key: cord-0998983-0omrgb5g authors: Otieno, Steve Biko; Altahan, Alaa; Kaweeta, Fnu; Karri, Saradasri; Alnoor, Fnu; Johnson, Robert title: Severe Hemolysis in a COVID-19 Patient with Paroxysmal Nocturnal Hemoglobinuria date: 2021-07-13 journal: Case Rep Hematol DOI: 10.1155/2021/6619177 sha: 6495becd95164c6867beedbf0e33f82a648e2f8c doc_id: 998983 cord_uid: 0omrgb5g Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease 2019 (COVID-19), has been demonstrated to be able to activate complement, making patients with deficiency in negative complement regulation, such as paroxysmal nocturnal hemoglobinuria (PNH), particularly vulnerable to complement-mediated cell damage. We report a case of a patient who presented with fatigue, facial swelling, and upper respiratory infection (URI) symptoms and was found to have COVID-19 with laboratory tests showing severe hemolysis and pancytopenia secondary to PNH. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected more than 150 million worldwide and caused over 3 million deaths since December 2019, and these numbers continue to rise. It was declared a pandemic by the World Health Organization (WHO) on March 11, 2020. SARS-CoV-2 has been shown to be able to activate complement, making patients with a deficiency in negative complement regulation, such as paroxysmal nocturnal hemoglobinuria (PNH), particularly vulnerable to complement-mediated cell damage [1, 2] Patients with PNH have a mutation in the PIG-A gene which controls a key step in the biosynthesis of cell surface linker glycosyl-phosphatidylinositol (GPI) which tethers the negative complement regulators CD55 and CD59 to cell surfaces. e lack of the GPI linker results in the absence of these two key negative complement regulators [3] . On erythrocytes, the absence of the GPI linker results in complement-mediated hemolysis which is a common presentation of PNH. We report a case of a patient with COVID-19 who was diagnosed with PNH after she presented with fatigue, facial swelling, and URI symptoms with laboratories showing severe hemolysis and pancytopenia. e patient is a 19-year-old female with no significant past medical history who presented to the Emergency Department (ED) with left-sided facial swelling. 3 weeks prior to presentation, she developed cough, subjective fever, severe fatigue, and swelling of the gums of her left teeth. e gum swelling got worse, and she started having facial swelling. She underwent a COVID-19 test in the community prior to presentation but had not received the results at the time of presentation. e jaw swelling worsened and started draining pus despite taking amoxicillin prescribed by her dentist. She presented to the ED for further evaluation. On review of systems, she denied any history of recurrent infections, anemia, bleeding, rashes, jaundice, or thrombosis. Her only medication was amoxicillin. She denied smoking, alcohol, or illicit drug use. Family history was notable for a cousin, aunt, and grandmother with leukemia. On exam, her temperature was 37.3°C, blood pressure was 114/75, heart rate was 130, and oxygen saturation was 99% on room air. She was noted to have left face and neck swelling. Lungs were clear to auscultation bilaterally. She had no bruises, petechiae, or lymphadenopathy. e rest of her exam was unremarkable. A maxillofacial computed tomographic scan (CT) showed diffuse soft tissue edema throughout the left face without drainable fluid collection to suggest an abscess. Initial labs showed pancytopenia with a white blood cell count of 2.6 × 10 3 per microliter (reference range 4.2 × 10 3 to 10.2 × 10 3 ), an absolute neutrophil count of 1.8 × 10 3 per microliter (reference range 1.8 × 10 3 to 7.1 × 10 3 ), a hemoglobin of 2.7 grams per deciliter (reference range 11.5 to 14.8), and a platelet count of 30 × 10 3 per microliter (reference range 150 × 10 3 to 400 × 10 3 ). Other notable laboratory results were a total bilirubin level of 1. Table 1 . She received four units of packed red blood cells (pRBCs) and was started on broad-spectrum antibiotics. e patient developed a fever with a maximum temperature of 38.5°C after admission. Her COVID-19 test result returned as positive. Since the initial labs were consistent with hemolysis in the context of pancytopenia, a peripheral smear was ordered as well as flow cytometry on peripheral blood and flow cytometry for PNH. A bone marrow aspiration and core biopsy were performed. A CT chest, abdomen, and pelvis did not reveal any adenopathy and was negative for pulmonary embolism. Flow cytometry was positive for PNH ( Figure 1 ). e peripheral blood smear showed leukopenia with absolute neutropenia and thrombocytopenia. e