Myelodysplastic syndrome with fibrosis and complex karyotype arising in a patient with essential thrombocythaemia
- Author:
Nor Ainiza Mansor
1
Author Information
1. Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre
- Collective Name:Nor Ainiza Mansor; Nurasyikin Yusof; Yee-Loong Tang; Azlin Ithnin; Raja Zahratul Azma; Nor Rafeah Tumian and Salwati Shuib
- Publication Type:Case Reports
- Keywords:
Myeloproliferative neoplasm;
essential thrombocythaemia;
myelodysplastic syndrome;
complex karyotype
- MeSH:
myelodysplastic syndrome
- From:The Malaysian Journal of Pathology
2018;40(2):191-197
- CountryMalaysia
- Language:English
-
Abstract:
Introduction: Essential thrombocythaemia (ET) is a chronic myeloproliferative neoplasm (MPN) characterised by persistent thombocytosis. It is an indolent disorder but transformation to myelofibrosis (MF), acute myeloid leukaemia (AML) or myelodyplastic syndrome (MDS) has been reported. Case Report: We described a patient with ET whose disease evolved into MDS with fibrosis and complex karyotype after 15 years of stable disease. She was asymptomatic and was on hydroxyurea (HU) treatment until recently when she presented with worsening anaemia. Physical examination showed mild splenomegaly. Full blood picture showed leukoerythroblastic picture with presence of 3% circulating blasts and background of dysplastic features such as hypogranular cytoplasm and nuclear hyposegmentation of neutrophils. The bone marrow aspiration was haemodiluted but revealed presence of 6% blast cells, trilineage dysplasia and predominant erythroid precursors (60%). Trephine biopsy showed no excess of blast cells and normal quantity of erythroid precursors, but there was increased in fibrosis (WHO grade 2) and presence of dysmegakaryopoeisis such as nuclear hypolobation, multinucleation and micromegakaryocytes. Cytogenetic study showed complex karyotype; monosomy of chromosome 2, chromosome 5, chromosome 18 and presence of a marker chromosome (42~44, XX,-2,-5,-18,+mar). Fluorescence in situ hybridisation (FISH) showed 5q deletion (CSF1R and EGR1). Conclusion: The findings were consistent with transformation of ET to MDS with fibrosis and complex karyotype. ET progression to MDS is considered rare. The presence of complex karyotype and fibrosis in MDS are associated with unfavourable outcome.
- Full text:5.2018my0967.pdf
