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首页> 外文期刊>Pediatric and developmental pathology: the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society >Concurrent infantile hemangioendothelioma and mesenchymal hamartoma in a developmentally arrested liver of an infant requiring hepatic transplantation.
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Concurrent infantile hemangioendothelioma and mesenchymal hamartoma in a developmentally arrested liver of an infant requiring hepatic transplantation.

机译:在需要肝移植的婴儿的发育停滞的肝脏中同时发生婴儿性血管内皮内皮瘤和间充质错构瘤。

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摘要

A newborn female underwent a surgical resection for a hepatic mass discovered prenatally by ultrasonography, and diagnosed pathologically as a mesenchymal hamartoma. Within 4 months after surgery, multiple cutaneous hemangiomas developed and a multinodular mass was detected in the liver. A liver biopsy showed an infantile hemangioendothelioma with type I features. An orthotopic liver transplant was performed due to the extensive nature of the hepatic involvement and progressive respiratory compromise. Virtually the entire liver was involved by a large infantile hemangioendothelioma. A multicystic mesenchymal hamartoma was also found on the left side. In addition, the uninvolved hepatic parenchyma had features recapitulating the fetal liver. This simultaneous involvement of the liver by a mesenchymal hamartoma and infantile hemangioendothelioma is unique. A review of the literature revealed only one incompletely characterized case with similar findings.
机译:一名刚出生的女性接受了超声检查,在手术前切除了肝脏,该肝脏肿块是在产前通过超声检查发现的,在病理上被诊断为间质错构瘤。手术后4个月内,出现多发性皮肤血管瘤,并在肝脏中检测到多结节性肿块。肝活检显示婴儿肝血管内皮瘤具有I型特征。由于肝受累的广泛性质和进行性呼吸损害,进行了原位肝移植。实际上,整个肝脏都被一个大的婴儿血管内皮瘤所累及。左侧还发现了多囊性间质错构瘤。另外,未受累的肝实质具有重现胎儿肝脏的特征。间充质错构瘤和婴儿血管内皮内皮瘤同时参与肝脏是独特的。文献回顾显示,只有一个特征不完全的病例具有相似的发现。

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