Myelofibrosis with myeloid metaplasia (MMM)
نویسندگان
چکیده
منابع مشابه
Myelofibrosis with myeloid metaplasia (MMM), Idiopathic myelofibrosis, Agnogenic myeloid metaplasia
MMM usually presents with fatigue, weight loss, splenomegaly with or without symptoms. Anemia and various alterations of the white blood cell and/or platelet count are frequently seen at diagnosis. Thrombocytopenia-related bleeding may occur. MMM must be distinguished from myelodysplasia with fibrosis, from acute megakayoblastic leukemia and acute myelofibrosis. As the disease progresses, incre...
متن کامل[Myelofibrosis with myeloid metaplasia].
Introduction Myelofibrosis with myeloid metaplasia (MMM) represents both agnogenic myeloid metaplasia (AMM) and the fibrotic stages of polycythemia vera (PV) and essential thrombocythemia (ET). The latter two conditions are also referred to as post polycythemic myelofibrosis (PPM) and post thrombocythemic myelofibrosis (PTM). MMM is currently classified under the broad category of chronic myelo...
متن کاملLenalidomide therapy in myelofibrosis with myeloid metaplasia.
We present results of 2 similarly designed but separate phase 2 studies involving single-agent lenalidomide (CC-5013, Revlimid) in a total of 68 patients with symptomatic myelofibrosis with myeloid metaplasia (MMM). Protocol treatment consisted of oral lenalidomide at 10 mg/d (5 mg/d if baseline platelet count < 100 x 10(9)/L) for 3 to 4 months with a plan to continue treatment for either 3 or ...
متن کاملExperimental Induction of Myelofibrosis with Myeloid Metaplasia
A LTHOUGH myelofibrosis with myeloid metaplasia ( MMM ) was first described nearly one hundred years ago, the etiology of this disturbance remains uncertain.1 Two interpretations have been offered: first, that there is a primary insult to bone marrow resulting in necrosis and necrobiosis followed by a reparative stage of fibrosis of marrow and compensatory cxtramedullary hematopoiesis in the li...
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ژورنال
عنوان ژورنال: Atlas of Genetics and Cytogenetics in Oncology and Haematology
سال: 2010
ISSN: 1768-3262
DOI: 10.4267/2042/32101