{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,10]],"date-time":"2025-10-10T01:48:59Z","timestamp":1760060939790,"version":"build-2065373602"},"reference-count":84,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Seminars in Diagnostic Pathology"],"published-print":{"date-parts":[[2023,7]]},"DOI":"10.1053\/j.semdp.2023.04.013","type":"journal-article","created":{"date-parts":[[2023,4,25]],"date-time":"2023-04-25T13:10:03Z","timestamp":1682428203000},"page":"258-266","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["The new and old in superficial mesenchymal tumors with uncertain origin and\/or melanocytic differentiation"],"prefix":"10.1053","volume":"40","author":[{"given":"Ahmad","family":"Alkashash","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Azadeh","family":"Samiei","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3776-5053","authenticated-orcid":false,"given":"Ahmed K.","family":"Alomari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"7","key":"10.1053\/j.semdp.2023.04.013_bib0001","doi-asserted-by":"crossref","first-page":"904","DOI":"10.1038\/modpathol.2015.49","article-title":"ALK rearrangement and overexpression in epithelioid fibrous histiocytoma","volume":"28","author":"Doyle","year":"2015","journal-title":"Mod Pathol"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0002","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1016\/j.path.2021.03.002","article-title":"Update on cutaneous soft tissue tumors","volume":"14","author":"Dermawan","year":"2021","journal-title":"Surg Pathol Clin"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0003","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1111\/j.1365-2133.1989.tb07782.x","article-title":"Epithelioid cell histiocytoma: A new entity","volume":"120","author":"Jones","year":"1989","journal-title":"Br J Dermatol"},{"issue":"5","key":"10.1053\/j.semdp.2023.04.013_bib0004","doi-asserted-by":"crossref","first-page":"1427","DOI":"10.1111\/bjd.13548","article-title":"Epithelioid cell histiocytoma of the skin with clonal ALK gene rearrangement resulting in VCL-ALK and SQSTM1-ALK gene fusions","volume":"172","author":"Jedrych","year":"2015","journal-title":"Br J Dermatol"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0005","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1111\/j.1365-2559.1994.tb01290.x","article-title":"Epithelioid benign fibrous histiocytoma of skin: clinico-pathological analysis of 20 cases of a poorly known variant","volume":"24","author":"Singh Gomez","year":"1994","journal-title":"Histopathology"},{"issue":"11","key":"10.1053\/j.semdp.2023.04.013_bib0006","doi-asserted-by":"crossref","first-page":"805","DOI":"10.1097\/DAD.0000000000001085","article-title":"ALK gene fusions in epithelioid fibrous histiocytoma: a study of 14 cases, with new histopathological findings","volume":"40","author":"Kazakov","year":"2018","journal-title":"Am J Dermatopathol"},{"issue":"7","key":"10.1053\/j.semdp.2023.04.013_bib0007","doi-asserted-by":"crossref","first-page":"837","DOI":"10.1111\/cup.13923","article-title":"Spindle cell variant of epithelioid cell histiocytoma (spindle cell histiocytoma) with ALK gene fusions: cases series and review of the literature","volume":"48","author":"Kazlouskaya","year":"2021","journal-title":"J Cutan Pathol"},{"issue":"5","key":"10.1053\/j.semdp.2023.04.013_bib0008","doi-asserted-by":"crossref","first-page":"753","DOI":"10.1038\/modpathol.2017.191","article-title":"Epithelioid fibrous histiocytoma: molecular characterization of ALK fusion partners in 23 cases","volume":"31","author":"Dickson","year":"2018","journal-title":"Mod Pathol"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0009","doi-asserted-by":"crossref","first-page":"243","DOI":"10.1016\/0190-9622(92)70034-D","article-title":"Epithelioid cell