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一名早产儿因心包内混合性生殖细胞肿瘤导致大量心包积液。

Massive pericardial effusion due to intrapericardial mixed germ cell tumor in a premature baby.

作者信息

Doksöz Önder, Terek Demet Tümay, Karaçelik Mustafa, Yıldırım Hülya Tosun, Demirağ Bengü, Meşe Timur, Sarıosmanoğlu Osman Nejat, Arslanoğlu Sertaç

机构信息

Departments of Pediatric Cardiology.

Neonatology.

出版信息

Pediatr Int. 2015 Oct;57(5):968-70. doi: 10.1111/ped.12655. Epub 2015 Jul 6.

Abstract

Primary cardiac tumor is uncommon in childhood, with an incidence of 0.06-0.32%, and intrapericardial teratoma represents an exceptional rarity among these entities. Germ cell tumors (GCT) are rare, representing only 1-3% of childhood tumors. Twenty per cent of GCT are malignant and are associated with age and location. Extragonadal involvement accounts for nearly half of the cases. Anterior mediastinum is a common location of malignant germ cell tumors, yet pericardial and aortic adventitia involvement have been rarely reported. Here we report the case of a preterm twin baby boy with intrapericardial mixed germ cell tumor who presented with hydrops fetalis and pericardial effusion.

摘要

原发性心脏肿瘤在儿童时期并不常见,发病率为0.06%-0.32%,而心包内畸胎瘤在这些肿瘤中极为罕见。生殖细胞肿瘤(GCT)很少见,仅占儿童肿瘤的1%-3%。20%的GCT是恶性的,且与年龄和部位有关。性腺外受累约占病例的一半。前纵隔是恶性生殖细胞肿瘤的常见部位,但心包和主动脉外膜受累的报道很少。在此,我们报告一例患有心包内混合性生殖细胞肿瘤的早产双胞胎男婴,其表现为胎儿水肿和心包积液。

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