Abnormal Eosinophils With Large, Distinctly Basophilic Granules (Harlequin Cells) on Peripheral Blood Smear: A Clue for Diagnosing Chronic Myeloid Leukemia.
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.
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.
- Abstract
3
- 10.1182/blood.v108.11.118.118
- Nov 16, 2006
- Blood
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
31
- 10.2353/jmoldx.2006.050064
- May 1, 2006
- The Journal of Molecular Diagnostics
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
7
- 10.1046/j.1365-2141.1999.14354210.x
- Jun 1, 1999
- British Journal of Haematology
Myelodysplasia and myeloproliferative disorders in childhood: an update
- Research Article
25
- 10.1046/j.1365-2141.2001.02994.x
- Sep 1, 2001
- British Journal of Haematology
Pitfalls in the diagnosis of childhood leukaemia.
- Research Article
38
- 10.1046/j.1365-2141.2002.03469.x
- May 19, 2002
- British journal of haematology
Receptor tyrosine kinase mutations in myeloid neoplasms.
- Abstract
3
- 10.1182/blood-2024-208963
- Nov 5, 2024
- Blood
Associations between Myeloid Malignancies and Osteoporosis Using Real-World Data from the Trinetx Database
- Research Article
48
- 10.4065/81.4.553
- Apr 1, 2006
- Mayo Clinic Proceedings
Atypical Myeloproliferative Disorders: Diagnosis and Management
- Research Article
95
- 10.1046/j.1365-2141.2002.03234.x
- Jan 1, 2002
- British Journal of Haematology
CHRONIC NEUTROPHILIC LEUKAEMIA: A DISTINCT CLINICAL ENTITY?
- Research Article
218
- 10.1046/j.1365-2141.2003.04195.x
- Apr 1, 2003
- British Journal of Haematology
The eosinophilias, including the idiopathic hypereosinophilic syndrome.
- Research Article
26
- 10.3324/haematol.2014.109199
- Jul 11, 2014
- Haematologica
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
7
- 10.1016/j.beha.2005.07.014
- Jun 14, 2006
- Best Practice & Research Clinical Haematology
Classic and atypical myeloproliferative disorders
- Abstract
- 10.1182/blood.v126.23.4444.4444
- Dec 3, 2015
- Blood
Are Chronic Myeloproliferative Neoplasms Associated with Age-Related Macular Degeneration?
- Abstract
6
- 10.1182/blood.v110.11.680.680
- Nov 16, 2007
- Blood
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
- Nov 2, 2023
- Blood
Understanding Thrombosis and Hemorrhage in Myeloproliferative Neoplasms through a Nationwide Study
- Abstract
1
- 10.1182/blood.v116.21.3078.3078
- Nov 19, 2010
- Blood
Familial Chronic Myeloproliferative Neoplasms