histiocytoma. A clinicopathologic and immunohistochemical study of eight cases","volume":"26","author":"Mehregan","year":"1992","journal-title":"J Am Acad Dermatol"},{"issue":"9","key":"10.1053\/j.semdp.2023.04.013_bib0010","doi-asserted-by":"crossref","first-page":"697","DOI":"10.1111\/j.1600-0560.2011.01747.x","article-title":"EMA positivity in epithelioid fibrous histiocytoma: a potential diagnostic pitfall","volume":"38","author":"Doyle","year":"2011","journal-title":"J Cutan Pathol"},{"issue":"8","key":"10.1053\/j.semdp.2023.04.013_bib0011","doi-asserted-by":"crossref","first-page":"471","DOI":"10.1002\/gcc.23038","article-title":"Molecular investigation of ALK-rearranged epithelioid fibrous histiocytomas identifies CLTC as a novel fusion partner and evidence of fusion-independent transcription activation","volume":"61","author":"Georgantzoglou","year":"2022","journal-title":"Genes Chromosomes Cancer"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0012","doi-asserted-by":"crossref","first-page":"9626","DOI":"10.1007\/s11357-014-9626-3","article-title":"P62\/SQSTM1 at the interface of aging, autophagy, and disease","volume":"36","author":"Bitto","year":"2014","journal-title":"Age (Dordr)"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0013","doi-asserted-by":"crossref","first-page":"430","DOI":"10.1038\/modpathol.2010.213","article-title":"Renal cell carcinoma with novel VCL-ALK fusion: new representative of ALK-associated tumor spectrum","volume":"24","author":"Debelenko","year":"2011","journal-title":"Mod Pathol"},{"key":"10.1053\/j.semdp.2023.04.013_bib0014","doi-asserted-by":"crossref","first-page":"475","DOI":"10.1016\/j.biocel.2014.03.027","article-title":"Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma","volume":"53","author":"Plaszczyca","year":"2014","journal-title":"Int J Biochem Cell Biol"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0015","doi-asserted-by":"crossref","first-page":"382","DOI":"10.1097\/PAS.0000000000000996","article-title":"Cutaneous melanocytoma with CRTC1-TRIM11 fusion: report of 5 cases resembling clear cell sarcoma","volume":"42","author":"Cellier","year":"2018","journal-title":"Am J Surg Pathol"},{"issue":"11","key":"10.1053\/j.semdp.2023.04.013_bib0016","doi-asserted-by":"crossref","first-page":"1457","DOI":"10.1097\/PAS.0000000000001952","article-title":"Cutaneous melanocytic tumor with CRTC1::TRIM11 translocation: an emerging entity analyzed in a series of 41 cases","volume":"46","author":"Hanna","year":"2022","journal-title":"Am J Surg Pathol"},{"issue":"12","key":"10.1053\/j.semdp.2023.04.013_bib0017","doi-asserted-by":"crossref","first-page":"1579","DOI":"10.1097\/00000478-200412000-00005","article-title":"Paraganglioma-like dermal melanocytic tumor: a unique entity distinct from cellular blue nevus, clear cell sarcoma, and cutaneous melanoma","volume":"28","author":"Deyrup","year":"2004","journal-title":"Am J Surg Pathol"},{"issue":"6","key":"10.1053\/j.semdp.2023.04.013_bib0018","doi-asserted-by":"crossref","first-page":"861","DOI":"10.1097\/PAS.0000000000001217","article-title":"CRTC1-TRIM11 fusion in a case of metastatic clear cell sarcoma: are CRTC1-TRIM11 fusion-bearing tumors melanocytomas or clear cell sarcomas?","volume":"43","author":"Bontoux","year":"2019","journal-title":"Am J Surg Pathol"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0019","doi-asserted-by":"crossref","first-page":"368","DOI":"10.1111\/his.14812","article-title":"Cutaneous melanocytic tumour with CRTC1::TRIM11 fusion in a case with recurrent local lymph node and distant pulmonary metastases at early stage: aggressive rather than indolent?","volume":"82","author":"Yang","year":"2023","journal-title":"Histopathology"},{"issue":"7","key":"10.1053\/j.semdp.2023.04.013_bib0020","doi-asserted-by":"crossref","first-page":"915","DOI":"10.1111\/cup.13984","article-title":"Dermal