TY - JOUR
T1 - A failed case to diagnose cardiac sarcoidosis presenting advanced atrioventricular block
AU - Morikawa, Mako
AU - Kato, Kimihiko
AU - Kako, Nobuo
AU - Hiramitsu, Shinya
AU - Oguri, Mitsutoshi
AU - Yajima, Kazuhiro
AU - Hibino, Takeshi
AU - Kato, Yasuchika
AU - Mizoguchi, Yoshikazu
AU - Kuroda, Makoto
AU - Yokoi, Kiyoshi
AU - Ichiro Morimoto, Shin
N1 - Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.
PY - 2008/9/26
Y1 - 2008/9/26
N2 - A 53-year-old-male developed atrioventricular block in January 2001. A chest X-ray and laboratory tests, including serum angiotensin converting enzyme, were normal. The patient underwent permanent pacemaker implantation and attended for semiannual follow-up after discharge since the etiology of advanced atrioventricular block remains unknown. One year later, the patient was diagnosed with uveitis related to sarcoidosis. No clinical finding specific to cardiac sarcoidosis was notable at that time. Four years after onset, the patient developed congestive heart failure. An echocardiogram revealed diffuse LV hypokinesis, but no asymmetric interventricular septal thinning. Laboratory tests showed normal angiotensin converting enzyme. Noncaseating granuloma was not confirmed by transbronchial biopsy. Despite normal myocardial uptake of gallium-67, uptake of 18F-Fluorodeoxyglucose increased in the myocardium. Nevertheless, clinical manifestations did not match the criteria for cardiac sarcoidosis. Prednisolone was administered daily. Two months after tapering dosage, the patient developed multiple organ failure and died. Post mortem histological findings were consistent with cardiac sarcoidosis. We experienced great difficulty in detecting cardiac involvement in the early stage of sarcoidosis. A specific method with greater sensitivity is required to diagnose cardiac involvement in the early stages of sarcoidosis.
AB - A 53-year-old-male developed atrioventricular block in January 2001. A chest X-ray and laboratory tests, including serum angiotensin converting enzyme, were normal. The patient underwent permanent pacemaker implantation and attended for semiannual follow-up after discharge since the etiology of advanced atrioventricular block remains unknown. One year later, the patient was diagnosed with uveitis related to sarcoidosis. No clinical finding specific to cardiac sarcoidosis was notable at that time. Four years after onset, the patient developed congestive heart failure. An echocardiogram revealed diffuse LV hypokinesis, but no asymmetric interventricular septal thinning. Laboratory tests showed normal angiotensin converting enzyme. Noncaseating granuloma was not confirmed by transbronchial biopsy. Despite normal myocardial uptake of gallium-67, uptake of 18F-Fluorodeoxyglucose increased in the myocardium. Nevertheless, clinical manifestations did not match the criteria for cardiac sarcoidosis. Prednisolone was administered daily. Two months after tapering dosage, the patient developed multiple organ failure and died. Post mortem histological findings were consistent with cardiac sarcoidosis. We experienced great difficulty in detecting cardiac involvement in the early stage of sarcoidosis. A specific method with greater sensitivity is required to diagnose cardiac involvement in the early stages of sarcoidosis.
UR - http://www.scopus.com/inward/record.url?scp=50349099374&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=50349099374&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2007.06.115
DO - 10.1016/j.ijcard.2007.06.115
M3 - Article
C2 - 17884196
AN - SCOPUS:50349099374
SN - 0167-5273
VL - 129
SP - e46-e49
JO - International Journal of Cardiology
JF - International Journal of Cardiology
IS - 2
ER -