Accelerate Literature Icon
Want to do a literature review? Try our new Literature Review workflow

Abnormal Eosinophils With Large, Distinctly Basophilic Granules (Harlequin Cells) on Peripheral Blood Smear: A Clue for Diagnosing Chronic Myeloid Leukemia.

  • TL;DR
  • Abstract
  • Literature Map
  • Similar Papers
TL;DR

Harlequin cells, abnormal eosinophils with large basophilic granules, were identified in 72% of CML cases and are rare in other myeloproliferative neoplasms, suggesting that their recognition on blood smears can serve as a sensitive and specific morphological marker to aid in the prompt diagnosis of CML and guide confirmatory testing.

Abstract
Translate article icon Translate Article Star icon

Chronic myeloid leukemia (CML) often presents with hematologic findings that overlap with reactive leukocytosis and other myeloproliferative neoplasms (MPNs), creating diagnostic uncertainty that may delay targeted therapy or prompt unnecessary molecular testing. Harlequin cells-abnormal eosinophils containing basophilic granules-are well described in acute myeloid leukemia (AML) with CBFB::MYH11 fusion, but their diagnostic relevance in CML has not been systematically assessed. We retrospectively reviewed 177 peripheral blood smears: 53 CML; 30 non-CML MPN and related disorders; 59 AML (including three with CBFB::MYH11 fusion); 11 eosinophilia; and 24 reactive cytosis cases. Harlequin cells were stringently defined as abnormal eosinophils containing both typical eosinophilic granules and large, distinctly basophilic (not purplish-orange) cytoplasmic granules to exclude reactive mimics. Harlequin cells were identified in 72% (38 out of 53) of CML cases, a frequency significantly higher than in non-CML MPN (10%, P < 0.01), AML without CBFB::MYH11 fusion (3.6%, P < 0.01), eosinophilia (0%), and reactive cytosis (0%) groups. They were also observed in 67% (2/3) of AML with CBFB::MYH11 fusion and in 20% (3/15) of primary myelofibrosis, but were absent in polycythemia vera, essential thrombocythemia, and chronic myelomonocytic leukemia. Strictly defined Harlequin cells were not found in any reactive condition. In the appropriate clinical context, strictly defined Harlequin cells on routine peripheral blood smears may serve as a sensitive and highly specific morphologic clue for CML. Recognition of this readily accessible feature may facilitate prompt BCR::ABL1 confirmatory testing, reduce diagnostic ambiguity, and help avoid unnecessary ancillary studies.

Similar Papers
  • Abstract
  • Cite Count Icon 3
  • 10.1182/blood.v108.11.118.118
Hypermethylation of SH2-Containing Phosphatase-1 (SHP-1) and Suppressor of Cytokine Signaling-1 and -3 (SOCS-1 and -3) in Philadelphia Negative Chronic Myeloproliferative Disorders (Ph-CMPD).
  • Nov 16, 2006
  • Blood
  • Davide Rossi + 11 more

Hypermethylation of SH2-Containing Phosphatase-1 (SHP-1) and Suppressor of Cytokine Signaling-1 and -3 (SOCS-1 and -3) in Philadelphia Negative Chronic Myeloproliferative Disorders (Ph-CMPD).

  • Research Article
  • Cite Count Icon 31
  • 10.2353/jmoldx.2006.050064
Detection of the Single Hotspot Mutation in the JH2 Pseudokinase Domain of Janus Kinase 2 in Bone Marrow Trephine Biopsies Derived from Chronic Myeloproliferative Disorders
  • May 1, 2006
  • The Journal of Molecular Diagnostics
  • Oliver Bock + 5 more

Detection of the Single Hotspot Mutation in the JH2 Pseudokinase Domain of Janus Kinase 2 in Bone Marrow Trephine Biopsies Derived from Chronic Myeloproliferative Disorders

  • Research Article
  • Cite Count Icon 7
  • 10.1046/j.1365-2141.1999.14354210.x
Myelodysplasia and myeloproliferative disorders in childhood: an update
  • Jun 1, 1999
  • British Journal of Haematology
  • Peter D Emanuel

Myelodysplasia and myeloproliferative disorders in childhood: an update

  • Research Article
  • Cite Count Icon 25
  • 10.1046/j.1365-2141.2001.02994.x
Pitfalls in the diagnosis of childhood leukaemia.
  • Sep 1, 2001
  • British Journal of Haematology
  • Judith M Chessells

Pitfalls in the diagnosis of childhood leukaemia.

  • Research Article
  • Cite Count Icon 38
  • 10.1046/j.1365-2141.2002.03469.x
Receptor tyrosine kinase mutations in myeloid neoplasms.
  • May 19, 2002
  • British journal of haematology
  • Rajeev Gupta + 2 more

Receptor tyrosine kinase mutations in myeloid neoplasms.

