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Differential diagnosis of myelofibrosis based on WHO 2008 criteria: acute panmyelosis with myelofibrosis, acute megakaryoblastic leukemia with myelofibrosis, primary myelofibrosis and myelodysplastic syndrome with myelofibrosis.
Bae, E; Park, C-J; Cho, Y-U; Seo, E-J; Chi, H-S; Jang, S; Lee, K-H; Lee, J-H; Lee, J-H; Suh, J-J; Im, H-J.
Afiliación
  • Bae E; Department of Laboratory Medicine, VHS Medical Center, Seoul, South Korea; Department of Laboratory Medicine, College of Medicine and Asan Medical Center, University of Ulsan, Seoul, South Korea.
Int J Lab Hematol ; 35(6): 629-36, 2013 Dec.
Article en En | MEDLINE | ID: mdl-23693053
INTRODUCTION: The aim of this study was to characterize clinicopathological features of acute panmyelosis with myelofibrosis (APMF), acute megakaryoblastic leukemia with myelofibrosis (AMKL-MF), primary myelofibrosis (PMF) and myelodysplastic syndrome with myelofibrosis (MDS-MF) in order to provide the keys to the differential diagnosis of bone marrow (BM) fibrosis. METHODS: We compared age, gender, splenomegaly, serum lactate dehydrogenase level, blood cell counts, blast counts in peripheral blood (PB) and BM, megakaryocyte counts, BM cellularity, dysplasia, and the karyotypes of patients with APMF (n = 6), AMKL-MF (n = 7), PMF (n = 44), and MDS-MF (n = 44). RESULTS: APMF showed hyperplasia of all three lineages, increase in megakaryocyte count with dysplasia and frequent abnormal karyotypes. AMKL-MF was associated with elevated BM blast counts, decreased BM megakaryocyte count with rare megakaryocytic dysplasia and chromosome 21 abnormality. PMF patients displayed splenomegaly, rare blasts in PB/BM, and JAK2 V617F mutation. MDS-MF patients showed pancytopenia, dysplasia in all three lineages and recurrent chromosomal abnormalities involving chromosome 5,7,12, and 17. CONCLUSIONS: Although differential diagnosis among APMF, AMKL-MF, PMF, and MDS-MF is very challenging due to the overlapping clinical and morphological features, meticulous investigation of the patient with respect to splenomegaly, blood cell count, PB and BM findings, and karyotype will serve as a guide to correct diagnosis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Leucemia Megacarioblástica Aguda / Mielofibrosis Primaria Tipo de estudio: Diagnostic_studies Límite: Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Int J Lab Hematol Asunto de la revista: HEMATOLOGIA Año: 2013 Tipo del documento: Article País de afiliación: Corea del Sur Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Leucemia Megacarioblástica Aguda / Mielofibrosis Primaria Tipo de estudio: Diagnostic_studies Límite: Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Int J Lab Hematol Asunto de la revista: HEMATOLOGIA Año: 2013 Tipo del documento: Article País de afiliación: Corea del Sur Pais de publicación: Reino Unido