Bessho T, Kubota K, Komori S, Ohtsuka Y, Uneo Y, Uematsu K, Koyama K
Department of Obstetrics and Gynecology, Hyogo College of Medicine, Nishinomiya, Japan.
Prenat Diagn. 1996 Apr;16(4):337-41. doi: 10.1002/(SICI)1097-0223(199604)16:4<337::AID-PD848>3.0.CO;2-U.
Although various conditions associated with non-immune hydrops have been reported, primary hepatic tumours are rare. As a mesenchymal hamartoma of the liver is a rare benign tumour, it has not been listed as a cause of hydrops. In this report we describe a case in which a large cystic mass in the fetal liver associated with non-immune hydrops was prenatally detected with sonography and magnetic resonance imaging, and histopathologically confirmed as a mesenchymal hamartoma of the liver.
尽管已有多种与非免疫性水肿相关的病症报道，但原发性肝肿瘤较为罕见。肝间叶性错构瘤作为一种罕见的良性肿瘤，尚未被列为水肿的病因。在本报告中，我们描述了一例产前通过超声和磁共振成像检测出胎儿肝脏内有一个与非免疫性水肿相关的巨大囊性肿块，并经组织病理学证实为肝间叶性错构瘤的病例。
