Publication:
Primary gastric synovial sarcoma

cris.lastimport.scopus2025-05-07T21:44:40Z
cris.virtual.departmentEmergency Medicine-NTUH
cris.virtual.departmentEmergency Medicine
cris.virtual.departmentSurgery
cris.virtual.departmentSurgery-NTUH
cris.virtual.departmentPathology
cris.virtual.departmentPathology-NTUH
cris.virtual.orcid0000-0002-9584-3486en_US
cris.virtual.orcid0000-0001-7313-7057en_US
cris.virtual.orcid0000-0001-7739-5934en_US
cris.virtualsource.departmentd7564346-494d-43f3-acf9-819c9af8debd
cris.virtualsource.departmentd7564346-494d-43f3-acf9-819c9af8debd
cris.virtualsource.departmentf758a324-b3cf-4753-aa13-79897165bd67
cris.virtualsource.departmentf758a324-b3cf-4753-aa13-79897165bd67
cris.virtualsource.department9de93d96-206b-4a25-9f23-a9ac5b8cb656
cris.virtualsource.department9de93d96-206b-4a25-9f23-a9ac5b8cb656
cris.virtualsource.orcidd7564346-494d-43f3-acf9-819c9af8debd
cris.virtualsource.orcidf758a324-b3cf-4753-aa13-79897165bd67
cris.virtualsource.orcid9de93d96-206b-4a25-9f23-a9ac5b8cb656
dc.contributor.authorWang C.-C.en_US
dc.contributor.authorMENG-CHE WUen_US
dc.contributor.authorMING-TSAN LINen_US
dc.contributor.authorJEN-CHIEH LEEen_US
dc.creatorLee J.-C.;Lin M.-T.;MENG-CHE WU;Wang C.-C.
dc.date.accessioned2020-03-25T08:01:00Z
dc.date.available2020-03-25T08:01:00Z
dc.date.issued2012
dc.description.abstractSynovial sarcoma is a malignant soft tissue neoplasm that may arise from a variety of sites in the human body. It is typically characterized by its biphasic histological pattern, but a monophasic type composed entirely of spindle cells also exists. The diagnosis of monophasic synovial sarcoma can be very challenging and often requires molecular diagnostic techniques, especially for tumors arising in rare locations such as the gastrointestinal tract. We report here the case of a 38-year-old woman with a primary gastric monophasic synovial sarcoma confirmed by reverse transcriptase polymerase chain reaction that revealed t(X;18) (SYT-SSX1) translocation. To our knowledge, only 11 synovial sarcomas arising in the stomach have previously been reported. The pathologic features, differential diagnoses, and clinical manifestations are discussed. ? 2012.
dc.identifier.doi10.1016/j.jfma.2012.07.010
dc.identifier.issn0929-6646
dc.identifier.pmid23021509
dc.identifier.scopus2-s2.0-84867025225
dc.identifier.urihttps://scholars.lib.ntu.edu.tw/handle/123456789/479102
dc.relation.ispartofJournal of the Formosan Medical Association
dc.relation.journalissue9
dc.relation.journalvolume111
dc.relation.pages516-520
dc.subject.classification[SDGs]SDG3
dc.subject.otherbarium; CD99 antigen; cytokeratin AE1; cytokeratin AE3; doxorubicin; ifosfamide; adult; article; cancer chemotherapy; cancer diagnosis; case report; computer assisted tomography; female; follow up; histopathology; human; immunohistochemistry; liver metastasis; primary gastric synovial sarcoma; spindle cell sarcoma; stomach biopsy; stomach sarcoma; synovial sarcoma; wedge resection; Adult; Female; Humans; Oncogene Proteins, Fusion; Reverse Transcriptase Polymerase Chain Reaction; Sarcoma, Synovial; Stomach; Stomach Neoplasms; Translocation, Genetic; Tumor Markers, Biological
dc.titlePrimary gastric synovial sarcomaen_US
dc.typejournal articleen
dspace.entity.typePublication

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