Myelodysplastic Syndromes (MDS); diagnosis, classification, treatment and monitoring

نویسندگان

چکیده

Due to the neoplastic nature of myelodysplastic syndromes (MDS), they have been renamed as neoplasms in World Health Organization (WHO) 2022 classification. These are heterogeneous groups myeloid disorders characterized by dysplasia bone marrow cells, ineffective hematopoiesis, increased apoptosis, peripheral blood cytopenia, and risk progression acute leukemia (AML). The recent progress understanding pathogenesis these diseases is due emergence next-generation sequencing (NGS) simultaneous interpretation changes cell morphologies, cytogenetics, molecular mutations, which provided conditions for better classification determination efficient prognosis. Based on Revised International Prognostic Scoring System (IPSS-R) system, MDS treatment approaches were divided into two groups: low-risk MDS, high-risk MDS. In not main cause death, most patients die a result cytopenia quality life. Therefore, goal improve life patients. However, with possibility AML life-threatening. clinical decisions aim course disease.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Azacitidine for the treatment of myelodysplastic syndromes (MDS).pub

Azacitidine is a pyrimidine nucleoside analogue with multiple mechanisms involved in its antineoplastic action. There is evidence that RNA metabolism is the primary target of this antimetabolite, although its inhibition of DNA methylation has been proposed as the main effect responsible for its clinical efficacy in myelodysplastic syndromes. In patients with myelodysplastic syndromes (MDS), aza...

متن کامل

Myelodysplastic syndromes (MDS) in Central Africans.

Forty two patients who were seen and satisfied the French-American-British (FAB) diagnostic criteria for myelodysplastic syndromes (MDS) over a 6-year period at the University of Zimbabwe's Department of Haematology, Harare, are presented. Their overall ages ranged from 29 to 75 years with a mean +/- SD of 57.8 +/- 11.2 years. Males outnumbered females with a male to female ratio of 1.2:1. Refr...

متن کامل

Myelodysplastic syndromes (MDS) in Zimbabweans--preliminary observations.

Twenty three Zimbabwean African patients who satisfied the French-American-British(FAB) diagnostic criteria for the myelodysplastic syndromes(MDS) at Godfrey Huggins School of Medicine, University of Zimbabwe, between July 1985 and June 1987 are presented. The disorders appear not to behave differently from those reported in Caucasian populations with regard to clinical and haematological featu...

متن کامل

Myelodysplastic syndromes: diagnosis and staging.

Myelodysplastic syndromes (MDS) represent a heterogeneous group of hematologic disorders characterized by ineffective hematopoiesis and an increased risk of developing acute myelogenous leukemia (AML). Accurate diagnosis of MDS can be difficult, and its classification requires evaluation of cytopenias, bone marrow morphology, blast percentage, and cytogenetics. These factors, as well as patient...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Iranian Journal of Blood and Cancer

سال: 2022

ISSN: ['2008-4595', '2008-4609']

DOI: https://doi.org/10.58209/ijbc.14.3.71