Related Experiment Video
Updated: Aug 25, 2026

Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome
Published on: October 3, 2018
[Myelodysplastic syndromes--an overview for the practitioner]
1Hämatologisches Zentrallabor, Inselspital, Bern. max.solenthaler@insel.ch
Abstract:
Myelodysplastic syndromes (MDS) comprise a heterogeneous group of hematological diseases deriving from a clonally expanded precursor bone marrow cell. MDS are characterized by ineffective hematopoiesis, peripheral cytopenias of various degrees and increased risk for transformation into acute myeloid leukemia. The incidence is highest in elderly people. Diagnosis is based on morphology, exclusion of reactive causes of dyshematopoiesis and cytogenetics/FISH. Allogeneic stem cell transplantation, the only curative therapy so far, is not feasible for most of the patients. Other therapeutic options include supportive therapy such as blood transfusions and antibiotics, hematopoietic growth factors (rHuEPO, G-CSF), immunomodulating agents and chemotherapy. It is important to install iron chelation therapy in cases with long term transfusion dependency.
Insights
Myelodysplastic syndromes (MDS) are bone marrow disorders affecting older adults, characterized by ineffective blood cell production and a risk of developing into leukemia. Treatment options are limited, with stem cell transplant being the only cure, while other therapies focus on symptom management.
Area of Science:
- Hematology
- Oncology
- Bone Marrow Disorders
Context:
- Myelodysplastic syndromes (MDS) are a group of clonal bone marrow diseases.
- Characterized by ineffective hematopoiesis, peripheral cytopenias, and a high risk of transformation to acute myeloid leukemia.
- Primarily affect elderly individuals, posing diagnostic and therapeutic challenges.
Purpose:
- To provide a comprehensive overview of myelodysplastic syndromes.
- To highlight diagnostic criteria including morphology, exclusion of reactive causes, and cytogenetics/FISH.
- To outline current therapeutic strategies for MDS patients.
Summary:
- MDS involves a clonal expansion of abnormal bone marrow precursor cells, leading to insufficient blood cell production.
- Diagnosis relies on morphological assessment, excluding other causes, and cytogenetic analysis.
- Curative treatment like allogeneic stem cell transplantation is limited; supportive care (transfusions, growth factors, iron chelation) and other therapies (immunomodulation, chemotherapy) are crucial.
Impact:
- Improved understanding of MDS heterogeneity and pathogenesis.
- Guidance for accurate diagnosis and risk stratification.
- Informed therapeutic decision-making for MDS management, emphasizing supportive care and tailored treatments.
Related Concept Videos
Cellular Adaptation IV: Dysplasia and Metaplasia
Satellite Stem Cells and Muscular Dystrophy
Disorders of the Skeletal Muscle
Musculoskeletal disorders
Musculoskeletal disorders involve injuries and conditions affecting the skeletal muscles and associated connective tissues. These disorders can arise from acute biomechanical stresses or chronic overuse and can occur across different age groups. Common injuries include sprains, fractures, and muscular strains, often resulting from...
Bone Marrow Sampling and Transplants
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy the...
Parkinson's Disease: Overview
Disorders of Erythrocytes
Erythrocyte disorders can be broadly categorized into two main types: anemic and polycythemic conditions.
A low oxygen-carrying capacity of the blood due to the loss, lower production, or destruction of erythrocytes is termed anemia. Hemorrhagic anemia, for example, occurs when bleeding from an external wound or internal ulcer reduces erythrocyte counts.
On the other...

