Ann Lab Med.  2015 Nov;35(6):651-653. 10.3343/alm.2015.35.6.651.

Straightforward Identification of Masked Polycythemia Vera Based on Proposed Revision of World Health Organization Diagnostic Criteria for BCR-ABL1-Negative Myeloproliferative Neoplasms

Affiliations
  • 1Department of Laboratory Medicine, University of Ulsan, College of Medicine and Asan Medical Center, Seoul, Korea. yucho@amc.seoul.kr

Abstract

No abstract available.


MeSH Terms

Adult
Biomarkers, Tumor/genetics
Bone Marrow/pathology
Calreticulin/genetics
Erythropoietin/blood
Female
Fusion Proteins, bcr-abl/*genetics
Hematocrit
Hemoglobins/analysis
Humans
Janus Kinase 2/genetics
Male
Middle Aged
Mutation
Myeloproliferative Disorders/*diagnosis/genetics
Polycythemia Vera/*diagnosis/genetics
Receptors, Thrombopoietin/genetics
Thrombocythemia, Essential/diagnosis
World Health Organization
Biomarkers, Tumor
Calreticulin
Erythropoietin
Fusion Proteins, bcr-abl
Hemoglobins
Janus Kinase 2
Receptors, Thrombopoietin

Figure

  • Fig. 1 Bone marrow histomorphology of essential thrombocythemia (ET) and masked polycythemia vera (PV). (A) Bone marrow morphology of ET shows normocellular marrow with an increased number of large and mature megakaryocytes. Note the hyperlobulated megakaryocytes without significant pleomorphism (bone marrow biopsy, hematoxylin and eosin [H&E] stain, ×200). (B) Bone marrow morphology of masked PV (patient 1) shows a trilineage proliferation. Note the higher cellularity compared with that in (A) and an increased number of megakaryocytes displaying cytologic pleomorphism with mild atypia (bone marrow biopsy, H&E stain, ×200).


Reference

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