  • Abstract
  • Cite Count Icon 3
  • 10.1182/blood-2024-208963
Associations between Myeloid Malignancies and Osteoporosis Using Real-World Data from the Trinetx Database
  • Nov 5, 2024
  • Blood
  • Shireen J Usman + 4 more

Associations between Myeloid Malignancies and Osteoporosis Using Real-World Data from the Trinetx Database

  • Research Article
  • Cite Count Icon 48
  • 10.4065/81.4.553
Atypical Myeloproliferative Disorders: Diagnosis and Management
  • Apr 1, 2006
  • Mayo Clinic Proceedings
  • Ayalew Tefferi + 2 more

Atypical Myeloproliferative Disorders: Diagnosis and Management

  • Research Article
  • Cite Count Icon 95
  • 10.1046/j.1365-2141.2002.03234.x
CHRONIC NEUTROPHILIC LEUKAEMIA: A DISTINCT CLINICAL ENTITY?
  • Jan 1, 2002
  • British Journal of Haematology
  • John T Reilly

CHRONIC NEUTROPHILIC LEUKAEMIA: A DISTINCT CLINICAL ENTITY?

  • Research Article
  • Cite Count Icon 218
  • 10.1046/j.1365-2141.2003.04195.x
The eosinophilias, including the idiopathic hypereosinophilic syndrome.
  • Apr 1, 2003
  • British Journal of Haematology
  • Finella Brito‐Babapulle

The eosinophilias, including the idiopathic hypereosinophilic syndrome.

  • Research Article
  • Cite Count Icon 26
  • 10.3324/haematol.2014.109199
Clinical importance of different calreticulin gene mutation types in wild-type JAK2 essential thrombocythemia and myelofibrosis patients.
  • Jul 11, 2014
  • Haematologica
  • C Qiao + 6 more

The Janus kinase 2 (JAK2) V617F mutation (JAK2 V617F), JAK2 exon 12 mutations and myeloproliferative leukemia virus oncogene W515L/K mutation (MPL W515L/K) have become three major molecular diagnosis criteria for myeloproliferative neoplasms (MPNs) including polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF) from 2005. 1 However, diagnosing MPNs with non-mutated JAK2 and MPL remains a major diagnostic challenge. 2-4 6] Here, we report our data on CALR mutation in wild-type (wt) JAK2 MPN on patients. It should also be mentioned that this is undoubtedly the first report regarding CALR mutations in Chinese MPN patients.

  • Front Matter
  • Cite Count Icon 7
  • 10.1016/j.beha.2005.07.014
Classic and atypical myeloproliferative disorders
  • Jun 14, 2006
  • Best Practice & Research Clinical Haematology
  • Ayalew Tefferi

Classic and atypical myeloproliferative disorders

  • Abstract
  • 10.1182/blood.v126.23.4444.4444
Are Chronic Myeloproliferative Neoplasms Associated with Age-Related Macular Degeneration?
  • Dec 3, 2015
  • Blood
  • Marie Bak + 6 more

Are Chronic Myeloproliferative Neoplasms Associated with Age-Related Macular Degeneration?

  • Abstract
  • Cite Count Icon 6
  • 10.1182/blood.v110.11.680.680
Increased Risks of Polycythemia Vera (PV), Essential Thrombocythemia (ET), and Myelofibrosis (MF) among 24577 First-Degree Relatives of 11039 Patients with Chronic Myeloproliferative Disorders (MPD) in Sweden.
  • Nov 16, 2007
  • Blood
  • Ola Landgren + 4 more

Increased Risks of Polycythemia Vera (PV), Essential Thrombocythemia (ET), and Myelofibrosis (MF) among 24577 First-Degree Relatives of 11039 Patients with Chronic Myeloproliferative Disorders (MPD) in Sweden.

  • Research Article
  • 10.1182/blood-2023-185924
Understanding Thrombosis and Hemorrhage in Myeloproliferative Neoplasms through a Nationwide Study
  • Nov 2, 2023
  • Blood
  • Joon Young Hur + 4 more

Understanding Thrombosis and Hemorrhage in Myeloproliferative Neoplasms through a Nationwide Study

  • Abstract
  • Cite Count Icon 1
  • 10.1182/blood.v116.21.3078.3078
Familial Chronic Myeloproliferative Neoplasms
  • Nov 19, 2010
  • Blood
  • Caterina Alati + 5 more

Familial Chronic Myeloproliferative Neoplasms

Save Icon
Up Arrow
Open/Close
Notes

Save Important notes in documents

Highlight text to save as a note, or write notes directly

You can also access these Documents in Paperpal, our AI writing tool

Powered by our AI Writing Assistant