Skip to main content

Late-onset myocardial infarction and autoimmune haemolytic anaemia in a COVID-19 patient without respiratory symptoms, concomitant with a paradoxical increase in inflammatory markers: a case report



In December 2019, a new coronavirus (named severe acute respiratory syndrome coronavirus 2, SARS-CoV-2) spread from China, causing a pandemic in a very short time. The main clinical presentation of SARS-CoV-2 infection (COVID-19, coronavirus disease-2019) is pneumonia, but several cardiovascular complications may also occur (e.g., acute coronary syndromes, pulmonary embolism, stroke, arrhythmias, heart failure and cardiogenic shock). Direct or indirect mechanisms induced by SARS-CoV-2 could be implicated in the pathogenesis of these events.

Case presentation

We report herein the third case of COVID-19 autoimmune haemolytic anaemia (AIHA) reported so far, which occurredwithout any other possible explanations in a Caucasian patient. The patient also suffered from ST-elevation myocardial injury.


Both complications occurred quite late after COVID-19 diagnosis and were probably precipitated by systemic inflammation, as indicated by a significant delayed increase in inflammatory markers, including interleukin-6 (IL-6).

Peer Review reports


The main serious clinical presentation of COVID-19 is pneumonia, but several cardiovascular complications may also occur (e.g., acute coronary syndromes, pulmonary embolism, stroke, arrhythmias, heart failure and cardiogenic shock) [1]. Moreover, there are few studies describing AIHA during COVID-19 [2]. We report herein the third case of COVID-19 autoimmune haemolytic anaemia, which occurred after an ST-elevation myocardial injury in a patient without any respiratory symptoms.

Clinical case presentation

An 86-year-old Caucasian woman suffering from hypertension and anxiety-depressive syndrome was admitted to our Infectious and Tropical Disease Unit on April 1st, 2020. She tested positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nasopharyngeal swab on March 26th, 2020, and did not report any symptoms other than nausea. Physical and neurological examinations on admission were normal, blood pressure was 120/85 mmHg, heart rate was 92 beats per minute, and temperature was 36.8°C. She resided in a long-term care facility and was on treatment with trazodone 60 mg/ml 3 drops daily and delorazepam 1 mg/ml 5 drops daily for an anxiety syndrome and furosemide 25 mg 1 tablet three times a week for high blood pressure. She was unmarried, had no children, was a housewife and lived in an urban area. She did not smoke and did not consume alcohol. In Table 1, we report the main laboratory findings at diagnosis and during the course of her hospital stay. The baseline twelve-lead electrocardiogram was normal (Fig 1a). Although she was asymptomatic, we performed a chest X-ray, which showed a“thickening of the interstitial design, in particular at the bases”. Due to this finding, antiviral treatment with hydroxychloroquine and azithromycin was started according to a protocol reported elsewhere and clinical guidelines [3, 4]. Due to hypomobility, thromboprophylaxis with enoxaparin 4000 IU once daily was also started (Padua score = 4) [5]. During hospitalization, the patient did not need any oxygen support. Swabs were persistently positive over time until they became negative on May, 15th, 2020. Therefore, positivity lasted for a total of 54 days. Despite a favourable clinical course without any respiratory symptoms, c-reactive protein (CRP) and IL-6 increased progressively, with IL-6 reaching a peak of 165 pg/ml, concomitant with the occurrence of the complications described below (in particular AIHA).

Table 1. Haemato-biochemical values at hospitalization and at the occurrence of complications.
Figure 1.
figure 1

Baseline electrocardiogram (a) and the occurrence of myocardial infarction (b)

On April 11th, for abdominal and right shoulder pain, the patient underwent a computerized tomography (CT) scan, which demonstrated gallbladder lithiasis and areas of ground glass opacity in the lungs. A few days later, due to an accidental fall, she underwent a cerebral CT scan, which showed evidence of only chronic cerebral vasculopathy. As a precaution, due to the traumatic event, given the improvement in patient mobility, enoxaparin was stopped.

