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心脏并存肿瘤与心脏畸形

Coexistent cardiac tumours and malformations of the heart.

作者信息

Russell G A, Dhasmana J P, Berry P J, Gilbert-Barness E F

机构信息

Department of Paediatric Pathology, Bristol Maternity Hospital, U.K.

出版信息

Int J Cardiol. 1989 Jan;22(1):89-98. doi: 10.1016/0167-5273(89)90140-x.

Abstract

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.

摘要

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。

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