},{"key":"10.1053\/j.semdp.2019.02.008_bib0025","doi-asserted-by":"crossref","first-page":"838","DOI":"10.1080\/02841860601080415","article-title":"Irradiation of myxoid\/round cell liposarcoma induces volume reduction and lipoma-like morphology","volume":"46","author":"Engstr\u00f6m","year":"2007","journal-title":"Acta Oncol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0026","doi-asserted-by":"crossref","first-page":"1868","DOI":"10.1002\/cncr.27847","article-title":"Localized and metastatic myxoid\/round cell liposarcoma: clinical and molecular observations","volume":"119","author":"Hoffman","year":"2013","journal-title":"Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0027","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1097\/00000478-199602000-00005","article-title":"Myxoid\/round cell liposarcoma of the extremities. A clinicopathologic study of 29 cases with particular attention to extent of round cell liposarcoma","volume":"20","author":"Smith","year":"1996","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0028","doi-asserted-by":"crossref","first-page":"1442","DOI":"10.5858\/2008-132-1442-LAOAES","article-title":"Lipoblastoma. Appreciation of an expanded spectrum of disease through cytogenetic analysis","volume":"132","author":"Ende","year":"2008","journal-title":"Arch Pathol Lab Med"},{"key":"10.1053\/j.semdp.2019.02.008_bib0029","doi-asserted-by":"crossref","first-page":"1705","DOI":"10.1097\/PAS.0b013e3181b76462","article-title":"Lipoblastoma: a clinicopathologic and immunohistochemical analysis of 59 cases","volume":"33","author":"Coffin","year":"2009","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0030","doi-asserted-by":"crossref","first-page":"211","DOI":"10.2350\/10-05-0836-PB.1","article-title":"Adipose and myxoid tumors of childhood and adolescence","volume":"15","author":"Coffin","year":"2012","journal-title":"Pediatr Dev Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0031","doi-asserted-by":"crossref","first-page":"42","DOI":"10.1186\/s13104-018-3153-8","article-title":"Lipoblastoma: a clinicopathologic review of 23 cases from a major tertiary care center plus detailed review of literature","volume":"11","author":"Abdul-Ghafar","year":"2018","journal-title":"BMC Res Notes"},{"key":"10.1053\/j.semdp.2019.02.008_bib0032","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1007\/s00428-003-0799-x","article-title":"Lipoblastoma in a 23-year-old male: distinction from atypical lipomatous tumor using cytogenetic and fluorescence in-situ hybridization analysis","volume":"442","author":"Sciot","year":"2003","journal-title":"Virchows Arch"},{"key":"10.1053\/j.semdp.2019.02.008_bib0033","doi-asserted-by":"crossref","first-page":"294","DOI":"10.1111\/j.1365-2559.2007.02954.x","article-title":"Lipoblastoma in adolescents and young adults: report of six cases with FISH analysis","volume":"52","author":"De Saint Aubain Somerhausen","year":"2008","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0034","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1111\/pin.12077","article-title":"Desmin-positivity in spindle cells: under-recognized immunophenotype of lipoblastoma","volume":"63","author":"Kubota","year":"2013","journal-title":"Pathol Int"},{"key":"10.1053\/j.semdp.2019.02.008_bib0035","first-page":"4869","article-title":"PLAG1 fusion oncogenes in lipoblastoma","volume":"60","author":"Hibbard","year":"2000","journal-title":"Cancer Res"},{"key":"10.1053\/j.semdp.2019.02.008_bib0036","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1016\/j.cancergencyto.2004.04.017","article-title":"PLAG1-HAS2 fusion in lipoblastoma with masked 8q intrachromosomal rearrangement","volume":"156","author":"Morerio","year":"2005","journal-title":"Cancer Genet Cytogenet"},{"key":"10.1053\/j.semdp.2019.02.008_bib0037","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1002\/path.1879","article-title":"Rearrangement of chromosomal region 8q11-13 in lipomatous tumours: correlation with lipoblastoma morphology","volume":"208","author":"Brandal","year":"2006","journal-title":"J Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0038","doi-asserted-by":"crossref","first-page":"60","DOI":"10.1016\/j.cancergencyto.2008.01.017","article-title":"Cytogenetic