On May 8th, the patient developed paraesthesia of the left arm; therefore, an electrocardiogram was performed and showed evidence of an ST-elevation myocardial injury (Fig 1b). Cardiac biomarkers were elevated: the highest value of high-sensitivity troponin T was 268.3 ng/L, myoglobin was 128 ng/ml and creatine kinase-MB was 12.4 ng/ml, with a progressive reduction over the following days. Taking into account advanced age and patient fragility, cardiologists advised against a more aggressive approach, limiting medical therapy to intravenous acetylsalicylic acid 125 mg on the first day, followed by oral administration100 mg/day; oral clopidogrel 75 mg 4 tablets on the first day, followed by 75 mg/day; subcutaneous enoxaparin 4000 IU twice daily for 7 days; oral ramipril 5 mg once daily and oral atorvastatin 40 mg once daily. The patient was then transferred to the intensive care unit (ICU) for clinical and instrumental monitoring. An echocardiogram was performed, showing a hypertrophic left ventricle with normal systolic function (ejection fraction, EF, 55%), a normokinetic left ventricle apex, and normal right sections. The level of NT-proBNP was 5404 pg/ml. Moreover, for marked hypotension, therapy with norepinephrine (0.2 γ/kg/min) was prescribed.

After three days in the Intensive Care Unit (ICU), the patient’s clinical condition improved; therefore, she was transferred again to our unit. A reduction in haemoglobin of 2 grams was found on May 13th, 2020, compared to a value of 10 grams/dl 5 days before. To understand the aetiology of anaemia, ferritin, sideraemia, vitamin B12, folic acid were measured, but only folic acid was low. Haemophagocytic lymphohistiocytosis syndrome was excluded [6]. Direct and indirect Coombs tests were performed as well, and the direct Coombs test was highly positive (i.e., 4+) for immunoglobulin (IgG). The consulting haematologist performed a peripheral blood smear, which indicated “anisopoikilocytosis of erythrocytes, several acanthocytes, some schistocytes”. After consideration of this result, the consulting haematologist decided against a diagnosis of a lymphoproliferative disorder, there by suggesting the avoidance of bone biopsy and possible contraindications, such as the need for antiplatelet therapy for recent myocardial infarction. Since antibodies (IgG) against Cytomegalovirus (CMV) were positive, although IgM were negative, to exclude a possible role of Cytomegalovirus reactivation in the genesis of AIHA, CMV, Deoxyribo Nucleic Acid (DNA) was tested in serum using real time Polymerase Chain Reaction (PCR) (CMV Elite MGB® Kit, Elitech Group, Italia). With this method, CMV DNA was undetectable. Also, IgG for Parvovirus B-19 were positive, IgM were negative, and Parvovirus B19 DNA was undetectable in serum by real time PCR. Therefore, diagnosis of these two active infections was excluded.

High-dose corticosteroid treatment (prednisolone 0.8 mg/kg) was started, although anaemia was only mild because the patient had worsening asthenia and dyspnoea, while transfusion would have been dangerous due to the presence of IgG autoantibodies. Rapid improvement in haemoglobin levels was obtained (Table 1). On May, 27th 2020, echocardiogram was performed, which showed a hypokinetic cardiac apex and mild mitral regurgitation. The patient’s clinical condition improved; therefore, the patient was discharged on July 3rd 2020 in good conditions and then hosted in a long-term care facility. The patient did not carry out follow-up visits.


Herein, we report a case of AIHA occurring during COVID-19 concomitant with myocardial infarction. These complications occurred when IL-6 peaked at a high plasma concentration late during the course of COVID-19. To the best of our knowledge, this is the first report showing late-onset AIHA occurring during COVID-19 concomitant with myocardial infarction, another complication that may be due to a hyperinflammatory status. Moreover, AIHA occurred in a patient who did not have any pre-existing haematological diseases or predisposing conditions, while in most similar cases reported so far, patients suffered from neoplastic or lymphoproliferative disorders.

