1. Introduction
Here we report the case of a middle aged woman presenting with repeated syncopes, even after pacemaker implantation. Following several diagnostic investigations an unexpected diagnosis was made.
2. Case Presentation
A 66-year-old woman presented with complaints of lightheadedness and palpitations followed by abrupt loss of consciousness while sitting. There were no bladder or bowel incontinence or seizure-like movements. She had no chest pain or dyspnea. She experienced repeated syncopes in the two days prior to admission. Her past medical history was significant for a syncope nine years ago and a hysterectomy. There was no family history of sudden cardiac death nor medication use. On examination she had blood pressure of 140/60 mmHg, a regular heart rhythm of 73/min, no fever, 97% oxygen saturation; with normal heart and lung sounds on auscultation. There were no neurological abnormalities. The electrocardiogram at the emergency department revealed a sinus rhythm, 77/min, with a left axis and left anterior hemiblock. She was admitted at our department and during her hospital stay symptomatic sinus arrest and junctional bradycardia were documented on telemetry. We therefore decided to implant a pacemaker. She was discharged from the hospital after uneventful observation post-device implantation.
One month later the pacemaker analysis revealed three episodes of asymptomatic nonsustained ventricular tachycardia. Coronary angiography was performed to exclude myocardial ischemia and showed diffuse moderate coronary stenosis without significant ischemia on invasive physiological coronary assessment.
Transthoracic echocardiography showed normal heart structure and function. Three months after the pacemaker implantation she experienced a syncope. The pacemaker analysis at this time again showed runs of nonsustained ventricular tachycardia with a ventricular rate up to 300 bpm (
Figure 1).
The combination of brady- and tachyarrhythmias raised the concern for cardiac sarcoidosis (CS), for which a 18F-fluorodeoxyglucose (FDG)-positron emission tomography (PET) scan was scheduled.
The measured standardized uptake value (SUV) max was 4.33 g/mL and the left ventricular blood pool threshold 2.11 g/mL (cardiac SUV max greater than a 1.5-times left ventricular blood pool threshold are considered quantitatively positive) [
1].
The images showed FDG uptake in the basal segments of the anterolateral, inferolateral and inferior wall and in the basal segment of the anteroseptal wall, compatible with an inflammatory myocardial disease. There was no tracer uptake in other organs or mediastinal structures (
Figure 2).
The diagnosis of CS was suspected, based on the recent history of ventricular arrhythmia and sinus arrest in the absence of echocardiographic structural heart disease and hemodynamically significant myocardial ischemia. Laboratory results showed normal inflammatory parameters and normal troponin levels. The patient was admitted for device explantation, performance of cardiac magnetic resonance (CMR), diagnostic invasive electrophysiologic study and upgrade to a dual chamber implantable cardioverter defibrillator. During electrophysiologic study, sustained ventricular tachycardia could be induced. CMR showed prolonged myocardial relaxation up to 62–64 msec on T2 mapping in the inferolateral basal segment of the left ventricle, suggesting acute myocardial inflammation In addition, midmyocardial and subepicardial late gadolinium enhancement (LGE) was demonstrated in the same inferolateral basal segment of the left ventricle (
Figure 3 and
Figure 4).
Taken together these findings were strongly suggestive for myocardial inflammation/necrosis compatible with CS. Because of the localization of the lesions, an endomyocardial biopsy was not performed. A dual chamber implantable cardioverter defibrillator was implanted and corticosteroids were initiated, with a gradual tapering over 12 weeks. She did not experience syncope again, nor did she have any other symptoms suggestive of heart arrhythmias. A PET-scan three months after the cessation of corticosteroids showed the regression of all lesions (
Figure 5).
3. Discussion
Here we report a case of an isolated CS. Sarcoidosis is a multisystem inflammatory granulomatous disease of unknown origin. Up to 5% of patients with sarcoidosis present with clinical symptoms of cardiac involvement: ventricular arrythmias, conduction abnormalities and heart failure. About 20–25% of patients have clinical silent cardiac involvement [
2,
3]. The true prevalence of isolated CS is not known, as illustrated by a huge variability (27–45%) in the reporting of all cases with cardiac sarcoidosis [
4].
Diagnosis of CS is challenging. An endomyocardial biopsy provides a high specificity for diagnosis but this invasive test has documented limited sensitivity, due to the patchy nature of the disease. Advanced cardiac imaging with CMR and/or FDG-PET are therefore valuable tools for the detection of CS. The use of CMR clearly has increased the diagnostic yield in recent years [
3,
5]. In particular, the combination of detecting myocardial scarring/fibrosis by LGE and quantitative tissue characterization detecting myocardial inflammation by T2 mapping has shown added value in the diagnosis of CS [
6].
Although current recommendations require histological confirmation for diagnosis of sarcoidosis, either (A) histological diagnosis from myocardial tissue or (B) histological diagnosis from extra cardiac sarcoidosis in combination with other criteria with noninvasive studies [
2], we did not take a biopsy because of the difficult-to-reach cardiac localization of the lesions and the lack of extracardiac involvement.
Despite the fact that an atrioventricular block is considered typical for CS, the presence of ventricular tachycardia and sinus node dysfunction—after excluding other causes, such as ischemia and structural heart disease—in combination with late gadolinium enhancement (LGE) on CMR and uptake on cardiac FDG-PET led to the diagnosis of CS.
The combination of FDG-PET and CMR has contributed to diagnostic and therapeutic progress in CS. This is mainly due to the complementary information of both imaging modalities, with CMR demonstrating myocardial fibrosis and FDG-PET showing active inflammation [
7]. This distinction between active and nonactive lesions impacts therapeutic decision making, both with regard to systemic immunosuppressive therapy and cardiac specific therapy (implantable cardioverter defibrillator).
Management of CS is based on (A) immunosuppressive therapy for the treatment of active sarcoidosis and (B) cardiac-specific therapies including medication to treat ventricular dysfunction and device therapy (pacemaker/ICD) for heart blocks and heart rhythm disturbances [
2,
8].
4. Conclusions
Isolated cardiac sarcoidosis is a rare and underdiagnosed disease. Clinical presentation may include AV block, sinus node dysfunction, tachyarrythmias and heart failure. Multimodality imaging with CMR and PET-CT is very important for diagnosis and therapeutic decision making.
Author Contributions
L.B. wrote the manuscript. P.T.J. revised the manuscript. D.D.-B. revised the manuscript. O.G. and A.J. provided the images. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
No new data were created or analyzed in this study. Data sharing is not applicable to this article.
Conflicts of Interest
The authors declare no conflict of interest.
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