and molecular cytogenetic findings in lipoblastoma","volume":"183","author":"Bartuma","year":"2008","journal-title":"Cancer Genet Cytogenet"},{"key":"10.1053\/j.semdp.2019.02.008_bib0039","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1016\/j.jss.2013.05.010","article-title":"Cytogenetic analysis in the diagnosis and management of lipoblastomas: results from a single institution","volume":"184","author":"Fallon","year":"2013","journal-title":"J Surg Res"},{"key":"10.1053\/j.semdp.2019.02.008_bib0040","doi-asserted-by":"crossref","first-page":"731","DOI":"10.1111\/his.12317","article-title":"Diagnostic utility of molecular and cytogenetic analysis in lipoblastoma: a study of two cases and review of the literature","volume":"64","author":"Choi","year":"2014","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0041","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1016\/j.cancergen.2013.05.019","article-title":"A novel PLAG1-RAD51L1 gene fusion resulting from a t(8;14)(q12;q24) in a case of lipoblastoma","volume":"206","author":"Deen","year":"2013","journal-title":"Cancer Genet"},{"key":"10.1053\/j.semdp.2019.02.008_bib0042","doi-asserted-by":"crossref","first-page":"606","DOI":"10.1002\/gcc.22170","article-title":"Identification of COL3A1 and RAB2A as novel translocation partner genes of PLAG1 in lipoblastoma","volume":"53","author":"Yoshida","year":"2014","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0043","doi-asserted-by":"crossref","first-page":"469","DOI":"10.1016\/j.cancergen.2015.06.005","article-title":"Molecular cytogenetics of pediatric adipocytic tumors","volume":"208","author":"Dadone","year":"2015","journal-title":"Cancer Genet"},{"key":"10.1053\/j.semdp.2019.02.008_bib0044","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/j.1440-1827.2011.02740.x","article-title":"PLAG1 expression in mesenchymal tumors: an immunohistochemical study with specific emphasis on the pathogenetical distinction between soft tissue myoepithelioma and pleomorphic adenoma of the salivary gland","volume":"62","author":"Matsuyama","year":"2012","journal-title":"Pathol Int"},{"key":"10.1053\/j.semdp.2019.02.008_bib0045","doi-asserted-by":"crossref","first-page":"798","DOI":"10.1002\/pbc.23335","article-title":"Rearrangement of HMGA2 in a case of infantile lipoblastoma without Plag1 alteration","volume":"58","author":"P\u00e9deutour","year":"2012","journal-title":"Pediatr Blood Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0046","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1046\/j.1365-2559.2002.01409.x","article-title":"Lipoblastoma-like tumor of the vulva: report of three cases of a distinctive mesenchymal neoplasm of adipocytic differentiation","volume":"40","author":"Lae","year":"2002","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0047","doi-asserted-by":"crossref","first-page":"1290","DOI":"10.1097\/PAS.0000000000000448","article-title":"Lipoblastoma-like tumor of the vulva: further characterization in 8 new cases","volume":"39","author":"Mirkovic","year":"2015","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0048","doi-asserted-by":"crossref","first-page":"204","DOI":"10.1097\/PGP.0000000000000486","article-title":"Lipoblastoma-like tumor of the vulva, an important benign mimic of myxoid liposarcoma","volume":"38","author":"Creytens","year":"2019","journal-title":"Int J Gynecol Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0049","doi-asserted-by":"crossref","first-page":"1862","DOI":"10.1038\/s41379-018-0102-y","article-title":"Lipoblastoma-like tumor of the vulva: a clinicopathologic, immunohistochemical, fluorescence in situ hybridization and genomic copy number profiling study of seven cases","volume":"31","author":"Schoolmeester","year":"2019","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0050","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1097\/01.pas.0000190784.18198.d8","article-title":"Primitive myxoid mesenchymal tumor of infancy: a clinicopathologic report of 6 cases","volume":"30","author":"Alaggio","year":"2006","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0051","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1016\/j.cancergen.2015.11.004","article-title":"Undifferentiated