key: cord-0708230-33f5iawt authors: Ehrlich, Peter; Klingel, Karin; Ohlmann-Knafo, Susanne; Hüttinger, Sebastian; Sood, Nitin; Pickuth, Dirk; Kindermann, Michael title: Biopsy-proven lymphocytic myocarditis following first mRNA COVID-19 vaccination in a 40-year-old male: case report date: 2021-09-06 journal: Clin Res Cardiol DOI: 10.1007/s00392-021-01936-6 sha: 5badec701b9f45b8fbdca541226dc9d3e9adf80f doc_id: 708230 cord_uid: 33f5iawt nan were all normal. Blood cultures remained sterile. The SARS-CoV-2 PCR of a nasopharyngeal swap was negative as well as SARS-CoV-2 antibody testing (IgG and IgA). Pulmonary embolism was ruled out by CT angiography and sinus vein thrombosis was excluded by a cranial MRI scan. Transthoracic echocardiograpy in the emergency unit showed a normally sized left ventricle (end-diastolic diameter 52 mm) with a moderately reduced ejection fraction of 45% (biplane Simpson method) without regional wall motion abnormalities. The thickness of the basal septum was slightly increased to 13 mm. Pericardial effusion could be ruled out as well as a valvular heart disease. The patient was transferred to the intermediate care unit with the working diagnosis of "non-ST segment elevation myocardial infarction (NSTEMI)" versus "myocarditis", and therapy with acetylsalicylic acid, unfractionated heparin, an ACE inhibitor, a beta-blocker and a mineralocorticoid antagonist was started. On the next morning, chest pain worsened and ECG showed ST elevations in leads I, II, aVL, V5-V6 and ST depression in leads III and aVR (ECG 2 in Fig. 2 ), which prompted emergency coronary angiography using transradial access. As no coronary artery disease could be diagnosed and laevo-cardiography showed a globally reduced ejection fraction of 43% (see supplementary data file), left ventricular endomyocardial biopsy was performed to exclude a potentially life-threatening type of myocarditis. Histology and immuno-histology of the biopsies revealed acute lymphocytic myocarditis (Fig. 3) . (RT-)PCRs for common cardiotropic viruses or bacteria were negative. Conservative heart failure therapy achieved complete remission of all symptoms within two days. Left ventricular ejection fraction normalized to 60% forty-eight hours after admission. On day four after admission, the patient was discharged from hospital free of symptoms. Heart failure medication was continued. He was advised to refrain from high-intense physical activity in the upcoming 3 months until cardiological follow-up. A cardiac MRI study was carried out post-inpatient on day eight after admission. Cine images confirmed a normalized left ventricular ejection fraction (69%) without regional wall motion abnormalities. However, it revealed increased left ventricular wall thickness with a septal thickness of 16 mm at maximum and a persistent myocardial inflammation throughout the left ventricle: myocardial hyper-intensities on T2w images indicating myocardial edema were detected in the left ventricle, primarily in the basal and mid inferoseptal and anterolateral segments as well as in the apical lateral segment. Diffuse late gadolinium enhancement was noted in the basal and mid anteroseptal and inferoseptal segments as well as in the apical septal segment. Focal enhancement was mainly seen in the basal and mid anterolateral segments, in the apical lateral segment as well as in the apical cap. Approximately 90% of the total left ventricular mass was affected. There was no increased pericardial enhancement. Likewise, no pericardial effusion was evident (Fig. 4) . A follow-up cardiac MRI study will be scheduled three months after hospital discharge. The first reports of a small number of cases of suspected myocarditis after administration of the BioNTech/Pfizer COVID-19 vaccine came from Israel. A total of 275 cases of myocarditis were reported in Israel between December 2020 and May 2021 among more than five million vaccinated people. More than four-fifth of these cases occurred after the second vaccination dose and most cases were reported among men aged 16-19 years who had a mild clinical course with a hospital stay no longer than four days [2] . The US American CDC data (thru June 11, 2021) showed that after 5.8 million first doses of an mRNA COVID-19 vaccine administered to men aged 18-24 there were 47 reports of myocarditis or pericarditis, when three to 34 would have been expected. After the second vaccination dose, 233 cases were reported among 4.3 million vaccinated men, while two to 25 cases of myocarditis or pericarditis would have been expected. For females, the reported event rates after the first mRNA vaccination dose were within the expected event range for all age groups. But after the second vaccination dose, the number of reported myocarditis/ pericarditis cases in females aged 18-24 years went up to 27, slightly exceeding the rate in the general population which is two to 18 cases [3] . The US American Vaccine Safety Datalink (VSD) has repeatedly calculated the relative risk for developing myocarditis/pericarditis according to the CDC case definition after mRNA COVID-19 vaccination compared with individuals who got any other vaccination on the same calendar days. While the overall adjusted risk ratio for myocarditis/pericarditis after either dose of any mRNA COVID-19 vaccine was not significantly increased at 1.07 (95% CI 0.70-1.67; data from June 5, 2021), this looks different for the young: for 12-39-year-old individuals, the risk of getting myocarditis or pericarditis within 