Будь ласка, використовуйте цей ідентифікатор, щоб цитувати або посилатися на цей матеріал: http://ir.librarynmu.com/handle/123456789/12827
Повний запис метаданих
Поле DCЗначенняМова
dc.contributor.authorKhurdepa, K.-
dc.contributor.authorKarnabeda, O.-
dc.date.accessioned2024-10-15T08:21:22Z-
dc.date.available2024-10-15T08:21:22Z-
dc.date.issued2024-
dc.identifier.issnUDC: 616.155-018.1:575.224]:616-085 https://doi.org/10.32345/USMYJ.1(149).2024.75-80-
dc.identifier.urihttp://ir.librarynmu.com/handle/123456789/12827-
dc.description.abstractThis clinical case report presents a patient diagnosed with a myelodysplastic syndrome (MDS)/myeloproliferative neoplasm (MPN), specifically myelofibrosis with a deletion of the long arm of chromosome 5 (del 5q), an exceedingly rare anomaly in chronic myeloproliferative disorders. We performed a thorough analysis of the patient’s clinical, laboratory, and molecular-genetic characteristics to evaluate their impact on prognosis, treatment decisions, and therapeutic outcomes. After excluding other genetic abnormalities, the patient was treated with lenalidomide and prednisolone, resulting in improved clinical and hematological parameters. These findings are consistent with previous studies and suggest the potential efficacy of lenalidomide in treating patients with MDS/MPN characterized by del 5q, especially when no additional genetic abnormalities are present.uk_UA
dc.language.isoenuk_UA
dc.publisherUkrainian Scientific Medical Youth Journal Issue 3 (149), 2024uk_UA
dc.subjectChronic Myeloproliferative Neoplasm; Myelofibrosis; Myelodysplastic Syndromes; Del 5q; Lenalidomide.uk_UA
dc.titleMyelodysplastic syndrome (MDS)/Myeloproliferative neoplasm (MPN) with loss of long arm of chromosome 5 (del 5q): Clinical case and treatment perspectivesuk_UA
dc.typeArticleuk_UA
Розташовується у зібраннях:2024 УНММЖ №3



Усі матеріали в архіві електронних ресурсів захищені авторським правом, всі права збережені.