نتایج جستجو برای: raeb

تعداد نتایج: 214  

Journal: :Leukemia research 2010
Rami S Komrokji Gina M Matacia-Murphy Najla H Al Ali M S Beg Malek M Safa Dana E Rollison Alan F List

PURPOSE Epidemiology and outcome of myelodysplastic syndromes (MDS) in the United States is not well recognized. MDS became reportable to the Surveillance, Epidemiology, and End Results Program (SEER) in 2001. We report first study of MDS among large population in the Veteran Affair system. PATIENTS AND METHODS There are approximately 127 VA Medical Centers diagnosing and/or treating Cancer p...

2013
Tathagata Chatterjee Srishti Gupta Ajay Sharma Sanjeevan Sharma Devika Gupta

One case of acute panmyelosis with myelofibrosis (APMF) is here reported. A 45 year old male presented with abrupt onset of rapidly progressing low backache, weakness and pancytopenia. On examination there was no organomegaly. Peripheral blood examination revealed normocytic normochromic red blood cells with 10% circulating blasts. Flowcytometric examination of peripheral blood revealed blasts ...

Journal: :Journal of clinical pathology 1983
S Martin S C Baldock A T Ghoneim J A Child

Neutrophil function studies have been carried out in a series of 44 patients with primary myelodysplastic syndromes (MDS). In vitro tests of phagocytosis and killing of Candida guilliermondii and Staphylococcus aureus identified 13 patients with abnormal neutrophil function at presentation and a further 10 who developed abnormalities during the course of their disease. The incidence of defectiv...

2012
Torrey M Parker Mylene Bassal Robert Klaassen Sarah M Nikkel Michaela Cada Donna L Johnston

Myelodysplastic Syndrome (MDS) is a problem of ineffective hematopoesis, due to a clonal disorder of the hematopoetic stem cells. MDS is rare in children and considered premalignant as it often progresses to leukemia over time. There are known inherited predisposing conditions to MDS that have been reported in the literature. We describe the case of a 12-year-old girl with multiple dysmorphic f...

2003
Maarten van der Keur Esther de Graaff

To determine the clonal nature of hematopoiesis and to assess lineage involvement in patients with myelodysplastic syndromes (MDS), we used restriction fragment length polymorphisms of the X-linked genes phosphoglycerate kinase (PGK,) and hypoxanthine phosphoribosyltransferase (HPRT) and the X-linked probe M27P. Eleven female MDS patients heterozygousfor at least one of these probes were studie...

Journal: :Blood 2003
Mario Cazzola Rosangela Invernizzi Gaetano Bergamaschi Sonia Levi Barbara Corsi Erica Travaglino Valeria Rolandi Giorgio Biasiotto Jim Drysdale Paolo Arosio

The sideroblastic anemias are characterized by ring sideroblasts, that is, red cell precursors with mitochondrial iron accumulation. We therefore studied the expression of mitochondrial ferritin (MtF) in these conditions. Erythroid cells from 13 patients with refractory anemia with ring sideroblasts (RARS) and 3 patients with X-linked sideroblastic anemia (XLSA) were analyzed for the distributi...

2015
Şinasi Özsoylu

1. Patnaik MM, Parikh SA, Hanson CA, Tefferi A. Chronic myelomonocytic leukaemia: a concise clinical and pathophysiological review. Br J Haematol 2014;165:273-286. 2. Xu Z, Shier L. Auer rods in a patient with chronic myelomonocytic leukemia type 2. Blood 2014;124:3828. 3. Willis MS, McKenna RW, Peterson LC, Coad JE, Kroft SH. Low blast count myeloid disorders with Auer rods: a clinicopathologi...

2012
Sun Young Cho Tae Sung Park

which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. A 57-year-old man was diagnosed with myelodysplastic syndrome (refractory anemia with excess blasts [RAEB]-2) in April, 2007. As leukopenia gradually aggravated along with pneumonia overlap, we suspended the 12 th cycle of azacitidine therapy and administere...

Journal: :American journal of blood research 2015
Zaher K Otrock Nabil Chamseddine Ziad M Salem Tarek Wehbe Mouna Al-Ayoubi Moussa Dhaini Joseph Kattan Walid Mokaddem Therese Abi Nasr Oussama Jradi Fadi S Farhat Mahmoud Wehbe Mohammad H Haidar Mohamed A Kharfan-Dabaja Nizar Bitar Mirna El Hajj Adel M Kadri Francois G Kamar Hanan Yassine Hassan Khodr Ali T Taher Noha Hakime Rami Ar Mahfouz Wassim Serhal Ali Bazarbachi Hussein Z Farhat

Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematopoietic disorders characterized by peripheral blood cytopenias, blood cells dysplasia, and increased risk for progression to acute leukemia.Physicians should be vigilant in diagnosing MDS and should be aware of the contemporary therapies that are always in progress. Most of the data on MDS epidemiology and management come...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Wendy W Pang John V Pluvinage Elizabeth A Price Kunju Sridhar Daniel A Arber Peter L Greenberg Stanley L Schrier Christopher Y Park Irving L Weissman

Myelodysplastic syndromes (MDS) are a group of disorders characterized by variable cytopenias and ineffective hematopoiesis. Hematopoietic stem cells (HSCs) and myeloid progenitors in MDS have not been extensively characterized. We transplanted purified human HSCs from MDS samples into immunodeficient mice and show that HSCs are the disease-initiating cells in MDS. We identify a recurrent loss ...

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