Peripheral eosinophilia and eosinophilic bronchopneumopathy in a dog with chronic lymphocytic leukaemia

2020 ◽  
Vol 8 (2) ◽  
pp. e000961
Author(s):  
Cecilia Alexandra Stilwell ◽  
Jessica Florey

An eight-year-old, male neutered, crossbreed dog presented for evaluation of exercise intolerance, tachypnoea and cough. Initial haematology revealed moderate lymphocytosis (8.58 x 109/l, reference interval (RI) 1.0–4.8) and eosinophilia (2.74 x 109/l, RI 0.1–1.2). Thoracic radiographs revealed a generalised interstitial pattern with several ill-defined nodules. Cytology of the nodules identified a mixed inflammatory population consisting of 60 per cent eosinophils. In the absence of an underlying cause, a diagnosis of eosinophilic bronchopneumopathy (EBP) was made. Five weeks after the introduction of prednisolone (2 mg/kg/day), repeated haematology revealed persistent lymphocytosis (6.89 x 109/l). Blood flow cytometry was consistent with chronic lymphocytic leukaemia (CLL). Chlorambucil (6 mg/m2/day) was introduced and the haematological abnormalities and clinical signs resolved. The dog was euthanased 15 months after diagnosis due to acute clinical deterioration. To the authors’ knowledge this is the first report of concurrent eosinophilia and EBP in a dog with CLL. The possibility of a paraneoplastic peripheral eosinophilia and EBP was considered.

2003 ◽  
Vol 120 (6) ◽  
pp. 1017-1025 ◽  
Author(s):  
Eric D. Hsi ◽  
Kenneth J. Kopecky ◽  
Frederick R. Appelbaum ◽  
David Boldt ◽  
Tom Frey ◽  
...  

Methods ◽  
2018 ◽  
Vol 134-135 ◽  
pp. 32-40 ◽  
Author(s):  
Henry Hui ◽  
Kathryn A. Fuller ◽  
Hun Chuah ◽  
James Liang ◽  
Hasib Sidiqi ◽  
...  

2018 ◽  
Vol 463 ◽  
pp. 97-104
Author(s):  
Chia Sharpe ◽  
Joanne Davis ◽  
Kylie Mason ◽  
Constantine Tam ◽  
David Ritchie ◽  
...  

2004 ◽  
Vol 127 (4) ◽  
pp. 425-428 ◽  
Author(s):  
A. Carter ◽  
K. Lin ◽  
P. D. Sherrington ◽  
A. R. Pettitt

Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 4685-4685
Author(s):  
Catherine Wiseman ◽  
Jerome Giustiniani ◽  
Lene Mikkelsen ◽  
Marion Macey ◽  
Lindsey Goff ◽  
...  

Abstract Background: A common diagnostic feature of chronic lymphocytic leukaemia (CLL) is the weak surface immunoglobulin (sIg) expression of the IgM/D isotypes. The occurrence of sIgG is believed to be an atypical finding in CLL. Aims: To demonstrate that sIgG expression is a real and not artefactual by molecular and functional assays. Methods: 194 unselected, consecutive cases of CLL were analysed during routine diagnostic testing for sIgG and sIgM. Flow cytometry was performed using fresh whole blood and red cell lysis (Pharmalyse solution, BD). For confirmation of these results and demonstration of functionality, we used 4-colour flow cytometry, PCR for mRNA detection, proliferation assay (3H incorporation), and calcium flux assay. Results: 23% (44/194) of all CLL cases displayed sIgG, with 39 being sIgG+ alone. PCR results showed a distinct band indicating the presence of mRNA for IgG. Four-colour flow cytometry identified single cells that co-expressed CD19/CD160/sIgG and ruled out sIgM expression. In vitro proliferation assays demonstrated that sIgG is functional when triggered by F(Ab’)2 fragments specific for sIgG isotype. The strength of the signal in one case after stimulation via sIgG led to a 3.5-fold increase in cellular proliferation. Calcium flux assays also demonstrated that the IgG isotype was functional, one case showing a 50% increase in fluorescence intensity after stimulation via sIgG. Discussion: 23% of CLL cases have sIgG expression. In addition to a high frequency of sIgG expression, this study has shown sIgG to be capable of signalling. If antigen-drive is important in CLL, an IgG B-cell receptor should have higher affinity for a putative antigen, which potentially would be a poor prognostic feature. However, such cases would also be expected to show mutated VH genes, indicating a better prognosis. Further study is required to elucidate the pathological significance of sIgG expression and its role in CLL.


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