Zusammenfassung
Klinisches/methodisches Problem
Die Sarkoidose und Amyloidose sind Multisystemerkrankungen, in deren Verlauf es zu einer kardialen Beteiligung kommen kann.
Radiologische Standardverfahren
Bildgebend wird als primäres Verfahren die Echokardiographie eingesetzt. Zur weiteren Diagnostik wird neben der Biopsie und nuklearmedizinischen Verfahren v. a. die MRT herangezogen.
Methodische Innovationen
Als neuere Technik zur Darstellung globaler diffuser Kontrastmittelanreicherungen, wie sie im Rahmen der Amyloidose vorkommen, wird z. Z. das T1-Mapping evaluiert.
Leistungsfähigkeit
Durch den Einsatz der MRT, insbesondere des Late-Gadolinium-Enhancements (LGE), können die Sensitivität und Spezifität in der Diagnostik der kardialen Sarkoidose und Amyloidose entscheidend verbessert werden. Bei der Sarkoidose stellt das Vorhandensein eines LGE einen prognostischen Faktor bzgl. des Outcomes dar, während bei der kardialen Amyloidose durch Analyse des T1-Mappings eine bessere Abschätzung der Prognose möglich erscheint.
Empfehlung für die Praxis
Bei Verdacht auf kardiale Beteiligung im Rahmen einer Sarkoidose oder Amyloidose sollte als bildgebendes Verfahren eine MRT mit Kontrastmittel durchgeführt werden.
Abstract
Clinical/methodical issue
Sarcoidosis and amyloidosis are both multisystem disorders, which may involve the heart; however, isolated cardiac disease is rare. Diagnosis of cardiac sarcoidosis and amyloidosis is crucial because the patient prognosis is dependent on cardiac involvement and early treatment.
Standard radiological methods
Echocardiography is the first line imaging modality in the diagnostic work-up of both diseases, possibly giving hints towards the correct diagnosis. Besides myocardial biopsy and radionuclide studies cardiac magnetic resonance imaging (MRI) is routinely performed in patients suspect of having infiltrative cardiomyopathy.
Methodical innovations
The T1 mapping procedure is currently being evaluated as a new technique for detection and quantification of global myocardial enhancement, as seen in cardiac amyloidosis.
Performance
Sensitivities and specificities for detection of cardiac sarcoidosis and amyloidosis can be significantly improved by MRI, especially with late gadolinium enhancement (LGE) imaging. In cardiac sarcoidosis the use of LGE is outcome-related while in amyloidosis analysis of T1-mapping may be of prognostic value.
Practical recommendations
If cardiac involvement in sarcoidosis or amyloidosis is suspected cardiac MRI including LGE should be performed for establishing the diagnosis.
Literatur
Ahmad K, Kim YH, Spitzer AR et al (1992) Total nodal radiation in progressive sarcoidosis. Case report. Am J Clin Oncol 15:311–313
Anonymous (2007) Diagnostic standard and guidelines for sarcoidosis. Jpan J Sarcoidosis Granulomatous Disord 27:13
Austin BA, Tang WH, Rodriguez ER et al (2009) Delayed hyper-enhancement magnetic resonance imaging provides incremental diagnostic and prognostic utility in suspected cardiac amyloidosis. JACC Cardiovasc Imaging 2:1369–1377
Connors LH, Lim A, Prokaeva T et al (2003) Tabulation of human transthyretin (TTR) variants, 2003. Amyloid 10:160–184
Di Bella G, Minutoli F, Mazzeo A et al (2010) MRI of cardiac involvement in transthyretin familial amyloid polyneuropathy. AJR Am J Roentgenol 195:W394–399
Dubrey SW, Cha K, Anderson J et al (1998) The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement. QJM 91:141–157
Hiraga A (1993) Guideline for diagnosis of cardiac sarcoidosis: study report on diffuse pulmonary diseases. Ministry of Health, Labour and Welfare 2, Japan
Klein AL, Hatle LK, Taliercio CP et al (1990) Serial Doppler echocardiographic follow-up of left ventricular diastolic function in cardiac amyloidosis. J Am Coll Cardiol 16:1135–1141
Koivuniemi R, Paimela L, Suomalainen R et al (2008) Amyloidosis is frequently undetected in patients with rheumatoid arthritis. Amyloid 15:262–268