myxoid lipoblastoma with PLAG1-HAS2 fusion in an infant; morphologically mimicking primitive myxoid mesenchymal tumor of infancy (PMMTI)-diagnostic importance of cytogenetic and molecular testing and literature review","volume":"209","author":"Warren","year":"2016","journal-title":"Cancer Genet"},{"key":"10.1053\/j.semdp.2019.02.008_bib0052","doi-asserted-by":"crossref","first-page":"884","DOI":"10.1038\/modpathol.2017.12","article-title":"Recurrent BCOR internal tandem duplication and BCOR or BCL6 expression distinguish primitive myxoid mesenchymal tumor of infancy from congenital infantile fibrosarcoma","volume":"30","author":"Santiago","year":"2017","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0053","doi-asserted-by":"crossref","first-page":"1257","DOI":"10.1097\/01.pas.0000135524.73447.4a","article-title":"Pleomorphic liposarcoma. Clinicopathologic analysis of 57 cases","volume":"28","author":"Hornick","year":"2004","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0054","doi-asserted-by":"crossref","first-page":"523","DOI":"10.1111\/pin.12104","article-title":"Pleomorphic liposarcoma: a clinicopathological, immunohistochemical and molecular cytogenetic study of 32 additional cases","volume":"63","author":"Wang","year":"2013","journal-title":"Pathol Int"},{"key":"10.1053\/j.semdp.2019.02.008_bib0055","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1200\/JCO.2017.74.9598","article-title":"Clinical and molecular spectrum of liposarcoma","volume":"36","author":"Lee","year":"2018","journal-title":"J Clin Oncol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0056","doi-asserted-by":"crossref","first-page":"601","DOI":"10.1097\/00000478-200205000-00006","article-title":"Pleomorphic liposarcoma: clinicopathologic, immunohistochemical, and follow-up analysis of 63 cases","volume":"25","author":"Gebhard","year":"2002","journal-title":"Am J surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0057","doi-asserted-by":"crossref","first-page":"1047","DOI":"10.1097\/PAS.0b013e3182517b96","article-title":"Cutaneous and subcutaneous pleomorphic liposarcoma. A clinicopathologic study of 29 cases with evaluation of MDM2 gene amplification in 26","volume":"36","author":"Gardner","year":"2012","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0058","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1002\/cncy.21362","article-title":"Dedifferentiated liposarcoma and pleomorphic liposarcoma: a comparative study of cytomorphology and MDM2\/CDK4 expression on fine-needle aspiration","volume":"122","author":"Mari\u00f1o-Enr\u00edquez","year":"2014","journal-title":"Cancer Cytopathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0059","doi-asserted-by":"crossref","first-page":"e3179","DOI":"10.1371\/journal.pone.0003179","article-title":"Functional copy-number alterations in cancer","volume":"3","author":"Taylor","year":"2008","journal-title":"PLoS One"},{"key":"10.1053\/j.semdp.2019.02.008_bib0060","doi-asserted-by":"crossref","first-page":"329","DOI":"10.1111\/j.1440-1827.2008.02232.x","article-title":"Aberrant MAD2 expression in soft-tissue sarcoma","volume":"58","author":"Hisaoka","year":"2008","journal-title":"Pathol Int"},{"key":"10.1053\/j.semdp.2019.02.008_bib0061","doi-asserted-by":"crossref","first-page":"715","DOI":"10.1038\/ng.619","article-title":"Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy","volume":"42","author":"Barretina","year":"2010","journal-title":"Nat Genet"},{"issue":"1","key":"10.1053\/j.semdp.2019.02.008_bib0062","doi-asserted-by":"crossref","first-page":"S39","DOI":"10.1038\/modpathol.2013.174","article-title":"An approach to pleomorphic sarcomas: can we subclassify, and does it matter?","volume":"27","author":"Goldblum","year":"2014","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0063","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1016\/j.anndiagpath.2018.10.006","article-title":"Subclassification of pleomorphic sarcoma: how and why should we care?","volume":"37","author":"Hornick","year":"2018","journal-title":"Ann Diagn Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0064","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1097\/PAS.0b013e3181963c9c","article-title":"Liposarcomas