Koponen M A, Siegel R J
Fulton County Office of the Medical Examiner, Atlanta, GA 30303, USA.
Hum Pathol. 1996 Apr;27(4):420-3. doi: 10.1016/s0046-8177(96)90117-3.
We present a case of histiocytoid cardiomyopathy resulting in sudden and unexpected death in a 4-month-old infant with Peter's Anomaly and congenital glaucoma. At autopsy, the granular histiocytoid cells that define this entity were found predominantly involving the conduction system, with encasement and partial replacement the His' Bundle. Large aggregates of these cells formed atrioventricular and nodoventricular connections, indicating a possible mechanism for the arrhythmias characteristic of the condition. The striking propensity for involvement of the conduction system in this case lends further support to the view that this disorder represents a developmental anomaly of the Purkinje cell system of the heart.
我们报告了一例组织细胞样心肌病导致一名患有彼得异常和先天性青光眼的4个月大婴儿突然意外死亡的病例。尸检时,发现定义该疾病的颗粒状组织细胞样细胞主要累及传导系统,包绕并部分替代希氏束。这些细胞的大量聚集形成房室和结室连接,提示了该疾病特征性心律失常的一种可能机制。在该病例中传导系统受累的显著倾向进一步支持了这种疾病代表心脏浦肯野细胞系统发育异常的观点。