Saalouke M G, Perry L W, Okoroma E O, Shapiro S R, Scott L P
Br Heart J. 1978 Jan;40(1):49-54. doi: 10.1136/hrt.40.1.49.
Four patients with primitive ventricle and normally related great vessels with stenotic subpulmonary outlet chamber (Holmes' heart with pulmonary stenosis) are reported. The history, physical examination, and chest x-ray film are not helpful in distinguishing Holmes' heart with pulmonary stenosis from tetralogy of Fallot. Electrocardiogram often provides the first clue to the presence of Holmes' heart; left axis deviation with or without left ventricular hypertrophy is an unusual finding in tetralogy of Fallot, but common in Holmes' heart. Selective ventriculography is diagnostic: the right ventricular outflow chamber overlies the aortic root and aortic valve in the frontal view in Holmes' heart with pulmonary stenosis, but is to the left of the aortic valve in tetralogy of Fallot; no ventricular septum can be identified in Holmes' heart. The diagnosis can be suspected in a child with clinical features of tetralogy of Fallot but atypical electrocardiogram, and can be established by angiography.
本文报道了4例具有原始心室、大血管关系正常但存在肺动脉瓣下狭窄腔室的患者(即合并肺动脉狭窄的霍姆斯心脏)。病史、体格检查及胸部X线片对于鉴别合并肺动脉狭窄的霍姆斯心脏与法洛四联症并无帮助。心电图往往是提示霍姆斯心脏存在的首要线索;电轴左偏伴或不伴左心室肥厚在法洛四联症中并不常见,但在霍姆斯心脏中较为常见。选择性心室造影具有诊断价值:在合并肺动脉狭窄的霍姆斯心脏正位片上,右心室流出腔室位于主动脉根部及主动脉瓣上方,而在法洛四联症中则位于主动脉瓣左侧;在霍姆斯心脏中无法识别室间隔。对于具有法洛四联症临床特征但心电图不典型的儿童,可怀疑该病,并通过血管造影确诊。