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Hematology
Showing posts with label Hematology. Show all posts
Showing posts with label Hematology. Show all posts
Myelodysplastic Syndromes / Myeloproliferative Disorders
What are myelodysplastic syndromes?
Myelodysplastic syndromes are clonal marrow stem-cell disorders, characterized by ineffective hemopoiesis leading to blood cytopenias, and by progression to acute myeloid leukemia in a third of patients.
Who is affected?
15% of cases occur after chemotherapy or radiotherapy for a previous cancer. The syndromes are most common in elderly people.
What is the cause?
The pathophysiology involves cytogenetic changes with or without gene mutations and widespread gene hypermethylation at advanced stages.
What are the symptoms?
Clinical manifestations result from cytopenias (anemia, infection, and bleeding).
How to make the diagnosis?
Diagnosis is based on examination of blood and bone marrow showing blood cytopenias and hypercellular marrow with dysplasia, with or without excess of blasts. Prognosis depends largely on the marrow blast percentage, number and extent of cytopenias, and cytogenetic abnormalities.
What is the treatment?
Treatment of patients with lower-risk myelodysplastic syndromes, especially for anaemia, includes growth factors, lenalidomide, and transfusions.
Treatment of higher-risk patients is with hypomethylating agents and, whenever possible, allogeneic stem-cell transplantation.
In this first video in the series, Myeloproliferative Neoplasms 2015 - Mayo Clinic, Ruben Mesa, M.D., professor and hematologist at Mayo Clinic in Arizona, discusses the treatment and management of myeloproliferative neoplasms as well as shares highlights from the 56th Annual American Society of Hematology (ASH) meeting in San Francisco, December 2014.
Here is the complete playlist:
https://www.youtube.com/playlist?list=PLSWR1ylG_6JZKr0ChD4N_8MJ3g3FnF08S
References:
Myelodysplastic syndromes : The Lancet http://buff.ly/VwiRor
Myelodysplastic syndromes are clonal marrow stem-cell disorders, characterized by ineffective hemopoiesis leading to blood cytopenias, and by progression to acute myeloid leukemia in a third of patients.
Who is affected?
15% of cases occur after chemotherapy or radiotherapy for a previous cancer. The syndromes are most common in elderly people.
What is the cause?
The pathophysiology involves cytogenetic changes with or without gene mutations and widespread gene hypermethylation at advanced stages.
What are the symptoms?
Clinical manifestations result from cytopenias (anemia, infection, and bleeding).
How to make the diagnosis?
Diagnosis is based on examination of blood and bone marrow showing blood cytopenias and hypercellular marrow with dysplasia, with or without excess of blasts. Prognosis depends largely on the marrow blast percentage, number and extent of cytopenias, and cytogenetic abnormalities.
What is the treatment?
Treatment of patients with lower-risk myelodysplastic syndromes, especially for anaemia, includes growth factors, lenalidomide, and transfusions.
Treatment of higher-risk patients is with hypomethylating agents and, whenever possible, allogeneic stem-cell transplantation.
In this first video in the series, Myeloproliferative Neoplasms 2015 - Mayo Clinic, Ruben Mesa, M.D., professor and hematologist at Mayo Clinic in Arizona, discusses the treatment and management of myeloproliferative neoplasms as well as shares highlights from the 56th Annual American Society of Hematology (ASH) meeting in San Francisco, December 2014.
Here is the complete playlist:
https://www.youtube.com/playlist?list=PLSWR1ylG_6JZKr0ChD4N_8MJ3g3FnF08S
References:
Myelodysplastic syndromes : The Lancet http://buff.ly/VwiRor
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