melanocytic tumor with CRTC1-TRIM11 fusion: report of two additional cases with review of the literature of an emerging entity","volume":"48","author":"Parra","year":"2021","journal-title":"J Cutan Pathol"},{"issue":"1","key":"10.1053\/j.semdp.2023.04.013_bib0021","doi-asserted-by":"crossref","first-page":"1223","DOI":"10.1038\/s41467-018-03499-z","article-title":"TRIM11 activates the proteasome and promotes overall protein degradation by regulating USP14","volume":"9","author":"Chen","year":"2018","journal-title":"Nat Commun"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0022","doi-asserted-by":"crossref","first-page":"266","DOI":"10.1111\/ijd.15448","article-title":"Balloon cell melanoma: a systematic review","volume":"61","author":"Wei","year":"2022","journal-title":"Int J Dermatol"},{"issue":"18","key":"10.1053\/j.semdp.2023.04.013_bib0023","doi-asserted-by":"crossref","first-page":"5356","DOI":"10.1158\/1078-0432.CCR-05-2811","article-title":"EWS-CREB1: a recurrent variant fusion in clear cell sarcoma\u2013association with gastrointestinal location and absence of melanocytic differentiation","volume":"12","author":"Antonescu","year":"2006","journal-title":"Clin Cancer Res"},{"issue":"6","key":"10.1053\/j.semdp.2023.04.013_bib0024","doi-asserted-by":"crossref","first-page":"1127","DOI":"10.1016\/j.jaad.2014.08.016","article-title":"Primary cutaneous perivascular epithelioid cell tumor: a clinicopathological and molecular reappraisal","volume":"71","author":"Charli-Joseph","year":"2014","journal-title":"J Am Acad Dermatol"},{"issue":"1","key":"10.1053\/j.semdp.2023.04.013_bib0025","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1159\/000510650","article-title":"Sequencing PEComas: viewing Unicorns through the Molecular Looking Glass","volume":"99","author":"Groisberg","year":"2021","journal-title":"Oncology"},{"issue":"6","key":"10.1053\/j.semdp.2023.04.013_bib0026","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1111\/cup.13647","article-title":"Cutaneous \"fibroma-like\" perivascular epithelioid cell tumor: a case report and review of literature","volume":"47","author":"Odono","year":"2020","journal-title":"J Cutan Pathol"},{"issue":"7","key":"10.1053\/j.semdp.2023.04.013_bib0027","doi-asserted-by":"crossref","first-page":"962","DOI":"10.1097\/PAS.0000000000001630","article-title":"Clear cell tumor with melanocytic differentiation and ACTIN-MITF translocation: report of 7 cases of a novel entity","volume":"45","author":"de la Fouchardiere","year":"2021","journal-title":"Am J Surg Pathol"},{"issue":"4","key":"10.1053\/j.semdp.2023.04.013_bib0028","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1007\/s00428-021-03027-3","article-title":"Clear cell tumor with melanocytic differentiation and MITF-CREM translocation: a novel entity similar to clear cell sarcoma","volume":"479","author":"de la Fouchardiere","year":"2021","journal-title":"Virchows Arch"},{"key":"10.1053\/j.semdp.2023.04.013_bib0029","unstructured":"1932;35(3):351-7. MWAmmtogcafatsgTJoPaB."},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0030","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1111\/cup.13385","article-title":"Cutaneous myxomas and a psammomatous melanotic schwannoma in a patient with Carney complex","volume":"46","author":"Sarfo","year":"2019","journal-title":"J Cutan Pathol"},{"issue":"1","key":"10.1053\/j.semdp.2023.04.013_bib0031","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1097\/PAS.0b013e3182a0a150","article-title":"Malignant melanotic schwannian tumor: a clinicopathologic, immunohistochemical, and gene expression profiling study of 40 cases, with a proposal for the reclassification of \"melanotic schwannoma\"","volume":"38","author":"Torres-Mora","year":"2014","journal-title":"Am