Home | Volume 36 | Article number 286

Case report

COVID-19 and fortuitous discovery of chronic lymphocytic leukemia: biological findings and therapeutic challenges

COVID-19 and fortuitous discovery of chronic lymphocytic leukemia: biological findings and therapeutic challenges

Boubaker Charra1, Ayman Ellouadghiri1,&, Abdellah Magramane1, Touda Kebbou2, Kenza Damaan1, Abdeljabbar Maghfour1, Kamal Seddiki1, Hanane Ezzouine1


1Department of Anesthesiology and Intensive Care, Ibn Rochd University Hospital of Casablanca, Hassan II University, Casablanca, Morocco, 2Department of Radiology, Ibn Rochd University Hospital of Casablanca, Hassan II University, Casablanca, Morocco



&Corresponding author
Ayman Ellouadghiri, Department of Anesthesiology and Intensive Care, Ibn Rochd University Hospital of Casablanca, Hassan II University, Casablanca, Morocco




With the major spread of SARS-COV-2 around the world, its association with various pathologies has been reported. However, hemopathy has rarely been revealed during a coronavirus infection. The authors of this article aim to emphasize the diagnostic and therapeutic challenges faced while treating COVID/hemopathy patients.



Introduction    Down

Since December 2019, at the beginning of the outbreak in Wuhan China, SARS-COV-2 has been a one the biggest challenges public health has faced. As of today, over 7.8 million people have been infected and we deplore more than 450,000 deaths. Immunodeficient individuals are considered at high risk of developing severe forms of COVID-19. The association COVID-19 haemopathy is more frequent nowadays and is considered as a real challenge for physicians. The authors report the case of fortuitous discovery of chronic lymphocytic leukemia in a COVID-19 patient, emphasizing the difficulties of therapeutic care.



Patient and observation Up    Down

A 76-year-old male, with a history of colon cancer treated in 2013 (surgery), admitted in the intensive care unit for SARS-CoV-2 pneumonia. The patient has reported a stay in an endemic country 21 days before the admission. The main symptoms were dry cough, 40°C fever, multiples adenopathies and diarrhea. The patient´s state worsened and complicated by respiratory distress leading to a transfer to intensive care unit. A PCR test was conducted and came back positive. Chest CT scan showed bilateral ground glass opacities with consolidation (Figure 1). During his admission, the patient was conscious, GCS at 15/15, polypneic at 30 cycles/min, SpO2 of 85% at breathing room air with intercostal retraction, stable hemodynamics: BP 140/75mmHg, HR at 90bpm and 39°C fever. EKG showed normal sinus rhythm, fixed duration of PR interval, QTc at 475. Transthoracic echocardiography was normal. Arterial blood gas showed pH at 7.46, PaCO2 at 48mmHg, HCO3- at 26mmol/L, PaO2 at 131mmHg, PaO2/FiO2 ratio at 257.


Lab tests conducted at D1 of admission, revealed elevated WBC at 140020el/mm3 and lymphocytes 129660el/mm3 (vs 154000el/mm3 at D7), low hemoglobin at 8.9g/dL, platelets at 464000el/mm3, PT at 64%, fibrinogen at 6.77g/L, CRP at 130mg/L, BNP at 249pcg/L, PCT at 0.017μg/L, LDH at 331UI/L, ferritin at 563μg/L, troponin at 8.2ng/L. Blood smear showed small lymphocytes with rounded nucleus and reduced cytoplasm. Immunophenotyping of peripheral blood confirmed the presence of B-cell population; expressing one light chain immunoglobulin. Our therapeutic care was based on four daily noninvasive ventilation (NIV) sessions, hydroxychloroquine (200mg, twice a day), azythromycin (500mg per day), ceftriaxon (2g per day) and moxifloxacin (400mg, twice a day). The patient also received preventive dose of human immunoglobulins (0.5g/kg single dose), anti-coagulation, PPI, vitamin C, vitamin D and zinc. The patient´s respiratory status worsened leading to intubation and mechanical ventilation. Severe ARDS followed and 10 days after his admission, the patient expired.


Ethical approval: informed consent was obtained from the patient´s family for publication of this case.