in young patients. A study of 82 cases occurring in patients younger than 22 years of age","volume":"33","author":"Alaggio","year":"2009","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0065","doi-asserted-by":"crossref","first-page":"1395","DOI":"10.1097\/PAS.0b013e3182562bc1","article-title":"Liposarcomas of the mediastinum and thorax: a clinicopathologic and molecular cytogenetic study of 24 cases, emphasizing unusual and diverse histologic features","volume":"36","author":"Boland","year":"2012","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0066","doi-asserted-by":"crossref","first-page":"834","DOI":"10.1136\/jclinpath-2014-202420","article-title":"Array-based comparative genomic hybridisation analysis of a pleomorphic myxoid liposarcoma","volume":"67","author":"Creytens","year":"2014","journal-title":"J Clin Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0067","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1111\/his.12913","article-title":"Comprehensive genetic analysis of a paediatric pleomorphic myxoid liposarcoma reveals near-haploidization and loss of the RB1 gene","volume":"69","author":"Hofvander","year":"2016","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0068","first-page":"258","article-title":"Well differentiated liposarcoma (atypical lipomatous tumors)","volume":"18","author":"Laurino","year":"2001","journal-title":"Semin Diagn Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0069","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1007\/s00428-009-0815-x","article-title":"Well-differentiated and dedifferentiated liposarcomas","volume":"456","author":"Coindre","year":"2010","journal-title":"Virchows Arch"},{"key":"10.1053\/j.semdp.2019.02.008_bib0070","doi-asserted-by":"crossref","first-page":"4","DOI":"10.3389\/fsurg.2015.00004","article-title":"Retroperitoneal liposarcoma: current insights in diagnosis and treatment","volume":"2","author":"Matthyssens","year":"2015","journal-title":"Front Surg"},{"key":"10.1053\/j.semdp.2019.02.008_bib0071","doi-asserted-by":"crossref","first-page":"1213","DOI":"10.1097\/00000478-199412000-00004","article-title":"Dedifferentiated liposarcoma. Clinicopathologic analysis of 32 cases suggesting a better prognostic subgroup among pleomorphic sarcomas","volume":"18","author":"McCormick","year":"1994","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0072","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1097\/00000478-199703000-00002","article-title":"Dedifferentiated liposarcoma: a clinicopathological analysis of 155 cases with a proposal for an expanded definition of dedifferentiation","volume":"21","author":"Henricks","year":"1997","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0073","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1097\/PAP.0000000000000101","article-title":"Dedifferentiated liposarcoma: updates on morphology, genetics, and therapeutic strategies","volume":"23","author":"Thway","year":"2016","journal-title":"Adv Anat Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0074","doi-asserted-by":"crossref","first-page":"1122","DOI":"10.1097\/PAS.0b013e3181e5dc49","article-title":"Dedifferentiated liposarcoma with \u201chomologous\u201d lipoblastic (pleomorphic liposarcoma-like) differentiation: clinicopathologic and molecular analysis of a series suggesting revised diagnostic criteria","volume":"34","author":"Mari\u00f1o-Enr\u00edquez","year":"2010","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0075","doi-asserted-by":"crossref","first-page":"837","DOI":"10.1097\/PAS.0b013e3181dbf2f7","article-title":"Liposarcomas with mixed well-differentiated and pleomorphic features: a clinicopathologic study of 12 cases","volume":"34","author":"Boland","year":"2010","journal-title":"Am j Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0076","doi-asserted-by":"crossref","first-page":"1523","DOI":"10.1097\/PAS.0000000000000910","article-title":"Dedifferentiated liposarcoma with epithelioid\/epithelial features","volume":"41","author":"Makise","year":"2017","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0077","doi-asserted-by":"crossref","first-page":"20","DOI":"10.1016\/j.humpath.2017.12.025","article-title":"Dedifferentiated