J Surg Pathol"},{"issue":"12","key":"10.1053\/j.semdp.2023.04.013_bib0032","doi-asserted-by":"crossref","first-page":"1696","DOI":"10.3174\/ajnr.A7691","article-title":"Malignant melanotic nerve sheath tumor","volume":"43","author":"Benson","year":"2022","journal-title":"AJNR Am J Neuroradiol"},{"issue":"8","key":"10.1053\/j.semdp.2023.04.013_bib0033","doi-asserted-by":"crossref","first-page":"850","DOI":"10.1177\/1066896920923146","article-title":"Melanotic schwannoma, a deceptive misnomer for a tumor with relative aggressive behavior: a series of 7 cranial and spinal cases","volume":"28","author":"Sahay","year":"2020","journal-title":"Int J Surg Pathol"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0034","doi-asserted-by":"crossref","first-page":"299","DOI":"10.1007\/s11060-017-2653-z","article-title":"Intracranial melanotic schwannomas: a rare variant with unusual adherent features","volume":"136","author":"Mahato","year":"2018","journal-title":"J Neurooncol"},{"issue":"12","key":"10.1053\/j.semdp.2023.04.013_bib0035","doi-asserted-by":"crossref","first-page":"1661","DOI":"10.1097\/DSS.0000000000003267","article-title":"Cutaneous melanotic schwannoma in a pediatric patient","volume":"47","author":"Nguyen","year":"2021","journal-title":"Dermatol Surg"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0036","doi-asserted-by":"crossref","first-page":"317","DOI":"10.4103\/1793-5482.148789","article-title":"Non psammomatous melanocytic schwannoma presenting as a subcutaneous nodule: a rare presentation of a rare lesion","volume":"11","author":"Gulati","year":"2016","journal-title":"Asian J Neurosurg"},{"issue":"8","key":"10.1053\/j.semdp.2023.04.013_bib0037","doi-asserted-by":"crossref","first-page":"747","DOI":"10.1111\/cup.14232","article-title":"Nevus, melanoma, or something else? Mesenchymal neoplasms with melanocytic differentiation","volume":"49","author":"Evangelou","year":"2022","journal-title":"J Cutan Pathol"},{"issue":"6","key":"10.1053\/j.semdp.2023.04.013_bib0038","doi-asserted-by":"crossref","first-page":"558","DOI":"10.1046\/j.1365-2559.1999.00786.x","article-title":"Spinal melanotic schwannoma: a tumour with poor prognosis","volume":"35","author":"Vallat-Decouvelaere","year":"1999","journal-title":"Histopathology"},{"issue":"17","key":"10.1053\/j.semdp.2023.04.013_bib0039","first-page":"1451","article-title":"Clinicopathological, immunohistochemical, and ultrastructural study of 13 cases of melanotic schwannoma","volume":"118","author":"Zhang","year":"2005","journal-title":"Chin Med J (Engl)"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0040","doi-asserted-by":"crossref","first-page":"206","DOI":"10.1097\/00000478-199003000-00002","article-title":"Psammomatous melanotic schwannoma. A distinctive, heritable tumor with special associations, including cardiac myxoma and the Cushing syndrome","volume":"14","author":"Carney","year":"1990","journal-title":"Am J Surg Pathol"},{"issue":"6","key":"10.1053\/j.semdp.2023.04.013_bib0041","doi-asserted-by":"crossref","first-page":"E1334","DOI":"10.1227\/01.NEU.0000245608.07570.D2","article-title":"Melanotic nonpsammomatous trigeminal schwannoma as the first manifestation of Carney complex: case report","volume":"59","author":"Carrasco","year":"2006","journal-title":"Neurosurgery"},{"issue":"4","key":"10.1053\/j.semdp.2023.04.013_bib0042","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1097\/00005792-198507000-00007","article-title":"The complex of myxomas, spotty pigmentation, and endocrine overactivity","volume":"64","author":"Carney","year":"1985","journal-title":"Medicine (Baltimore)"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0043","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1007\/s00401-009-0611-3","article-title":"Activating mutations of the