Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anastasios I, Kyriazoglou"'
Autor:
Nektarios I. Koufopoulos, Menelaos G. Samaras, Christakis Kotanidis, Konstantinos Skarentzos, Abraham Pouliakis, Ioannis Boutas, Adamantia Kontogeorgi, Magda Zanelli, Andrea Palicelli, Maurizio Zizzo, Giuseppe Broggi, Rosario Caltabiano, Anastasios I. Kyriazoglou, Dimitrios Goutas
Publikováno v:
Diagnostics, Vol 14, Iss 23, p 2694 (2024)
Ewing sarcomas are rare tumors arising mainly in the bones and the surrounding soft tissues. Primary extraosseous Ewing sarcomas have also been described in several other organs and locations other than bones, including the pancreas. These tumors hav
Externí odkaz:
https://doaj.org/article/c0d1b075347b488ab2a323870e9fd12b
Autor:
Anastasios I. Kyriazoglou, Joana Vieira, Manuel R. Teixeira, Niki Arnogiannaki, Efthimios Dimitriadis, Nikos Pandis
Publikováno v:
Cancer Genetics. 205:332-336
Extraskeletal osteosarcomas are rare tumors with neoplastic cells synthesizing bone, usually associated with poor prognosis. We present the case of a 40-year-old man with an extraskeletal osteosarcoma that was treated by surgery and adjuvant radiothe
Autor:
Nikos Pandis, Sverre Heim, Efthimios Dimitriadis, Petter Brandal, Niki Arnogiannaki, Anastasios I. Kyriazoglou
Publikováno v:
Cancer Genetics. 204:677-681
Secondary peripheral chondrosarcoma is a malignant chondroid tumor arising in a benign precursor, either an osteochondroma or an enchondroma. Multiple osteochondromas syndrome (MO) is an autosomal dominant skeletal disorder associated with bony growt
Autor:
Anastasios I, Kyriazoglou, Helen, Rizou, Efthimios, Dimitriadis, Niki, Arnogiannaki, Niki, Agnantis, Nikos, Pandis
Publikováno v:
In vivo (Athens, Greece). 27(1)
Secondary chondrosarcoma is a malignant chondroid tumor arising in a benign precursor. Synovial chondromatosis is a benign chondroid lesion that rarely transforms to chondrosarcoma. We present the case of a 54-year-old male with the diagnosis of low-
Autor:
Anna Takou, Theoni Trangas, Kostantina Frangia, Demetra Rontogianni, Euthimios Dimitriadis, Nikolaos Pandis, Anastasios I. Kyriazoglou
Publikováno v:
Cancer genetics and cytogenetics. 195(1)
Synovial sarcoma (SS) is characterized by the t(X;18)(p11.2;q11.2) chromosomal translocation detected in >95% of cases. Through this translocation, one of the SYT genes, SYT4 on chromosome 18, is fused to one of the SSX genes on chromosome X. SYT4–