liposarcoma composed predominantly of rhabdoid\/epithelioid cells: a frequently misdiagnosed highly aggressive variant","volume":"77","author":"Agaimy","year":"2018","journal-title":"Hum Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0078","doi-asserted-by":"crossref","first-page":"1159","DOI":"10.5858\/arpa.2018-0205-RA","article-title":"Dedifferentiated liposarcoma with myofibroblastic differentiation","volume":"142","author":"Wang","year":"2018","journal-title":"Arch Pathol Lab Med"},{"issue":"2","key":"10.1053\/j.semdp.2019.02.008_bib0079","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1016\/0165-4608(93)90001-3","article-title":"Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors","volume":"68","author":"Dal Cin","year":"1993","journal-title":"Cancer Genet Cytogenet"},{"issue":"10","key":"10.1053\/j.semdp.2019.02.008_bib0080","doi-asserted-by":"crossref","first-page":"1182","DOI":"10.1097\/00000478-199610000-00002","article-title":"Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tum ors (a report of the CHAMP Study Group)","volume":"20","author":"Rosai","year":"1996","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0081","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1002\/gcc.2870100203","article-title":"Complex composition and co-amplification of SAS and MDM2 in ring and giant rod marker chromosomes in well-differentiated liposarcoma","volume":"10","author":"P\u00e9detour","year":"1994","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0082","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1002\/(SICI)1098-2264(199901)24:1<30::AID-GCC5>3.0.CO;2-P","article-title":"Structure of the supernumerary ring and giant rod chromosomes in adipose tissue tumors","volume":"24","author":"P\u00e9detour","year":"1999","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0083","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1002\/(SICI)1098-2264(199811)23:3<203::AID-GCC1>3.0.CO;2-5","article-title":"Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization","volume":"23","author":"Gisselsson","year":"1998","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0084","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1002\/gcc.20835","article-title":"Evaluation of well-differentiated\/de-differentiated liposarcomas by high-resolution oligonucleotide array-based comparative genomic hybridization","volume":"50","author":"Tap","year":"2011","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0085","doi-asserted-by":"crossref","first-page":"531","DOI":"10.1002\/(SICI)1096-9896(200004)190:5<531::AID-PATH579>3.0.CO;2-W","article-title":"Coordinated expression and amplification of the MDM2, CDK4, and HMGI-C genes in atypical lipomatous tumours","volume":"190","author":"Dei Tos","year":"2000","journal-title":"J Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0086","doi-asserted-by":"crossref","first-page":"2233","DOI":"10.1002\/ijc.23380","article-title":"HMGA2 is the partner of MDM2 in well-differentiated and dedifferentiated liposarcomas whereas CDK4 belongs to a distinct inconsistent amplicon","volume":"122","author":"Italiano","year":"2008","journal-title":"Int J Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0087","doi-asserted-by":"crossref","first-page":"1476","DOI":"10.1097\/PAS.0b013e3180581fff","article-title":"Detection of MDM2-CDK4 amplification by fluorescence in situ hybridization in 200 paraffin-embedded tumor samples: utility in diagnosing adipocytic lesions and comparison with immunohistochemistry and real-time PCR","volume":"31","author":"Sirvent","year":"2007","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0088","doi-asserted-by":"crossref","DOI":"10.1155\/2011\/483154","article-title":"Liposarcoma: molecular genetics and therapeutics","volume":"2011","author":"Conyers","year":"2011","journal-title":"Sarcoma"},{"key":"10.1053\/j.semdp.2019.02.008_bib0089","doi-asserted-by":"crossref","first-page":"5696","DOI":"10.1158\/1078-0432.CCR-08-3185","article-title":"Clinical and biological significance of CDK4 amplification in well-differentiated and dedifferentiated liposarcomas","volume":"15","author":"Italiano","year":"2009","journal-title":"Clin