Blood Res.  2014 Jun;49(2):134-137. 10.5045/br.2014.49.2.134.

Simultaneous presentation of JAK2 V617F mutation-related essential thrombocythemia and B-cell chronic lymphocytic leukemia

Affiliations
  • 1Laboratorio di Chimica-Clinica, Ematologia e Microbiologia (Ematologia/Coagulazione), Azienda Ospedaliera "S. Antonio Abate" - Gallarate, Italy. guido.dangelo@aogallarate.it
  • 2Anatomia Patologica, Azienda Ospedaliera "S. Antonio Abate" - Gallarate, Italy.
  • 3Oncologia - Ematologia, Azienda Ospedaliera "S. Antonio Abate" - Gallarate, Italy.

Abstract

No abstract available.


MeSH Terms

Leukemia, Lymphocytic, Chronic, B-Cell*
Thrombocythemia, Essential*

Figure

  • Fig. 1 (A) Bone marrow aspirate (May-Grünwald-Giemsa, MGG) showing lymphoid hyperplasia represented by small cells with scant cytoplasm (magnification 400×); (B) Bone marrow biopsy (hematoxylin-eosin) showing lymphoid hyperplasia and simultaneous megakaryocytic hyperplasia, isolated and in groups (magnification 200×); (C) Bone marrow biopsy showing a population of small lymphoid cells that were CD5+ (magnification 200×); and (D) Bone marrow aspirate (MGG) showing large megakaryocyte with hyperlobated nucleus (magnification 1,000×).

  • Fig. 2 Pathogenetic hypothesis of the simultaneous presence of myeloid and lymphoid disease. Abbreviation: EPMH-SC, early progenitor multipotential hematopoietic stem cell.


Reference

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