GNAQ gene: a frequent event in primary melanocytic neoplasms of the central nervous system","volume":"119","author":"Kusters-Vandevelde","year":"2010","journal-title":"Acta Neuropathol"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0044","doi-asserted-by":"crossref","first-page":"202","DOI":"10.1111\/bpa.12228","article-title":"Melanotic tumors of the nervous system are characterized by distinct mutational, chromosomal and epigenomic profiles","volume":"25","author":"Koelsche","year":"2015","journal-title":"Brain Pathol"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0045","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1007\/s00401-012-0948-x","article-title":"GNAQ and GNA11 mutations in melanocytomas of the central nervous system","volume":"123","author":"Murali","year":"2012","journal-title":"Acta Neuropathol"},{"issue":"9","key":"10.1053\/j.semdp.2023.04.013_bib0046","doi-asserted-by":"crossref","first-page":"1201","DOI":"10.1038\/modpathol.2009.85","article-title":"Detection and characterization of EWSR1\/ATF1 and EWSR1\/CREB1 chimeric transcripts in clear cell sarcoma (melanoma of soft parts)","volume":"22","author":"Wang","year":"2009","journal-title":"Mod Pathol"},{"issue":"12","key":"10.1053\/j.semdp.2023.04.013_bib0047","doi-asserted-by":"crossref","first-page":"943","DOI":"10.1097\/DAD.0000000000002311","article-title":"Plexiform melanocytic schwannoma: Report of a second case and overview of a rare entity","volume":"44","author":"Ranson","year":"2022","journal-title":"Am J Dermatopathol"},{"key":"10.1053\/j.semdp.2023.04.013_bib0048","doi-asserted-by":"crossref","first-page":"1163","DOI":"10.1002\/1097-0142(196509)18:9<1163::AID-CNCR2820180916>3.0.CO;2-0","article-title":"Clear-cell sarcoma of tendons and aponeuroses. An analysis of 21 cases","volume":"18","author":"Enzinger","year":"1965","journal-title":"Cancer"},{"issue":"5","key":"10.1053\/j.semdp.2023.04.013_bib0049","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1097\/00000478-198307000-00003","article-title":"Malignant melanoma of soft parts. A reassessment of clear cell sarcoma","volume":"7","author":"Chung","year":"1983","journal-title":"Am J Surg Pathol"},{"issue":"9","key":"10.1053\/j.semdp.2023.04.013_bib0050","doi-asserted-by":"crossref","first-page":"1775","DOI":"10.1200\/JCO.2003.10.108","article-title":"Classification of clear-cell sarcoma as a subtype of melanoma by genomic profiling","volume":"21","author":"Segal","year":"2003","journal-title":"J Clin Oncol"},{"key":"10.1053\/j.semdp.2023.04.013_bib0051","doi-asserted-by":"crossref","DOI":"10.1155\/2012\/984096","article-title":"Clear cell sarcoma (malignant melanoma) of soft parts: a clinicopathologic study of 52 cases","volume":"2012","author":"Hocar","year":"2012","journal-title":"Dermatol Res Pract"},{"issue":"7","key":"10.1053\/j.semdp.2023.04.013_bib0052","doi-asserted-by":"crossref","first-page":"800","DOI":"10.1016\/j.ejso.2007.10.006","article-title":"Clear cell sarcoma (melanoma of soft parts): the Royal Marsden Hospital experience","volume":"34","author":"Clark","year":"2008","journal-title":"Eur J Surg Oncol"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0053","doi-asserted-by":"crossref","first-page":"452","DOI":"10.1097\/PAS.0b013e31814b18fb","article-title":"Clear cell sarcoma of soft tissue: a clinicopathologic, immunohistochemical, and molecular analysis of 33 cases","volume":"32","author":"Hisaoka","year":"2008","journal-title":"Am J Surg Pathol"},{"issue":"5","key":"10.1053\/j.semdp.2023.04.013_bib0054","doi-asserted-by":"crossref","first-page":"416","DOI":"10.1136\/jcp.2008.057471","article-title":"Clear cell sarcoma of tendons and aponeuroses, and osteoclast-rich tumour of the gastrointestinal tract with features resembling clear cell sarcoma of soft parts: a review and