Cancer Res"},{"key":"10.1053\/j.semdp.2019.02.008_bib0090","doi-asserted-by":"crossref","first-page":"896","DOI":"10.1002\/gcc.20909","article-title":"The CDKN2A\/CDKN2B\/CDK4\/CCND1 pathway is pivotal in well-differentiated and dedifferentiated liposarcoma oncogenesis. An analysis of 104 tumors","volume":"50","author":"Louis-Brennetot","year":"2011","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0091","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1097\/PDM.0000000000000041","article-title":"Detection of MDM2\/CDK4 amplification in lipomatous soft tissue tumors from formalin-fixed, paraffin-embedded tissue: comparison of multiplex ligation-dependent probe amplification (MLPA) and fluorescence in situ hybridization (FISH)","volume":"23","author":"Creytens","year":"2015","journal-title":"Appl Immunohistochem Mol Morphol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0092","first-page":"1835","article-title":"Characterization of the 12q amplicons in lipomatous soft tissue tumors by multiplex ligation-dependent probe amplification-based copy number analysis","volume":"35","author":"Creytens","year":"2015","journal-title":"Anticancer Res"},{"key":"10.1053\/j.semdp.2019.02.008_bib0093","doi-asserted-by":"crossref","first-page":"1868","DOI":"10.1097\/PAS.0b013e318093f925","article-title":"Primary mediastinal liposarcoma: clinicopathologic analysis of 24 cases","volume":"31","author":"Hahn","year":"2007","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0094","doi-asserted-by":"crossref","first-page":"721","DOI":"10.1038\/modpathol.2014.152","article-title":"Liposarcomas of the posterior mediastinum: clinicopathologic study of 18 cases","volume":"28","author":"Ortega","year":"2015","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0095","doi-asserted-by":"crossref","DOI":"10.1038\/s41379-018-0171-y","article-title":"Amplification of DNA damage-inducible transcript 3 (DDIT3) is associated with myxoid liposarcoma-like morphology and homologous lipoblastic differentiation in dedifferentiated liposarcoma","author":"Mantilla","year":"2019","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0096","doi-asserted-by":"crossref","first-page":"1103","DOI":"10.1097\/00000478-199311000-00003","article-title":"Chondroid lipoma. A unique tumor simulating liposarcoma and myxoid chondrosarcoma","volume":"17","author":"Meis","year":"1993","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0097","doi-asserted-by":"crossref","first-page":"330","DOI":"10.1007\/s002920050366","article-title":"Chondroid lipoma. Clinicopathological, immunohistochemical and ultrastructural analysis of six cases of a distinct entity in the spectrum of lipomas","volume":"20","author":"Mentzel","year":"1999","journal-title":"Pathologe"},{"key":"10.1053\/j.semdp.2019.02.008_bib0098","doi-asserted-by":"crossref","first-page":"925","DOI":"10.1111\/his.12100","article-title":"Presence of C11orf95-MKL2 fusion is a consistent finding in chondroid lipomas: a study of eight cases","volume":"62","author":"Flucke","year":"2013","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0099","doi-asserted-by":"crossref","first-page":"230","DOI":"10.1016\/j.anndiagpath.2012.01.002","article-title":"Chondroid lipoma: an update and review","volume":"16","author":"Thway","year":"2012","journal-title":"Ann Diagn Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0100","first-page":"88","article-title":"Cytogenetic and cytologic features of chondroid lipoma of soft tissue","volume":"12","author":"Thompson","year":"1999","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0101","doi-asserted-by":"crossref","first-page":"208","DOI":"10.1007\/s00428-003-0946-4","article-title":"Chondroid lipoma is characterized by t(11;16)(q13:p12-13)","volume":"444","author":"Ballaux","year":"2004","journal-title":"Virchows Arch"},{"key":"10.1053\/j.semdp.2019.02.008_bib0102","doi-asserted-by":"crossref","first-page":"810","DOI":"10.1002\/gcc.20788","article-title":"C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13:p13) in chondroid lipoma","volume":"49","author":"Huang","year":"2010","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0103","first-page":"2011","article-title":"Delineation