Table 2

Diagnostic studies

TestComment
All patients with HES  
 Complete blood count*  
 Routine chemistries, including liver function tests*  
 Quantitative serum immunoglobulin levels, including IgE  
 Serum troponin*, echocardiogram If abnormal, cardiac MRI should be considered as this may show characteristic features of eosinophilic involvement; tissue involvement may be patchy limiting the utility of biopsy 
 Pulmonary function tests*  
 Chest/abdomen/pelvis CT* To assess for splenomegaly, lymphadenopathy, and occult neoplasms 
 Bone marrow biopsy, including cytogenetics* Recommended in all patients with AEC > 5.0 × 109/L and features of M-HES or L-HES. Should be considered in other patients 
 Biopsies of affected tissues (if possible)*  
 Other testing as indicated by history, signs, and symptoms Including parasitic serologies, anti-neutrophil cytoplasmic antibodies, and HIV 
 Serum tryptase and B12 levels  
FIP1L1/PDGFRA analysis by FISH or RT-PCR Testing of peripheral blood is sufficient 
 T- and B-cell receptor rearrangement studies  
 Lymphocyte phenotyping by flow cytometry* At a minimum CD3, CD4, and CD8 and CD19 or 20 staining should be performed to assess for aberrant CD3CD4+, CD3+CD4+CD8+, and CD3+CD4CD8 populations and B-cell lymphoproliferative disorders 
Patients with features of M-HES  
 Additional testing for BCR-ABL1, PDGFRB, JAK2, FGFR1, and KIT mutations by PCR, FISH, or other methods, as appropriate Testing should be guided by bone marrow findings 
Patients with evidence of L-HES  
 Consider PET scan,* lymph node biopsy*  
 EBV viral load  
TestComment
All patients with HES  
 Complete blood count*  
 Routine chemistries, including liver function tests*  
 Quantitative serum immunoglobulin levels, including IgE  
 Serum troponin*, echocardiogram If abnormal, cardiac MRI should be considered as this may show characteristic features of eosinophilic involvement; tissue involvement may be patchy limiting the utility of biopsy 
 Pulmonary function tests*  
 Chest/abdomen/pelvis CT* To assess for splenomegaly, lymphadenopathy, and occult neoplasms 
 Bone marrow biopsy, including cytogenetics* Recommended in all patients with AEC > 5.0 × 109/L and features of M-HES or L-HES. Should be considered in other patients 
 Biopsies of affected tissues (if possible)*  
 Other testing as indicated by history, signs, and symptoms Including parasitic serologies, anti-neutrophil cytoplasmic antibodies, and HIV 
 Serum tryptase and B12 levels  
FIP1L1/PDGFRA analysis by FISH or RT-PCR Testing of peripheral blood is sufficient 
 T- and B-cell receptor rearrangement studies  
 Lymphocyte phenotyping by flow cytometry* At a minimum CD3, CD4, and CD8 and CD19 or 20 staining should be performed to assess for aberrant CD3CD4+, CD3+CD4+CD8+, and CD3+CD4CD8 populations and B-cell lymphoproliferative disorders 
Patients with features of M-HES  
 Additional testing for BCR-ABL1, PDGFRB, JAK2, FGFR1, and KIT mutations by PCR, FISH, or other methods, as appropriate Testing should be guided by bone marrow findings 
Patients with evidence of L-HES  
 Consider PET scan,* lymph node biopsy*  
 EBV viral load  
*

Substantially affected by corticosteroid therapy.

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