Several studies highlighted that cardiovascular complications may occur in patients with SARS-CoV-2 infection. Indeed, SARS-CoV-2 can cause direct myocardial damage. In fact, the virus uses the angiotensin-enzyme-2 (ACE-2) host protein as a coreceptor to enter human cells, and this receptor is overexpressed in the heart and vascular system [7, 8]. Additionally, the cardiovascular system may be affected by systemic inflammation, causing organ damage as an effect of a cytokine storm [9, 10]. In addition, systemic inflammation can facilitate the rupture of pre-existing plaques, resulting in acute myocardial infarction. Concomitant causes of myocardial damage can be the altered ratio of myocardial demand-supply and increased cardiometabolic demand and hypoxia induced by lung disease [1]. Last, pre-existing cardiovascular diseases may have an impact on inducing heart injury [10, 11]. Our patient had hypertension and advanced age as risk factors. A cerebral CT scan evidenced chronic cerebral vasculopathy, possibly indicating a polyvascular atherosclerosis. Additionally, ongoing inflammation could have facilitated the rupture of pre-existing plaques. Therefore, myocardial infarction was somehow predictable. Even though the actual incidence of ST-segment elevation myocardial infarction in COVID-19 (as occurred in our patient) has not been described [12], the prevalence of acute myocardial injury in COVID-19 patients was reported to range from 7.2% to 17% [9, 10, 13]. Given the high incidence of myocardial infarction, especially in patients with underlying cardiovascular risks (as was the case in the patient presented herein), we should probably not have stopped enoxaparin when the accidental fall occurred, notwithstanding the risk of haemorrhagic events [14]. This consideration further confirms the need for improved algorithms and guidelines for the use of heparin in COVID-19 patients.

Immediately after myocardial infarction, our patient developed AIHA. This is an uncommon disorder characterized by the production of antibodies directed against self-red blood cells, which are destroyed through complement-mediated mechanisms and the reticuloendothelial system. Concurrent lymphoproliferative diseases, autoimmune diseases, Mycoplasma and infections due to several viruses, such as Epstein-Barr virus, Coxsackie, Cytomegalovirus, hepatitis C virus, and Parvovirus B19, may trigger AIHA. A possible aetiological mechanism is molecular mimicry, since these viruses possess structures that mimic normal host self-proteins, so the immune system activated against the pathogen may cross-react with self-antigens [15, 16]. Since we excluded possible alternative causes, we conclude that persistent inflammation due to SARS-CoV-2 infection was responsible for AIHA.

There are few studies describing AIHA during COVID-19. In particular, Lazarian et al. [17] described 7 cases of AIHA associated with COVID-19. These cases occurred during the course of the disease earlier (i.e., a median of 9 days) after diagnosis, and in only one case did the patient not suffer from neoplastic diseases (mainly lymphoproliferative disorders), which may explain the occurrence of AIHA. In contrast, our patient suffered from AIHA later on during the course of COVID-19, and no other obvious explanations were found for AIHA. Lopez et al. [18] described another case of direct Coombs test positive for IgG and C3 during COVID-19, but this patient had a medical history of congenital thrombocytopenia. Last, Hindilerden et al. [2] reported another case of AIHA during COVİD-19 in the absence of associated underlying disorders, showing a direct Coombs test positive for IgG and C3d. In conclusion, we present herein the third case of AIHA in a patient without underlying neoplastic or haematological concomitant disorders. Similar to the cases previously reported, our patient showed elevated markers of inflammation (i.e., ferritin, CRP, and D-dimers) at the time of AIHA diagnosis. Interestingly, at that point, IL-6 peaked at 165 pg/ml, starting from 22 pg/ml at the time of admission. We feel that hyperinflammation was pathogenically linked to both myocardial infarction and AIHA. Indeed, in our cohort, IL-6 appeared to be an independent predictor of death, together with elevated CRP [19].