of chondroid lipoma: an immunohistochemical and molecular biological analysis","author":"De Vreeze","year":"2011","journal-title":"Sarcoma"},{"key":"10.1053\/j.semdp.2019.02.008_bib0104","first-page":"477","article-title":"Spindle cell lipoma","volume":"84","author":"Angervall","year":"1976","journal-title":"Acta Pathol Microbiol Scand"},{"key":"10.1053\/j.semdp.2019.02.008_bib0105","doi-asserted-by":"crossref","first-page":"1852","DOI":"10.1002\/1097-0142(197511)36:5<1852::AID-CNCR2820360542>3.0.CO;2-U","article-title":"Spindle cell lipoma","volume":"36","author":"Enzinger","year":"1975","journal-title":"Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0106","doi-asserted-by":"crossref","first-page":"803","DOI":"10.1111\/j.1365-2559.1987.tb01884.x","article-title":"Spindle cell lipoma: a clinicopathological study with some original observations","volume":"11","author":"Fletcher","year":"1987","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0107","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1002\/1097-0142(19810101)47:1<126::AID-CNCR2820470121>3.0.CO;2-K","article-title":"Pleomorphic lipoma: a benign tumor simulating liposarcoma. A clinicopathologic analysis of 48 cases","volume":"47","author":"Shmookler","year":"1981","journal-title":"Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0108","doi-asserted-by":"crossref","first-page":"1267","DOI":"10.1097\/PAS.0000000000000915","article-title":"Spindle cell lipomas in women: a report of 53 cases","volume":"41","author":"Ko","year":"2017","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0109","doi-asserted-by":"crossref","first-page":"483","DOI":"10.1136\/jclinpath-2017-204975","article-title":"Tumours composed of fat are no longer a simple diagnosis: an overview of fatty tumours with a spindle cell component","volume":"71","author":"McCarthy","year":"2018","journal-title":"J Clin Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0110","doi-asserted-by":"crossref","first-page":"430","DOI":"10.1111\/his.12548","article-title":"Spindle cell\/pleomorphic lipomas of the face: an under-recognized diagnosis","volume":"66","author":"Cheah","year":"2015","journal-title":"Histopathology"},{"key":"10.1053\/j.semdp.2019.02.008_bib0111","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1093\/ajcp\/aqw137","article-title":"Spindle cell lipomas arising at atypical locations","volume":"146","author":"Ud Din","year":"2016","journal-title":"Am J Clin Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0112","doi-asserted-by":"crossref","first-page":"e122","DOI":"10.1097\/DAD.0000000000000546","article-title":"Uncommon tumor, uncommon location: dermal-based spindle cell\/pleomorphic lipoma","volume":"38","author":"Lincoln","year":"2016","journal-title":"Am J Dermatopathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0113","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1097\/00000478-199702000-00009","article-title":"Immunoreactivity for the human hematopoietic progenitor cell antigen (CD34) in lipomatous tumors","volume":"21","author":"Suster","year":"1997","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0114","doi-asserted-by":"crossref","first-page":"546","DOI":"10.1111\/j.1600-0560.1996.tb01447.x","article-title":"Spindle cell lipoma is strongly CD34 positive. An immunohistochemical study","volume":"23","author":"Templeton","year":"1996","journal-title":"J Cutan Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0115","doi-asserted-by":"crossref","first-page":"1119","DOI":"10.1097\/PAS.0b013e31825d532d","article-title":"Loss of retinoblastoma protein expression in spindle cell\/pleomorphic lipomas and cytogenetically related tumors: an immunohistochemical study with diagnostic implications","volume":"38","author":"Chen","year":"2012","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0116","doi-asserted-by":"crossref","first-page":"435","DOI":"10.1007\/s00428-016-1996-8","article-title":"S100 protein expressing spindle cells in spindle cell lipoma: a diagnostic pitfall","volume":"469","author":"Mentzel","year":"2016","journal-title":"Virchows