observed neutrophils and lymphocytes were mature without significant morphological abnormality. Schistocytes were not present ( Figure 2 (a)). Bone marrow biopsy showed large areas of the marrow that were less than 10% cellular (Figure 2 (b)); however, focally, the marrow is 40-50% cellular with erythroid predominant trilineage hematopoiesis (Figure 2 (c)). Megakaryocytes were present but markedly decreased without any significant dysplasia. Few mature neutrophils were present. Blasts were not increased. Immunohistochemical stains performed with appropriate controls demonstrated numerous E-cadherin-positive erythroid precursors ( Figure 2 (d)). ere were rare CD34-positive blasts and few scattered CD3-positive T cells and CD20-positive B cells. Terminal deoxynucleotidyl transferase (TdT) stain was negative. Bone marrow aspirate showed small hypocellular spicules with erythroid predominance. Some of these erythroid precursors were binucleated and had nuclear budding or irregular nuclear contours. Neutrophil precursors were present but infrequent. Blasts were not increased. A cytogenetics study revealed normal female karyotype (46XX). No mutations were detected by targeted nextgeneration sequencing. e patient was treated with 2 doses of 600 milligrams of the C5 complement inhibitor eculizumab as inpatient with improvement in counts. She was seen in clinic after discharge, and she received 2700 mg of the longer acting C5 complement inhibitor ravulizumab a week after the last dose of eculizumab and a 3300 mg dose 2 weeks later. Her last blood counts showed a white blood cell count of 4 × 10 3 per microliter, absolute neutrophil count of 2.2 × 10 3 per microliter, hemoglobin level of 7.8 grams deciliter, and platelet count of 50 × 10 3 per microliter. Haptoglobin was 30, and LDH was normal. In the subsequent visits, the patient's pancytopenia persisted, and she was referred to a transplant center for evaluation. e patient in this case presented with a tooth infection, severe fatigue, and upper respiratory infection symptoms with work-up revealing severe hemolysis in the setting of COVID-19. Flow cytometry analysis of peripheral blood revealed a PNH clone. PNH is characterized by severe fatigue, smooth muscle dystonias, hemolysis, and thrombosis [3] . e patient did not have a history of hemolysis or thrombosis. Iron studies were not consistent with a chronic blood loss process as the patient had a normal mean corpuscular volume (MCV). e underlying pathophysiology of PNH is the absence of the negative complement regulatory proteins CD55 and CD59 on the surface of erythrocytes ( Figure 3 ). Processes that activate the complement pathway make these erythrocytes vulnerable to complement-mediated hemolysis. SARS-CoV-2 has been implicated in overactivation of the complement system. Gao et al. reported that SARS-CoV-2 can activate the lectin complement pathway [1] . In another study, Yu et al. demonstrated that the SARS-CoV-2 spike proteins can activate the alternative complement pathway and also showed that disrupting interaction of the spike proteins and factor D or C5 inhibited this immunopathology [2] . e COVID-19 of this patient activated complement, resulting in the diagnosis of PNH in this previously asymptomatic patient. A complement-mediated thrombotic microangiopathy (TMA) has also been described in COVID-19 [4] . is type of TMA is usually characterized by hemolytic anemia, thrombocytopenia, and end-organ damage [4] . While the patient in this case had hemolytic anemia and thrombocytopenia, she did not have any endorgan damage suggesting that her pathophysiology was not driven by a TMA. In addition, TMAs usually have schistocytes on the peripheral blood smear. No schistocytes were observed on the peripheral blood smear for the patient in this case report. Case Reports in Hematology PNH is classified into 3 groups: (1) subclinical PNH which usually has few PNH clones but no clinical or laboratory manifestation of hemolysis or thrombosis; (2) classical PNH, which has clinical and laboratory manifestations of hemolysis and thrombosis; and (3) PNH in the setting of other marrow failure syndromes such as aplastic anemia or myelodysplastic syndrome [5] . It is important to note that a bone marrow biopsy in cases on PNH typically reveals a normal to increased cellularity with erythroid predominance [3] . e patient in this case had a hypocellular marrow suggesting a secondary process. She had likely had a concomitant severe aplastic anemia. Since the predominant clinical presentation of this patient was complement-mediated hemolysis, the goal of primary treatment was to control the hemolysis through complement inhibition. e