Search results for " Myxoid"

showing 5 items of 5 documents

Differential diagnosis of myxoid soft tissue tumors. Experience in the Clinical University Hospital of Valencia.

2018

Abstract Soft tissue tumors with myxoid components are often a diagnostic challenge for the pathologist. We retrospectively reviewed 41 cases of soft tissue tumors with myxoid components diagnosed in our center over a five-year period. The most frequent diagnoses were myxofibrosarcoma and myxoid liposarcoma, followed by low-grade fibromyxoid sarcoma, low-grade fibromyxoid tumor and myxoid neurofibroma. Other diagnoses included were extraskeletal myxoid chondrosarcoma, myxoinflammatory fibroblastic sarcoma, low-grade myxoliposarcoma, myofibrosarcoma, fibromatosis, solitary fibrous tumor, non-ossifying variant of ossifying fibromyxoid tumor and ancient neurinoma with myxoid degeneration. Immu…

0301 basic medicineAdultSolitary fibrous tumorPathologymedicine.medical_specialtySoft Tissue NeoplasmsPathology and Forensic MedicineDiagnosis Differential03 medical and health sciences0302 clinical medicinemedicineHumansRetrospective StudiesMyxoid liposarcomabusiness.industryFibromatosisFibromyxoid TumorMyxofibrosarcomaSarcomaExtraskeletal Myxoid Chondrosarcomamedicine.diseaseHospitals030104 developmental biology030220 oncology & carcinogenesisSarcomaDifferential diagnosisbusinessRevista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia
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Postoperative Radiation Therapy in Patients with Extracranial Chondrosarcoma: A Joint Study of the French Sarcoma Group and Rare Cancer Network

2020

International audience; PurposePostoperative radiation therapy (poRT) of intracranial/skull base chondrosarcomas (CHSs) is standard treatment. However, consensus is lacking for poRT in extracranial CHS (eCHS) owing to their easier resectability and intrinsic radioresistance. We assessed the practice and efficacy of poRT in eCHS.Methods and MaterialsThis multicentric retrospective study of the French Sarcoma Group/Rare Cancer Network included patients with eCHS who were operated on between 1985 and 2015. Inverse propensity score weighting (IPTW) was used to minimize poRT allocation biases.ResultsOf 182 patients, 60.4% had bone and 39.6% had soft-tissue eCHS. eCHS were of conventional (31.9%)…

MaleCancer Researchmedicine.medical_specialtyChondrosarcomaBone Neoplasmsmesenchymalbonesurvivalddc:616.0757030218 nuclear medicine & medical imagingsurgery03 medical and health sciences0302 clinical medicinePort (medical)adjuvantmedicinepostoperativeHumansRadiology Nuclear Medicine and imagingPostoperative PeriodradiotherapyRetrospective Studies[PHYS]Physics [physics]Radiationbusiness.industryadjuvant; bone; chondrosarcoma; mesenchymal; myxoid; postoperative; radioresistance; radiotherapy; soft tissue; surgery; survivalStandard treatmentIncidence (epidemiology)Hazard ratioRetrospective cohort studyMiddle Agedmedicine.diseasePrognosisConfidence interval3. Good healthradioresistanceTreatment OutcomeOncology030220 oncology & carcinogenesisFemaleRadiologySarcomaFranceChondrosarcomasoft tissuebusinessmyxoid
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Myxoid liposarcoma of the spermatic cord: US and MR imaging findings.

2013

We report a patient with myxoid liposarcoma of the spermatic cord in whom combined use of both ultrasound (US) and MRI helped to suggest the diagnosis. The lesion was solid at US and vascularized at color Doppler. T1-weighted MRI did not show fat within it; on T2-weighted images it had high signal intensity, with a cyst-like appearance. It is known that fat-poor myxoid liposarcomas with high water content may mimic a cystic lesion on non-contrast-enhanced MR; then, a combination of MRI findings, suggesting a cyst, and of US findings, showing the mass was actually solid and vascularized, allowed preoperatively the diagnosis of fat-poor myxoid liposarcoma. © 2013 Wiley Periodicals, Inc.

MaleSpermatic CordRadiology Nuclear Medicine and ImagingMyxoid liposarcomaGenital Neoplasms MaleHumansUltrasonography Doppler ColorMagnetic Resonance ImagingLiposarcoma MyxoidMR imagingUltrasonographyAgedJournal of clinical ultrasound : JCU
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Extraskeletal myxoid chondrosarcoma of the masticator space in a pediatric patient

2017

Extraskeletal myxoid chondrosarcoma (EMC) is a malignant soft-tissue neoplasm rarely described in the head and neck region of children and adolescents. We describe a case of EMC affecting the masticator space and a literature review. A 13-year-old boy who presented a large painless, diffuse mass causing progressive midfacial asymmetry of 6 months duration. Histopathological evaluation revealed a multinodular lesion, containing scattered round vacuolated tumor cells dispersed in an abundant myxoid stroma, separated by fibrous septae. Immunohistochemical analysis revealed positivity for vimentin, neuron-specific enolase, and chromogranin. The Ki-67 labelling index was 42%. The patient was tre…

Pathologymedicine.medical_specialtyOral Medicine and PathologybiologyMasticator spacebusiness.industryChromogranin AVimentinCase ReportExtraskeletal Myxoid Chondrosarcoma:CIENCIAS MÉDICAS [UNESCO]03 medical and health sciencesPediatric patient0302 clinical medicine030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASbiology.proteinmedicineParapharyngeal spaceImmunohistochemistryDifferential diagnosisbusinessGeneral Dentistry030217 neurology & neurosurgeryJournal of Clinical and Experimental Dentistry
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Soft tissue myoepithelial carcinoma with rhabdoid-like features andEWSR1rearrangement: Fine needle aspiration cytology with histologic correlation

2015

A new case of soft tissue myoepithelial carcinoma (MEC) with rhabdoid-like differentiation is presented including cytologic, histopathologic, immunohistochemical, and molecular biologic features. A 45-year-old woman was admitted to the Hospital with nodular mass involving the lower part of the abdominal wall. Fine-needle aspiration cytology showed a round cell tumor with abundant cytoplasm in the myxoid background. The nuclei were uniform, round to ovoid, with finely distributed chromatin, nucleoli, and pale, vacuolated, or eosinophilic cytoplasm with rhabdoid-like appearance resembling a soft tissue malignant rhabdoid tumor. The surgically removed tumor was poorly demarcated, yellow, soft,…

medicine.medical_specialtyPathologyHistologybiologymedicine.diagnostic_testEpithelioid sarcomaCD99Soft tissueVimentinGeneral MedicineExtraskeletal Myxoid Chondrosarcomamedicine.diseasePathology and Forensic MedicineMalignant Myoepitheliomabiology.proteinmedicineHistopathologyFluorescence in situ hybridizationDiagnostic Cytopathology
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