Veinot J P, Johnston B
Department of Laboratory Medicine, University of Ottawa Heart Institute at the Ottawa Civic Hospital, Ontario, Canada.
J Forensic Sci. 1998 May;43(3):715-7.
Sarcoidosis is a multi-systemic granulomatous disease of unknown cause. It commonly involves lymph nodes, lungs, eyes, and skin. Cardiac sarcoid may be isolated, or associated with systemic involvement. Cardiac involvement is found in 20-50% of autopsied patients with sarcoidosis. However, it only gives rise to clinical manifestations in about 5% of patients. Cardiac involvement by sarcoid has been reported to manifest as complete heart block, papillary muscle dysfunction, congestive heart failure, pericarditis and/or effusion, conduction abnormality or arrhythmia, chest pain, and sudden death. The most common site of involvement is the interventricular septum base, which when involved may lead to heart block or arrhythmia. We report a case of sudden death in a 33-year-old male with a history of surgically repaired congenital heart disease. Although his congenital heart disease was originally postulated to be important in his death, autopsy examination revealed cardiac sarcoid with prominent involvement of the conduction system.
结节病是一种病因不明的多系统肉芽肿性疾病。它通常累及淋巴结、肺、眼和皮肤。心脏结节病可能是孤立的,也可能与全身受累相关。在结节病尸检患者中,20% - 50%发现有心脏受累。然而,只有约5%的患者会出现临床表现。据报道,结节病累及心脏表现为完全性心脏传导阻滞、乳头肌功能障碍、充血性心力衰竭、心包炎和/或心包积液、传导异常或心律失常、胸痛以及猝死。最常受累的部位是室间隔基部,受累时可能导致心脏传导阻滞或心律失常。我们报告一例33岁男性猝死病例,该患者有先天性心脏病手术修复史。尽管最初推测其先天性心脏病在其死亡中起重要作用,但尸检发现心脏结节病,传导系统受累明显。