update","volume":"63","author":"Kosemehmetoglu","year":"2010","journal-title":"J Clin Pathol"},{"issue":"5","key":"10.1053\/j.semdp.2023.04.013_bib0055","doi-asserted-by":"crossref","first-page":"505","DOI":"10.1016\/j.ejso.2014.01.016","article-title":"Clear cell sarcoma of soft tissue: a retrospective review and analysis of 31 cases treated at Istituto Ortopedico Rizzoli","volume":"40","author":"Bianchi","year":"2014","journal-title":"Eur J Surg Oncol"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0056","doi-asserted-by":"crossref","first-page":"859","DOI":"10.1007\/s12032-010-9502-7","article-title":"Chemotherapy in clear cell sarcoma","volume":"28","author":"Jones","year":"2011","journal-title":"Med Oncol."},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0057","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1097\/PAS.0b013e3181c7d8b2","article-title":"Cutaneous clear cell sarcoma: a clinicopathologic, immunohistochemical, and molecular analysis of 12 cases emphasizing its distinction from dermal melanoma","volume":"34","author":"Hantschke","year":"2010","journal-title":"Am J Surg Pathol"},{"issue":"1","key":"10.1053\/j.semdp.2023.04.013_bib0058","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1097\/PAS.0000000000001404","article-title":"Compound clear cell sarcoma of the skin-a potential diagnostic pitfall: report of a series of 4 new cases and a review of the literature","volume":"44","author":"Luzar","year":"2020","journal-title":"Am J Surg Pathol"},{"issue":"12","key":"10.1053\/j.semdp.2023.04.013_bib0059","doi-asserted-by":"crossref","first-page":"1226","DOI":"10.1111\/cup.13812","article-title":"Diffuse PRAME expression is highly specific for malignant melanoma in the distinction from clear cell sarcoma","volume":"47","author":"Raghavan","year":"2020","journal-title":"J Cutan Pathol"},{"issue":"6","key":"10.1053\/j.semdp.2023.04.013_bib0060","doi-asserted-by":"crossref","first-page":"404","DOI":"10.1097\/DAD.0000000000002128","article-title":"PRAME expression in challenging dermal melanocytic neoplasms and soft tissue tumors with melanocytic differentiation","volume":"44","author":"Kline","year":"2022","journal-title":"Am J Dermatopathol"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0061","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1111\/his.14814","article-title":"PRAME is a useful marker for the differential diagnosis of melanocytic tumours and histological mimics","volume":"82","author":"Chen","year":"2023","journal-title":"Histopathology"},{"issue":"6","key":"10.1053\/j.semdp.2023.04.013_bib0062","doi-asserted-by":"crossref","first-page":"473","DOI":"10.1016\/j.ccr.2006.04.021","article-title":"Oncogenic MITF dysregulation in clear cell sarcoma: defining the MiT family of human cancers","volume":"9","author":"Davis","year":"2006","journal-title":"Cancer Cell"},{"issue":"7","key":"10.1053\/j.semdp.2023.04.013_bib0063","doi-asserted-by":"crossref","first-page":"e1","DOI":"10.1097\/PAS.0b013e31825485c5","article-title":"Tumors with EWSR1-CREB1 and EWSR1-ATF1 fusions: the current status","volume":"36","author":"Thway","year":"2012","journal-title":"Am J Surg Pathol"},{"key":"10.1053\/j.semdp.2023.04.013_bib0064","doi-asserted-by":"crossref","DOI":"10.1111\/cup.14390","article-title":"Compound clear cell sarcoma with EWSR1::CREM fusion","author":"Li","year":"2023","journal-title":"J Cutan Pathol"},{"issue":"12","key":"10.1053\/j.semdp.2023.04.013_bib0065","doi-asserted-by":"crossref","first-page":"1622","DOI":"10.1097\/PAS.0000000000001331","article-title":"Expanding the phenotypic spectrum of mesenchymal tumors harboring the EWSR1-CREM fusion","volume":"43","author":"Yoshida","year":"2019","journal-title":"Am J Surg Pathol"},{"issue":"12","key":"10.1053\/j.semdp.2023.04.013_bib0066","doi-asserted-by":"crossref","first-page":"905","DOI":"10.1111\/cup.13345","article-title":"Review