With regard to therapy, corticosteroids are recommended as the first-line treatment for AIHA [20]. In line with this recommendation, our patient was treated with high-dose prednisolone (0.8 mg/kg/day), while in the other case series reported so far, intravenous immunoglobulin at 1 g/kg/day was used first, with suboptimal response. Only when corticosteroids were prescribed was a significant response obtained, and in only one case was rituximab used after a poor response to corticosteroids [16, 17]. Therefore, our case appears to support current guidelines [20] indicating that corticosteroids should be the first-line treatment in AIHA, even when this complication occurs after COVID-19. However, as highlighted in the clinical case presentation, corticosteroid treatment was prescribed in our patient not withstanding mild anaemia because the patient was symptomatic, probably for concomitant myocardial damage, so further studies are necessary to validate this treatment in patients with more severe anaemia.


Although the underlying mechanisms are not well known, we confirm that SARS-CoV-2 infection may trigger AIHA, as well as other complications, such as myocardial infarction, possibly related to cytokine storm and hyperinflammation. This is further supported by the concomitant increase in inflammatory markers such as IL-6 in our patient. Moreover, our case highlights the need for laboratory and clinical surveillance of patients hospitalized for COVID-19 for a prompt diagnosis of late-onset complications, especially when markers such as IL-6 do not return to normal or paradoxically increase during the course of an otherwise benign disease.

Availability of data and materials

All data generated or analysed during this study are included in this article.



Severe acute respiratory syndrome coronavirus 2


Coronavirus disease-2019


Autoimmune haemolytic anaemia


C-reactive protein; IL-6: interleukin-6


Computed tomography


Intensive care unit


  1. Manish Bansal. Cardiovascular disease and COVID-19. Diabetes & Metabolic Syndrome: Clinical Research & Reviews. Volume 14, Issue 3, May–June 2020, Pages 247-250.

  2. Hindilerden F, Yonal-Hindilerden I, Akar E, Yesilbag Z, Kart-Yasar K. Severe autoimmune haemolytic anemia in COVID-19 infection, safely treated with steroids. Mediterr J Hematol Infect Dis. 2020;12(1):e2020053.

    Article  Google Scholar 

  3. Gautret P, Lagier JC, Parola P, et al. Hydroxychloroquine and azithromycin as a treatment of COVID-19: results of an open-label non-randomized clinical trial [published online ahead of print, 2020 Mar 20]. Int J Antimicrob Agents. 2020;2020:105949.

    Article  Google Scholar 

  4. Vademecum for the treatment of people with COVID-19 disease. Edition 2.0, 13 March 2020. Lombardy Section of the Italian Society of Infectious and Tropical Diseases. InfezMed 2020; 28 (2), 143-152

  5. SmilgNicolás C, TornelSánchez G. Javier Trujillo Santos Concordance Among Venous Thromboembolism Risk Assessment Models. Med Clin (Barc). 2018;150(2):61–3.

    Article  Google Scholar 

  6. La Rosée P, Horne A, Hines M, et al. Recommendations for the management of hemophagocytic lymphohistiocytosis in adults. Blood. 2019;133(23):2465–77.

    Article  Google Scholar 

  7. Xu H, Zhong L, Deng J, Peng J, Dan H, Zeng X, Li T, Chen Q. High expression of ACE2 receptor of 2019-nCoV on the epithelial cells of oral mucosa. Int J Oral Sci. 2020;12:8–15.

    Article  CAS  Google Scholar 

  8. Zou X, Chen K, Zou J, Han P, Hao J, Han Z. Single-cell RNA-seq data analysis on the receptor ACE2 expression reveals the potential risk of different human organs vulnerable to 2019-nCoV infection. Front Med, 2020.

  9. Zhou F, Yu T, Du R, et al. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study [published correction appears in Lancet. 2020 Mar 28;395(10229):1038]. Lancet. 2020;395(10229):1054-1062.

  10. Huang C, Wang Y, Li X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan China [published correction appears in Lancet. 2020 Jan 30]. Lancet. 2020;395(10223):497–506.