Koyama J, Falk RH (2010) Prognostic significance of strain Doppler imaging in light-chain amyloidosis. JACC Cardiovasc Imaging 3:333–342
Kristen AV, Dengler TJ, Katus HA (2007) Suspected cardiac amyloidosis: endomyocardial biopsy remains the diagnostic gold-standard. Am J Hematol 82:328
Kristen AV, Perz JB, Schonland SO et al (2007) Rapid progression of left ventricular wall thickness predicts mortality in cardiac light-chain amyloidosis. J Heart Lung Transplant 26:1313–1319
Krombach GA, Hahn C, Tomars M et al (2007) Cardiac amyloidosis: MR imaging findings and T1 quantification, comparison with control subjects. J Magn Reson Imaging 25:1283–1287
Lyne JC, Petryka J, Pennell DJ (2008) Atrial enhancement by cardiovascular magnetic resonance in cardiac amyloidosis. Eur Heart J 29:212
Maceira AM, Joshi J, Prasad SK et al (2005) Cardiovascular magnetic resonance in cardiac amyloidosis. Circulation 111:186–193
Maceira AM, Prasad SK, Hawkins PN et al (2008) Cardiovascular magnetic resonance and prognosis in cardiac amyloidosis. J Cardiovasc Magn Reson 10:54
Mccrohon JA, Moon JC, Prasad SK et al (2003) Differentiation of heart failure related to dilated cardiomyopathy and coronary artery disease using gadolinium-enhanced cardiovascular magnetic resonance. Circulation 108:54–59
Okayama K, Kurata C, Tawarahara K et al (1995) Diagnostic and prognostic value of myocardial scintigraphy with thallium-201 and gallium-67 in cardiac sarcoidosis. Chest 107:330–334
Robbers LF, Baars EN, Brouwer WP et al (2012) T1 mapping shows increased extracellular matrix size in the myocardium due to amyloid depositions. Cir Cardiovasc Imaging 5:423–426
Roberts WC, Waller BF (1983) Cardiac amyloidosis causing cardiac dysfunction: analysis of 54 necropsy patients. Am J Cardiol 52:137–146
Sato T, Kanzaki H, Ishida Y et al (2010) Second left ventricular aneurysm newly developed in a patient with untreated cardiac sarcoidosis. Circ J 74:2477–2478
Smedema JP, Snoep G, Van Kroonenburgh MP et al (2005) The additional value of gadolinium-enhanced MRI to standard assessment for cardiac involvement in patients with pulmonary sarcoidosis. Chest 128:1629–1637
Steckman DA, Schneider PM, Schuller JL et al (2012) Utility of cardiac magnetic resonance imaging to differentiate cardiac sarcoidosis from arrhythmogenic right ventricular cardiomyopathy. Am J Cardiol 110:575–579
Syed IS, Glockner JF, Feng D et al (2010) Role of cardiac magnetic resonance imaging in the detection of cardiac amyloidosis. JACC Cardiovas Imaging 3:155–164
Uemura A, Morimoto S, Hiramitsu S et al (1999) Histologic diagnostic rate of cardiac sarcoidosis: evaluation of endomyocardial biopsies. Am Heart J 138:299–302
Uemura A, Morimoto S, Kato Y et al (2005) Relationship between basal thinning of the interventricular septum and atrioventricular block in patients with cardiac sarcoidosis. Sarcoidosis Vasc Diffuse Lung Dis 22:63–65
Vignaux O (2005) Cardiac sarcoidosis: spectrum of MRI features. AJR Am J Roentgenol 184:249–254
Vignaux O, Dhote R, Duboc D et al (2002) Clinical significance of myocardial magnetic resonance abnormalities in patients with sarcoidosis: a 1-year follow-up study. Chest 122:1895–1901
Yazaki Y, Isobe M, Hiroe M et al (2001) Prognostic determinants of long-term survival in Japanese patients with cardiac sarcoidosis treated with prednisone. Am J Cardiol 88:1006–1010
Youssef G, Leung E, Mylonas I et al (2012) The use of 18F-FDG PET in the diagnosis of cardiac sarcoidosis: a systematic review and metaanalysis including the Ontario experience. J Nucl Med 53:241–248
Interessenkonflikt
Die korrespondierende Autorin gibt für sich und ihre Koautoren an, dass kein Interessenkonflikt besteht.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Bauner, K., Wintersperger, B. MRT bei kardialer Sarkoidose und Amyloidose. Radiologe 53, 54–60 (2013). https://doi.org/10.1007/s00117-012-2386-0
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00117-012-2386-0