of the medical literature and assessment of current utilization patterns regarding the use of two common fluorescence in situ hybridization assays in the diagnosis of dermatofibrosarcoma protuberans and clear cell sarcoma","volume":"45","author":"Linos","year":"2018","journal-title":"J Cutan Pathol"},{"issue":"10","key":"10.1053\/j.semdp.2023.04.013_bib0067","doi-asserted-by":"crossref","first-page":"817","DOI":"10.1097\/00000478-198910000-00001","article-title":"Ossifying fibromyxoid tumor of soft parts. A clinicopathological analysis of 59 cases","volume":"13","author":"Enzinger","year":"1989","journal-title":"Am J Surg Pathol"},{"issue":"8","key":"10.1053\/j.semdp.2023.04.013_bib0068","doi-asserted-by":"crossref","first-page":"1294","DOI":"10.1016\/S0022-3468(99)90175-6","article-title":"Ossifying fibromyxoid tumor of soft parts in a child: a case report","volume":"34","author":"Ijiri","year":"1999","journal-title":"J Pediatr Surg"},{"issue":"4","key":"10.1053\/j.semdp.2023.04.013_bib0069","doi-asserted-by":"crossref","first-page":"421","DOI":"10.1097\/00000478-200304000-00001","article-title":"Ossifying fibromyxoid tumor of soft parts: a clinicopathologic study of 70 cases with emphasis on atypical and malignant variants","volume":"27","author":"Folpe","year":"2003","journal-title":"Am J Surg Pathol"},{"issue":"1","key":"10.1053\/j.semdp.2023.04.013_bib0070","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1017\/S0022215100122200","article-title":"Ossifying fibromyxoid tumour (of soft parts) of the head and neck: a clinicopathological and immunohistochemical study of nine cases","volume":"107","author":"Williams","year":"1993","journal-title":"J Laryngol Otol"},{"issue":"9","key":"10.1053\/j.semdp.2023.04.013_bib0071","doi-asserted-by":"crossref","first-page":"1039","DOI":"10.1097\/00000478-199509000-00007","article-title":"Atypical and malignant variants of ossifying fibromyxoid tumor. Clinicopathologic analysis of six cases","volume":"19","author":"Kilpatrick","year":"1995","journal-title":"Am J Surg Pathol"},{"issue":"6","key":"10.1053\/j.semdp.2023.04.013_bib0072","first-page":"480","article-title":"Ossifying fibromyxoid tumor of soft parts","volume":"41","author":"Yoshida","year":"1991","journal-title":"Acta Pathol Jpn"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0073","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1016\/S1092-9134(97)80011-1","article-title":"Ossifying fibromyxoid tumor of soft parts: a report of 17 cases with emphasis on unusual histological features","volume":"1","author":"Zamecnik","year":"1997","journal-title":"Ann Diagn Pathol"},{"key":"10.1053\/j.semdp.2023.04.013_bib0074","doi-asserted-by":"crossref","first-page":"52","DOI":"10.1016\/j.anndiagpath.2015.11.002","article-title":"Ossifying fibromyxoid tumor: morphology, genetics, and differential diagnosis","volume":"20","author":"Schneider","year":"2016","journal-title":"Ann Diagn Pathol"},{"issue":"11","key":"10.1053\/j.semdp.2023.04.013_bib0075","doi-asserted-by":"crossref","first-page":"1615","DOI":"10.1097\/PAS.0b013e3182284a3f","article-title":"Ossifying fibromyxoid tumor of soft parts: a clinicopathologic, proteomic, and genomic study","volume":"35","author":"Graham","year":"2011","journal-title":"Am J Surg Pathol"},{"issue":"11","key":"10.1053\/j.semdp.2023.04.013_bib0076","doi-asserted-by":"crossref","first-page":"1751","DOI":"10.1097\/PAS.0b013e31829644b4","article-title":"PHF1 rearrangements in ossifying fibromyxoid tumors of soft parts: a fluorescence in situ hybridization study of 41 cases with emphasis on the malignant variant","volume":"37","author":"Graham","year":"2013","journal-title":"Am J Surg