use of complement inhibitors such as eculizumab or ravulizumab is well established in treating PNH. Both drugs are monoclonal antibodies against the C5 component of complement preventing its cleavage into to C5a and C5b. is prevents the terminal complement cascade and the formation of the membrane attack complex (MAC), as shown in Figure 3 (c) (d) Figure 2 : Peripheral blood and bone marrow biopsy. e peripheral blood smear showed leukopenia with absolute neutropenia and thrombocytopenia. e observed neutrophils and lymphocytes were mature without significant morphological abnormality. Schistocytes were not present (a). Bone marrow biopsy showed large areas of the marrow that are less than 10% cellular (b); however, focally, the marrow is 40-50% cellular with erythroid predominant trilineage hematopoiesis (c). Immunohistochemical stains performed with appropriate controls demonstrated numerous E-cadherin-positive erythroid precursors (d). experience of 4 patients with COVID-19 who had a history of PNH and were on complement inhibitors [6] . Kulasekararaj et al. also reported an institutional experience of another 4 patients with COVID-19 and a history of PNH [7] . Two of these patients were treatment naïve, and two were established on complement inhibitor therapy [7] . e results of a small study of 80 patients suggested that eculizumab may improve survival and reduce hypoxia in patients with severe COVID-19 [8] . However, there is no approved indication yet for use in COVID-19 patients. Clinical trials Other potential therapeutic agents targeting the complement pathway include narsoplimab which is a fully human Ig4 monoclonal antibody directed against the mannan-binding lectin-associated serine protease-2 (MASP-2), an effector enzyme of the lectin pathway of the complement system [9] , AMY-101, a peptide inhibitor of the C3 complement [10] , and Zilucoplan, a C5 complement inhibitor [11] . is 19-year-old female with undiagnosed PNH became symptomatic in the context of a SARS-COV-2 infection. Management of PNH in the setting of SARS-CoV-2 infection poses a great challenge. SARS-CoV-2 has been shown to activate complement, and patients with PNH lack key inhibitors of complement regulation, CD55 and CD59, and are, therefore, predisposed to complement-mediated damage. is case raises a great concern for patients who, at baseline, have clinically evident PNH. In such patients, a SARS-CoV-2 infection would potentially cause significant morbidity and mortality. In this patient population, it may be prudent to consider anticomplement therapy, for patients not on this therapy, to mitigate potentially catastrophic SARS-CoV-2-mediated complement activation. is case shows that complement inhibitors may potentially be effective in controlling SARS-CoV-2-mediated complementactivation-dependent hemolysis in PNH patients. All data analyzed during this study are included in this published article. No written consent has been obtained from the patient as there are no patient identifiable data included in the case report. e authors declare no conflicts of interest. Steve Biko Otieno, MD, PhD, Alaa Altahan, MD, Fnu Kaweeta, MD, and Saradasri Karri, MD, wrote and edited the article Fnu Alnoor, MD, wrote and edited the section on pathology. Robert Johnson, MD, reviewed the article and provided comments. Highly pathogenic coronavirus N protein aggravates lung injury by MASP-2-mediated complement over-activation Direct activation of the alternative complement pathway by SARS-CoV-2 spike proteins is blocked by factor D inhibition How I treat paroxysmal nocturnal hemoglobinuria Severe COVID-19 infection and thrombotic microangiopathy: success does not come easily Update on the diagnosis and management of paroxysmal nocturnal hemoglobinuria COVID-19 infection in patients on anti-complement therapy: the Leeds National Paroxysmal Nocturnal Haemoglobinuria service experience Terminal complement inhibition dampens the inflammation during COVID-19 Eculizumab as an emergency treatment for adult patients with severe COVID-19 in the intensive care unit: a proof-ofconcept study Endothelial injury and thrombotic microangiopathy in COVID-19: treatment with the lectin-pathway inhibitor narsoplimab e first case of COVID-19 treated with the complement C3 inhibitor AMY-101 Zilucoplan in patients with acute hypoxic respiratory failure due to COVID-19 (ZILU-COV): a structured summary of a study protocol for a randomised controlled trial Acknowledgments e authors would like to acknowledge the Centers of Disease Control (https://www.cdc.gov/media/subtopic/ images.htm) for making publicly available images of the SARS-CoV-2 virus used in making Figure 3 .