Case Report
Ann Hematol Oncol. 2017; 4(1): 1128.
Detection of Pleural Fluid Involvement by Flow Cytometry Method in a Patient with Acute Myeloid Leukemia
Keklik M1*, Kalan U2, Camlica D3 and Keklik E4
1Department of Hematology, Kayseri Education and Research Hospital, Turkey
2Department of Internal Medicine, Kayseri Education and Research Hospital, Turkey
3Flow Cytometry Unit, Erciyes University, Turkey
4Department of Physiology, Erciyes University, Turkey
*Corresponding author: Muzaffer Keklik, Department of Hematology, Kayseri Education and Research Hospital, Turkey
Received: December 16, 2016; Accepted: January 24, 2017; Published: January 27, 2017
Abstract
Acute leukaemias rarely present with or develop pleural effusion during their clinical course. Flow Cytometry (FC) is a potentially useful diagnostic tool for clinical practice. We report a case in which pleural effusion of an acute myeloid leukaemia (AML) was confirmed as pleural fluid involvement by FC method. A 27-years old female presented with fever and shortness of breath. On thorax CT, pleural effusion was detected in both hemithorax. Peripheral blood and pleural fluid FC was performed: CD4 (+), HLA DR (+), CD34 (+), CD33 (+), CD117 (+), CD38 (+), CD11b (+) and MPO (+) were found and these findings were considered as consistent with AML and pleural involvement. Flow cytometry is a potentially useful diagnostic tool for clinical practice and it is a convenient method which has an important role in detection of AML in patients with pleural effusion.
Keywords: Acute myeloid leukemia; Flow cytometry; Pleural effusion
Introduction
Acute myeloid leukemia (AML) is a hematologic malignancy that carries a poor prognosis in adults. Pleural effusion in patients with AML is a rare occurrence. After a thorough search of the literature, only few cases/research articles have been found [1-3]. Recently, flow cytometry (FC) has increasingly become important in the diagnosis, prognostication and follow-up of AML [4-6]. In this study, we presented an adult AML case, in which pleural fluid involvement was detected by FC evaluation.
Case Presentation
A 27-years old female presented to emergency department with fever and shortness of breath lasting for 3-5 days. She was conscious with vital signs as follows: body temperature 38.3°C, heart rate 100 beats per minute; blood pressure 110/60 mmHg. Breath sounds were bilaterally fainted at basal regions of lung. On chest radiography, pleural effusion was observed. On thorax CT, pleural fluid was detected in both hemithorax (Figure 1). The following findings were detected in peripheral blood analysis: hemoglobin (Hb): 11.4 g/L (13–16 g/L); white blood cells (WBC): 76x109/L, (5.8–10.8x109/L); platelet count:145x109/L (150–400x109/L). Blast cells were observed in the peripheral blood smear. A pleural tap was performed, which revealed serofibrinous fluid with a protein level of 6.2 g/dL, Hb: 0 g/ L, red blood cell: 0.01 cells/lL, and WBC: 5.5x109/L. FC evaluation of peripheral blood and pleural fluid was performed by using FACS Calibur flow cytometer (Becton–Dickinson, Erembodegem, Belgium). CD4 (+), HLA DR (+), CD34 (+), CD33 (+), CD117 (+), CD38 (+), CD11b (+) and MPO (+) were detected in myeloid series. CD4:CD8 ratio was 38:66. Figure 2 shows these findings of FC in the pleural fluid. These findings were considered as consistent with pleural involvement of AML. Galactomannan, tuberculosis and viral evaluations of pleural fluid were found to be negative. Also, bacterial and mycobacterial culture tests were reported as negative. Diagnosis of AML was confirmed on bone marrow aspiration. Shortness of breath was relieved in patient after removing 300 cc fluids by pleural tap. For the patient a parenteral induction chemotherapy protocol consisting of cytarabine and daunorubicin was scheduled. However, the patient developed progression of disease and she died of sepsis on the 20th hospital day.
Figure 1: Axial section of a CT of the thorax showing bilateral pleural effusion.
Figure 2: Findings of flowcytometry in pleural fluid.
Discussion
Acute leukaemias rarely present with or are accompanied by pleural fluid involvement. Possible causes of pleural effusion include extramedullary proliferation of a quiescent leukaemic clone with metastasis to the bone marrow, infections, other solid tumours, and complication of chemotherapy [7]. In our case, resistant or progressive disease might be the possible aetiology. In some patients, the pleural effusion responds to treatment, whereas the resistant or the relapsing patients may necessitate a pleurodesis [8,9]. However, according to the literature, presence of pleural effusion may be a poor prognostic factor, as most cases sooner succumb to disease [10-12]. Likewise our patient died a short time due to the progression. The clinician should be alert for any signs of pleural effusion in AML patients during the treatment.
Flow cytometry is an effective method for the characterization of malignant cells in effusion specimens in both the diagnostic and research settings, and this method is comparable to immunohistochemistry in terms of sensitivity and specificity, with the additional advantage of providing quantitative data [13-15]. In our case, AML diagnosis and pleural involvement were supported by FC analysis in both peripheral blood and pleural fluid.
In conclusion, in leukaemic patients, FC is frequently used as an ancillary technique for the diagnosis of hematological malignancies and it has become the most important method for diagnosis of AML. Also, it is a method than can contribute in management of malignancies as it is widely available, which can be used in analysis of all other body fluids as well as peripheral blood and bone marrow.
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