Russell G A, Dhasmana J P, Berry P J, Gilbert-Barness E F
Department of Paediatric Pathology, Bristol Maternity Hospital, U.K.
Int J Cardiol. 1989 Jan;22(1):89-98. doi: 10.1016/0167-5273(89)90140-x.
Cardiac tumours and anatomical malformations of the heart may produce similar clinical signs and symptoms. The coexistence of these two abnormalities complicates diagnosis and probably adversely affects prognosis. We present a review of four cases of this rare combination. In the first case, Ebstein's malformation was present in a child with tuberous sclerosis and cardiac rhabdomyomata. Right ventricular rhabdomyomata were associated with a hypoplastic tricuspid valve in the second case. In the third case, cardiac myxomas were detected in a child with a double-chambered right ventricle. The fourth case was a child with a fibroma of the right ventricle with pulmonary atresia. We propose that, in some circumstances, a space-occupying lesion may be associated with, or possibly induce, a malformation within the developing heart.
心脏肿瘤和心脏解剖畸形可能产生相似的临床体征和症状。这两种异常情况并存会使诊断复杂化,并且可能对预后产生不利影响。我们对这种罕见组合的四个病例进行了综述。第一个病例中,一名患有结节性硬化症和心脏横纹肌瘤的儿童存在埃布斯坦畸形。第二个病例中,右心室横纹肌瘤与发育不全的三尖瓣相关。第三个病例中,在一名患有双腔右心室的儿童中检测到心脏黏液瘤。第四个病例是一名患有右心室纤维瘤并伴有肺动脉闭锁的儿童。我们提出,在某些情况下,占位性病变可能与发育中的心脏内的畸形相关,或者可能诱发这种畸形。