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C L I N I C A L V I G N E T T E Nuclear medicine modalities in myocarditis 1297 A follow ‑up visit after 3 months showed: clin‑

ical improvement; normal resting electrocardio‑

gram; normalization of left ventricular ejection fraction (54%) and persistent right ventricular systolic dysfunction (tricuspid annular plane systolic excursion of 5 mm); persistent LGE areas on CMR. The patient was included in the ongoing, prospective clinical trial STREAM (ClinicalTri‑

als.gov identifier: NCT04 085 718),4 and referred for resting single ‑photon emission computed to‑

mography (to assess possible myocardial perfu‑

sion defects) and 18F‑2‑fluoro‑2‑deoxy ‑D‑glucose positron emission tomography (FDG ‑PET) (per‑

formed within 2 days). To suppress physiologi‑

cal glucose uptake in the myocardium, 2 days of a low ‑carbohydrate ‑high ‑fat diet, followed by prolonged fasting, and intravenous heparin (50 IU per kilogram) just before FDG ‑PET imag‑

ing were administered. FDG ‑PET revealed exten‑

sive areas of high FDG uptake in the apex, inter‑

ventricular septum, lateral and postero ‑lateral LV walls (Figure 1C). High FDG uptake corresponded with the resting single ‑photon emission comput‑

ed tomography perfusion defect after a 99mTc‑

‑MIBI injection (total extent of perfusion defect was 47%), as well as with LGE at CMR (Supple‑

mentary material, Figure S1), suggesting active myocardial inflammation. Based on these re‑

sults, the patient was referred for a right ven‑

tricular endomyocardial biopsy which revealed virus ‑negative, chronic ‑active myocarditis and myocardial fibrosis; other diseases with cardi‑

ac involvement were excluded. Immunosuppres‑

sive therapy for inflammatory cardiomyopathy was not started because of the breast cancer ac‑

cidentally detected by FDG ‑PET. The standard Nuclear medicine modalities are not included

in the routine diagnostic work ‑up of clinically suspected myocarditis due to limited evidence.1‑3 A 35‑year ‑old woman with a history of a recent respiratory infection was admitted to the hos‑

pital with dyspnea, palpitations, increased ab‑

dominal girth. Her electrocardiogram showed atrial flutter (with ventricular rate, 140 bpm) and left bundle branch block. Echocardiography showed globally decreased contractility of both ventricles with left ventricular (LV) ejection frac‑

tion of 28% and tricuspid annular plane systol‑

ic excursion of 5 mm; severe tricuspid regurgi‑

tation, mild pericardial, pleural, and abdominal effusions, and 2 hyperechogenic thrombi fixed to the LV apex. Invasive coronary angiography showed no changes. Laboratory investigations showed the following abnormalities: a N ‑termi‑

nal pro ‑B‑type natriuretic peptide concentra‑

tion of 5785 pg/ml (reference range <125 pg/ml);

a troponin I concentration of 4.213 ng/ml (refer‑

ence range <0.05 ng/ml); a D‑dimer concentra‑

tion of 5597 ng/ml. Cardiac magnetic resonance (CMR) findings confirmed a depression of the bi‑

ventricular systolic function and a nondilated LV. Notably, no myocardial edema was observed but subepicardial and mid ‑wall (nonischemic distribution) diffused areas of late gadolinium enhancement (LGE) in the anterior, lateral, and postero ‑lateral walls, interventricular septum, and apex were observed (Figure 1A and 1B). The pa‑

tient was discharged in a stable general condition after 6 weeks of hospitalization. She was pre‑

scribed standard guideline ‑recommended treat‑

ment for heart failure as well as warfarin and re‑

striction of physical activity for 3 to 6 months.

Correspondence to:

Krzysztof Ozierański, MD, PhD,  1st Department of Cardiology,  Medical university of Warsaw,  ul. Banacha 1a, 

02‑097 Warszawa, Poland,  phone: +48 22 599 29 58, email: 

krzysztof.ozieranski@wum.edu.pl Received: September 7, 2020.

Revision accepted:

October 8, 2020.

Published online:

October 15, 2020.