21 days after any of both doses of an mRNA COVID-19 vaccine was 3.5 times higher (95% CI 1.1-15.0; data from June 5, 2021) than with any other vaccination. There was a predominance of cases in young and male patients, especially after administration of the second dose and a clustering of cases within the first week following vaccination. Outcome data indicated that patients generally recovered from symptoms quickly [3] . Recent data gathered from more than 2 million people, who received at least one COVID-19 vaccination at 40 hospitals from Washington, Oregon, Montana and California, reported an incidence rate for post-COVID-19 vaccination myocarditis of 1 per 100,000 and of post-vaccination pericarditis of 1.8 per 100,000 [4] . The study confirms that myocarditis after mRNA COVID-19 vaccination occurs preferably in younger (median age 36 years) men (75%), soon after a median delay of 3.5 days after immunization and mostly (80%) after the second dose, but pericarditis occurs preferably in older (median age 59 years) men (73%) and later at a median value of 20 days after immunization with either the first (41%) or the second dose (59%). Hospitalization rate of myocarditis/pericarditis patients was 95% and 35%, Fig. 3 Endomyocardial biopsy reveals areas of inflammation and myocyte necrosis (arrows in A, Giemsa stain). The majority of immune cells represent CD68-positive macrophages (B) but also numerous CD3-positive T cells (C) are present in the interstitium respectively. Hospitalized patients were discharged after a median of 2 days and after one day, respectively. None of the patients died. To the best of our knowledge, this is the first case of a biopsy-proven myocarditis after the first dose of COVID-19 vaccination with an mRNA vaccine. In most reported cases of suspected post COVID-19 vaccination myocarditis, endomyocardial biopsy was not performed, but diagnosis of myocarditis was based on elevated myocardial necrosis markers and "typical" cardiac MRI findings. In the recent case series of Larson et al. [5] and Rosner et al. [6] , only two patients underwent endomyocardial biopsy-however, histology did not reveal myocarditis in either case. Although the authors explain the negative results with the sampling bias, the shortcoming of a lack of confirmation of the diagnosis of myocarditis by definite histological evidence remains. Although we cannot definitely rule out the possibility that the myocarditis in our patient was just a coincidental association with COVID-19 vaccination, the close temporal relationship, which is also reported in other case series and the lack of a specific cardiotropic virus in the biopsies argue for a vaccine reaction. Some points in our case deserve to be highlighted: As the patient developed myocarditis a few days after the first vaccination in absence of anti-SARS-CoV-2-antibodies, the pathogenesis of mRNA COVID-19 vaccine associated myocarditis does not appear to depend on anti-SARS CoV-2 spike protein antibodies. Thus, the hypothesis of crossreactivity of antibodies induced by mRNA vaccination with myocardial antigens (molecular mimicry [7] ) is not corroborated by our case. Rather, the quick cardiac infiltration of immune cells after vaccination suggests that myocarditis may be caused by other mechanisms. Unlike myocarditis associated with smallpox vaccination [8] , the myocarditis following mRNA COVID-19 vaccination in our case was not an eosinophilic but a pure lymphocytic myocarditis. As acute lymphocytic myocarditis has a better prognosis with a high potential of healing under supportive and heart failure therapy compared with eosinophilic or giant-cell myocarditis [9] this might explain the more benign course of myocarditis associated with mRNA COVID-19 vaccination. In our case, there was a discrepancy between rapid improvement of symptoms and left ventricular function despite persistent myocardial inflammation as documented by extensive late gadolinium enhancement (LGE) in the cardiac MRI study. This finding should prompt caution when deciding whether to continue drug therapy or to allow the patient to resume intense sporting activities. As both, the presence of LGE [10] as well as the detection of an inflammatory infiltrate in the endomyocardial biopsy [11] confer an increased risk for cardiac death and major adverse cardiac events, clinical decision making in these patients should not rely solely on symptom status and left ventricular ejection fraction. Cardiovascular magnetic resonance in nonischemic myocardial inflammation. Expert Recommendations Surveillance of myocarditis (inflammation of the heart muscle) cases between Centres for Disease Control and Prevention. Clinical considerations: myocarditis and pericarditis after receipt of mRNA COVID-19 vaccines among adolescents and young adults Myocarditis and pericarditis after vaccination for COVID-19 Myocarditis after BNT162b2 and mRNA-1273 vaccination Myocarditis temporally associated with COVID-19 vaccination From anti-SARS-CoV-2 immune responses to COVID-19 via molecular mimicry Eosinophilic-lymphocytic myocarditis after smallpox vaccination Myocarditis and inflammatory cardiomyopathy: current evidence and future directions Prognostic impact of late gadolinium enhancement by cardiovascular magnetic resonance in myocarditis. A systematic review and meta-analysis Predictors of outcome in patients with suspected myocarditis The online version contains supplementary material available at https:// doi. org/ 10. 1007/ s00392-021-01936-6.