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https://read.qxmd.com/read/34969238/raeb-ii-type-of-myelodysplastic-syndrome-associated-with-axillary-abscesses-case-report
#1
Bożena Sokołowska, Daria Majowicz, Magdalena Kozioł, Olga Czabak, Ewa Wąsik-Szczepanek, Adrian Juda, Maria Soroka-Wojtaszko, Marek Hus
Myelodysplastic syndromes (MDS) are clonal haematopoetic stem cells disorders, characterized by bone marrow dysplasia, ineffecitive haematopoesis and cytopenias. Due to neutropenia, infections are common. A case is presented of a patient with high-risk myelodysplastic syndrome (MDS) complicated by hidradenitis suppurativa that developed in both axillae. Abscesses required multiple incisions and drainage. After five cycles of treatment with azacitidine, the patient underwent allogenic bone marrow transplantation...
December 29, 2021: Annals of Agricultural and Environmental Medicine: AAEM
https://read.qxmd.com/read/27642338/linezolid-induced-twice-pure-red-cell-aplasia-in-a-patient-with-central-nervous-system-infection-after-allogeneic-stem-cell-transplantation
#2
JOURNAL ARTICLE
Wenqing Hu, Bing Shi, Lihui Liu, Shengke He, Liping Ye, DengMei Tian, Yongqing Zhang
Linezolid (LZD), severed as the first oxazolidinone antibiotic, was active against multidrug-resistant gram-positive strains. LZD can induce thrombocytopenia, anemia and leukocytopenia. Currently, reports on pure red cell aplasia (PRCA) cases induced by LZD are relatively rare (4-7). In this paper, we reported a patient with PRCA twice induced by LZD. A 37-year-old man was diagnosed with myelodysplatic syndrome (MDS) and underwent allo-HSCT from an unrelated donor with ABO blood type and leukocyte antigen (HLA)-matching...
2016: Iranian Journal of Pharmaceutical Research: IJPR
https://read.qxmd.com/read/26812791/laboratory-and-clinical-risk-assessment-to-treat-myelodysplatic-syndromes
#3
REVIEW
Antonio Gidaro, Giorgio Lambertenghi Deliliers, Paolo Gallipoli, Massimo Arquati, Maddalena Alessandra Wu, Roberto Castelli
Myelodisplastic syndromes (MDS) are heterogeneous myeloid disorders characterized by peripheral cytopenias and increased risk of transformation into acute myelogenous leukemia (AML). MDS are generally suspected in the presence of cytopenia on routine analysis and the evaluation of bone marrow cells morphology and cellularity leads to correct diagnosis of MDS. The incidence of MDS is approximately five cases per 100,000 people per year in the general population, but it increases up to 50 cases per 100,000 people per year after 60 years of age...
September 1, 2016: Clinical Chemistry and Laboratory Medicine: CCLM
https://read.qxmd.com/read/24688752/outcomes-of-patients-with-myelodysplatic-syndrome-and-chronic-myelomonocytic-leukemia-post-clofarabine-failure
#4
JOURNAL ARTICLE
Hady Ghanem, Guillermo Garcia-Manero, Stefan Faderl, Farhad Ravandi, Jorge Cortes, Lakshmikanth Katragadda, Susan O'Brien, Naval Daver, Sherry Pierce, Tapan Kadia, Hagop Kantarjian, Elias Jabbour
BACKGROUND: The outcome of patients with myelodysplastic syndrome (MDS) and chronic myelomonocytic leukemia (CMML) post clofarabine is unknown. METHODS: We reviewed 109 patients with MDS or CMML with a median age of 67 years, treated with a clofarabine-based chemotherapy as frontline (n = 38) or salvage (n = 71) therapy. A total of 58 (53%) patients received salvage therapy after clofarabine failure: 13 allogeneic stem cell transplant (ASCT), 18 high-dose cytarabine-containing regimen, 10 hypomethylating agents and 17 investigational treatments...
April 2014: Therapeutic Advances in Hematology
https://read.qxmd.com/read/10067093/-allogeneic-peripheral-blood-stem-cell-transplantation-in-an-elderly-patient-with-myelodysplatic-syndrome-with-myelofibrosis
#5
JOURNAL ARTICLE
H Sawada, A Wake, Y Yamasaki, Y Izumi
Allogeneic peripheral blood stem cell transplantation (Allo-PBSCT) has in recent years become an alternative to allogeneic bone marrow transplantation because it facilitates rapid hematopoietic reconstitution without an increase in the incidence of severe graft-versus-host disease (GVHD). We report on a 61-year-old man with myelodysplastic syndrome (MDS) and myelofibrosis who received an allo-PBSCT from his HLA-matched 68-year-old brother. The preparative regimen consisted of busulfan and cyclophosphamide. Cyclosporin A and methotrexate were administered for GVHD prophylaxis...
January 1999: [Rinshō Ketsueki] the Japanese Journal of Clinical Hematology
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