Kardiol Pol. 2020; 

78 (12): 1297‑1298 doi:10.33963/KP.15647 Copyright by the Author(s), 2020

C L I N I C A L V I G N E T T E

Emerging nuclear medicine modalities

to improve diagnostic accuracy in myocarditis

Agata Tymińska1, Krzysztof Ozierański1, Alida L. P. Caforio2, Małgorzata Kobylecka3, Vadym Matsibora4, Robert Kowalik1, Marcin Grabowski1, Grzegorz Opolski1

1  1st Department of Cardiology, Medical university of Warsaw, Warsaw, Poland

2  Division of Cardiology, Department of Cardiac, Thoracic, and Vascular Sciences and Public Health, university of Padova, Padova, italy 3  Department of Nuclear Medicine, Medical university of Warsaw, Warsaw, Poland

4  2nd Department of Clinical radiology, Medical university of Warsaw, Warsaw, Poland

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KARDIOLOGIA POLSKA 2020; 78 (12) 1298

5  Piriou N, Sassier J, Pallardy A, et al. utility of cardiac FDg ‑PeT imaging cou‑

pled to magnetic resonance for the management of an acute myocarditis with non‑

‑informative endomyocardial biopsy. eur Heart J Cardiovasc imaging. 2015; 16: 574.

treatment for heart failure and scheduled follow‑

‑up were continued, and the patient was referred to an oncologist.

In our case, baseline and follow ‑up CMR showed LGE areas, but in keeping with the pres‑

ent state of knowledge, failed to show active in‑

flammation, confirming that it has limited val‑

ue in the diagnosis of chronic ‑active myocardi‑

tis.1‑3 We would like to highlight the potential role of the application of a new noninvasive di‑

agnostic method, FDG ‑PET, in order to facili‑

tate an appropriate selection of patients with low ‑intermediate probability of ongoing myo‑

carditis to endomyocardial biopsy.5 According to the European Society of Cardiology recom‑

mendations, endomyocardial biopsy is the gold standard for diagnosis of myocarditis,1 which confirmed the suspicion made with FDG ‑PET.

Supplementary material

Supplementary material is available at www.mp.pl/kardiologiapolska.

article information

conflict of intereSt  None declared.

open acceSS  This is an Open Access article distributed under the terms  of  the  Creative  Commons  Attribution ‑NonCommercial ‑NoDerivatives  4.0  in‑

ternational License (CC BY ‑NC ‑ND 4.0), allowing third parties to download ar‑

ticles and share them with others, provided the original work is properly cited,  not changed in any way, distributed under the same license, and used for non‑

commercial purposes only. For commercial use, please contact the journal office  at kardiologiapolska@ptkardio.pl.

How to cite  Tymińska A, Ozierański K, Caforio ALP, et al. emerging nucle‑

ar medicine modalities to improve diagnostic accuracy in myocarditis. Kardiol Pol. 

2020; 78: 1297‑1298. doi:10.33963/KP.15647

referenceS

1  Caforio ALP, Pankuweit S, Arbustini e, et al. Current state of knowledge on ae‑

tiology, diagnosis, management, and therapy of myocarditis: a position statement  of the european Society of Cardiology Working group on Myocardial and Pericar‑

dial Diseases. eur Heart J. 2013; 34: 2636‑2648.

2  Ferreira VM, Schulz ‑Menger J, Holmvang g, et al. Cardiovascular magnetic res‑

onance in nonischemic myocardial inflammation: expert recommendations. J Am  Coll Cardiol. 2018; 72: 3158‑3176.

3  Caforio ALP, Cheng C, Perazzolo M, et al. How to improve therapy in myocardi‑

tis: role of cardiovascular magnetic resonance and of endomyocardial biopsy. eur  Heart J Suppl. 2019; 21: B19‑B22.

4  FDg ‑PeT/CT images comparing to Mri and endomyocardial biopsy in myocardi‑

tis (STreAM), identifier NCT04 085 718. ClinicalTrials.gov. u.S. National Library of Med‑

icine. https://clinicaltrials.gov/ct2/show/NCT04085718. Accessed November 1, 2020.

figure 1 A, B – cardiac magnetic resonance images with late enhancement techniques; A – the long ‑axis 2‑chamber view demonstrating subepicardial and mid‑wall late gadolinium enhancement in the left ventricular wall (arrow); B – the short ‑axis demonstrating diffuse areas of late gadolinium enhancement representing bands of increased signal running in the short axis plane (arrow); c – fusion positron emission tomography images (sagittal, coronal, and axial presentation, left, middle, and right, respectively) of myocardial 18F‑2‑fluoro‑2‑deoxy ‑D‑glucose uptake showing the area of high preferential glucose uptake in the apex (white arrows), lateral and postero ‑lateral walls (red arrows). High 18F‑2‑fluoro‑2‑deoxy ‑D‑glucose uptake area corresponds with the decreased single‑

‑photon emission computed tomography perfusion area (Supplementary material, Figure S1). Green arrow shows low septal 18F‑2‑fluoro‑2‑deoxy ‑D‑glucose uptake, corresponding with normal single ‑photon emission computed tomography perfusion.

A B c

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