    Article  CAS  Google Scholar 

  11. Li B, Yang J, Zhao F, et al. Prevalence and impact of cardiovascular metabolic diseases on COVID-19 in China. Clin Res Cardiol. 2020;109(5):531–8.

    Article  CAS  Google Scholar 

  12. Dehghani P, Davidson LJ, Grines CL, et al. North American COVID-19 ST-segment elevation myocardial infarction (NACMI) registry: Rationale, design, and implications [published online ahead of print, 2020 May 16]. Am Heart J. 2020.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Wang D, Hu B, Hu C, et al. Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus-Infected Pneumonia in Wuhan China [published online ahead of print, 2020 Feb 7]. JAMA. 2020;323(11):1061–9.

    Article  CAS  Google Scholar 

  14. M. Mazzitelli, F. Serapide, B. Tassone, D. Laganà, E. M. Trecarichi, and C. Torti, “Spontaneous and severe haematomas in patients with COVID-19 on low-molecular-weight heparin for paroxysmal atrial fibrillation” Mediterr. J. Hematol. Infect. Dis., vol. 12, no. 1, Art. no. 1, Jun. 2020.

  15. Matthias G, von Herrath MG, Oldstone MB. Virus-induced autoimmune disease. Curr Opin Immunol. 1996;8(6):878–85.

    Article  Google Scholar 

  16. Meite M, Léonard S, Idrissi ME, Izui S, Masson PL, Coutelier JP. Exacerbation of autoantibody-mediated hemolyticanemia by viral infection. J Virol. 2000;74(13):6045–9.

    Article  CAS  Google Scholar 

  17. Lazarian G, Quinquenel A, Bellal M, Siavellis J, Jacquy C, Re D et al. Autoimmune haemolytic anemia associated with Covid-19 infection. Br J Haematol. 2020.

  18. Lopez C, Kim J, Pandey A, Huang T, DeLoughery TG. Simultaneous Onset of COVID-19 and Autoimmune Haemolytic Anaemia. Br J Haematol. 2020.

  19. E. M. Trecarichi et al. Characteristics, outcome and predictors of in-hospital mortality in an elderly population from a SARS-CoV-2 outbreak in a long-term care facility. MedRxiv 2020.06.30.20143701 [preprint]

  20. Lechner K, Jäger U. How I treat autoimmune haemolytic anemias in adults. Blood. 2010;116(11):1831–8.

    Article  CAS  Google Scholar 

Download references


The authors thank all our patients, our nurses in the Infectious Diseases and Tropical Medicine Unit and the University “Magna Graecia” (UMG) COVID-19 Group. This group is composed, in addition to the main authors, by the following individuals: Eugenio Arrighi, Bernardo Bertucci, Maria Teresa Busceti, Claudio Carallo, Francesco Saverio Costanzo, Adele De Francesco, Paolo Fusco, Luigia Gallo, Aida Giancotti, Amerigo Giudice, Giuseppe Greco, Domenico Laganà, Angelo Lamberti, Maria Carla Liberto, Rosaria Lionello, Nadia Marascio, Giuseppina Marrazzo, Maria Petullà, Graziella Perri, Vincenzo Scaglione, Francesca Serapide, Ciro Indolfi, Federico Longhini, Andrea Bruni, and Eugenio Garofalo.


This study did not receive any funding and was conducted as a part of routine clinical practice.

Author information

Authors and Affiliations




MCP, BT and MR designed the study. MCP, BT, MR, MM, CD, GP, AC, VLG, EL, CT, EMT, GM, AQ and GSB collected the data and managed the clinical case. MCP wrote the draft. CT and EMT critically revised the manuscript. All authors have read and approved the submitted version.

Corresponding author

Correspondence to Maria Chiara Pelle.

Ethics declarations

Ethics approval and consent to participate

Not applicable

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pelle, M.C., Tassone, B., Ricchio, M. et al. Late-onset myocardial infarction and autoimmune haemolytic anaemia in a COVID-19 patient without respiratory symptoms, concomitant with a paradoxical increase in inflammatory markers: a case report. J Med Case Reports 14, 246 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: