Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Michael, Michal"'
Autor:
Michel-Edwar Mickael, Norwin Kubick, Atanas G. Atanasov, Petr Martinek, Jarosław Olav Horbańczuk, Nikko Floretes, Michael Michal, Tomas Vanecek, Justyna Paszkiewicz, Mariusz Sacharczuk, Piotr Religa
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 8, Pp 8301-8319 (2024)
The accurate identification of the primary tumor origin in metastatic cancer cases is crucial for guiding treatment decisions and improving patient outcomes. Copy number alterations (CNAs) and copy number variation (CNV) have emerged as valuable geno
Externí odkaz:
https://doaj.org/article/e6185171faa7413aaa28f25c0fe5414d
Autor:
Jiri Molacek, Vladislav Treska, Tomas Skalicky, Josef Vodicka, Jiri Ferda, Eva Ferdova, Jan Baxa, Christiana Mach, Alexandra Jungova, Michael Michal
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundCastleman´s disease is an extremely rare heterogenous lymphoproliferative pathology with a mostly benign behavior. It is a localized or generalized lymph node enlargement of an unknown aetiology. Unicentric form is typically a slow-growing
Externí odkaz:
https://doaj.org/article/d976299f467d48eda88f9cd9e4e0bc31
Publikováno v:
Bone Reports, Vol 16, Iss , Pp 101180- (2022)
Tumor-induced osteomalacia (TIO) is an uncommon type of osteomalacia associated with phosphaturic mesenchymal tumors (PMTs). Due to nonspecific symptoms, the diagnosis and appropriate management of the disease is often delayed for many years. Involve
Externí odkaz:
https://doaj.org/article/2dabc43d44b84167a4ecff2bb3ebdfa3
Autor:
Michael E. Kallen, Michael Michal, Anders Meyer, David I. Suster, Nicholas J. Olson, Gregory W. Charville, Raul Perret, John M. Gross
Publikováno v:
American Journal of Surgical Pathology. 47:725-737
Autor:
Jiří Lenz, Natálie Klubíčková, Nikola Ptáková, Veronika Hájková, Petr Grossmann, Petr Šteiner, Zdeněk Kinkor, Marián Švajdler, Michal Michal, Petra Konečná, Dominika Macháčová, Pavel Hurník, Michal Tichý, František Tichý, Michal Kyllar, Luděk Fiala, Miroslav Kavka, Michael Michal
Publikováno v:
Human Pathology. 134:19-29
Extraskeletal myxoid chondrosarcoma (EMC) is a rare sarcoma of uncertain lineage. Insulinoma-associated protein 1 (INSM1) has recently been described as a highly specific and sensitive immunohistochemical marker for EMC. The goal of this study was to
Autor:
Anders Meyer, Natálie Klubíčková, Elaheh Mosaieby, Petr Grossmann, Antonina Kalmykova, Olena Koshyk, Michael Michal
Publikováno v:
Virchows Archiv. 482:777-782
We report a case of a 67-year-old male patient with a sinonasal tumor that showed areas of classic biphenotypic sinonasal sarcoma (BSNS) which in some sections sharply transitioned into high-grade rhabdomyosarcoma. Immunohistochemically, the conventi
Autor:
Michael Michal, Nasir Ud Din, Marián Švajdler, Natálie Klubíčková, Nikola Ptáková, Veronika Hájková, Michal Michal, Abbas Agaimy
Publikováno v:
Genes, Chromosomes and Cancer. 62:290-296
This article presents 2 cases of TFG::MET-rearranged mesenchymal tumor, an extremely rare molecular subset among an emerging group of mesenchymal neoplasms with kinase gene (NTRK, BRAF, RET and others) alterations. Both tumors were congenital, occurr
Autor:
Małgorzata Chłopek, Jerzy Lasota, Lester D.R. Thompson, Magdalena Szczepaniak, Alina Kuźniacka, Kinga Hińcza, Kamila Kubicka, Maciej Kaczorowski, Michael Newford, Yalan Liu, Abbas Agaimy, Wojciech Biernat, Monika Durzyńska, Ireneusz Dziuba, Arndt Hartmann, Shingo Inaguma, Ewa Iżycka-Świeszewska, Hiroyuki Kato, Janusz Kopczyński, Michal Michal, Michael Michal, Rafał Pęksa, Monika Prochorec-Sobieszek, Anna Starzyńska, Satoru Takahashi, Bartosz Wasąg, Artur Kowalik, Markku Miettinen
Publikováno v:
Modern Pathology. 35:1609-1617
Sinonasal mucosal melanoma is a rare tumor arising within the nasal cavity, paranasal sinuses, or nasopharynx (sinonasal tract). This study evaluated 90 cases diagnosed in 29 males and 61 females with median age 68 years. Most tumors involved the nas
Autor:
Boulos, Mansour, Michele, Donati, Květoslava, Michalová, Michal, Michal, Nikola, Ptáková, Veronika, Hájková, Michael, Michal
Publikováno v:
Virchows Archiv. 481:751-757
Epithelioid fibrous histiocytoma (EFH) is a distinctive cutaneous neoplasm with a relatively variable morphological appearance. Recently, it has been shown that this tumor is molecularly characterized by ALK gene fusions. We report three EFHs with un
Autor:
Natálie Klubíčková, Michael Michal, Abbas Agaimy, Nina Zidar, Michal Pavlovský, Kenji Yorita, Petr Grossmann, Veronika Hájková, Nikola Ptáková, Petr Šteiner, Michal Michal
Publikováno v:
Virchows Archiv. 481:721-729
We report 7 cases of an indolent, variably myxoid tumor of the vocal cords, characterized by overt cellular atypia with large cells containing intranuclear and intracytoplasmic vacuoles, delicate curvilinear vessels, and sparse inflammatory infiltrat