Zobrazeno 1 - 10
of 111
pro vyhledávání: '"epithelioid inflammatory myofibroblastic sarcoma"'
Autor:
David Zezoff, DO, Stefanie Lowas, MD, Muriel Cleary, MD, Ali Akalin, MD, Farhana Riaz, MD, Jean-Marc Gauguet, MD/PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 6199-6204 (2024)
Epithelioid inflammatory myofibroblastic sarcoma, a variant of the inflammatory myofibroblastic tumor, is a rare tumor that is not well described in the radiologic literature. We present a case of a 14-year-old male adolescent who presented with feve
Externí odkaz:
https://doaj.org/article/09b6bcfc3b154af497859eebc75f2b42
Publikováno v:
Discover Oncology, Vol 15, Iss 1, Pp 1-7 (2024)
Abstract Epithelioid inflammatory myofibroblastic sarcoma (EIMS) is a rare subtype of inflammatory myofibroblastic tumor, characterized to be an aggressive disease with high frequency of ALK rearrangement, rapid recurrence, and poor prognosis. Primar
Externí odkaz:
https://doaj.org/article/81268a47bb3c4a13aac672d12b7e0003
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Epithelioid inflammatory myofibroblastic sarcoma (EIMS) is a distinct subtype of inflammatory myofibroblastoma tumor (IMT) that is recognized as a rare malignant tumor characterized by anaplastic lymphoma kinase (ALK) positivity, significant aggressi
Externí odkaz:
https://doaj.org/article/bd09fc572cdc4c9d84571296c926e7e4
Publikováno v:
Journal of Pathology and Translational Medicine, Vol 58, Iss 3, Pp 141-145 (2024)
An aggressive subtype of inflammatory myofibroblastic tumor, epithelioid inflammatory myofibroblastic sarcoma occurs primarily inside the abdominal cavity, followed by a pulmonary localization. Most harbor anaplastic lymphoma kinase (ALK) gene rearra
Externí odkaz:
https://doaj.org/article/fbad169d6c6e429eb9ca1da6f26ca747
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Epithelioid inflammatory myofibroblastic sarcoma (EIMS) is an extremely rare and aggressive form of inflammatory myofibroblastic tumor. Clinically, it has a high risk of relapse and peripheral organ infiltration, and it responds poorly to conventiona
Externí odkaz:
https://doaj.org/article/b5c787c134bf4cb4892f4f95f39aef5e
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
Inflammatory myofibroblastic tumor (IMT) is a rare tumor originating from mesenchymal tissue. Epithelioid inflammatory myofibroblastic sarcoma (EIMS) represents a rare and particularly aggressive variant, associated with a worse prognosis. Almost all
Externí odkaz:
https://doaj.org/article/526d3b3419c244238bd988373ec54efd
Publikováno v:
Human Pathology Reports, Vol 35, Iss , Pp 300726- (2024)
Inflammatory myofibroblastic tumors are mesenchymal neoplasms made up of spindle cells with inflammatory infiltrates and are intermediate-grade tumors. Inflammatory Myofibroblastic Tumor (IMT) has a variant known as Epithelioid Inflammatory Myofibrob
Externí odkaz:
https://doaj.org/article/b67796485de94b02a32407da103d9e9a
Publikováno v:
Respirology Case Reports, Vol 12, Iss 1, Pp n/a-n/a (2024)
Abstract Epithelioid inflammatory myofibroblastic sarcoma (EIMS) is an aggressive subtype of inflammatory myofibroblastic tumour which rarely affects the chest cavity. We, for the first time, report a case of mediastinal EIMS with the EML4‐ALK fusi
Externí odkaz:
https://doaj.org/article/9479c15e35124aa998e9ddb4aab41bd2
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Epithelioid inflammatory myofibroblastic sarcoma (EIMS) is a highly aggressive malignant subtype of inflammatory myofibroblastoma (IMT) associated with poor prognosis. IMT can occur in various parts of the body, most frequently in the lungs, followed
Externí odkaz:
https://doaj.org/article/91bff3409f624d91a98c1205e8a402f6
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