Arch"},{"key":"10.1053\/j.semdp.2019.02.008_bib0117","doi-asserted-by":"crossref","first-page":"619","DOI":"10.1002\/gcc.20884","article-title":"Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion","volume":"50","author":"Bartuma","year":"2011","journal-title":"Genes Chromosom Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0118","doi-asserted-by":"crossref","first-page":"616","DOI":"10.1002\/ijc.10864","article-title":"Custering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors","volume":"103","author":"Dahlen","year":"2003","journal-title":"Int J Cancer"},{"key":"10.1053\/j.semdp.2019.02.008_bib0119","first-page":"97","article-title":"Atypical spindle cell lipoma: a clinicopathologic, immunohistochemical, and molecular study emphasizing its relationship to classical spindle cell lipoma","volume":"465","author":"Creytens","year":"2014","journal-title":"Virchows Arch"},{"key":"10.1053\/j.semdp.2019.02.008_bib0120","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1097\/PAS.0000000000000770","article-title":"Atypical spindle cell lipomatous tumor: clinicopathologic characterization of 232 cases demonstrating a morphologic spectrum","volume":"14","author":"Mari\u00f1o-Enr\u00edquez","year":"2017","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0121","doi-asserted-by":"crossref","first-page":"288","DOI":"10.1097\/PAS.0000000000001156","article-title":"Fat-rich (spindle cell-poor) variants of atypical spindle cell lipomatous tumors show similar morphologic, immunohistochemical and molecular features as \u201cdysplastic lipomas\u201d: are they related lesions? Comment on Michal et al (2018)","volume":"43","author":"Creytens","year":"2019","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0122","doi-asserted-by":"crossref","DOI":"10.1177\/1066896918809189","article-title":"Atypical spindle cell lipomatous tumor with benign heterologous (metaplastic) cartilagenous diferentiation","author":"Creytens","year":"2019","journal-title":"Int J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0123","doi-asserted-by":"crossref","first-page":"550","DOI":"10.1111\/pin.12719","article-title":"Atypical spindle cell\/pleomorphic lipomatous tumor: a clinicopathologic, immunohistochemical, and molecular study of 20 cases","volume":"68","author":"Bahadir","year":"2019","journal-title":"Pathol Int"},{"key":"10.1053\/j.semdp.2019.02.008_bib0124","doi-asserted-by":"crossref","first-page":"300","DOI":"10.1016\/j.humpath.2018.04.032","article-title":"Atypical mitoses are present in otherwise classical pleomorphic lipomas-reply","volume":"81","author":"Creytens","year":"2019","journal-title":"Hum Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0125","doi-asserted-by":"crossref","first-page":"1443","DOI":"10.1097\/PAS.0000000000000936","volume":"41","author":"Creytens","year":"2017","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2019.02.008_bib0126","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1016\/j.humpath.2017.11.023","article-title":"Atypical multivacuolated lipoblasts and atypical mitoses are not compatible with the diagnosis of spindle cell\/pleomorphic lipoma","volume":"74","author":"Creytens","year":"2018","journal-title":"Hum Pathol"}],"container-title":["Seminars in Diagnostic Pathology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0740257019300188?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0740257019300188?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,7,15]],"date-time":"2024-07-15T03:18:25Z","timestamp":1721013505000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0740257019300188"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,3]]},"references-count":126,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2019,3]]}},"alternative-id":["S0740257019300188"],"URL":"https:\/\/doi.org\/10.1053\/j.semdp.2019.02.008","relation":{},"ISSN":["0740-2570"],"issn-type":[{"value":"0740-2570","type":"print"}],"subject":[],"published":{"date-parts":[[2019,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"A contemporary review of myxoid adipocytic tumors","name":"articletitle","label":"Article Title"},{"value":"Seminars in Diagnostic Pathology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1053\/j.semdp.2019.02.008","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}