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Successful treatment of acquired amegakaryocytic thrombocytopenia with cyclosporine in adult onset Still's disease
- Issue Date
- Jan-2007
- Publisher
- SPRINGER
- Keywords
- acquired amegakaryocytic thrombocytopenia; autoimmune hemolytic anemia; adult-onset Still' s disease; cyclosporine
- Citation
- RHEUMATOLOGY INTERNATIONAL, v.27, no.3, pp.295 - 298
- Indexed
- SCIE
SCOPUS
- Journal Title
- RHEUMATOLOGY INTERNATIONAL
- Volume
- 27
- Number
- 3
- Start Page
- 295
- End Page
- 298
- ISSN
- 0172-8172
- Abstract
- Acquired amegakaryocytic thrombocytopenia (AAT) is a rare disorder, characterized by severe thrombocytopenia and selective, marked decrease or absence of megakaryocytes in the bone marrow. We describe a 29-year-old female with adult onset Still's disease preceding a diagnosis of AAT and autoimmune hemolytic anemia, which was successfully treated with cyclosporine. This is the first case of AAT in a patient with adult onset Still's disease.
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Related Researcher
- Yoo, Dae Hyun
- COLLEGE OF MEDICINE (DEPARTMENT OF INTERNAL MEDICINE)