Pathol"},{"issue":"11","key":"10.1053\/j.semdp.2023.04.013_bib0077","doi-asserted-by":"crossref","first-page":"2603","DOI":"10.1016\/j.humpath.2013.04.003","article-title":"Ossifying fibromyxoid tumor presenting EP400-PHF1 fusion gene","volume":"44","author":"Endo","year":"2013","journal-title":"Hum Pathol"},{"issue":"7","key":"10.1053\/j.semdp.2023.04.013_bib0078","doi-asserted-by":"crossref","first-page":"1331","DOI":"10.1038\/s41379-020-0457-8","article-title":"PHF1 fusions cause distinct gene expression and chromatin accessibility profiles in ossifying fibromyxoid tumors and mesenchymal cells","volume":"33","author":"Hofvander","year":"2020","journal-title":"Mod Pathol"},{"issue":"3","key":"10.1053\/j.semdp.2023.04.013_bib0079","doi-asserted-by":"crossref","first-page":"1069","DOI":"10.1016\/j.ajpath.2012.05.030","article-title":"Recurrent rearrangement of the PHF1 gene in ossifying fibromyxoid tumors","volume":"181","author":"Gebre-Medhin","year":"2012","journal-title":"Am J Pathol"},{"issue":"10","key":"10.1053\/j.semdp.2023.04.013_bib0080","doi-asserted-by":"crossref","first-page":"934","DOI":"10.1111\/cup.13728","article-title":"Superficial malignant ossifying fibromyxoid tumors harboring the rare and recently described ZC3H7B-BCOR and PHF1-TFE3 fusions","volume":"47","author":"Linos","year":"2020","journal-title":"J Cutan Pathol"},{"issue":"2","key":"10.1053\/j.semdp.2023.04.013_bib0081","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1002\/gcc.22132","article-title":"Novel ZC3H7B-BCOR, MEAF6-PHF1, and EPC1-PHF1 fusions in ossifying fibromyxoid tumors\u2013molecular characterization shows genetic overlap with endometrial stromal sarcoma","volume":"53","author":"Antonescu","year":"2014","journal-title":"Genes Chromosomes Cancer"},{"key":"10.1053\/j.semdp.2023.04.013_bib0082","doi-asserted-by":"crossref","DOI":"10.1016\/j.yexmp.2021.104686","article-title":"A PHF1-TFE3 fusion atypical ossifying fibromyxoid tumor with prominent collagenous rosettes: case report with a brief review","volume":"123","author":"Zou","year":"2021","journal-title":"Exp Mol Pathol"},{"issue":"9","key":"10.1053\/j.semdp.2023.04.013_bib0083","doi-asserted-by":"crossref","first-page":"643","DOI":"10.1002\/gcc.22755","article-title":"Novel recurrent PHF1-TFE3 fusions in ossifying fibromyxoid tumors","volume":"58","author":"Suurmeijer","year":"2019","journal-title":"Genes Chromosomes Cancer"},{"issue":"12","key":"10.1053\/j.semdp.2023.04.013_bib0084","doi-asserted-by":"crossref","first-page":"1504","DOI":"10.5858\/arpa.2019-0371-RA","article-title":"Ossifying fibromyxoid tumor: a review with emphasis on recent molecular advances and differential diagnosis","volume":"143","author":"Carter","year":"2019","journal-title":"Arch Pathol Lab Med"}],"container-title":["Seminars in Diagnostic Pathology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0740257023000424?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0740257023000424?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,9]],"date-time":"2025-10-09T19:24:33Z","timestamp":1760037873000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0740257023000424"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,7]]},"references-count":84,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2023,7]]}},"alternative-id":["S0740257023000424"],"URL":"https:\/\/doi.org\/10.1053\/j.semdp.2023.04.013","relation":{},"ISSN":["0740-2570"],"issn-type":[{"type":"print","value":"0740-2570"}],"subject":[],"published":{"date-parts":[[2023,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"The new and old in superficial mesenchymal tumors with uncertain origin and\/or melanocytic differentiation","name":"articletitle","label":"Article Title"},{"value":"Seminars in Diagnostic Pathology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1053\/j.semdp.2023.04.013","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}