Discussion Up    Down

Chronic lymphocytic leukemia (CLL) is the most frequent leukemia during adulthood. Eighty percent of the patients are asymptomatic at the moment of the diagnosis and 30% will never receive a treatment [1]. CLL is characterized with a clonal proliferation and accumulation of mature B cells, usually CD5 positive, in the bloodstream, bone marrow, lymph nodes and spleen [2]. The diagnosis of CLL is based on the presence of at least 5000 B-cell lymphocytes/μL in peripheral blood stream for at least three months. Clonality of circulating B cells must be confirmed by flow cytometry. The abnormal cells found at a blood smear test are typically mature small lymphocytes with a cytoplasmic border and dense nucleus deprived of nucleoli with partially aggregated chromatin [2, 3]. Treatment is based on immunochemotherapy (Table 1) for 90% of the patients with no genetic abnormalities associated with chemo resistance [4, 5]. The use of new therapies cibling different pathways is more frequent nowadays and could become an alternative to chemotherapy in the future. The association SARS-COV-2/CLL is a real challenge for physicians as they both have their own specific therapies.


Individuals with a compromised immunity can have longer incubation period of the virus [6]. Our patient had an incubation period of 21 days. SARS-COV-2 induced lymphopenia is correlated with severe forms of the disease in general population [7, 8]. In our case, we have noted a significant increase of lymphocyte population after a week. This increase has been previously reported by a British study [9], however the mechanisms are still unknown. The main therapeutic challenge in this case is due to the lack of consensus regarding COVID-19 and hemopathies. The treatment should therefore be personalized. The association of intravenous human immunoglobulins is highly recommended in patients presenting repeated infections, in order to boost their immunity [10]. However, the administration of chemotherapy is still controversed, as it can worsen SARS-COV-2 immunodeficiency, lead to cardiotoxicity and aggravate the prognosis. Chemotherapy should be avoided for CLL patients presenting COVID-19 to restrain treatment-related immunodeficiency and prevent drug interactions [10].



Conclusion Up    Down

Clinical and biological symptoms of COVID-19 can be concealed due to its coexistence with malignant hemopathies such as chronic lymphocytic leukemia. Treatment should be personalized according to the patient´s immune status and comorbidities.



Competing interests Up    Down

The authors declare no competing interests.



Authors' contributions Up    Down

This case report was written by Ayman Ellouadghiri; the references were assured by Abdellah Magramane; the first review was assured by Touda Kebbou; our work was closely supervised by Pr Boubaker Charra and Hanane Ezzouine. All the authors have read and agreed to the final manuscript.



Table and figure Up    Down

Table 1: US food and drug administration-approved drugs for the treatment of chronic lymphocytic leukemia

Figure 1: chest CT scan showing bilateral ground glass opacities with consolidation



References Up    Down

  1. Jacque N, Leblond V. La leucémie lymphoïde chronique: mise au point. Presse Med. 2019;48(7-8 Pt 1):807-815. PubMed | Google Scholar

  2. Melo JV, Catovsky D, Galton DAG. The relationship between chronic lymphocytic leukaemia and prolymphocytic leukaemia IV: analysis of survival and prognostic features. Br J Haematol. 1986;63(2):377-387. PubMed | Google Scholar

  3. Hallek M. Chronic lymphocytic leukemia: 2020 update on diagnosis, risk stratification and treatment. Am J Hematol. 2019;94(11):1266-1287. PubMed | Google Scholar

  4. Parikh SA. Chronic lymphocytic leukemia treatment algorithm 2018. Blood Cancer J. 2018;8(10):93. PubMed | Google Scholar

  5. Sharma S, Rai KR. Chronic lymphocytic leukemia (CLL) treatment: so many choices, such great options. Cancer. 2019;125(9):1432-1440. PubMed | Google Scholar

  6. Jin XH, Zheng KI, Pan KH, Xie YP, Zheng MH. COVID-19 in a patient with chronic lymphocytic leukaemia. Lancet Haematol. 2020;7(4):e351-e352. PubMed | Google Scholar

  7. Verity R, Okell LC, Dorigatti I, Winskill P, Whittaker C, Imai N et al. Estimates of the severity of coronavirus disease 2019: a model-based analysis. Lancet Infect Dis. 2020;20(6):669-677. PubMed | Google Scholar

  8. Erpos E, Ntanasis-Stathopoulos I, Elalamy I, Kastritis E, Sergentanis TN, Politou M et al. Hematological findings and complications of COVID-19. Am J Hematol. 2020;95(7):834-847. PubMed | Google Scholar

  9. Paneesha S, Pratt G, Parry H, Moss P. COVID-19 infection in therapy-naive patients with B-cell chronic lymphocytic leukemia. Leuk Res. 2020;93:106366. PubMed | Google Scholar

  10. Di Ciaccio P, McCaughan G, Trotman J, Ho PJ, Cheah CY, Gangatharan S et al. Australian and New Zealand consensus statement on the management of lymphoma, chronic lymphocytic leukaemia and myeloma during the COVID-19 pandemic. Intern Med J. 2020;50(6):667-679. PubMed | Google Scholar