Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Miłosz Jazdon"'
Publikováno v:
American Journal of Medical and Clinical Sciences. 7
Soft tissue sarcomas (STS) are rare malignant neoplasms, accounting for approximately 7-8% of childhood cancers. The 5-year survival rate varies from 15-90% depending on the severity of the disease. The purpose of our study was to assess the therapeu
Autor:
Katarzyna Derwich, Julita Janura-Szymańska, Wiesław Smoczyk, Miłosz Jazdon, Klaudia Kończak, Agata Adamczewska
Publikováno v:
Nowotwory. Journal of Oncology. 66:322-325
Rhabdomyosarcoma (RMS) is the most common type of soft tissue sarcoma in children. There are two main types of RMS: embryonal and alveolar (having a worse prognosis). The treatment for childhood RMS is based on surgery, chemotherapy and radiation. In
Autor:
Miłosz Jazdon, Bogna Ukielska, Łukasz Kałużny, Ewelina Gowin, Olga Zajac-Spychala, Danuta Januszkiewicz-Lewandowska, Katarzyna Jończyk-Potoczna, Benigna Konatkowska, Alicja Bartkowska-Śniatkowska, Joanna Kędzierska, Przemysław Mańkowski
Publikováno v:
Pediatria Polska. 90:236-240
We present a case of a 9-month-old boy referred to hospital with suspicion for malignancy. Additional tests revealed hepatomegaly, laboratory markers of liver failure and elevated levels of alpha-fetoprotein. During hospitalization patient's conditio