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Soft tissue sarcoma with ZC3H7B::BCOR fusion in a male mimicking low-grade fibromyxoid sarcoma - A case report

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F23%3A00079173" target="_blank" >RIV/00159816:_____/23:00079173 - isvavai.cz</a>

  • Alternative codes found

    RIV/61383082:_____/23:00001315 RIV/00216224:14110/23:00133286 RIV/00216208:11110/23:10469566 RIV/00216208:11150/23:10469566 and 2 more

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/abs/pii/S0344033823005319" target="_blank" >https://www.sciencedirect.com/science/article/abs/pii/S0344033823005319</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.prp.2023.154831" target="_blank" >10.1016/j.prp.2023.154831</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Soft tissue sarcoma with ZC3H7B::BCOR fusion in a male mimicking low-grade fibromyxoid sarcoma - A case report

  • Original language description

    Diagnosis of soft tissue tumors is often challenging, given the large number of entities, often with non-specific or overlapping morphology. Although morphology still plays an important part in diagnostic process, additional studies including immunohistochemistry and molecular genetics are often needed to arrive at correct diagnosis. We report a case of 61-year-old male with subcutaneous tumor in right hip area, that was surgically removed. The tumor was composed of uniform bland spindle cells in mild to moderately cellular myxoid nodules, with limited areas of collagenization and the diagnosis of low grade fibromyxoid sarcoma was made. The tumor recurred 3 years after the initial diagnosis and the new sample showed a high-grade round cell sarcoma with limited residual low-grade areas and non-specific immunoprofile after extended immunohistochemical work-up. Molecular analysis demonstrated ZC3H7B::BCOR fusion. Sarcomas with ZC3H7B::BCOR fusion occurring outside of uterus are exceedingly rare. A comprehensive review of previously published cases and a short discussion about classification of the entity is provided, together with data about morphology and immunoprofile of the lesions. The case also underscores the necessity of extended work up of soft tissue tumors with unusual immunohistochemical or morphological features in order to accurately assess their biological potential.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30109 - Pathology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Pathology research and practice

  • ISSN

    0344-0338

  • e-ISSN

    1618-0631

  • Volume of the periodical

    251

  • Issue of the periodical within the volume

    NOV 2023

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    5

  • Pages from-to

    154831

  • UT code for WoS article

    001098794100001

  • EID of the result in the Scopus database